CN117694408A - Edible plant blend oil capable of reducing hyperlipidemia - Google Patents
Edible plant blend oil capable of reducing hyperlipidemia Download PDFInfo
- Publication number
- CN117694408A CN117694408A CN202410048746.3A CN202410048746A CN117694408A CN 117694408 A CN117694408 A CN 117694408A CN 202410048746 A CN202410048746 A CN 202410048746A CN 117694408 A CN117694408 A CN 117694408A
- Authority
- CN
- China
- Prior art keywords
- oil
- hyperlipidemia
- blend
- mlct
- blend oil
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 94
- 208000031226 Hyperlipidaemia Diseases 0.000 title claims abstract description 34
- 230000001603 reducing effect Effects 0.000 title claims abstract description 22
- 235000018927 edible plant Nutrition 0.000 title claims abstract description 10
- 239000003921 oil Substances 0.000 claims abstract description 128
- 238000002156 mixing Methods 0.000 claims abstract description 13
- 235000013305 food Nutrition 0.000 claims abstract description 12
- 235000016709 nutrition Nutrition 0.000 claims abstract description 6
- 235000019198 oils Nutrition 0.000 claims description 124
- 235000020664 gamma-linolenic acid Nutrition 0.000 claims description 28
- 238000003756 stirring Methods 0.000 claims description 28
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 claims description 27
- VZCCETWTMQHEPK-QNEBEIHSSA-N gamma-linolenic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/CCCCC(O)=O VZCCETWTMQHEPK-QNEBEIHSSA-N 0.000 claims description 27
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 23
- 229930195729 fatty acid Natural products 0.000 claims description 23
- 239000000194 fatty acid Substances 0.000 claims description 23
- VZCCETWTMQHEPK-UHFFFAOYSA-N gamma-Linolensaeure Natural products CCCCCC=CCC=CCC=CCCCCC(O)=O VZCCETWTMQHEPK-UHFFFAOYSA-N 0.000 claims description 23
- 229960002733 gamolenic acid Drugs 0.000 claims description 23
- 235000013311 vegetables Nutrition 0.000 claims description 19
- 238000001914 filtration Methods 0.000 claims description 17
- 235000020661 alpha-linolenic acid Nutrition 0.000 claims description 15
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 15
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 14
- 229960004488 linolenic acid Drugs 0.000 claims description 14
- 239000010473 blackcurrant seed oil Substances 0.000 claims description 13
- 150000004665 fatty acids Chemical class 0.000 claims description 13
- 239000000944 linseed oil Substances 0.000 claims description 12
- 235000021388 linseed oil Nutrition 0.000 claims description 12
- 239000008158 vegetable oil Substances 0.000 claims description 12
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 8
- 235000019484 Rapeseed oil Nutrition 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000003549 soybean oil Substances 0.000 claims description 6
- 235000012424 soybean oil Nutrition 0.000 claims description 6
- 235000020235 chia seed Nutrition 0.000 claims description 4
- 238000009472 formulation Methods 0.000 claims description 4
- 235000006484 Paeonia officinalis Nutrition 0.000 claims description 3
- 244000170916 Paeonia officinalis Species 0.000 claims description 3
- 235000021324 borage oil Nutrition 0.000 claims description 3
- 239000003240 coconut oil Substances 0.000 claims description 3
- 235000019864 coconut oil Nutrition 0.000 claims description 3
- 239000010475 evening primrose oil Substances 0.000 claims description 3
- 235000019482 Palm oil Nutrition 0.000 claims description 2
- 235000008524 evening primrose extract Nutrition 0.000 claims description 2
- 229940089020 evening primrose oil Drugs 0.000 claims description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 2
- 239000002540 palm oil Substances 0.000 claims description 2
- 239000001335 perilla frutescens leaf extract Substances 0.000 claims description 2
- 241000195493 Cryptophyta Species 0.000 claims 2
- VMPHSYLJUKZBJJ-UHFFFAOYSA-N trilaurin Chemical compound CCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC)COC(=O)CCCCCCCCCCC VMPHSYLJUKZBJJ-UHFFFAOYSA-N 0.000 claims 2
- 235000019774 Rice Bran oil Nutrition 0.000 claims 1
- 239000010495 camellia oil Substances 0.000 claims 1
- 235000005687 corn oil Nutrition 0.000 claims 1
- 239000002285 corn oil Substances 0.000 claims 1
- 239000002385 cottonseed oil Substances 0.000 claims 1
- 235000012343 cottonseed oil Nutrition 0.000 claims 1
- 239000004006 olive oil Substances 0.000 claims 1
- 235000008390 olive oil Nutrition 0.000 claims 1
- 239000003346 palm kernel oil Substances 0.000 claims 1
- 235000019865 palm kernel oil Nutrition 0.000 claims 1
- 239000008165 rice bran oil Substances 0.000 claims 1
- 239000003813 safflower oil Substances 0.000 claims 1
- 235000020238 sunflower seed Nutrition 0.000 claims 1
- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 claims 1
- VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical compound CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 24
- 210000004369 blood Anatomy 0.000 abstract description 14
- 239000008280 blood Substances 0.000 abstract description 14
- 150000002632 lipids Chemical class 0.000 abstract description 11
- 239000008157 edible vegetable oil Substances 0.000 abstract description 5
- 239000003963 antioxidant agent Substances 0.000 abstract description 4
- 239000002994 raw material Substances 0.000 abstract description 4
- 230000002195 synergetic effect Effects 0.000 abstract description 4
- 230000003078 antioxidant effect Effects 0.000 abstract description 3
- 230000035764 nutrition Effects 0.000 abstract description 3
- 239000010773 plant oil Substances 0.000 abstract description 2
- 241000699670 Mus sp. Species 0.000 description 23
- 230000000052 comparative effect Effects 0.000 description 22
- 235000019197 fats Nutrition 0.000 description 17
- 210000002966 serum Anatomy 0.000 description 17
- 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 16
