CN114984196B - Natural plant composition for preventing and treating arteriosclerosis, preparation method and application - Google Patents
Natural plant composition for preventing and treating arteriosclerosis, preparation method and application Download PDFInfo
- Publication number
- CN114984196B CN114984196B CN202210757395.4A CN202210757395A CN114984196B CN 114984196 B CN114984196 B CN 114984196B CN 202210757395 A CN202210757395 A CN 202210757395A CN 114984196 B CN114984196 B CN 114984196B
- Authority
- CN
- China
- Prior art keywords
- parts
- extract
- arteriosclerosis
- mangosteen
- natural plant
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 206010003210 Arteriosclerosis Diseases 0.000 title claims abstract description 54
- 208000011775 arteriosclerosis disease Diseases 0.000 title claims abstract description 54
- 239000000203 mixture Substances 0.000 title claims abstract description 29
- 230000003405 preventing effect Effects 0.000 title claims abstract description 18
- 238000002360 preparation method Methods 0.000 title claims abstract description 13
- 239000000284 extract Substances 0.000 claims abstract description 70
- 235000011299 Brassica oleracea var botrytis Nutrition 0.000 claims abstract description 33
- 235000017647 Brassica oleracea var italica Nutrition 0.000 claims abstract description 33
- 240000003259 Brassica oleracea var. botrytis Species 0.000 claims abstract description 32
- 240000006053 Garcinia mangostana Species 0.000 claims abstract description 31
- 235000017048 Garcinia mangostana Nutrition 0.000 claims abstract description 31
- 229940072113 onion extract Drugs 0.000 claims abstract description 29
- 239000000843 powder Substances 0.000 claims abstract description 27
- 235000021323 fish oil Nutrition 0.000 claims abstract description 24
- 239000003094 microcapsule Substances 0.000 claims abstract description 24
- 229940109529 pomegranate extract Drugs 0.000 claims abstract description 24
- 241000196324 Embryophyta Species 0.000 claims abstract description 22
- 229940086319 nattokinase Drugs 0.000 claims abstract description 22
- 108010073682 nattokinase Proteins 0.000 claims abstract description 22
- 229920001184 polypeptide Polymers 0.000 claims abstract description 21
- 102000004196 processed proteins & peptides Human genes 0.000 claims abstract description 21
- 108090000765 processed proteins & peptides Proteins 0.000 claims abstract description 21
- 229940026314 red yeast rice Drugs 0.000 claims abstract description 20
- 238000000034 method Methods 0.000 claims description 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 16
- 235000013336 milk Nutrition 0.000 claims description 16
- 239000008267 milk Substances 0.000 claims description 16
- 210000004080 milk Anatomy 0.000 claims description 16
- 238000002156 mixing Methods 0.000 claims description 16
- 230000002829 reductive effect Effects 0.000 claims description 16
- 238000010298 pulverizing process Methods 0.000 claims description 15
- 235000013305 food Nutrition 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 10
- 235000002378 plant sterols Nutrition 0.000 claims description 7
- 238000001035 drying Methods 0.000 claims description 5
- 238000001914 filtration Methods 0.000 claims description 5
- 230000002265 prevention Effects 0.000 claims description 5
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 claims description 4
- 239000002775 capsule Substances 0.000 claims description 3
- 235000013399 edible fruits Nutrition 0.000 claims description 3
- 239000006228 supernatant Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 239000006057 Non-nutritive feed additive Substances 0.000 claims description 2
- 239000008187 granular material Substances 0.000 claims description 2
- 239000002994 raw material Substances 0.000 claims description 2
- 238000001694 spray drying Methods 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims description 2
- 244000062241 Kaempferia galanga Species 0.000 claims 1
- 235000013421 Kaempferia galanga Nutrition 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 abstract description 5
- 230000007246 mechanism Effects 0.000 abstract description 4
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 66
- 235000012000 cholesterol Nutrition 0.000 description 35
- 230000000694 effects Effects 0.000 description 26
- 230000003110 anti-inflammatory effect Effects 0.000 description 20
- 230000000052 comparative effect Effects 0.000 description 19
- 108010028554 LDL Cholesterol Proteins 0.000 description 18
- 210000004204 blood vessel Anatomy 0.000 description 16
- 101000588302 Homo sapiens Nuclear factor erythroid 2-related factor 2 Proteins 0.000 description 10
- 102100031701 Nuclear factor erythroid 2-related factor 2 Human genes 0.000 description 10
- 206010061218 Inflammation Diseases 0.000 description 9
- 210000004369 blood Anatomy 0.000 description 9
- 239000008280 blood Substances 0.000 description 9
- 239000003814 drug Substances 0.000 description 9
- 230000004054 inflammatory process Effects 0.000 description 9
- 210000004185 liver Anatomy 0.000 description 9
- 210000004027 cell Anatomy 0.000 description 8
- 108010022197 lipoprotein cholesterol Proteins 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- SUVMJBTUFCVSAD-UHFFFAOYSA-N sulforaphane Chemical compound CS(=O)CCCCN=C=S SUVMJBTUFCVSAD-UHFFFAOYSA-N 0.000 description 8
- 241000700159 Rattus Species 0.000 description 7
- 201000010099 disease Diseases 0.000 description 7
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 7
- 229940079593 drug Drugs 0.000 description 7
- 230000036541 health Effects 0.000 description 7
- 208000010110 spontaneous platelet aggregation Diseases 0.000 description 7
- 230000002195 synergetic effect Effects 0.000 description 7
- 230000002194 synthesizing effect Effects 0.000 description 7
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 6
- 230000003078 antioxidant effect Effects 0.000 description 6
- 210000001367 artery Anatomy 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 108090000623 proteins and genes Proteins 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- SUVMJBTUFCVSAD-JTQLQIEISA-N 4-Methylsulfinylbutyl isothiocyanate Natural products C[S@](=O)CCCCN=C=S SUVMJBTUFCVSAD-JTQLQIEISA-N 0.000 description 5
- 102000004889 Interleukin-6 Human genes 0.000 description 5
- 108090001005 Interleukin-6 Proteins 0.000 description 5
- 102000003945 NF-kappa B Human genes 0.000 description 5
- 108010057466 NF-kappa B Proteins 0.000 description 5
- 108090000854 Oxidoreductases Proteins 0.000 description 5
- 102000004316 Oxidoreductases Human genes 0.000 description 5
- 108060008682 Tumor Necrosis Factor Proteins 0.000 description 5
- 102000000852 Tumor Necrosis Factor-alpha Human genes 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 5
- 210000000170 cell membrane Anatomy 0.000 description 5
- 235000019197 fats Nutrition 0.000 description 5
- 235000020660 omega-3 fatty acid Nutrition 0.000 description 5
- 230000028327 secretion Effects 0.000 description 5
- 238000007873 sieving Methods 0.000 description 5
- 229960005559 sulforaphane Drugs 0.000 description 5
- 235000015487 sulforaphane Nutrition 0.000 description 5
- 210000004026 tunica intima Anatomy 0.000 description 5
- CABVTRNMFUVUDM-VRHQGPGLSA-N (3S)-3-hydroxy-3-methylglutaryl-CoA Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)C[C@@](O)(CC(O)=O)C)O[C@H]1N1C2=NC=NC(N)=C2N=C1 CABVTRNMFUVUDM-VRHQGPGLSA-N 0.000 description 4
- 241000234282 Allium Species 0.000 description 4
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 4
- REFJWTPEDVJJIY-UHFFFAOYSA-N Quercetin Chemical compound C=1C(O)=CC(O)=C(C(C=2O)=O)C=1OC=2C1=CC=C(O)C(O)=C1 REFJWTPEDVJJIY-UHFFFAOYSA-N 0.000 description 4
- 230000009471 action Effects 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 4
- 235000006708 antioxidants Nutrition 0.000 description 4
- 210000001168 carotid artery common Anatomy 0.000 description 4
- 229940088598 enzyme Drugs 0.000 description 4
- 210000001105 femoral artery Anatomy 0.000 description 4
- 230000006870 function Effects 0.000 description 4
- 230000002401 inhibitory effect Effects 0.000 description 4
- 150000002632 lipids Chemical class 0.000 description 4
- 239000012528 membrane Substances 0.000 description 4
- 210000005087 mononuclear cell Anatomy 0.000 description 4
- 230000037361 pathway Effects 0.000 description 4
- 235000013824 polyphenols Nutrition 0.000 description 4
- 210000000329 smooth muscle myocyte Anatomy 0.000 description 4
- 230000002792 vascular Effects 0.000 description 4
- 201000001320 Atherosclerosis Diseases 0.000 description 3
- 241000721047 Danaus plexippus Species 0.000 description 3
- 206010012735 Diarrhoea Diseases 0.000 description 3
- 241000219991 Lythraceae Species 0.000 description 3
- 102100029438 Nitric oxide synthase, inducible Human genes 0.000 description 3
- 101710089543 Nitric oxide synthase, inducible Proteins 0.000 description 3
- 235000014360 Punica granatum Nutrition 0.000 description 3
- 102000040945 Transcription factor Human genes 0.000 description 3
- 108091023040 Transcription factor Proteins 0.000 description 3
- 230000003064 anti-oxidating effect Effects 0.000 description 3
- 230000002146 bilateral effect Effects 0.000 description 3
- 230000036772 blood pressure Effects 0.000 description 3
- 206010008118 cerebral infarction Diseases 0.000 description 3
- 210000001035 gastrointestinal tract Anatomy 0.000 description 3
- 229940100601 interleukin-6 Drugs 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- -1 polyphenol compounds Chemical class 0.000 description 3
- 150000008442 polyphenolic compounds Chemical class 0.000 description 3
- 230000000770 proinflammatory effect Effects 0.000 description 3
- HSINOMROUCMIEA-FGVHQWLLSA-N (2s,4r)-4-[(3r,5s,6r,7r,8s,9s,10s,13r,14s,17r)-6-ethyl-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]-2-methylpentanoic acid Chemical compound C([C@@]12C)C[C@@H](O)C[C@H]1[C@@H](CC)[C@@H](O)[C@@H]1[C@@H]2CC[C@]2(C)[C@@H]([C@H](C)C[C@H](C)C(O)=O)CC[C@H]21 HSINOMROUCMIEA-FGVHQWLLSA-N 0.000 description 2
- MZOFCQQQCNRIBI-VMXHOPILSA-N (3s)-4-[[(2s)-1-[[(2s)-1-[[(1s)-1-carboxy-2-hydroxyethyl]amino]-4-methyl-1-oxopentan-2-yl]amino]-5-(diaminomethylideneamino)-1-oxopentan-2-yl]amino]-3-[[2-[[(2s)-2,6-diaminohexanoyl]amino]acetyl]amino]-4-oxobutanoic acid Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@@H](N)CCCCN MZOFCQQQCNRIBI-VMXHOPILSA-N 0.000 description 2
- 206010067484 Adverse reaction Diseases 0.000 description 2
- 101710095342 Apolipoprotein B Proteins 0.000 description 2
- 102100040202 Apolipoprotein B-100 Human genes 0.000 description 2
- 235000011331 Brassica Nutrition 0.000 description 2
- 241000219198 Brassica Species 0.000 description 2
- 108010074051 C-Reactive Protein Proteins 0.000 description 2
- 102100032752 C-reactive protein Human genes 0.000 description 2
- 102000004127 Cytokines Human genes 0.000 description 2
- 108090000695 Cytokines Proteins 0.000 description 2
- AFSDNFLWKVMVRB-UHFFFAOYSA-N Ellagic acid Chemical compound OC1=C(O)C(OC2=O)=C3C4=C2C=C(O)C(O)=C4OC(=O)C3=C1 AFSDNFLWKVMVRB-UHFFFAOYSA-N 0.000 description 2
- ATJXMQHAMYVHRX-CPCISQLKSA-N Ellagic acid Natural products OC1=C(O)[C@H]2OC(=O)c3cc(O)c(O)c4OC(=O)C(=C1)[C@H]2c34 ATJXMQHAMYVHRX-CPCISQLKSA-N 0.000 description 2
- 229920002079 Ellagic acid Polymers 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 108010023302 HDL Cholesterol Proteins 0.000 description 2
- 208000031226 Hyperlipidaemia Diseases 0.000 description 2
- 102100030412 Matrix metalloproteinase-9 Human genes 0.000 description 2
- 108010015302 Matrix metalloproteinase-9 Proteins 0.000 description 2
- PCZOHLXUXFIOCF-UHFFFAOYSA-N Monacolin X Natural products C12C(OC(=O)C(C)CC)CC(C)C=C2C=CC(C)C1CCC1CC(O)CC(=O)O1 PCZOHLXUXFIOCF-UHFFFAOYSA-N 0.000 description 2
- 241000228347 Monascus <ascomycete fungus> Species 0.000 description 2
- 206010028813 Nausea Diseases 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 229920000241 Punicalagin Polymers 0.000 description 2
- ZVOLCUVKHLEPEV-UHFFFAOYSA-N Quercetagetin Natural products C1=C(O)C(O)=CC=C1C1=C(O)C(=O)C2=C(O)C(O)=C(O)C=C2O1 ZVOLCUVKHLEPEV-UHFFFAOYSA-N 0.000 description 2
- QNVSXXGDAPORNA-UHFFFAOYSA-N Resveratrol Natural products OC1=CC=CC(C=CC=2C=C(O)C(O)=CC=2)=C1 QNVSXXGDAPORNA-UHFFFAOYSA-N 0.000 description 2
- HWTZYBCRDDUBJY-UHFFFAOYSA-N Rhynchosin Natural products C1=C(O)C(O)=CC=C1C1=C(O)C(=O)C2=CC(O)=C(O)C=C2O1 HWTZYBCRDDUBJY-UHFFFAOYSA-N 0.000 description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
- LUKBXSAWLPMMSZ-OWOJBTEDSA-N Trans-resveratrol Chemical compound C1=CC(O)=CC=C1\C=C\C1=CC(O)=CC(O)=C1 LUKBXSAWLPMMSZ-OWOJBTEDSA-N 0.000 description 2
- 206010047700 Vomiting Diseases 0.000 description 2
- 230000006838 adverse reaction Effects 0.000 description 2
- 235000010208 anthocyanin Nutrition 0.000 description 2
- 229930002877 anthocyanin Natural products 0.000 description 2
- 239000004410 anthocyanin Substances 0.000 description 2
- 150000004636 anthocyanins Chemical class 0.000 description 2
- 210000000702 aorta abdominal Anatomy 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 210000000941 bile Anatomy 0.000 description 2
- 239000003613 bile acid Substances 0.000 description 2
- 210000003855 cell nucleus Anatomy 0.000 description 2
- 208000026106 cerebrovascular disease Diseases 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 238000005345 coagulation Methods 0.000 description 2
- 230000001120 cytoprotective effect Effects 0.000 description 2
- 238000001784 detoxification Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 208000002173 dizziness Diseases 0.000 description 2
- 235000004132 ellagic acid Nutrition 0.000 description 2
- 229960002852 ellagic acid Drugs 0.000 description 2
- 239000002158 endotoxin Substances 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 230000001815 facial effect Effects 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 210000000497 foam cell Anatomy 0.000 description 2
- 229930182470 glycoside Natural products 0.000 description 2
- 210000002216 heart Anatomy 0.000 description 2
- 229910001385 heavy metal Inorganic materials 0.000 description 2
- 210000002865 immune cell Anatomy 0.000 description 2
- 230000002757 inflammatory effect Effects 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- MWDZOUNAPSSOEL-UHFFFAOYSA-N kaempferol Natural products OC1=C(C(=O)c2cc(O)cc(O)c2O1)c3ccc(O)cc3 MWDZOUNAPSSOEL-UHFFFAOYSA-N 0.000 description 2
- 150000002617 leukotrienes Chemical class 0.000 description 2
- 230000003859 lipid peroxidation Effects 0.000 description 2
- 210000005229 liver cell Anatomy 0.000 description 2
- PCZOHLXUXFIOCF-BXMDZJJMSA-N lovastatin Chemical compound C([C@H]1[C@@H](C)C=CC2=C[C@H](C)C[C@@H]([C@H]12)OC(=O)[C@@H](C)CC)C[C@@H]1C[C@@H](O)CC(=O)O1 PCZOHLXUXFIOCF-BXMDZJJMSA-N 0.000 description 2
- FAARLWTXUUQFSN-UHFFFAOYSA-N methylellagic acid Natural products O1C(=O)C2=CC(O)=C(O)C3=C2C2=C1C(OC)=C(O)C=C2C(=O)O3 FAARLWTXUUQFSN-UHFFFAOYSA-N 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000002107 myocardial effect Effects 0.000 description 2
- 229930014626 natural product Natural products 0.000 description 2
- 230000008693 nausea Effects 0.000 description 2
- 210000004940 nucleus Anatomy 0.000 description 2
- 229940094443 oxytocics prostaglandins Drugs 0.000 description 2
- 231100000915 pathological change Toxicity 0.000 description 2
- 230000036285 pathological change Effects 0.000 description 2
- 150000003180 prostaglandins Chemical class 0.000 description 2
- ZJVUMAFASBFUBG-OGJBWQGYSA-N punicalagin Chemical compound C([C@H]1O[C@@H]([C@@H]2OC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)O[C@H]2[C@@H]1OC(=O)C1=CC(O)=C(O)C(O)=C11)O)OC(=O)C2=CC(O)=C(O)C(O)=C2C2=C(O)C(O)=C(OC3=O)C4=C2C(=O)OC2=C4C3=C1C(O)=C2O ZJVUMAFASBFUBG-OGJBWQGYSA-N 0.000 description 2
- LMIBIMUSUFYFJN-RSVYENFWSA-N punicalagin Natural products O[C@@H]1O[C@@H]2COC(=O)c3cc(O)c(O)c(O)c3c4c(O)cc5OC(=O)c6c(c(O)c(O)c7OC(=O)c4c5c67)c8c(O)c(O)c(O)cc8C(=O)O[C@H]2[C@@H]9OC(=O)c%10cc(O)c(O)c(O)c%10c%11c(O)c(O)c(O)cc%11C(=O)O[C@@H]19 LMIBIMUSUFYFJN-RSVYENFWSA-N 0.000 description 2
- ZRKSVMFLACVUIU-UHFFFAOYSA-N punicalagin isomer Natural products OC1=C(O)C(=C2C3=4)OC(=O)C=4C4=C(O)C(O)=C3OC(=O)C2=C1C1=C(O)C(O)=C(O)C=C1C(=O)OC1C2OC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(O)OC1COC(=O)C1=CC4=C(O)C(O)=C1O ZRKSVMFLACVUIU-UHFFFAOYSA-N 0.000 description 2
- 235000005875 quercetin Nutrition 0.000 description 2
- 229960001285 quercetin Drugs 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 235000021283 resveratrol Nutrition 0.000 description 2
- 229940016667 resveratrol Drugs 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 210000001519 tissue Anatomy 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 239000003053 toxin Substances 0.000 description 2
- 231100000765 toxin Toxicity 0.000 description 2
- 238000013518 transcription Methods 0.000 description 2
- 230000035897 transcription Effects 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 230000032258 transport Effects 0.000 description 2
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 2
- 210000004231 tunica media Anatomy 0.000 description 2
- 238000001291 vacuum drying Methods 0.000 description 2
- 210000002385 vertebral artery Anatomy 0.000 description 2
- 230000008673 vomiting Effects 0.000 description 2
- 240000002234 Allium sativum Species 0.000 description 1
- 102000015427 Angiotensins Human genes 0.000 description 1
- 108010064733 Angiotensins Proteins 0.000 description 1
- 208000037260 Atherosclerotic Plaque Diseases 0.000 description 1
- 244000308180 Brassica oleracea var. italica Species 0.000 description 1
- 208000024172 Cardiovascular disease Diseases 0.000 description 1
- 108010012236 Chemokines Proteins 0.000 description 1