- 210000004185 liver Anatomy 0.000 description 12
- 150000003626 triacylglycerols Chemical class 0.000 description 12
- 241000024188 Andala Species 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 235000012000 cholesterol Nutrition 0.000 description 8
- 241000196324 Embryophyta Species 0.000 description 7
- 102000004889 Interleukin-6 Human genes 0.000 description 7
- 108090001005 Interleukin-6 Proteins 0.000 description 7
- 239000000306 component Substances 0.000 description 7
- 230000006870 function Effects 0.000 description 7
- 229940100601 interleukin-6 Drugs 0.000 description 7
- 108060008682 Tumor Necrosis Factor Proteins 0.000 description 6
- 102000000852 Tumor Necrosis Factor-alpha Human genes 0.000 description 6
- 238000009825 accumulation Methods 0.000 description 6
- -1 carbon chain fatty acids Chemical class 0.000 description 6
- 201000010099 disease Diseases 0.000 description 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 6
- 230000004060 metabolic process Effects 0.000 description 6
- 241000699666 Mus <mouse, genus> Species 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 230000002829 reductive effect Effects 0.000 description 5
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 5
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 5
- 206010019708 Hepatic steatosis Diseases 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 230000002401 inhibitory effect Effects 0.000 description 4
- 210000005228 liver tissue Anatomy 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 210000001519 tissue Anatomy 0.000 description 4
- GOZMBJCYMQQACI-UHFFFAOYSA-N 6,7-dimethyl-3-[[methyl-[2-[methyl-[[1-[3-(trifluoromethyl)phenyl]indol-3-yl]methyl]amino]ethyl]amino]methyl]chromen-4-one;dihydrochloride Chemical compound Cl.Cl.C=1OC2=CC(C)=C(C)C=C2C(=O)C=1CN(C)CCN(C)CC(C1=CC=CC=C11)=CN1C1=CC=CC(C(F)(F)F)=C1 GOZMBJCYMQQACI-UHFFFAOYSA-N 0.000 description 3
- 208000008589 Obesity Diseases 0.000 description 3
- 206010012601 diabetes mellitus Diseases 0.000 description 3
- 235000004626 essential fatty acids Nutrition 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 230000002757 inflammatory effect Effects 0.000 description 3
- 230000037356 lipid metabolism Effects 0.000 description 3
- 235000020824 obesity Nutrition 0.000 description 3
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 description 3
- 230000000770 proinflammatory effect Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 208000024172 Cardiovascular disease Diseases 0.000 description 2
- 208000004930 Fatty Liver Diseases 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 101001076414 Mus musculus Interleukin-6 Proteins 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- MBMBGCFOFBJSGT-KUBAVDMBSA-N all-cis-docosa-4,7,10,13,16,19-hexaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 description 2
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000033228 biological regulation Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 235000005911 diet Nutrition 0.000 description 2
- 230000037213 diet Effects 0.000 description 2
- 208000010706 fatty liver disease Diseases 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- 230000028709 inflammatory response Effects 0.000 description 2
- 208000030159 metabolic disease Diseases 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 description 2
- LCPDWSOZIOUXRV-UHFFFAOYSA-N phenoxyacetic acid Chemical compound OC(=O)COC1=CC=CC=C1 LCPDWSOZIOUXRV-UHFFFAOYSA-N 0.000 description 2
- 239000002504 physiological saline solution Substances 0.000 description 2
- 230000008092 positive effect Effects 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 230000001502 supplementing effect Effects 0.000 description 2
- 230000009885 systemic effect Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229940126672 traditional medicines Drugs 0.000 description 2
- 210000004881 tumor cell Anatomy 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- HVCOBJNICQPDBP-UHFFFAOYSA-N 3-[3-[3,5-dihydroxy-6-methyl-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxydecanoyloxy]decanoic acid;hydrate Chemical compound O.OC1C(OC(CC(=O)OC(CCCCCCC)CC(O)=O)CCCCCCC)OC(C)C(O)C1OC1C(O)C(O)C(O)C(C)O1 HVCOBJNICQPDBP-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 102100034542 Acyl-CoA (8-3)-desaturase Human genes 0.000 description 1
- 108010071619 Apolipoproteins Proteins 0.000 description 1
- 102000007592 Apolipoproteins Human genes 0.000 description 1
- 240000004355 Borago officinalis Species 0.000 description 1
- 235000007689 Borago officinalis Nutrition 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 208000017667 Chronic Disease Diseases 0.000 description 1
- 108010073542 Delta-5 Fatty Acid Desaturase Proteins 0.000 description 1
- 238000008157 ELISA kit Methods 0.000 description 1
- 229930186217 Glycolipid Natural products 0.000 description 1
- 229940121710 HMGCoA reductase inhibitor Drugs 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 241000219925 Oenothera Species 0.000 description 1
- 235000004496 Oenothera biennis Nutrition 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 235000021319 Palmitoleic acid Nutrition 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 235000004347 Perilla Nutrition 0.000 description 1
- 244000124853 Perilla frutescens Species 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000009102 absorption Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 210000000577 adipose tissue Anatomy 0.000 description 1
- JAZBEHYOTPTENJ-JLNKQSITSA-N all-cis-5,8,11,14,17-icosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O JAZBEHYOTPTENJ-JLNKQSITSA-N 0.000 description 1
- 230000033115 angiogenesis Effects 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000002785 anti-thrombosis Effects 0.000 description 1
- 230000006907 apoptotic process Effects 0.000 description 1
- 235000021342 arachidonic acid Nutrition 0.000 description 1