- 102000019034 Chemokines Human genes 0.000 description 1
- 208000016192 Demyelinating disease Diseases 0.000 description 1
- 206010012305 Demyelination Diseases 0.000 description 1
- 208000032928 Dyslipidaemia Diseases 0.000 description 1
- 102000016942 Elastin Human genes 0.000 description 1
- 108010014258 Elastin Proteins 0.000 description 1
- 206010048554 Endothelial dysfunction Diseases 0.000 description 1
- 208000007530 Essential hypertension Diseases 0.000 description 1
- 208000004930 Fatty Liver Diseases 0.000 description 1
- 206010019468 Hemiplegia Diseases 0.000 description 1
- 206010019708 Hepatic steatosis Diseases 0.000 description 1
- 206010020772 Hypertension Diseases 0.000 description 1
- 208000017170 Lipid metabolism disease Diseases 0.000 description 1
- 108010075520 Nitric Oxide Synthase Type III Proteins 0.000 description 1
- 102100028452 Nitric oxide synthase, endothelial Human genes 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- 206010030113 Oedema Diseases 0.000 description 1
- 206010030124 Oedema peripheral Diseases 0.000 description 1
- NPGIHFRTRXVWOY-UHFFFAOYSA-N Oil red O Chemical compound Cc1ccc(C)c(c1)N=Nc1cc(C)c(cc1C)N=Nc1c(O)ccc2ccccc12 NPGIHFRTRXVWOY-UHFFFAOYSA-N 0.000 description 1
- 235000007189 Oryza longistaminata Nutrition 0.000 description 1
- 206010057249 Phagocytosis Diseases 0.000 description 1
- CWEZAWNPTYBADX-UHFFFAOYSA-N Procyanidin Natural products OC1C(OC2C(O)C(Oc3c2c(O)cc(O)c3C4C(O)C(Oc5cc(O)cc(O)c45)c6ccc(O)c(O)c6)c7ccc(O)c(O)c7)c8c(O)cc(O)cc8OC1c9ccc(O)c(O)c9 CWEZAWNPTYBADX-UHFFFAOYSA-N 0.000 description 1
- KNAHARQHSZJURB-UHFFFAOYSA-N Propylthiouracile Chemical compound CCCC1=CC(=O)NC(=S)N1 KNAHARQHSZJURB-UHFFFAOYSA-N 0.000 description 1
- OKYHUOHBRKWCQJ-FTJYXMLISA-N S-1-propenyl-L-cysteine sulfoxide zwitterion Chemical compound C\C=C\S(=O)C[C@H](N)C(O)=O OKYHUOHBRKWCQJ-FTJYXMLISA-N 0.000 description 1
- ZZLHPCSGGOGHFW-UHFFFAOYSA-N S-methyl-L-cysteine sulphoxide Natural products CS(=O)CC(N)C(O)=O ZZLHPCSGGOGHFW-UHFFFAOYSA-N 0.000 description 1
- 208000007536 Thrombosis Diseases 0.000 description 1
- 102100040247 Tumor necrosis factor Human genes 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 210000002551 anterior cerebral artery Anatomy 0.000 description 1
- 229940121363 anti-inflammatory agent Drugs 0.000 description 1
- 239000002260 anti-inflammatory agent Substances 0.000 description 1
- 210000000709 aorta Anatomy 0.000 description 1
- 230000004900 autophagic degradation Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- 230000002308 calcification Effects 0.000 description 1
- 150000001765 catechin Chemical class 0.000 description 1
- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 description 1
- 235000005487 catechin Nutrition 0.000 description 1
- 230000002490 cerebral effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000005482 chemotactic factor Substances 0.000 description 1
- 230000001684 chronic effect Effects 0.000 description 1
- OKYHUOHBRKWCQJ-UHFFFAOYSA-N cis S-1-Propenyl-L-cystein Natural products CC=CS(=O)CC(N)C(O)=O OKYHUOHBRKWCQJ-UHFFFAOYSA-N 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 210000002808 connective tissue Anatomy 0.000 description 1
- 230000002079 cooperative effect Effects 0.000 description 1
- 210000000805 cytoplasm Anatomy 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000034994 death Effects 0.000 description 1
- 230000003412 degenerative effect Effects 0.000 description 1
- CYQFCXCEBYINGO-IAGOWNOFSA-N delta1-THC Chemical compound C1=C(C)CC[C@H]2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3[C@@H]21 CYQFCXCEBYINGO-IAGOWNOFSA-N 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 206010012601 diabetes mellitus Diseases 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 201000006549 dyspepsia Diseases 0.000 description 1
- 230000000001 effect on platelet aggregation Effects 0.000 description 1
- 229920002549 elastin Polymers 0.000 description 1
- 230000008694 endothelial dysfunction Effects 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 208000010706 fatty liver disease Diseases 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 230000020764 fibrinolysis Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000004611 garlic Nutrition 0.000 description 1
- 238000007490 hematoxylin and eosin (H&E) staining Methods 0.000 description 1
- 206010020718 hyperplasia Diseases 0.000 description 1
- 238000002991 immunohistochemical analysis Methods 0.000 description 1
- 208000027866 inflammatory disease Diseases 0.000 description 1
- 230000028709 inflammatory response Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 239000007928 intraperitoneal injection Substances 0.000 description 1
- 208000002551 irritable bowel syndrome Diseases 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 235000020667 long-chain omega-3 fatty acid Nutrition 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229940057059 monascus purpureus Drugs 0.000 description 1
- 210000001616 monocyte Anatomy 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 239000002773 nucleotide Substances 0.000 description 1
- 125000003729 nucleotide group Chemical group 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 229940012843 omega-3 fatty acid Drugs 0.000 description 1
- 235000020665 omega-6 fatty acid Nutrition 0.000 description 1
- 210000003463 organelle Anatomy 0.000 description 1
- 108010071584 oxidized low density lipoprotein Proteins 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000008506 pathogenesis Effects 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 230000008782 phagocytosis Effects 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 230000007505 plaque formation Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 229920002414 procyanidin Polymers 0.000 description 1
- 230000002062 proliferating effect Effects 0.000 description 1
- 229960002662 propylthiouracil Drugs 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 210000002460 smooth muscle Anatomy 0.000 description 1
- NRHMKIHPTBHXPF-TUJRSCDTSA-M sodium cholate Chemical compound [Na+].C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 NRHMKIHPTBHXPF-TUJRSCDTSA-M 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 231100000240 steatosis hepatitis Toxicity 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 230000009747 swallowing Effects 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 230000002537 thrombolytic effect Effects 0.000 description 1
- RZWIIPASKMUIAC-VQTJNVASSA-N thromboxane Chemical compound CCCCCCCC[C@H]1OCCC[C@@H]1CCCCCCC RZWIIPASKMUIAC-VQTJNVASSA-N 0.000 description 1
- 150000003595 thromboxanes Chemical class 0.000 description 1
- 238000002137 ultrasound extraction Methods 0.000 description 1
- 238000010200 validation analysis Methods 0.000 description 1
- 208000019553 vascular disease Diseases 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 210000004885 white matter Anatomy 0.000 description 1
- 150000007964 xanthones Chemical class 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/575—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of three or more carbon atoms, e.g. cholane, cholestane, ergosterol, sitosterol
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
- A23L33/11—Plant sterols or derivatives thereof, e.g. phytosterols
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/17—Amino acids, peptides or proteins
- A23L33/18—Peptides; Protein hydrolysates
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/17—Amino acids, peptides or proteins
- A23L33/19—Dairy proteins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/56—Materials from animals other than mammals
- A61K35/60—Fish, e.g. seahorses; Fish eggs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/06—Fungi, e.g. yeasts
- A61K36/062—Ascomycota
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/31—Brassicaceae or Cruciferae (Mustard family), e.g. broccoli, cabbage or kohlrabi
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/38—Clusiaceae, Hypericaceae or Guttiferae (Hypericum or Mangosteen family), e.g. common St. Johnswort
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/88—Liliopsida (monocotyledons)
- A61K36/896—Liliaceae (Lily family), e.g. daylily, plantain lily, Hyacinth or narcissus
- A61K36/8962—Allium, e.g. garden onion, leek, garlic or chives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/88—Liliopsida (monocotyledons)
- A61K36/899—Poaceae or Gramineae (Grass family), e.g. bamboo, corn or sugar cane
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/01—Hydrolysed proteins; Derivatives thereof
- A61K38/012—Hydrolysed proteins; Derivatives thereof from animals
- A61K38/018—Hydrolysed proteins; Derivatives thereof from animals from milk
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/43—Enzymes; Proenzymes; Derivatives thereof
- A61K38/46—Hydrolases (3)
- A61K38/48—Hydrolases (3) acting on peptide bonds (3.4)
- A61K38/482—Serine endopeptidases (3.4.21)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/30—Extraction of the material
- A61K2236/33—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones
- A61K2236/331—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones using water, e.g. cold water, infusion, tea, steam distillation, decoction
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/30—Extraction of the material
- A61K2236/33—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones
- A61K2236/333—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones using mixed solvents, e.g. 70% EtOH
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Mycology (AREA)
- Epidemiology (AREA)
- Botany (AREA)
- Alternative & Traditional Medicine (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Medical Informatics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Polymers & Plastics (AREA)
- Nutrition Science (AREA)
- Food Science & Technology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Gastroenterology & Hepatology (AREA)
- Cardiology (AREA)
- Zoology (AREA)
- Marine Sciences & Fisheries (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Obesity (AREA)
- Molecular Biology (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
The invention provides a natural plant composition for preventing and treating arteriosclerosis, a preparation method and application thereof, wherein the natural plant composition comprises the following components in parts by mass: 100-200 parts of phytosterol, 100-200 parts of fish oil microcapsule powder, 10-40 parts of milk-benefiting polypeptide, 10-30 parts of red yeast rice, 30-70 parts of nattokinase, 1-5 parts of onion extract, 5-15 parts of mangosteen extract, 2-8 parts of broccoli seed extract and 5-25 parts of pomegranate extract. The natural plant composition can treat arteriosclerosis from the aspect of the formation mechanism of arteriosclerosis, thereby achieving the purpose of radical treatment.
Description
Technical Field
The invention relates to the technical field of treatment of arteriosclerosis, and particularly relates to a natural plant composition for preventing and treating arteriosclerosis, a preparation method and application thereof.
Background
Arteriosclerosis is a non-inflammatory disease of an artery, is a general name of degenerative and proliferative diseases of thickening, hardening and losing elasticity of an artery wall and narrowing a lumen, and is commonly known as atherosclerosis, medial calcification of an artery and arteriosclerotic 3. Arteriosclerosis is a vascular disease which appears with age, and the rule of the arteriosclerosis is usually that the arteriosclerosis occurs in adolescents, wherein the arteriosclerosis aggravates and develops in the elderly. The most important causes of arteriosclerosis are hypertension, hyperlipidemia and smoking. Other conditions such as obesity, diabetes, lack of exercise, stress, advanced age, family history, and irritable bowel syndrome can cause arteriosclerosis. In recent years, the disease is gradually increased in China and becomes one of the main causes of death of the old.
The mechanism of arteriosclerosis formation is that various pathogenic factors cause intimal damage to generate inflammation, mononuclear cells enter the intimal membrane, low-density lipoprotein cholesterol is oxidized, platelets are adhered and aggregated, smooth muscle cells proliferate and migrate to form a fibrous cap, vascular connective tissues are damaged, elastin cannot be well used, and then arteriosclerosis formation is caused.
The existing method for treating arteriosclerosis mainly treats arteriosclerosis symptomatically by using medicines, but the existing medicine treatment mode only prevents and treats arteriosclerosis by reducing indexes such as blood pressure, blood fat, blood sugar and the like, can relieve the disease condition, but often causes adverse reactions such as diarrhea, nausea, dizziness and the like, and cannot prevent and treat the arteriosclerosis fundamentally and needs to be taken for a lifetime.
In view of the above, the present invention is particularly proposed.
Disclosure of Invention
The invention aims to provide a natural plant composition for preventing and treating arteriosclerosis, which can effectively reduce the content of total cholesterol and low-density lipoprotein cholesterol and prevent platelet aggregation through mutual compatibility of a plurality of components, and can play roles in resisting inflammation and oxidation, repairing vascular intima and increasing vascular elasticity, thereby effectively preventing and treating arteriosclerosis.
The second purpose of the invention is to provide a preparation method of the natural plant composition, the preparation method is simple and convenient to operate, and the prepared composition has good prevention and treatment effects on arteriosclerosis.
The third purpose of the invention is to provide the application of the natural plant composition in medicines or health-care foods for treating diseases related to arteriosclerosis.
In order to achieve the above purpose of the present invention, the following technical solutions are adopted:
the invention provides a natural plant composition for preventing and treating arteriosclerosis, which comprises the following components in parts by mass: 100-200 parts of phytosterol, 100-200 parts of fish oil microcapsule powder, 10-40 parts of milk-benefiting polypeptide, 10-30 parts of red yeast rice, 30-70 parts of nattokinase, 1-5 parts of onion extract, 5-15 parts of mangosteen extract, 2-8 parts of broccoli seed extract and 5-25 parts of pomegranate extract.
Preferably, the food comprises 120-170 parts of phytosterol, 120-170 parts of fish oil microcapsule powder, 20-30 parts of milk polypeptide, 15-25 parts of red yeast rice, 40-60 parts of nattokinase, 1.5-4 parts of onion extract, 7-12 parts of mangosteen extract, 3-7 parts of broccoli seed extract and 10-20 parts of pomegranate extract.
Preferably 150 parts of phytosterol, 150 parts of fish oil microcapsule powder, 25 parts of milk benefiting polypeptide, 20 parts of red yeast rice, 50 parts of nattokinase, 2 parts of onion extract, 10 parts of mangosteen extract, 5 parts of broccoli seed extract and 15 parts of pomegranate extract.
In the prior art, arteriosclerosis is treated symptomatically mainly by using medicines, particularly, the arteriosclerosis is prevented and treated by reducing indexes such as blood pressure, blood fat, blood sugar and the like, although the mode can relieve the disease condition, adverse reactions such as diarrhea, nausea, dizziness and the like are often caused, the mode cannot be fundamentally prevented and treated, the treatment is not thorough, and the medicines are required to be taken for the whole life to control the disease condition.
In order to solve the above technical problems, the present invention provides a natural plant composition for preventing and treating arteriosclerosis, which prevents and treats arteriosclerosis from the viewpoint of arteriosclerosis formation mechanism, and achieves radical treatment of arteriosclerosis by:
1. reducing total cholesterol and low density lipoprotein cholesterol levels;
2. removing heavy metal toxin and endotoxin;
3. preventing platelet aggregation;
4. anti-inflammatory;
5. oxidation resistance;
6. repair the blood vessel intima and increase the blood vessel elasticity.
Specifically, when the components are compatible, the plant sterol and the red yeast rice are mutually cooperated as main materials, wherein the plant sterol mainly aims at exogenous cholesterol, can reduce the secretion of apolipoprotein B of intestinal tracts and liver cells, reduce the absorption of dietary cholesterol and the entrance of bile cholesterol into microbubbles, further reduce the absorption of the cholesterol, increase the secretion of bile acid, further improve the reverse transport of the cholesterol, and also can inhibit key enzyme (hydroxymethyl glutaryl coenzyme A reductase HMG-COA-R) for synthesizing the cholesterol to block the pathway for synthesizing the cholesterol. Monascus fungi in red yeast are inoculated to rice and prepared by fermentation, and contain a key enzyme (hydroxymethyl glutaryl coenzyme A reductase HMG-COA-R) specific inhibitor for human body to synthesize cholesterol, so that the endogenous pathway for synthesizing cholesterol can be blocked, and the monascus fungi not only can reduce total cholesterol, low density lipoprotein cholesterol and arteriosclerosis index, but also can reduce triglyceride and improve the remarkable comprehensive effect of high density lipoprotein cholesterol. The plant sterol and red rice can cooperate to play a synergistic role and inhibit endogenous cholesterol and exogenous cholesterol at the same time.