- 229940114079 arachidonic acid Drugs 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 239000010474 borage seed oil Substances 0.000 description 1
- 210000005252 bulbus oculi Anatomy 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 230000033366 cell cycle process Effects 0.000 description 1
- 208000026106 cerebrovascular disease Diseases 0.000 description 1
- SECPZKHBENQXJG-UHFFFAOYSA-N cis-palmitoleic acid Natural products CCCCCCC=CCCCCCCCC(O)=O SECPZKHBENQXJG-UHFFFAOYSA-N 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 235000013367 dietary fats Nutrition 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 238000005906 dihydroxylation reaction Methods 0.000 description 1
- 235000020669 docosahexaenoic acid Nutrition 0.000 description 1
- 229940090949 docosahexaenoic acid Drugs 0.000 description 1
- 230000002526 effect on cardiovascular system Effects 0.000 description 1
- 230000001729 effect on metabolism Effects 0.000 description 1
- 235000020673 eicosapentaenoic acid Nutrition 0.000 description 1
- 229960005135 eicosapentaenoic acid Drugs 0.000 description 1
- JAZBEHYOTPTENJ-UHFFFAOYSA-N eicosapentaenoic acid Natural products CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O JAZBEHYOTPTENJ-UHFFFAOYSA-N 0.000 description 1
- IQLUYYHUNSSHIY-HZUMYPAESA-N eicosatetraenoic acid Chemical compound CCCCCCCCCCC\C=C\C=C\C=C\C=C\C(O)=O IQLUYYHUNSSHIY-HZUMYPAESA-N 0.000 description 1
- 235000020774 essential nutrients Nutrition 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000004129 fatty acid metabolism Effects 0.000 description 1
- 125000001924 fatty-acyl group Chemical group 0.000 description 1
- 235000004426 flaxseed Nutrition 0.000 description 1
- 235000012041 food component Nutrition 0.000 description 1
- 239000005428 food component Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 235000013402 health food Nutrition 0.000 description 1
- 235000004280 healthy diet Nutrition 0.000 description 1
- 235000009200 high fat diet Nutrition 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 230000013632 homeostatic process Effects 0.000 description 1
- 239000002471 hydroxymethylglutaryl coenzyme A reductase inhibitor Substances 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 230000036737 immune function Effects 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000037353 metabolic pathway Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 208000008338 non-alcoholic fatty liver disease Diseases 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 235000020660 omega-3 fatty acid Nutrition 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 150000003180 prostaglandins Chemical class 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229960004274 stearic acid Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 231100000240 steatosis hepatitis Toxicity 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 210000001835 viscera Anatomy 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
Landscapes
- Edible Oils And Fats (AREA)
Abstract
The invention provides edible plant blend oil for reducing hyperlipidemia, which belongs to the field of oil nutrition, and comprises 6-8% of GLA, 8-20% of DAG, 8-16% of MLCT and 3.25-6.5% of ALA in percentage by weight of various raw materials; the food plant blend oil provided by the invention is reasonable in collocation, and the synergistic effect between lipid concomitants is utilized, so that the food plant blend oil can achieve the effect of reducing blood fat, meets the expectations of consumers for healthy plant oil, and has good application value and market prospect; the invention does not contain any antioxidant and is prepared by blending pure natural edible oil.
Description
Technical Field
The invention belongs to the field of grease nutrition, and particularly relates to edible plant blend oil capable of reducing hyperlipidemia.
Background
Hyperlipidemia is a complex and persistent metabolic disorder that has posed a major threat to human health. The early stages of hyperlipidemia are usually free of obvious clinical symptoms, but their damage to the body is hidden, systemic. When endogenous lipid metabolism is disturbed or exogenous lipid is taken too much, blood lipid composition is markedly abnormal, and hyperlipidemia is formed. Hyperlipidemia including disturbed glycolipid metabolism and systemic homeostasis is a high risk factor for metabolic diseases such as obesity, diabetes, nonalcoholic fatty liver disease, and cardiovascular disease. However, the traditional medicines for the disease, such as phenoxyacetic acid, antioxidants, statins and the like, have certain side effects after being taken for a long time. Therefore, the development of green, healthy natural foods instead of traditional medicines is one of the methods for intervention in hyperlipidemia in the future, and the regulation of diet is also the most direct way to intervene or prevent diseases.
The grease is one of three essential nutrients for human body, mainly comprises triglyceride and trace active accompanying substances, can provide energy and essential fatty acid for the human body, and is vital to the healthy development of the human body. Such as gamma-linolenic acid (GLA), essential fatty acid of human body, can prevent fatty acid oxidation, and has blood lipid reducing effect; and GLA and derivative molecules thereof can also influence the expression of various genes involved in immune functions and apoptosis, and inhibit the tumor cell cycle process and tumor cell angiogenesis. Alpha-linolenic acid (ALA) can regulate blood lipid and blood sugar, reduce cholesterol, triglyceride, LDL and VLDL, raise HDL, and exert antithrombotic effect. Because a single oil is difficult to be rich in multiple nutritional ingredients, the vegetable blend oil is generated in order to make the edible oil more comprehensive in nutrition.