In the components of the invention, the broccoli seed extract is adopted to remove heavy metal toxin and endotoxin. Specifically, sulforaphane in broccoli seed extract can up-regulate transcription factor Nrf2, and can activate transcription of more than 500 genes in human genome, and most of the genes have cytoprotective function. Nrf2 produces cytoprotective effects through detoxification mechanisms that enhance detoxification and excretion of harmful foreign materials and toxic metals; nrf2 increases highly coordinated antioxidant activity through the action of more than 20 genes, which also has anti-inflammatory effects; in addition, nrf2 also enhances autophagy of cells to clear toxic protein aggregates and dysfunctional organelles, and the healthy nutrients (phenolic antioxidants, long-chain omega 3 fatty acids DHA and EPA, sulfides and terpenoids in allium sativum vegetables) are all acted upon by Nrf2 activity.
In the components of the invention, the nattokinase and the onion extract have the synergistic and cooperative effect. Specifically, nattokinase not only dissolves thrombus, but also inhibits platelet coagulation. The onion extract contains multiple active ingredients, wherein the polyphenol quercetin and sulfide isoalliin can inhibit platelet coagulation, and also has effects of inhibiting cholesterol oxidation, softening blood vessel, and inhibiting blood pressure increase. The two are matched with each other, so that good thrombolysis and platelet aggregation prevention effects can be achieved.
In the components of the invention, the fish oil microcapsule powder and the broccoli seed extract are compatible to play an anti-inflammatory role. In particular, the fish oil microcapsule powder contains omega 3 (EPA and DHA) fatty acids, which are capable of alleviating chronic inflammatory reactions. In fact, during the development of arteriosclerosis, the cell membrane and nucleus of immune cells are involved in inflammatory reactions, and when the vascular intima is damaged, monocytes in immune cells are activated. There are two molecules of inflammation, one is that inflammatory mediators acting on the cell membrane directly produce an inflammatory response including Prostaglandins (PG), leukotrienes (LT), and Thromboxanes (TX); the other is cell factor acting on cell nucleus, including tumor necrosis factor (TNF-alpha), interleukin IL-6, etc. Omega 3 polyunsaturated fatty acids can act not only on the nucleus but also on the cell membrane. Specifically, the omega 3 polyunsaturated fatty acid can inhibit NF-kB through PPARY, and can inhibit the nuclear expression of excessive proinflammatory cytokines, such as tumor necrosis factor TNF-alpha, interleukin IL-6 and the like. Meanwhile, omega 3 polyunsaturated fatty acids (EPA and DHA) competitively inhibit proinflammatory mediators derived from omega 6 polyunsaturated fatty acids (AA) on cell membranes, and the production of the proinflammatory mediators can be reduced. Omega 3 polyunsaturated fatty acids are furthermore capable of producing anti-inflammatory mediators with a direct resolution validation. The broccoli seed extract can play an anti-inflammatory role by up-regulating Nrf2 and reducing the activity of NF-kB and a series of inflammatory mediators (cytokines, chemokines, adhesion factors, COM-2, MMP-9, iNOS and the like). The two components cooperate with each other to achieve good anti-inflammatory effect.
The components of the invention also contain pomegranate extract and mangosteen extract. The two can be mutually compatible with broccoli seed extract to improve the multi-target synergistic antioxidation. Specifically, pomegranate extracts contain unique mixed polyphenols (punicalagin, anthocyanins, resveratrol and ellagic acid). Wherein, the punicalagin not only can activate the antioxidase, but also can inhibit the activity of lipid peroxidation; the anthocyanin is a strong antioxidant and has the functions of reducing the permeability and weakness of capillary vessels; resveratrol is a strong antioxidant and has the effects of inhibiting nucleotide reductase, and inhibiting low density lipoprotein cholesterol oxidation and lipid peroxidation; ellagic acid also has antioxidant and anti-inflammatory effects. The mangosteen extract contains various polyphenols such as xanthones, procyanidins, catechins, etc., which are good antioxidants. Nrf2 increases highly coordinated antioxidant activity through the action of more than 20 genes, which also has anti-inflammatory effects; the broccoli seed extract can up-regulate transcription factor Nrf2, and Nrf2 can play a role in increasing highly coordinated antioxidant activity through the action of more than 20 genes. The three components cooperate to achieve good synergistic antioxidation effect.
The health-care food is characterized in that the health-care food is prepared from the components of the health-care food, the components of the health-care food are added with milk-benefiting polypeptide, and the milk-benefiting polypeptide can be matched with pomegranate extracts, fish oil microcapsule powder and onion extracts to play a role in repairing blood vessel intima. In particular, atherosclerosis is induced by endothelial dysfunction that would result directly from insufficient nitric oxide production by endothelial nitric oxide synthase. The pomegranate extract contains various polyphenol compounds, the onion extract contains quercetin and sulfide, and the fish oil microcapsule powder contains omega-3 fatty acid, which can promote the production and secretion of nitric oxide. The functional factor of the milk-benefiting polypeptide is valine-proline tripeptide, which can effectively inhibit the generation of angiotensin, dilate blood vessels, stimulate the intimal cells of the blood vessels to efficiently synthesize nitric oxide, maintain the integrity of the intimal blood vessels, and increase the elasticity of the blood vessels. The components are compatible, so that the tunica intima can be repaired, and the elasticity of blood vessels can be increased.
The proportion of the components of the invention is not set at will, particularly, the main cause of the arteriosclerosis is that the excessive low-density lipoprotein cholesterol leads to direct swallowing and drinking of intima cells, when inflammation is caused, mononuclear cells can phagocytize a large amount of oxidized low-density lipoprotein cholesterol to form foam cells to deposit subcutaneous cells in blood vessels, and fibrous tissue hyperplasia is stimulated to promote the generation of atherosclerosis. A large amount of clinical practice data show that the normal standard reaching rate of low-density lipoprotein cholesterol index can be increased to more than 90% by using 100-200 parts of phytosterol and 10-30 parts of red yeast rice for 1-3 months, and the important reason is that the phytosterol can only achieve the optimal effect within the range of 100-200 parts. Aiming at exogenous cholesterol, the secretion of apolipoprotein B of intestinal tracts and liver cells can be reduced, the absorption of dietary cholesterol and the entrance of bile cholesterol into microbubbles are reduced, the absorption of cholesterol is further reduced, the secretion of bile acid is increased, the reverse transport of cholesterol is improved, a key enzyme (hydroxymethyl glutaryl coenzyme A reductase HMG-COA-R) for synthesizing the cholesterol can be inhibited, and the pathway for synthesizing the cholesterol is blocked. The indexes of the plant sterol are not obviously changed when the plant sterol is lower than 100 parts of low-density lipoprotein cholesterol, the low-density lipoprotein cholesterol is higher than 200 parts of low-density lipoprotein cholesterol, the metabolic burden of the liver is aggravated, the function of the liver is weakened, and the blood sugar of a few people is slightly increased. In fact, the phytosterol has more biological activity only when 100-200 parts, is more suitable for absorption and metabolism of human bodies, and is matched with 10-30 parts of red yeast rice, because the red yeast rice contains a key enzyme (hydroxymethyl glutaryl coenzyme A reductase HMG-COA-R) specific inhibitor for synthesizing the cholesterol by the human bodies, the endogenous pathway for synthesizing the cholesterol can be blocked, and the red yeast rice not only can reduce the total cholesterol, the low-density lipoprotein cholesterol and the arteriosclerosis index, but also can reduce triglyceride and improve the remarkable comprehensive effect of the high-density lipoprotein cholesterol. The ring-opening rate of the monacolin K of the selected red yeast rice is more than 65 percent, the bioavailability of the phytosterol to the liver is greatly improved, and the monacolin K are mutually cooperated and are monarch and minister in the range to exert the best effect on the inhibition of endogenous cholesterol and exogenous cholesterol.
According to the invention, the addition amount of the fish oil microcapsule powder is 100-200 parts, the broccoli seed extract is 2-8 parts, tumor necrosis factor alpha (TNF +) is clinically detected in 1-3 months, and C-reactive protein (CRP) and interleukin 6 (IL-6) are reduced by less than 58%, because the anti-inflammatory effect can only reach 3% when the fish oil microcapsule powder is less than 100 parts, and the anti-inflammatory effect is not substantially changed before when the fish oil microcapsule powder is more than 200 parts, so that omega 3 (EPA and DHA) fatty acid contained in the fish oil microcapsule powder has an obvious influence on mononuclear cell inflammation only when 100-200 parts is used, the optimal effect is achieved, and meanwhile, the broccoli seed extract is 2-8 parts, so that Nrf2 can be adjusted upwards, NF-kB and a series of inflammation media (cell factors, chemotactic factors, adhesion factors, COM-2, MMP-9, iNOS and the like) are reduced, so that the anti-inflammatory effect is achieved, and the activated transcription factor N2 accelerates the transcription of the fish oil microcapsule powder from cell membrane to nucleus to the anti-inflammatory effect, the broccoli seed extract is 2-8 parts, the anti-inflammatory agent, the COM-2, the iNOS and the monarch extract can achieve a synergistic effect when the anti-lipid-reducing effect is in a good range, so that the anti-reducing effect of the anti-inflammatory effect is achieved.
In the formula, 1-5 parts of onion extract, 5-15 parts of mangosteen extract and 5-25 parts of pomegranate extract are used as adjuvant medicines in the range, so that the lipid-lowering and anti-inflammatory effects of the monarch medicine are improved, the antioxidation effect is also realized, the oxidation of low-density lipoprotein cholesterol can be effectively reduced, the phagocytosis of mononuclear cells is reduced, the number of foam cell deposits is reduced, and the occurrence of arteriosclerosis is reduced.
In the formula of the invention, 30-70 parts of nattokinase and 10-40 parts of milk-benefiting polypeptide have the action principle that 30-70 parts of nattokinase can only act on fibrinolysis and platelet aggregation, and simultaneously the blood flow speed is increased, the lipid plaque reduction rate can reach 68.5 percent after the composition is used for 3 months, the plaque dissolving effect is not ideal when the composition is less than 30 parts, and the composition is more than 70 parts of nattokinase can cause diarrhea, vomiting and dyspepsia, and the main reason is that the nattokinase is digested and decomposed by intestinal tracts, and the excessive nattokinase easily stimulates intestines and stomach. The health milk polypeptide 10-40 parts can increase the blood vessel elasticity by more than 50% in 3 months, so that the health milk polypeptide and the health milk polypeptide can be used as a guiding drug together to enable all the natural active plants to better exert respective functions. The compatibility of the whole formula is to effectively intervene by using pure natural food materials according to the pathogenesis of arteriosclerosis and the whole process of arteriosclerosis formation, and meanwhile, the formula has innovative significance for preventing and treating 3 hundred million people's cardiovascular diseases at present.
The broccoli seed extract of the present invention is purchased from Korea-European trade (Shanghai) Co., ltd, or from Brassica corporation, shanghai Heat transfer industry Co., ltd. The content of sulforaphane and sulforaphane glycoside contained in the broccoli seed extract is not less than 13% as a purchase standard at the time of purchase.
Preferably, the pomegranate extract is prepared by the following method: pulverizing pericarpium Granati, drying to obtain powder, extracting with one or more of water, alcohol or other food processing aids, concentrating, and drying to obtain pericarpium Granati extract. Specifically, after the pomegranate peel is crushed and dried, 70% ethanol aqueous solution with the mass ratio of 1. Mixing filtrates, further concentrating under reduced pressure, and vacuum drying to obtain fructus Punicae Granati extract.
Preferably, the mangosteen extract is prepared by the following method: pulverizing mangosteen fruit shell, extracting with ethanol of 70% or more, filtering, centrifuging, concentrating under reduced pressure, and spray drying to obtain mangosteen extract. Specifically, mangosteen nutshell is smashed and then extracted by ethanol with the concentration of more than 70%, wherein the weight ratio of the mangosteen nutshell to the ethanol is 1.
Preferably, the onion extract is prepared by the following method: pulverizing Bulbus Allii Cepae, mixing with ethanol water solution, ultrasonic extracting, filtering, concentrating, centrifuging, and collecting supernatant to obtain Bulbus Allii Cepae extract. Specifically, the onion extract is obtained by taking fresh onions, crushing the onions by a food processor, adding 70% ethanol aqueous solution with the mass ratio of 1 to 10, carrying out ultrasonic extraction for 3 times at 40 ℃, wherein the ultrasonic power is 200W, combining extracting solutions, filtering, carrying out reduced pressure concentration, centrifuging concentrated solution, wherein the centrifugal speed is 4000r/min, the centrifugal time is 10min, and taking supernatant.
It is understood that the pomegranate extract, the mangosteen extract and the onion extract of the present invention can also be obtained commercially. For example, the mangosteen extract is available from Nippon Kabushiki Kaisha, the pomegranate extract is available from Mouthica Biotech, inc., and the onion extract is available from Shaanxi Fuwa Natural products, inc. In addition, the onion extract can be prepared by the extraction method described in JP4348425 or JP 2017-61431. In fact, these extracts, whether obtained from commercial products or extracted by themselves, are of uniform purity and with a certain guarantee, and therefore are all uniform as to the efficacy exerted by the composition after it has been prepared.
The invention also provides a preparation method of the natural plant composition for preventing and treating arteriosclerosis, which comprises the following steps:
pulverizing the above materials respectively, mixing, stirring, and making into preparation.
Preferably, the raw materials are mixed and sieved by a 60-100 mesh sieve.
Preferably, the preparation is any one of tablets, capsules and granules.
The preparation method is simple to operate, and the prepared composition has a good prevention and treatment effect on arteriosclerosis.
The invention also provides application of the natural plant composition for preventing and treating arteriosclerosis in medicines or health-care foods for treating diseases related to arteriosclerosis.
Compared with the prior art, the invention has the following beneficial effects:
the natural plant composition provided by the invention can effectively reduce the content of total cholesterol and low-density lipoprotein cholesterol and prevent platelet aggregation through mutual compatibility of various components, and can play roles in resisting inflammation and oxidation, repairing vascular intima and increasing vascular elasticity, thereby effectively preventing and treating arteriosclerosis.
Detailed Description
Embodiments of the present invention will be described in detail below with reference to examples, but it will be understood by those skilled in the art that the following examples are only illustrative of the present invention and should not be construed as limiting the scope of the present invention. The examples, in which specific conditions are not specified, were conducted under conventional conditions or conditions recommended by the manufacturer. The reagents or instruments used are not indicated by the manufacturer, and are all conventional products available commercially.
Example 1
The following components were weighed: 1000mg of phytosterol, 1000mg of fish oil microcapsule powder, 100mg of milk health polypeptide, 100mg of red yeast rice, 300mg of nattokinase, 10mg of onion extract, 50mg of mangosteen extract, 20mg of broccoli seed extract and 50mg of pomegranate extract.
Respectively pulverizing the above materials, mixing, sieving with 80 mesh sieve, and mixing with multidimensional mixer to obtain tablet with mass of 0.8 g/tablet.
Wherein the Broccoli seed extract is obtained from Korea-European trade (Shanghai) Co., or from Brassica corporation, shanghai Heat transfer industry Co., ltd. The content of sulforaphane and sulforaphane glycoside contained in the broccoli seed extract is not less than 13% as a purchase standard at the time of purchase.
The onion extract is purchased from Shaanxi forest Freund natural products, and can also be directly prepared by adopting the following method: crushing fresh onions by using a food processor, adding 70% ethanol water solution with the mass ratio of 1. In addition, the onion extract can be prepared by the extraction method described in the patent publication No. JP4348425 or the patent publication No. JP 2017-61431.
The mangosteen extract can be purchased from Nippon New drug Co., ltd, or can be directly prepared by the following method: pulverizing mangosteen fruit shell, extracting with ethanol with concentration of 70% or more at 80 deg.C for 1 hr at a weight ratio of 1.
The pomegranate extract can be purchased from Yuanhua Biotech limited, or can be directly prepared by the following method: pulverizing pericarpium Granati, drying, adding 70% ethanol water solution with mass ratio of 1. Mixing filtrates, further concentrating under reduced pressure, and vacuum drying to obtain fructus Punicae Granati extract.
Example 2
The following components were weighed: 1200mg of phytosterol, 1200mg of fish oil microcapsule powder, 200mg of AnYi milk polypeptide, 150mg of red yeast rice, 400mg of nattokinase, 15mg of onion extract, 70mg of mangosteen extract, 30mg of broccoli seed extract and 100mg of pomegranate extract.
Respectively pulverizing the above materials, mixing, sieving with 80 mesh sieve, adding into multidimensional mixer, mixing, and making into tablet with mass of 0.8 g/tablet.
The onion extract, the mangosteen extract, the broccoli seed extract, and the pomegranate extract were obtained in the same manner as in example 1.
Example 3
The following components were weighed: 1500mg of phytosterol, 1500mg of fish oil microcapsule powder, 250mg of milk health polypeptide, 200mg of red yeast rice, 500mg of nattokinase, 20mg of onion extract, 100mg of mangosteen extract, 50mg of broccoli seed extract and 150mg of pomegranate extract.
Respectively pulverizing the above materials, mixing, sieving with 80 mesh sieve, adding into multidimensional mixer, mixing, and making into tablet with mass of 0.8 g/tablet.
The onion extract, the mangosteen extract, the broccoli seed extract, and the pomegranate extract were obtained in the same manner as in example 1.
Example 4
The following components were weighed: 1700mg of phytosterol, 1700mg of fish oil microcapsule powder, 300mg of milk health polypeptide, 250mg of red yeast rice, 600mg of nattokinase, 40mg of onion extract, 120mg of mangosteen extract, 70mg of broccoli seed extract and 200mg of pomegranate extract.
Respectively pulverizing the above materials, mixing, sieving with 60 mesh sieve, and mixing with multidimensional mixer to obtain tablet with mass of 0.8 g/tablet.
The onion extract, the mangosteen extract, the broccoli seed extract, and the pomegranate extract were obtained in the same manner as in example 1.
Example 5
The following components were weighed: 2000mg of phytosterol, 2000mg of fish oil microcapsule powder, 400mg of AnYi milk polypeptide, 300mg of red yeast rice, 700mg of nattokinase, 50mg of onion extract, 150mg of mangosteen extract, 80mg of broccoli seed extract and 250mg of pomegranate extract.