The relationship between edible oil and fat metabolism has shown that polyunsaturated fatty acids have a profound effect on liver fatty acid metabolism. This is probably because the physiological activity of dietary fat rich in polyunsaturated fatty acids affects serum and tissue lipid levels; borage oil (BSO) not only contains various active ingredients, but also contains GLA, and can play a role in reducing blood fat. The ALA-rich oil can reduce cholesterol and regulate lipid metabolism.
The Diglyceride (DAG) is a product obtained by esterifying two fatty acids in oil with glycerol (glycerin), and is simply called diglyceride or diglyceride. It has been shown that DAG has important functions in reducing excess fat in viscera, reducing blood esters in the body, inhibiting body weight gain, etc., and this function is achieved mainly by inhibiting accumulation of Triglycerides (TG) in the body by such substances.
MLCT is a novel class of structural lipids formed from the binding of medium carbon chain fatty acids (MCFA) and long carbon chain fatty acids (LCFA) to the same glycerol molecule. MLCT has great significance in controlling weight, body fat and improving metabolism of apolipoprotein, and is a health food for preventing and controlling obesity and other chronic diseases. Nowadays, the consumption level of people is increased, and the diseases related to fat digestion, absorption, metabolism and the like are increased, and research and discovery of high fat diet is usually accompanied by diseases such as obesity, diabetes, hyperlipidemia, certain cancers and the like, so people are focusing on modifying natural fat to produce medium-long carbon chain triglyceride (MLCT) so as to achieve the purpose of healthy diet.
At present, research on edible vegetable blend oils has not focused on different fatty acid glyceride restrictions. For example, chinese patent CN201911125017.9 discloses a blood lipid-lowering oil and a preparation method thereof, which selects only the use of chia seed oil to provide omega-3 unsaturated fatty acids, and does not mention different fatty acid compositions and control the ratio between different fatty acids. Chinese patent CN202210165144.7 discloses a preparation method of unsaturated fatty acid with weight-reducing and lipid-lowering effects, the main component of the fatty acid obtained by the method is polyunsaturated fatty acid linoleic acid, but the proportion of fatty acid glyceride of the product is not limited and hyperlipidemia cannot be relieved. Although chinese patent CN202211225531.1 discloses a fatty acid ester compound and a preparation method thereof, the structure of the fatty acid ester compound may include fatty acyl groups formed by dehydroxylation of oleic acid, palmitoleic acid, linoleic acid, linolenic acid, stearic acid, arachidonic acid, eicosatetraenoic acid, eicosapentaenoic acid or docosahexaenoic acid, there is still no limitation on the proportion of different fatty acid glycerides and no effect of reducing hyperlipidemia.
Disclosure of Invention
This section is intended to outline some aspects of embodiments of the invention and to briefly introduce some preferred embodiments. Some simplifications or omissions may be made in this section as well as in the description summary and in the title of the application, to avoid obscuring the purpose of this section, the description summary and the title of the invention, which should not be used to limit the scope of the invention.
The present invention has been made in view of the above and/or problems occurring in the prior art.
Therefore, the invention aims to overcome the defects in the prior art and provide the edible plant blend oil with the function of reducing the hyperlipidemia.
In order to solve the technical problems, the invention provides the following technical scheme: an edible vegetable blend oil with the function of reducing hyperlipidemia, wherein the content of fatty acid glycerol in a finished product is calculated by percentage, and the blend oil comprises 6-8% of GLA from borage, evening primrose and blackcurrant seed oil, 8-20% of DAG from soybean oil, peanut oil and rapeseed oil, 8-16% of MLCT from coconut oil and palm oil, and 3.25-6.5% of ALA from chia seeds, perilla seeds, flax seeds and peony seed oil.
As a preferable scheme of the plant blend oil, the invention comprises the following steps: fatty acid glycerides contained in the blend oil composition: GLA, DAG, MLCT, ALA are not exogenously added.
As a preferable scheme of the plant blend oil, the invention comprises the following steps: the edible plant blend oil comprises borage oil, evening primrose oil, blackcurrant seed oil, diglyceride oil, medium-long chain triglyceride oil, chia seed oil, perilla seed oil, linseed oil and peony seed oil.
As a preferable scheme of the plant blend oil, the invention comprises the following steps: the blend oil is not specified for the fatty acid glyceride content, but defines the numerical ranges of GLA 6.9%, DAG 10%, MLCT 14% and ALA 4.95%.
Still another object of the present invention is to overcome the deficiencies in the prior art and to provide a method for preparing edible vegetable blend oil with reduced hyperlipidemia, comprising,
and mixing the nutritional oil according to a proportion at room temperature, fully stirring to obtain mixed oil, and further filtering to obtain a product.
As a preferable scheme of the preparation method of the plant blend oil, the invention comprises the following steps: the stirring speed is 65r/min, the stirring time is 25min, and the filtering is 300 mesh filtering.
The invention further aims to overcome the defects in the prior art and provide the application of the edible plant blend oil with the function of reducing the hyperlipidemia in preparing the formula food with special medical application for patients with the hyperlipidemia.
The invention has the beneficial effects that:
(1) The invention provides edible plant blend oil with blood fat reducing function, which comprises the following raw materials, by weight, 6-8% of GLA, 8-20% of DAG, 8-16% of MLCT and 3.25-6.5% of ALA; wherein, the fatty acid such as GLA, DAG, MLCT, ALA and the like are not exogenously added.
(2) The food plant blend oil provided by the invention is reasonable in collocation, and the synergistic effect between lipid concomitants is utilized, so that the food plant blend oil can achieve the effect of reducing blood fat, meets the expectations of consumers for healthy plant oil, and has good application value and market prospect; the invention does not contain any antioxidant and is prepared by blending pure natural edible oil.
(3) The fatty acid composition with good fat component can rapidly provide energy, and unsaturated fatty acid has antioxidant capacity, so that the degree of attack of cells by free radicals can be relieved; the blend oil contains MLCT, is a nutrient substance with special physiological functions, has a unique metabolic pathway in human body, can provide energy, and has the functions of inhibiting fat accumulation in the body, improving intestinal morphology and structure, regulating immunity, preventing and treating diseases and the like; DAG is a trace component of natural vegetable oil and fat, is a well-known and safe food component, and has positive effects in inhibiting accumulation of neutral fat, relieving diabetes mellitus, preventing or treating diseases caused by hyperlipidemia and cardiovascular and cerebrovascular diseases, and the like; the GLA, ALA and other unsaturated fatty acids can have good regulation effect on metabolism of human bodies, and have obvious blood fat reducing and anti-inflammatory effects. But only when GLA content is 6-8%, DAG content is 8-20%, MLCT content is 8-16%, ALA content is 3.25-6.5% can significant effect be achieved. For example, example 1, having 6.9% gla, 10% DAG, 14% MLCT and 4.95% ALA, shows the best lipid lowering effect among the selected experimental groups; an effect outside this range is poor, for example, comparative example 1, gla content is 3.75%, lower than recommended value content; in comparative example 2, the MLCT content was 6%, which was lower than the recommended value content, and from the experimental result, the lipid-lowering effect was not significant compared to example 1. This may be because different fatty acid glycerides have a synergistic effect in a certain concentration range, and the synergistic effect may be lost or antagonism may occur beyond this range, so that the effect of preventing hyperlipidemia is poor.
(4) The invention can be used as the fat component part of the special full-nutrition formula food of the formula food with special medical application for patients with hyperlipidemia, and can also be used as the fat component in the nutrient group of the non-full-nutrition formula food for patients with hyperlipidemia to be matched with other formula food with special medical application or common food; the blend oil provided by the invention does not bring any potential safety hazard to patients with hyperlipidemia.
Drawings
In order to more clearly illustrate the technical solutions of the embodiments of the present invention, the drawings that are needed in the description of the embodiments will be briefly described below, it being obvious that the drawings in the following description are only some embodiments of the present invention, and that other drawings may be obtained according to these drawings without inventive effort for a person skilled in the art. Wherein:
FIG. 1 is a graph showing the effect of vegetable oil blends in different proportions on weight change in mice according to the examples of the present invention.
FIG. 2 is a graph showing the effect of vegetable oil blends in different proportions on serum and liver lipid levels in mice in accordance with the examples of the present invention; wherein A is the influence of the vegetable blend oil with different proportions on the content of serum TC, B is the influence of the vegetable blend oil with different proportions on the content of serum TG, C is the influence of the vegetable blend oil with different proportions on the content of liver TC, and D is the influence of the vegetable blend oil with different proportions on the content of liver TG.
FIG. 3 is a graph showing the effect of the mixed vegetable oil in different proportions on the serum inflammatory factor of mice in the embodiment of the invention; wherein A is the influence of the vegetable blend oil with different proportions on the content of serum mouse interleukin-6 (IL-6), and B is the influence of the vegetable blend oil with different proportions on the content of serum tumor necrosis factor-alpha (TNF-alpha).
Detailed Description
In order that the above-recited objects, features and advantages of the present invention will become more apparent, a more particular description of the invention will be rendered by reference to specific embodiments thereof which are illustrated in the appended drawings.
In the following description, numerous specific details are set forth in order to provide a thorough understanding of the present invention, but the present invention may be practiced in other ways other than those described herein, and persons skilled in the art will readily appreciate that the present invention is not limited to the specific embodiments disclosed below.
Further, reference herein to "one embodiment" or "an embodiment" means that a particular feature, structure, or characteristic can be included in at least one implementation of the invention. The appearances of the phrase "in one embodiment" in various places in the specification are not necessarily all referring to the same embodiment, nor are separate or alternative embodiments mutually exclusive of other embodiments.
The edible vegetable blend oil is prepared by selecting high-quality edible vegetable oil, adding each vegetable oil into a stirring tank according to a certain proportion, stirring at the stirring speed of 65r/min for 25min at room temperature, and filtering to obtain the edible vegetable blend oil, wherein the filtering is performed by a 300-mesh screen, and the vegetable oil raw materials are all common commercial products.
Example 1
Raw materials: blackcurrant seed oil (GLA content 15%), soybean oil diglyceride oil (DAG content 40%), rapeseed oil MLCT oil (MLCT content 70%), linseed oil (ALA content 55%), and the above-mentioned high-quality edible blackcurrant seed oil 46%, diglyceride oil 25%, MLCT oil 20% and linseed oil 9% were added into a reaction kettle.
Mixing at room temperature of 25deg.C, stirring for 25min at a stirring speed of 65r/min, and filtering with 300 mesh net to obtain mixed oil.