Respectively pulverizing the above materials, mixing, sieving with 100 mesh sieve, adding into multidimensional mixer, mixing, and making into tablet with mass of 0.8 g/tablet.
The onion extract, the mangosteen extract, the broccoli seed extract, and the pomegranate extract were obtained in the same manner as in example 1.
Example 6
The specific operation process is the same as that of example 3, except that powder is prepared.
Example 7
The specific operation process is the same as that of example 3, and only capsules are prepared.
Comparative example 1
The specific procedure was as in example 3 except that the phytosterol was added at 2500mg.
Comparative example 2
The specific procedure was the same as in example 3 except that the broccoli seed extract was added in an amount of 100mg.
Comparative example 3
The specific procedure was the same as in example 3 except that the broccoli seed extract was not added.
Comparative example 4
The specific operation process is the same as that of example 3, except that the amount of nattokinase added is 100mg.
Comparative example 5
The specific operation process is the same as that of example 3, except that the addition amount of the fish oil microcapsule powder is 2500mg.
Comparative example 6
The specific operation process is the same as that of example 3, except that the addition amount of the milk benefiting polypeptide is 500mg.
Experimental example 1
The preparations of examples 1 to 7 and comparative examples 1 to 6 were tested for their effects on rat arteriosclerosis as follows: 150 rats were randomly divided into 15 groups of ten. One group was a control group, one group was a model group, and the other three groups were experimental groups. The control group is fed with basic feed, and the model group and the experimental group adopt a method of performing intraperitoneal injection on vitamin D60 ten thousand units/kg once, and simultaneously performing drenching on high-fat feed and 10 mL/kg of fat milk (each 500 mL of fat milk contains 30g of cholesterol, 5 g of sodium cholate, 3g of propylthiouracil and 50g of lard) every day to prepare the arteriosclerosis model.
The experimental group was administered with 0.2 g/(kg. D) of the formulations of examples 1 to 7 and comparative examples 1 to 6, respectively, and the control group and the model group were administered with the same amount of distilled water per day. The blood lipid, TNF-alpha, IL-6 and NF-kB are measured by taking blood from the ocular venous plexus 1 time per day for 60 days continuously after the last administration for 2 hours, and the abdominal aorta hemorheology index is measured. The rat is killed, abdominal aorta, heart, liver and the like are taken and soaked in 10% formalin, the pathological changes of the artery, the heart and the liver are observed through routine paraffin embedding, slicing and HE staining, the ratio of the mesolamella thickness to the radius of the inner cavity of the blood vessel is calculated, the positive expression of the mesolamella NF-kB in the artery is observed through immunohistochemical analysis by adopting an SABC method, and the pathological changes of the artery are observed.
The pathological morphological observation result shows that the control rat has clear vascular structure, complete internal elastic facial mask and regular arrangement of the smooth muscle cells of the mesolamella, and is parallel to the internal elastic facial mask. The aorta of the rat in the model group has atherosclerotic plaque, the elastic membrane in the blood vessel is damaged and broken, the tunica media is obviously irregularly thickened, the ratio of the thickness of the tunica media to the radius of the lumen of the blood vessel is obviously increased, the arrangement of smooth muscle cells is disordered, the cells tend to migrate to the tunica intima, and the smooth muscle fibers are obviously disordered; the lipid deposition of myocardial tissues is severe, and a large number of red-stained particles appear in cytoplasm of myocardial cells in a lesion area; liver sections were strongly positive by oil red O staining. Compared with the model group, the breakage of the elastic membrane in the blood vessel of rats in each experimental group is reduced, partial stretching is flat, the arrangement of the fibers of the smooth muscle of the mesolamella is slightly disordered, and compared with the effect of the example 3 and the comparative example 6, the repairing effect of the example 3 on the elastic membrane is not much different from that of the comparative example 6, which shows that the repairing effect cannot be improved by continuously increasing the amount of the milk polypeptide for benefiting health after the amount reaches a certain amount.
The lowering effect and anti-inflammatory effect on total cholesterol and low density lipoprotein cholesterol levels are shown in table 1 below:
TABLE 1
As can be seen from Table 1, the natural plant composition of the present invention can significantly reduce the total cholesterol and low density lipoprotein cholesterol levels and has significant anti-inflammatory effects. Comparing example 3 with comparative example 1, it can be seen that the results of example 3 and comparative example 1 are not very different in the performance of reducing the total cholesterol and low density lipoprotein cholesterol levels, and the effect of example 3 is slightly better than that of comparative example 1, probably because the excessive phytosterol is difficult to be absorbed by human body, and the synergistic promotion effect of red yeast rice on phytosterol is inhibited to a certain extent, which shows that the optimal effect of reducing the total cholesterol and low density lipoprotein cholesterol levels can be achieved only when the ratio of phytosterol to red yeast rice is a certain ratio.
Comparing the anti-inflammatory effects of example 3 with those of comparative examples 2, 3 and 5, it can be seen that the anti-inflammatory effect of example 3 is slightly superior to that of comparative examples 2 and 5, and is significantly superior to that of comparative example 3. The reason is that the broccoli seed extract and the fish oil microcapsule powder can mutually cooperate to achieve good anti-inflammatory effect, and the anti-inflammatory effect can be optimized only when the mass ratio of the broccoli seed extract to the fish oil microcapsule powder is maintained to be a certain ratio.
The effect on platelet aggregation in rats is shown in table 2 below:
TABLE 2
As can be seen from Table 2, the natural plant composition of the present invention can significantly inhibit the aggregation of platelets. Comparing example 3 with comparative example 4, it can be seen that in the case where the amount of nattokinase added is not as much as in comparative example 4, the platelet aggregation preventing effect of example 3 is slightly better than that of comparative example 4, probably because the excessive amount of nattokinase inhibits the synergistic effect with the onion extract to some extent, indicating that the platelet aggregation preventing effect is optimal only in the case where the two are in a certain ratio.
Experimental example 2
21 patients with arteriosclerosis were treated with the natural plant composition prepared in example 3, and serum was measured after a certain period of treatment, and the results are shown in Table 3.
TABLE 3
As can be seen from the above table, the natural plant composition of the present invention has a very good therapeutic effect on the significant reduction of total cholesterol and low density lipoprotein cholesterol, thereby having very good preventive and therapeutic effects on the prevention and recovery of arteriosclerosis.
Typical cases
Case 1: when a woman is 63 years old, CT shows that the liver is occupied and damaged, and regular examination is required. After taking the product for 1 month, the liver is rechecked to only leave uneven fatty liver, and other indexes are restored to normal.
Case 2: some Panzhi, male, 57 years old, the left common carotid artery intersection has plaque generation after blood vessel examination, the right side 1863 of the arteriosclerosis degree, the left side 1832, the product is taken for 3 months and then the double examination is carried out, the intima in the two common carotid arteries is thickened, the plaque disappears, the right side 1723 of the arteriosclerosis degree, and the left side 1667.
Case 3: for a certain woman in 53 years old with hyperlipidemia, the American direct marketing brand Yossana is taken for a long time, but the blood lipid is not obviously improved. After the product is taken for one month, the blood fat is recovered to be normal, and after the product is taken for three months, the liver index is recovered to be normal.
Case 4: some Hu, male, age 64, sudden cerebral infarction, inconvenient movement after discharge, unclear speaking and vomiting, edema of hands and feet on the affected side of hemiplegia and grade 3 grip strength. The hand and foot edema disappears after half a year of using the product, and the user can walk by himself.
Case 5: a certain horse, male, 62 years old, has been examined by physical examination to find subacute cerebral infarction, old cerebral infarction, cerebral white matter demyelination, essential hypertension, dyslipidemia, bilateral anterior cerebral artery A1 with far occlusion, internal carotid plaque formation and arteriosclerosis, left common carotid artery thickness 1.5mm, bilateral vertebral artery left 3.6mm, right 2.9mm, right femoral artery 2.0mm, left femoral artery 2.8mm, left common carotid artery thickness 1.1mm, bilateral vertebral artery left 3.5mm, right 3.0mm, right femoral artery 1.4mm, left femoral artery 2.3mm after half a year of conditioning by the product.
While particular embodiments of the present invention have been illustrated and described, it would be obvious that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention.
Claims (6)
1. A natural plant composition for preventing and treating arteriosclerosis is characterized by comprising the following components in parts by mass: 100-200 parts of phytosterol, 100-200 parts of fish oil microcapsule powder, 10-40 parts of milk-benefiting polypeptide, 10-30 parts of red yeast rice, 30-70 parts of nattokinase, 1-5 parts of onion extract, 5-15 parts of mangosteen extract, 2-8 parts of broccoli seed extract and 5-25 parts of pomegranate extract;
the pomegranate extract is prepared by the following method: pulverizing pericarpium Granati, drying to obtain powder, extracting with one or more of water, alcohol or other food processing aids, concentrating, and drying to obtain pericarpium Granati extract;
the mangosteen extract is prepared by adopting the following method: pulverizing mangosteen fruit shell, extracting with ethanol of 70% or more, filtering, centrifuging, concentrating under reduced pressure, and spray drying to obtain mangosteen extract;
the onion extract is prepared by the following method: pulverizing Bulbus Allii Cepae, mixing with ethanol water solution, ultrasonic extracting, filtering, concentrating, centrifuging, and collecting supernatant to obtain Bulbus Allii Cepae extract.