Comparative example 1
Blend oil: high-quality edible blackcurrant seed oil 25%, diglyceride oil 46%, MLCT oil 20% and linseed oil 9% are selected and added into a reaction kettle.
The difference is that: the GLA content provided by the blend oil is lower than the recommended range of the patent.
Mixing at room temperature of 25deg.C, stirring for 25min at a stirring speed of 65r/min, and filtering with 300 mesh net to obtain mixed oil.
Comparative example 2
Blend oil: the high-quality edible blackcurrant seed oil 46%, diglyceride oil 15%, soybean oil 10%, MLCT oil 20% and linseed oil 9% are selected and added into a reaction kettle.
The difference is that: the content of the diglyceride provided by the blend oil is lower than the recommended range of the patent, so that the consistency of the fatty acid composition of the blend oil is ensured, and soybean oil serving as the raw oil of the diglyceride is used for supplementing. Mixing at room temperature of 25deg.C, stirring for 25min at a stirring speed of 65r/min, and filtering with 300 mesh net to obtain mixed oil.
Comparative example 3
Blend oil: the high-quality edible blackcurrant seed oil 46%, diglyceride oil 25%, MLCT oil 8%, rapeseed oil 12% and linseed oil 9% are selected and added into a reaction kettle.
The difference is that: the MLCT content provided by the blend oil is lower than the recommended range of the patent, so that the consistency of the fatty acid composition of the blend oil is ensured, and the rapeseed oil serving as the MLCT raw oil is used for supplementing.
Mixing at room temperature of 25deg.C, stirring for 25min at a stirring speed of 65r/min, and filtering with 300 mesh net to obtain mixed oil.
Comparative example 4
Blend oil: high-quality edible blackcurrant seed oil 50%, diglyceride oil 25%, MLCT oil 20% and linseed oil 5% are selected and added into a reaction kettle.
The difference is that: the ALA content provided by the blend oil is lower than the recommended range of the patent. Mixing at room temperature of 25deg.C, stirring for 25min at a stirring speed of 65r/min, and filtering with 300 mesh net to obtain mixed oil.
Comparative example 5
Blend oil: high-quality edible blackcurrant seed oil 55%, diglyceride oil 30%, MLCT oil 23% and linseed oil 10% are selected and added into a reaction kettle.
The difference is that: the GLA content provided by the blend oil is higher than the recommended range of the patent. Mixing at room temperature of 25deg.C, stirring for 25min at a stirring speed of 65r/min, and filtering with 300 mesh net to obtain mixed oil.
Comparative example 6
Blend oil: high-quality edible blackcurrant seed oil 29%, diglyceride oil 55%, MLCT oil 10% and linseed oil 6% are selected and added into a reaction kettle.
The difference is that: the DAG content provided by the blend oil is higher than the recommended scope of the patent. Mixing at room temperature of 25deg.C, stirring for 25min at a stirring speed of 65r/min, and filtering with 300 mesh net to obtain mixed oil.
Comparative example 7
Blend oil: selecting 44% of high-quality edible blackcurrant seed oil, 20% of diglyceride oil, 28% of MLCT oil and 8% of linseed oil, and adding into a reaction kettle.
The difference is that: the MLCT content provided by the blend oil is higher than the recommended range of the patent. Mixing at room temperature of 25deg.C, stirring for 25min at a stirring speed of 65r/min, and filtering with 300 mesh net to obtain mixed oil.
Comparative example 8
Blend oil: 40% of high-quality edible blackcurrant seed oil, 25% of diglyceride oil, 20% of MLCT oil and 15% of linseed oil are selected and added into a reaction kettle.
The difference is that: the ALA content provided by the blend oil is higher than the recommended range of the patent. Mixing at room temperature of 25deg.C, stirring for 25min at a stirring speed of 65r/min, and filtering with 300 mesh net to obtain mixed oil.
According to national standards, GLA, DAG, MLCT and ALA contents in the blend oil were detected by gas chromatography and high performance liquid chromatography, as shown in Table 1.
Table 1 percentage of essential fatty acid glycerides for each example
The invention utilizes an animal high-fat model to evaluate the lipid consumption of a C57BL6J male mouse, and the specific method is as follows:
(1) Feed oil
The blend oils of example 1 and comparative examples 1 to 8 above were prepared as experimental diets, wherein GLA, DAG, MLCT and ALA contents are shown in table 1.
(2) Grouping animals
88C 57 male mice of 4-6 weeks old were selected, 8 were randomly selected as a blank control group (CON), and the remaining 80 were subjected to high-fat modeling, and after the high-fat model was established, they were randomly divided into 11 groups of high-fat model groups (HFD), example 1 and comparative examples 1-8. Wherein, the control group mice are fed with common feed, and the high-fat group mice are fed with high-fat feed. The general feed and the high fat feed formulations are shown in tables 2 and 3.
After the mice are separated into cages, natural illumination is carried out, and the mice can eat and drink water freely; the indoor environment temperature is controlled at 22+/-2 ℃ and the humidity is about 60 percent. Mice were kept for 12 weeks, weighed 1 time a week, and weight parameters were recorded.
(3) Inspection index and processing
After the test, the mice are fasted for 12 hours, eyeballs are taken for blood collection, serum is separated (3000 r/m and centrifuged for 10 min), the mice are killed after neck breaking, the livers are rapidly taken out, quick frozen by liquid nitrogen, and the mice are stored in a freezer at-80 ℃ for standby.
(3) Preparation of liver tissue homogenate
Rinsing fresh liver tissue in pre-cooled physiological saline, removing blood, wiping the filter paper, accurately weighing 0.5g (accurate to 0.0001 g) of tissue at the same part, preparing 10% tissue homogenate (w/v) in pre-cooled sterilized physiological saline ice bath, centrifuging the tissue homogenate at 4000r/m for 10min, taking supernatant, sub-packaging, and preserving at-20 ℃ for later use.
(4) Influence of blend oil with different compositions on blood fat and liver of mice
Serum and liver samples of mice were taken and Total Cholesterol (TC) and Triglyceride (TG) levels in the serum and liver of mice were determined using a test kit.
(5) Effect of blend oils of different compositions on TNF-alpha and IL-6 in serum of hyperlipidemic mice
The mouse liver tissue supernatant is weighed, and the two factor contents of the mouse liver tissue are respectively measured according to the steps of a tumor necrosis factor-alpha (TNF-alpha) and a mouse interleukin-6 (IL-6) ELISA kit instruction book.
Table 2 general feed formulation
Table 3 high fat feed formulation
FIG. 1 shows growth curves of mice, and the establishment of a high-fat model of the mice was performed in the first 8 weeks, and the establishment of the high-fat model was successful from the eighth week. The mice were fed with mixed vegetable oil feed in different proportions for 12 weeks. From the figure, it can be seen that the higher fat group of example 1 had significantly decreased weight, while the mice of each group of the comparative example had slightly decreased weight.
Effects of blend vegetable oils in different ratios on TC and TG content in mouse serum and liver:
as can be seen from fig. 2-a and 2-C, compared with the control group, the total cholesterol content of the high-fat building block is obviously accumulated, and after the dry state of the blend oil administration in different proportions, the total cholesterol content of the experimental group is reduced, and the total cholesterol accumulation of the experimental group is obviously improved by about 30% in the embodiment 1.
In contrast, the improvement effect of each group of the comparative examples on total cholesterol was not significant. Example 1 plant blend oil was GLA, DAG, MLCT and ALA ranges were within our limits and the proportions in the comparative groups were outside our limits. The results show that the blend oil has remarkable beneficial effects on the metabolism of serum and liver total cholesterol in mice only under the limited blend oil proportion range, and can play a role in promoting the metabolism of liver fatty acids.
Triglycerides are metabolized primarily by the liver, and high levels of triglycerides cause fatty liver-like changes, leading to increased incidence of fatty liver. As can be seen from fig. 2-B and 2-C, the triglyceride content of the modeling group was significantly accumulated compared with the control group, and the triglyceride content in the serum and liver of the mice was reduced after the administration of the blend oil in different proportions, wherein example 1 was most significant, while the TG content was not significantly affected by each of the control groups. The blend oil of example 1 showed the most remarkable improvement effect on TG accumulation, indicating that the fatty acid composition ratio had a positive effect on lipid metabolism. Compared with example 1, the GLA, DAG, MLCT and ALA ranges in the comparative examples are outside the range defined by the patent, so that the TG relieving effect is poor, and only GLA, DAG, MLCT and ALA components are in the proportion range defined by the patent from the side.
TNF-alpha and IL-6 are pro-inflammatory factors, and the content of the pro-inflammatory factors can primarily reflect the inflammatory change condition of the organism. As shown in FIGS. 3-A and 3-B, the levels of TNF- α and IL-6 in the serum of the model group were significantly increased as compared to the control group, indicating that hyperlipidemia would lead to the occurrence of inflammatory responses in the body. The levels of TNF- α and IL-6 were significantly reduced in example 1 compared to the modeling modules, whereas the levels of TNF- α and IL-6 were not significantly reduced in the comparative examples. Because the proportion of the blend oil in each group of the comparative example is outside the proportion range defined by us, the blend oil within the limit of the patent can be obtained to obviously reduce inflammatory factors in mouse serum, thereby improving hyperlipidemia.
Taken together, GLA, DAG, MLCT and ALA components only have certain improvement effects on accumulation of TC and TG in serum and liver of mice within the limit of the patent, and can obviously relieve inflammatory response.
Comparative examples 1 to 4 were poor in lipid-lowering effect due to insufficient amounts of these active ingredients to initiate lipid-lowering signals due to the GLA, DAG, MLCT and ALA content in the blend oil being too low. In contrast, the blend oil of comparative example 5 has a GLA content exceeding the range defined in this patent, and a certain amount of GLA is passed through Δ5 desaturase to produce proinflammatory factors such as prostaglandin 2. Comparative examples 6 and 7 show that the DAG and MLCT contents are not proportional to the lipid-lowering effect, and that too high a content does not make the lipid-lowering effect more remarkable. For comparative example 8, too high an ALA content increased the unsaturated fatty acid content in the blend oil, so that oxidation occurred in the body, and the generated free radicals attack the body to produce an inflammatory reaction. Finally, GLA, DAG, MLCT and ALA contents only exert the best lipid-lowering effect within the limits defined in this patent.
It should be noted that the above embodiments are only for illustrating the technical solution of the present invention and not for limiting the same, and although the present invention has been described in detail with reference to the preferred embodiments, it should be understood by those skilled in the art that the technical solution of the present invention may be modified or substituted without departing from the spirit and scope of the technical solution of the present invention, and it should be covered in the scope of the present invention.
Claims (10)
1. An edible plant blend oil with the function of reducing hyperlipidemia is characterized in that: the blend oil comprises, by volume, 40-53.3% of gamma-linolenic acid GLA-derived vegetable oil, 20-50% of diglyceride DAG-derived vegetable oil, 11.43-22.86% of medium-long chain triglyceride MLCT-derived vegetable oil, and 5.9-11.81% of alpha-linolenic acid ALA-derived vegetable oil.
2. The edible vegetable blend oil with hyperlipidemia reducing function according to claim 1, wherein: the content of the fatty acid glycerol in the finished product of the blend oil is calculated by percentage, and the blend oil comprises 6-8% of GLA, 8-20% of DAG, 8-16% of MLCT and 3.25-6.5% of ALA.
3. The edible vegetable blend oil with hyperlipidemia reducing function according to claim 1, wherein: the GLA is derived from one or more of borage oil, evening primrose oil, blackcurrant seed oil and algae oil.
4. The edible vegetable blend oil with hyperlipidemia reduction function according to claim 1 or 2, wherein: the DAG-derived oil comprises one or more of camellia oil, olive oil, soybean oil, corn oil, safflower seed oil, cotton seed oil and rapeseed oil.
5. The edible vegetable blend oil with hyperlipidemia reducing function according to claim 1, wherein: the medium MLCT-derived oil comprises one or more of coconut oil extract, lauric acid triglyceride, palm kernel oil extract, capric acid triglyceride, caprylic acid triglyceride, palm oil, rice bran oil, algae oil, coconut oil, high oleic sunflower seed oil, soybean oil and rapeseed oil.
6. The edible vegetable blend oil with hyperlipidemia reducing function according to claim 1, wherein: the ALA is derived from one or more of chia seed oil, perilla seed oil, linseed oil and peony seed oil.
7. The edible vegetable blend oil with hyperlipidemia reduction function according to any one of claims 1 to 3, 5 or 6, wherein: none of the GLA, DAG, MLCT, ALA was exogenously added.
8. The method for preparing the edible plant blend oil with the function of reducing hyperlipidemia according to any one of claims 1 to 7, which is characterized in that: mixing the nutritional oil according to a proportion at room temperature, fully stirring to obtain mixed oil, and further filtering to obtain a product.
9. The method of preparing as claimed in claim 8, wherein: the stirring speed of the stirring is 65r/min, and the stirring time is 25min; the filtration was 300 mesh filtration.
10. Use of the edible vegetable blend oil with hyperlipidemia reduction function according to any one of claims 1 to 3, 5 or 6 for preparing a formulation food for special medical use for hyperlipidemia patients.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202410048746.3A CN117694408A (en) | 2024-01-12 | 2024-01-12 | Edible plant blend oil capable of reducing hyperlipidemia |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202410048746.3A CN117694408A (en) | 2024-01-12 | 2024-01-12 | Edible plant blend oil capable of reducing hyperlipidemia |
Publications (1)
Publication Number | Publication Date |
---|---|
CN117694408A true CN117694408A (en) | 2024-03-15 |
Family
ID=90153591
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202410048746.3A Pending CN117694408A (en) | 2024-01-12 | 2024-01-12 | Edible plant blend oil capable of reducing hyperlipidemia |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN117694408A (en) |
-
2024
- 2024-01-12 CN CN202410048746.3A patent/CN117694408A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103891924B (en) | A kind of ready-mixed oil containing corn oil and preparation method thereof | |
CN103444911A (en) | Medicinal and edible health care blending oil | |
KR101362989B1 (en) | Lipid-improving agent and composition containing lipid-improving agent | |
US20100144878A1 (en) | Nutritional supplement or functional food comprising oil combination | |
CN101690526A (en) | Blend oil with proportional fatty acid prepared by walnut oil and other plant oils | |
WO2022156273A1 (en) | Functional edible oil, preparation method therefor and use thereof | |
CN109965031B (en) | Formula of fat component of formula food for special medical application for inflammatory bowel diseases and preparation method | |
CN101810226A (en) | Fatty acid component balanced children type nutrition blended oil containing multiple active ingredients | |
CN1806642A (en) | Nutritious health-caring vegetable blend oil | |
CN105707292A (en) | Camellia blend oil suitable for infants | |
CN103380826A (en) | Functional fat with cardiovascular and cerebrovascular disease risk factor prevention function and preparation method thereof | |
CN112273651A (en) | Soft capsule rich in microalgae oil DHA, DPA and EPA and preparation method thereof | |
CN112772924A (en) | Special grease base oil for functional food and preparation method and application thereof | |
CN101099562A (en) | Omega-3 unsaturated fatty acids appetizer oil and producing method and application thereof | |
JP2016202001A (en) | Fat composition | |
CN108782786B (en) | Healthy edible black garlic blend oil and preparation method thereof | |
CN117694408A (en) | Edible plant blend oil capable of reducing hyperlipidemia | |
CN105028680A (en) | Blend oil meeting essential fatty acid reference intake of Chinese residents | |
CN106260120B (en) | A kind of selenium-rich edible blend oil and preparation method thereof | |
CN112219902B (en) | Oil composition suitable for foods for infants of low-age | |
CN103766507A (en) | Edible oil with health-care function | |
CN109805108B (en) | Special medical application formula food fat component for inflammatory bowel diseases and preparation method thereof | |
Choudhary et al. | Blended rice bran and olive oil–moving towards a new cooking media | |
CN111513145A (en) | Edible blend oil containing lutein ester and preparation method thereof | |
CN117814321B (en) | Composite grease of chlamydomonas reinhardtii oil and corn diglyceride oil and preparation process thereof |
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 |