2. The natural plant composition for preventing and treating arteriosclerosis as set forth in claim 1, wherein the plant sterol is 120-170 parts, the fish oil microcapsule powder is 120-170 parts, the milk's galangal polypeptide is 20-30 parts, the red yeast rice is 15-25 parts, the nattokinase is 40-60 parts, the onion extract is 1.5-4 parts, the mangosteen extract is 7-12 parts, the broccoli seed extract is 3-7 parts, and the pomegranate extract is 10-20 parts.
3. The natural plant composition for preventing and treating arteriosclerosis as defined in claim 1, wherein the plant sterol is 150 parts, the fish oil microcapsule powder is 150 parts, the milk polypeptide is 25 parts, the red yeast rice is 20 parts, the nattokinase is 50 parts, the onion extract is 2 parts, the mangosteen extract is 10 parts, the broccoli seed extract is 5 parts, and the pomegranate extract is 15 parts.
4. A method for preparing the natural plant composition for the prevention and treatment of arteriosclerosis as defined in any one of claims 1-3, comprising the steps of:
pulverizing the above materials respectively, mixing, stirring, and making into preparation.
5. The method of claim 4, wherein the raw materials are mixed and then screened through a 60-100 mesh screen.
6. The method of claim 4, wherein the preparation is any one of a tablet, a capsule and a granule.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202210757395.4A CN114984196B (en) | 2022-06-30 | 2022-06-30 | Natural plant composition for preventing and treating arteriosclerosis, preparation method and application |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202210757395.4A CN114984196B (en) | 2022-06-30 | 2022-06-30 | Natural plant composition for preventing and treating arteriosclerosis, preparation method and application |
Publications (2)
Publication Number | Publication Date |
---|---|
CN114984196A CN114984196A (en) | 2022-09-02 |
CN114984196B true CN114984196B (en) | 2023-01-06 |
Family
ID=83019876
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202210757395.4A Active CN114984196B (en) | 2022-06-30 | 2022-06-30 | Natural plant composition for preventing and treating arteriosclerosis, preparation method and application |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN114984196B (en) |
Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6641850B1 (en) * | 1999-04-19 | 2003-11-04 | Stewart And Lynda Resnick Revocable Trust | Methods of using pomegranate extracts for causing regression in lesions due to arteriosclerosis in humans |
CN102349963A (en) * | 2011-10-20 | 2012-02-15 | 新时代健康产业(集团)有限公司 | Health care product for preventing microthrombus from forming and preparation method thereof |
CN102406115A (en) * | 2011-10-26 | 2012-04-11 | 江苏江大源生态生物科技有限公司 | Natural functional food for preventing cardiovascular and cerebrovascular diseases |
CN102526333A (en) * | 2011-01-04 | 2012-07-04 | 统欣生物科技股份有限公司 | Composition for regulating blood fat and protecting heart and blood vessels |
CN109259243A (en) * | 2018-09-26 | 2019-01-25 | 广州普维君健药业有限公司 | Composition of lower hyperlipidemia, hypertension, hyperglycemia and its preparation method and application |
CN109678834A (en) * | 2019-01-20 | 2019-04-26 | 林燕 | A kind of preparation method for extracting anthocyanidin from mangosteen peel |
CN110051826A (en) * | 2019-05-17 | 2019-07-26 | 广东双骏生物科技有限公司 | A kind of composition and preparation method thereof with improvement cardiovascular function |
CN111418851A (en) * | 2020-04-29 | 2020-07-17 | 私诺(北京)健康科技有限公司 | A nutritious food for protecting blood vessel |
CN111557407A (en) * | 2020-05-18 | 2020-08-21 | 碧豫药业有限责任公司 | Health food capable of reducing blood fat |
CN112075633A (en) * | 2020-09-18 | 2020-12-15 | 杭州衡美食品科技有限公司 | Natural extract and dietary fiber compounded weight-losing composition |
-
2022
- 2022-06-30 CN CN202210757395.4A patent/CN114984196B/en active Active
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6641850B1 (en) * | 1999-04-19 | 2003-11-04 | Stewart And Lynda Resnick Revocable Trust | Methods of using pomegranate extracts for causing regression in lesions due to arteriosclerosis in humans |
CN102526333A (en) * | 2011-01-04 | 2012-07-04 | 统欣生物科技股份有限公司 | Composition for regulating blood fat and protecting heart and blood vessels |
CN102349963A (en) * | 2011-10-20 | 2012-02-15 | 新时代健康产业(集团)有限公司 | Health care product for preventing microthrombus from forming and preparation method thereof |
CN102406115A (en) * | 2011-10-26 | 2012-04-11 | 江苏江大源生态生物科技有限公司 | Natural functional food for preventing cardiovascular and cerebrovascular diseases |
CN109259243A (en) * | 2018-09-26 | 2019-01-25 | 广州普维君健药业有限公司 | Composition of lower hyperlipidemia, hypertension, hyperglycemia and its preparation method and application |
CN109678834A (en) * | 2019-01-20 | 2019-04-26 | 林燕 | A kind of preparation method for extracting anthocyanidin from mangosteen peel |
CN110051826A (en) * | 2019-05-17 | 2019-07-26 | 广东双骏生物科技有限公司 | A kind of composition and preparation method thereof with improvement cardiovascular function |
CN111418851A (en) * | 2020-04-29 | 2020-07-17 | 私诺(北京)健康科技有限公司 | A nutritious food for protecting blood vessel |
CN111557407A (en) * | 2020-05-18 | 2020-08-21 | 碧豫药业有限责任公司 | Health food capable of reducing blood fat |
CN112075633A (en) * | 2020-09-18 | 2020-12-15 | 杭州衡美食品科技有限公司 | Natural extract and dietary fiber compounded weight-losing composition |
Non-Patent Citations (1)
Title |
---|
山竹壳中原花青素的提取及纯化工艺研究;孙冲霞;《江苏农业科学》;20120316;第39卷(第5期);第356-358页 * |
Also Published As
Publication number | Publication date |
---|---|
CN114984196A (en) | 2022-09-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Rajkapoor et al. | Effect of dried fruits of Carica papaya L INN on hepatotoxicity | |
CN103861070B (en) | Health product for preventing angiosclerosis | |
KR20120003693A (en) | Anti-obesity composition comprising red grape extracts, green tea extracts, soybean extracts, and l-carnitine | |
Marzaimi et al. | Current review on mangosteen usages in antiinflammation and other related disorders | |
JP2001342142A (en) | Composition for preventing and curing urologic disease | |
KR101672274B1 (en) | Compositions comprising a Viola Herba extract, or an extract of Viola Herba, Persicae Semen, Cinnamomi Ramulus, and Glycyrrhiza spp. for the prevention or treatment of lipid-related cardiovascular diseases and obesity | |
JP2004217559A (en) | Prophylactic and ameliorating agent for diabetic condition | |
JP2007269631A (en) | Agent for suppressing accumulation of neutral fat | |
CN114984196B (en) | Natural plant composition for preventing and treating arteriosclerosis, preparation method and application | |
Khongrum et al. | Antidyslipidemic, Antioxidant, and Anti‐inflammatory Effects of Jelly Drink Containing Polyphenol‐Rich Roselle Calyces Extract and Passion Fruit Juice with Pulp in Adults with Dyslipidemia: A Randomized, Double‐Blind, Placebo‐Controlled Trial | |
KR20210035592A (en) | galeusinialeul iyonghan biman haeso gineung-ui saengsigtaib cha joseongmul | |
Wan et al. | Effect of Lactobacillus acidophilus fermentation on the composition of chlorogenic acids and anti-hyperuricemia activity of Artemisia selengensis Turcz | |
JP2004352626A (en) | Anticholesterol agent containing plant-derived component | |
KR101934810B1 (en) | Preparation for improving blood circulation comprising oriental medicinal extracts | |
KR20180079920A (en) | Composition for preventing, improving or treating hepatic fibrosis or liver cirrhosis comprising Cuscuta Semen extract | |
CN109620858A (en) | The integration of drinking and medicinal herbs preparation for preventing and treating diabetes | |
KR100888068B1 (en) | Compositions for suppressing obesity | |
JP3980952B2 (en) | Enteric fat absorption inhibitor containing plant extract and food containing the same | |
KR100656241B1 (en) | The extract of Korean fermented soybean with inhibitory effect on hyperlipemia and platelet aggregation, and their composition | |
EP1433500B1 (en) | Blood fluidity-improving health foods | |
KR102161893B1 (en) | The food composition for anti-obesity comprising pine nut cones by-products | |
CN107335026B (en) | Medicine for treating focal segmental glomerulosclerosis | |
CN107456504A (en) | A kind of dietary supplements and its preparation method and application | |
WO2023217115A1 (en) | Composition of malus niedzwetzkyana dieck and prunus cerasifera ehrhart and use thereof in terms of resisting atherosclerosis | |
Atazadegan et al. | The Effect of Herbal Medicine and Natural Bioactive Compounds on Plasma Adiponectin: A Clinical |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |