CN116195747A - Composite dietary fiber nutrition powder for regulating blood glucose metabolism and preparation method and application thereof - Google Patents
Composite dietary fiber nutrition powder for regulating blood glucose metabolism and preparation method and application thereof Download PDFInfo
- Publication number
- CN116195747A CN116195747A CN202310243397.6A CN202310243397A CN116195747A CN 116195747 A CN116195747 A CN 116195747A CN 202310243397 A CN202310243397 A CN 202310243397A CN 116195747 A CN116195747 A CN 116195747A
- Authority
- CN
- China
- Prior art keywords
- dietary fiber
- powder
- composite
- wheat bran
- inulin
- 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.)
- Granted
Links
- 235000013325 dietary fiber Nutrition 0.000 title claims abstract description 87
- 239000000843 powder Substances 0.000 title claims abstract description 54
- 235000016709 nutrition Nutrition 0.000 title claims abstract description 35
- 239000002131 composite material Substances 0.000 title claims abstract description 29
- 230000035764 nutrition Effects 0.000 title claims abstract description 23
- 239000008280 blood Substances 0.000 title claims abstract description 22
- 210000004369 blood Anatomy 0.000 title claims abstract description 22
- 230000001105 regulatory effect Effects 0.000 title claims abstract description 20
- 238000002360 preparation method Methods 0.000 title claims abstract description 17
- 230000004153 glucose metabolism Effects 0.000 title claims abstract description 9
- 235000015099 wheat brans Nutrition 0.000 claims abstract description 37
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims abstract description 36
- JYJIGFIDKWBXDU-MNNPPOADSA-N inulin Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)OC[C@]1(OC[C@]2(OC[C@]3(OC[C@]4(OC[C@]5(OC[C@]6(OC[C@]7(OC[C@]8(OC[C@]9(OC[C@]%10(OC[C@]%11(OC[C@]%12(OC[C@]%13(OC[C@]%14(OC[C@]%15(OC[C@]%16(OC[C@]%17(OC[C@]%18(OC[C@]%19(OC[C@]%20(OC[C@]%21(OC[C@]%22(OC[C@]%23(OC[C@]%24(OC[C@]%25(OC[C@]%26(OC[C@]%27(OC[C@]%28(OC[C@]%29(OC[C@]%30(OC[C@]%31(OC[C@]%32(OC[C@]%33(OC[C@]%34(OC[C@]%35(OC[C@]%36(O[C@@H]%37[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O%37)O)[C@H]([C@H](O)[C@@H](CO)O%36)O)[C@H]([C@H](O)[C@@H](CO)O%35)O)[C@H]([C@H](O)[C@@H](CO)O%34)O)[C@H]([C@H](O)[C@@H](CO)O%33)O)[C@H]([C@H](O)[C@@H](CO)O%32)O)[C@H]([C@H](O)[C@@H](CO)O%31)O)[C@H]([C@H](O)[C@@H](CO)O%30)O)[C@H]([C@H](O)[C@@H](CO)O%29)O)[C@H]([C@H](O)[C@@H](CO)O%28)O)[C@H]([C@H](O)[C@@H](CO)O%27)O)[C@H]([C@H](O)[C@@H](CO)O%26)O)[C@H]([C@H](O)[C@@H](CO)O%25)O)[C@H]([C@H](O)[C@@H](CO)O%24)O)[C@H]([C@H](O)[C@@H](CO)O%23)O)[C@H]([C@H](O)[C@@H](CO)O%22)O)[C@H]([C@H](O)[C@@H](CO)O%21)O)[C@H]([C@H](O)[C@@H](CO)O%20)O)[C@H]([C@H](O)[C@@H](CO)O%19)O)[C@H]([C@H](O)[C@@H](CO)O%18)O)[C@H]([C@H](O)[C@@H](CO)O%17)O)[C@H]([C@H](O)[C@@H](CO)O%16)O)[C@H]([C@H](O)[C@@H](CO)O%15)O)[C@H]([C@H](O)[C@@H](CO)O%14)O)[C@H]([C@H](O)[C@@H](CO)O%13)O)[C@H]([C@H](O)[C@@H](CO)O%12)O)[C@H]([C@H](O)[C@@H](CO)O%11)O)[C@H]([C@H](O)[C@@H](CO)O%10)O)[C@H]([C@H](O)[C@@H](CO)O9)O)[C@H]([C@H](O)[C@@H](CO)O8)O)[C@H]([C@H](O)[C@@H](CO)O7)O)[C@H]([C@H](O)[C@@H](CO)O6)O)[C@H]([C@H](O)[C@@H](CO)O5)O)[C@H]([C@H](O)[C@@H](CO)O4)O)[C@H]([C@H](O)[C@@H](CO)O3)O)[C@H]([C@H](O)[C@@H](CO)O2)O)[C@@H](O)[C@H](O)[C@@H](CO)O1 JYJIGFIDKWBXDU-MNNPPOADSA-N 0.000 claims abstract description 33
- 229920001202 Inulin Polymers 0.000 claims abstract description 31
- 229940029339 inulin Drugs 0.000 claims abstract description 31
- 150000004666 short chain fatty acids Chemical class 0.000 claims abstract description 24
- 230000000968 intestinal effect Effects 0.000 claims abstract description 16
- 230000000694 effects Effects 0.000 claims abstract description 13
- 229920001542 oligosaccharide Polymers 0.000 claims abstract description 10
- 150000002482 oligosaccharides Chemical class 0.000 claims abstract description 10
- 239000002207 metabolite Substances 0.000 claims abstract description 8
- 239000002994 raw material Substances 0.000 claims abstract description 8
- 230000033228 biological regulation Effects 0.000 claims abstract description 6
- 230000004060 metabolic process Effects 0.000 claims abstract description 6
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 22
- 235000021391 short chain fatty acids Nutrition 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 15
- 239000000047 product Substances 0.000 claims description 15
- 235000019260 propionic acid Nutrition 0.000 claims description 11
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 10
- 108090000790 Enzymes Proteins 0.000 claims description 9
- 102000004190 Enzymes Human genes 0.000 claims description 9
- 229940088598 enzyme Drugs 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 9
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 8
- 239000008103 glucose Substances 0.000 claims description 8
- 239000004375 Dextrin Substances 0.000 claims description 7
- 229920001353 Dextrin Polymers 0.000 claims description 7
- 235000019425 dextrin Nutrition 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- UQZIYBXSHAGNOE-USOSMYMVSA-N Stachyose Natural products O(C[C@H]1[C@@H](O)[C@H](O)[C@H](O)[C@@H](O[C@@]2(CO)[C@H](O)[C@@H](O)[C@@H](CO)O2)O1)[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](CO[C@@H]2[C@@H](O)[C@@H](O)[C@@H](O)[C@H](CO)O2)O1 UQZIYBXSHAGNOE-USOSMYMVSA-N 0.000 claims description 6
- FTSSQIKWUOOEGC-RULYVFMPSA-N fructooligosaccharide Chemical compound OC[C@H]1O[C@@](CO)(OC[C@@]2(OC[C@@]3(OC[C@@]4(OC[C@@]5(OC[C@@]6(OC[C@@]7(OC[C@@]8(OC[C@@]9(OC[C@@]%10(OC[C@@]%11(O[C@H]%12O[C@H](CO)[C@@H](O)[C@H](O)[C@H]%12O)O[C@H](CO)[C@@H](O)[C@@H]%11O)O[C@H](CO)[C@@H](O)[C@@H]%10O)O[C@H](CO)[C@@H](O)[C@@H]9O)O[C@H](CO)[C@@H](O)[C@@H]8O)O[C@H](CO)[C@@H](O)[C@@H]7O)O[C@H](CO)[C@@H](O)[C@@H]6O)O[C@H](CO)[C@@H](O)[C@@H]5O)O[C@H](CO)[C@@H](O)[C@@H]4O)O[C@H](CO)[C@@H](O)[C@@H]3O)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@@H](O)[C@@H]1O FTSSQIKWUOOEGC-RULYVFMPSA-N 0.000 claims description 6
- 229940107187 fructooligosaccharide Drugs 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000002244 precipitate Substances 0.000 claims description 6
- 230000001737 promoting effect Effects 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- UQZIYBXSHAGNOE-XNSRJBNMSA-N stachyose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO[C@@H]3[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O3)O)O2)O)O1 UQZIYBXSHAGNOE-XNSRJBNMSA-N 0.000 claims description 6
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims description 6
- 235000013305 food Nutrition 0.000 claims description 5
- 230000036541 health Effects 0.000 claims description 5
- 239000012153 distilled water Substances 0.000 claims description 4
- 230000003914 insulin secretion Effects 0.000 claims description 4
- 238000004806 packaging method and process Methods 0.000 claims description 4
- 108091005658 Basic proteases Proteins 0.000 claims description 3
- 108010073178 Glucan 1,4-alpha-Glucosidase Proteins 0.000 claims description 3
- 102000004139 alpha-Amylases Human genes 0.000 claims description 3
- 108090000637 alpha-Amylases Proteins 0.000 claims description 3
- 229940024171 alpha-amylase Drugs 0.000 claims description 3
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 claims description 3
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 claims description 3
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 claims description 3
- 238000009835 boiling Methods 0.000 claims description 3
- 230000009849 deactivation Effects 0.000 claims description 3
- 238000004108 freeze drying Methods 0.000 claims description 3
- 238000000227 grinding Methods 0.000 claims description 3
- 230000000415 inactivating effect Effects 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000007873 sieving Methods 0.000 claims description 3
- 235000021255 galacto-oligosaccharides Nutrition 0.000 claims description 2
- 150000003271 galactooligosaccharides Chemical class 0.000 claims description 2
- DLRVVLDZNNYCBX-RTPHMHGBSA-N isomaltose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)C(O)O1 DLRVVLDZNNYCBX-RTPHMHGBSA-N 0.000 claims description 2
- 206010012601 diabetes mellitus Diseases 0.000 abstract description 13
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract description 6
- 230000002265 prevention Effects 0.000 abstract description 2
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000002609 medium Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- 241000699670 Mus sp. Species 0.000 description 8
- 238000012216 screening Methods 0.000 description 8
- 238000002474 experimental method Methods 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 235000005911 diet Nutrition 0.000 description 6
- 238000000855 fermentation Methods 0.000 description 6
- 230000004151 fermentation Effects 0.000 description 6
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 6
- 244000005700 microbiome Species 0.000 description 6
- 210000001035 gastrointestinal tract Anatomy 0.000 description 5
- 230000037213 diet Effects 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 229910021642 ultra pure water Inorganic materials 0.000 description 4
- 239000012498 ultrapure water Substances 0.000 description 4
- 102000004877 Insulin Human genes 0.000 description 3
- 108090001061 Insulin Proteins 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 230000002550 fecal effect Effects 0.000 description 3
- 238000000338 in vitro Methods 0.000 description 3
- 229940125396 insulin Drugs 0.000 description 3
- 210000002429 large intestine Anatomy 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 210000001072 colon Anatomy 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 230000000378 dietary effect Effects 0.000 description 2
- 150000002016 disaccharides Chemical class 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 210000004185 liver Anatomy 0.000 description 2
- 230000000813 microbial effect Effects 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 244000052769 pathogen Species 0.000 description 2
- 230000001717 pathogenic effect Effects 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 210000000813 small intestine Anatomy 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 208000031648 Body Weight Changes Diseases 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 208000027244 Dysbiosis Diseases 0.000 description 1
- 108090000604 Hydrolases Proteins 0.000 description 1
- 102000004157 Hydrolases Human genes 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 206010022489 Insulin Resistance Diseases 0.000 description 1
- ABSPRNADVQNDOU-UHFFFAOYSA-N Menaquinone 1 Natural products C1=CC=C2C(=O)C(CC=C(C)C)=C(C)C(=O)C2=C1 ABSPRNADVQNDOU-UHFFFAOYSA-N 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 238000011360 adjunctive therapy Methods 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 239000003472 antidiabetic agent Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000009704 beneficial physiological effect Effects 0.000 description 1
- 239000003833 bile salt Substances 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 230000004579 body weight change Effects 0.000 description 1
- 235000021152 breakfast Nutrition 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 210000004534 cecum Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000001684 chronic effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 229940097265 cysteamine hydrochloride Drugs 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
- 229910000396 dipotassium phosphate Inorganic materials 0.000 description 1
- 235000019797 dipotassium phosphate Nutrition 0.000 description 1
- 208000016097 disease of metabolism Diseases 0.000 description 1
- 230000007140 dysbiosis Effects 0.000 description 1
- 230000037149 energy metabolism Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000001610 euglycemic effect Effects 0.000 description 1
- 238000013401 experimental design Methods 0.000 description 1
- 230000004129 fatty acid metabolism Effects 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 235000013376 functional food Nutrition 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 244000005709 gut microbiome Species 0.000 description 1
- BTIJJDXEELBZFS-QDUVMHSLSA-K hemin Chemical compound CC1=C(CCC(O)=O)C(C=C2C(CCC(O)=O)=C(C)\C(N2[Fe](Cl)N23)=C\4)=N\C1=C/C2=C(C)C(C=C)=C3\C=C/1C(C)=C(C=C)C/4=N\1 BTIJJDXEELBZFS-QDUVMHSLSA-K 0.000 description 1
- 229940025294 hemin Drugs 0.000 description 1
- 150000004688 heptahydrates Chemical class 0.000 description 1
- 150000004687 hexahydrates Chemical class 0.000 description 1
- 230000007236 host immunity Effects 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 201000001421 hyperglycemia Diseases 0.000 description 1
- 229940126904 hypoglycaemic agent Drugs 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 208000028774 intestinal disease Diseases 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 208000030159 metabolic disease Diseases 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 230000008506 pathogenesis Effects 0.000 description 1
- 230000007119 pathological manifestation Effects 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 239000008055 phosphate buffer solution Substances 0.000 description 1
- SHUZOJHMOBOZST-UHFFFAOYSA-N phylloquinone Natural products CC(C)CCCCC(C)CCC(C)CCCC(=CCC1=C(C)C(=O)c2ccccc2C1=O)C SHUZOJHMOBOZST-UHFFFAOYSA-N 0.000 description 1
- MBWXNTAXLNYFJB-NKFFZRIASA-N phylloquinone Chemical compound C1=CC=C2C(=O)C(C/C=C(C)/CCC[C@H](C)CCC[C@H](C)CCCC(C)C)=C(C)C(=O)C2=C1 MBWXNTAXLNYFJB-NKFFZRIASA-N 0.000 description 1
- 235000019175 phylloquinone Nutrition 0.000 description 1
- 239000011772 phylloquinone Substances 0.000 description 1
- 229960001898 phytomenadione Drugs 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- 235000013406 prebiotics Nutrition 0.000 description 1
- 239000013630 prepared media Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
Images
Classifications
-
- 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
- A23L33/20—Reducing nutritive value; Dietetic products with reduced nutritive value
- A23L33/21—Addition of substantially indigestible substances, e.g. dietary fibres
-
- 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
- A23L33/125—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives containing carbohydrate syrups; containing sugars; containing sugar alcohols; containing starch hydrolysates
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/702—Oligosaccharides, i.e. having three to five saccharide radicals attached to each other by glycosidic linkages
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/733—Fructosans, e.g. inulin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- 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
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P60/00—Technologies relating to agriculture, livestock or agroalimentary industries
- Y02P60/80—Food processing, e.g. use of renewable energies or variable speed drives in handling, conveying or stacking
- Y02P60/87—Re-use of by-products of food processing for fodder production
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Diabetes (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Endocrinology (AREA)
- Mycology (AREA)
- Nutrition Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Emergency Medicine (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention belongs to the technical field of diabetes prevention and treatment, and particularly relates to compound dietary fiber nutrition powder for regulating blood glucose metabolism, and a preparation method and application thereof. The composite dietary fiber nutrition powder comprises the following raw materials in parts by weight: 3-9 parts of wheat bran dietary fiber powder; 1-3 parts of soluble dietary fiber (inulin); 0.05-1 part of functional oligosaccharide; the inulin has a molecular weight of 5-10kDa. The nutritional powder prepared by the invention improves intestinal canal ecological disturbance by improving the proportion of intestinal canal flora and host metabolite short chain fatty acid (acetic acid and butyric acid), thereby realizing the regulation effect on sugar metabolism and having better market popularization value.
Description
Technical Field
The invention belongs to the technical field of diabetes prevention and treatment, and particularly relates to composite dietary fiber nutrition powder for regulating blood glucose metabolism, and a preparation method and application of the nutrition powder.
Background
Diabetes is a chronic metabolic disease characterized mainly by hyperglycemia, and the worldwide incidence of which is rising. Diabetes is largely classified into type 1 diabetes, type 2 diabetes and other types of diabetes, with type 2 diabetes accounting for over 95% of patients. It is generally thought that its pathogenesis is related to insulin hyposecretion and/or islet resistance, and that abnormal glucose metabolism is one of the typical pathological manifestations of diabetes.
The aim of diabetes treatment is to control blood glucose, prevent or delay complications and reduce the death rate. In addition to the use of various hypoglycemic agents and insulin, early treatment of diabetes also involves dietary therapy, i.e., the use of adjunctive therapy or diet, health-related interventions are also indispensable.
Therefore, the development of functional foods with the function of mildly regulating blood sugar can meet the requirements and has clinical application value.
Epidemiological studies have shown that dietary fiber intake is inversely related to diabetes risk. The undigested dietary fiber of human body can be fermented by microorganisms in cecum and colon, and the main product is Short Chain Fatty Acid (SCFA), mainly comprising acetic acid, propionic acid and butyric acid, wherein the molar ratio of acetic acid, propionic acid and butyric acid in normal colon is 60:20:20. This ratio also changes as the body health and nutrient levels change. In clinical studies, it was found that increasing dietary fiber intake increases the synthesis of short chain fatty acids SCFAs, and enrichment of SCFA-producing bacteria by modulating intestinal inflammation and host immunity, even affecting insulin sensitivity and energy metabolism, thereby improving intestinal dysbiosis, promoting insulin secretion, and alleviating type ii diabetes.
Therefore, it is important to develop a dietary fiber composition that regulates blood glucose by regulating intestinal short chain fatty acid metabolism.
Disclosure of Invention
In view of the above, the present invention provides a composite dietary fiber nutritional powder for achieving a regulating effect on sugar metabolism by regulating intestinal flora and host metabolites, and a preparation method and application thereof; the nutritional powder can increase the ratio of acetic acid and propionic acid in short chain fatty acid metabolite, improve intestinal canal ecological disturbance, promote insulin secretion, effectively regulate blood sugar, and prevent and/or treat diabetes.
The specific preparation scheme of the invention is as follows:
the composite dietary fiber nutrition powder for regulating blood glucose metabolism comprises the following raw materials in parts by weight: 3-9 parts of insoluble dietary fiber; 1-3 parts of soluble dietary fiber; 0.05-1 part of functional oligosaccharide;
the composite dietary fiber nutrition powder realizes the regulation effect on sugar metabolism by regulating intestinal flora and host metabolites.
Preferably, the insoluble dietary fiber is wheat bran dietary fiber powder;
preferably, the soluble dietary fiber is inulin, and the molecular weight of the inulin is 5-10kDa; inulin of this molecular weight range has a stronger ability to promote the formation of short chain fatty acids (acetic acid, propionic acid) than other molecular weights.
Preferably, the functional oligosaccharide is at least one of isomaltooligosaccharide, resistant dextrin, stachyose, fructooligosaccharide, galactooligosaccharide and arabinose.
The functional oligosaccharides are low-calorie polymers, and only a small part of the functional oligosaccharides are digested and decomposed in the intestinal tract, so that the effect of continuously gradually supplying energy is achieved; most of the microbial substances in the intestinal tracts are used as fermentation substrates to generate short-chain fatty acids, so that the microbial substances can promote the propagation of beneficial microorganisms, prevent the propagation of harmful microorganisms, inhibit the synthesis of fat by the liver and further inhibit the occurrence of obesity.
Inulin is a dietary prebiotic fiber capable of modulating the composition and/or activity of intestinal microbiota, thereby producing beneficial physiological effects on the host.
Resistant dextrins, a low calorie dietary fiber, only 15% of which is digested by enzymes in the small intestine and the rest enters the large intestine, 75% of which is slowly and progressively fermented in the large intestine without causing digestive tract discomfort, 10% is excreted outside the body.
Arabinose, also called pectic sugar, acts in the body mainly through two ways, namely, inhibiting enzyme for hydrolyzing disaccharide and reducing sugar for inhibiting disaccharide hydrolysis; secondly, sucrose which is not decomposed in the small intestine is decomposed by microorganisms in the large intestine through the inhibition effect on the disaccharide hydrolase to generate a large amount of organic acids, and the organic acids have the inhibition effect on the liver synthetic fat, so that the generation of new fat in the body is reduced, and a good weight-losing effect is achieved.
The invention also provides a preparation method of the wheat bran insoluble dietary fiber powder, which specifically comprises the following steps:
(1) Wheat bran powder was mixed with 1: mixing 7-10 (w/t) with distilled water to form a mixture A;
the wheat bran powder is prepared by the inventor through purification, separation, washing, drying and crushing of wheat bran, and the related processes are more conventional and are not described in detail;
(2) Adding 1-3% of heat-resistant alpha-amylase into the mixture A, and performing enzymolysis for 10-30 minutes at 90-95 ℃; adding 0.5-1.5% of amyloglucosidase by weight of the mixture A, and reacting for 30 minutes at 40-60 ℃; adding alkaline protease accounting for 2-4% of the weight of the mixture A, and reacting for 1.5-2 hours at 45-55 ℃ to obtain an enzymolysis material;
(3) Adding pH regulator into the enzymolysis material to regulate pH to 7+ -0.5, inactivating enzyme in boiling water bath for 10-20min;
(4) Centrifuging the material subjected to enzyme deactivation for 10-30 minutes at 6000-10000 Xg, and collecting solid precipitate;
(5) Freeze drying the solid precipitate at-60 to-80 deg.c, grinding, and 80 mesh sieving to obtain insoluble wheat bran diet fiber powder.
The invention also provides a preparation method of the composite dietary fiber nutrition powder for regulating blood glucose metabolism, which specifically comprises the following steps:
(1) Firstly, uniformly mixing insoluble dietary fibers and soluble dietary fibers of wheat bran, and then adding the insoluble dietary fibers and the soluble dietary fibers and the functional oligosaccharides into a three-dimensional mixer for fully and uniformly mixing to obtain composite nutrition powder;
(2) Packaging the composite nutrition powder by adopting an aluminum-plastic composite bag, and storing at normal temperature.
The composite dietary fiber nutrition powder prepared by the invention can be applied to the preparation of health care products/foods/medicines with the effect of regulating blood sugar.
The composite dietary fiber nutrition powder prepared by the invention can also be applied to the preparation of products for promoting the generation of short-chain fatty acid SCFAs and relieving type II diabetes.
The composite dietary fiber nutrition powder prepared by the invention can also be applied to the preparation of products for regulating the SCFAs of short-chain fatty acids in intestinal tracts. The application is realized by improving the ecological disturbance of intestinal tracts and promoting the secretion of insulin by increasing the proportion of acetic acid and propionic acid in the short chain fatty acid metabolic products.
The beneficial effects are that:
1. the nutrition powder of the invention realizes the regulation of sugar metabolism by regulating intestinal flora and host metabolites, can obviously improve the proportion of acetic acid and propionic acid in short chain fatty acid metabolites, improve intestinal ecological disturbance, promote insulin secretion and relieve type II diabetes;
2. the dietary fiber product takes the wheat bran insoluble dietary fiber and inulin soluble dietary fiber with specific molecular weight as main efficacy factors, and has a synergistic effect on regulating and controlling blood sugar; the components are safe and effective, and the price is low;
3. the product stability is good, the state of the powder body of the nutritional powder prepared by the invention is kept stable after the nutritional powder is packaged for 6 months, the conditions of agglomeration and poor fluidity are avoided, and no peculiar smell is generated; no lump appears after brewing.
Drawings
FIG. 1 is a diagram showing the screening of the formation of short chain fatty acids of the wheat bran insoluble dietary fiber and soluble dietary fiber complex type;
FIG. 2 shows the formation of short chain fatty acids of wheat bran insoluble dietary fiber and inulin of varying molecular weight;
FIG. 3 shows the formation of short chain fatty acids in the different proportions of wheat bran insoluble dietary fiber and inulin;
FIG. 4 is a graph showing blood glucose changes in experimental mice;
fig. 5 shows the body weight change of the experimental mice.
Detailed Description
Example 1
In the embodiment, insoluble dietary fibers are compounded with other soluble dietary fibers, and intestinal microorganism effect is simulated in an in-vitro fermentation mode, so that the optimal combination is screened. The screening process is as follows:
1. bacterial collection
Three healthy volunteers without intestinal diseases, without edible drugs and antibiotics for three months were recruited, informed consent was filled in, fecal samples were collected, and in vitro fermentation experiments were performed. The volunteer feces 10g+100ml PBS phosphate buffer (pH=7.0) was homogenized, prepared as a 10% fecal homogenate, and then filtered using 4 layers of gauze to obtain fecal bacterial solution (IGF).
2. Preparation of the culture Medium
2g of peptone, 2g of yeast powder, 0.05g of hemin, 0.5g of bile salt, 0.1g of sodium chloride, 2g of sodium bicarbonate, 2mL of tween-80, 0.04g of monopotassium phosphate, 0.04g of dipotassium phosphate, 0.0051g of calcium chloride (hexahydrate), 0.01g of magnesium sulfate (heptahydrate), and dissolving in 1L of PBS phosphate buffer solution, and sterilizing for later use.
After the prepared medium was autoclaved at 121℃for 20 minutes, vitamin K1. Mu.L and L-cysteamine hydrochloride 0.5g were dissolved in ultrapure water and passed through a 0.22 μm filter membrane, and the medium was added.
3. Preparation of wheat bran insoluble dietary fiber
Wheat bran powder was mixed with 1:8 (w/t) and distilled water to form a mixture A;
the wheat bran powder is prepared by the inventor through purification, separation, washing, drying and crushing of wheat bran, and the related processes are more conventional and are not described in detail;
(2) Adding 1% by weight of heat-resistant alpha-amylase into the mixture A, and carrying out enzymolysis for 20 minutes at 92 ℃; adding 0.5% of amyloglucosidase by weight of the mixture A, and reacting for 30 minutes at 60 ℃; adding alkaline protease accounting for 3% of the weight of the mixture A, and reacting for 2 hours at 50 ℃ to obtain an enzymolysis material;
(3) Adding a pH regulator into the enzymolysis material to regulate the pH to 7+/-0.5, and inactivating enzyme in a boiling water bath for 10min;
(4) Centrifuging the material subjected to enzyme deactivation for 20 minutes at 6000 Xg, and collecting solid precipitate;
(5) Freeze drying the solid precipitate at-80deg.C, grinding, and sieving with 80 mesh sieve to obtain testa Tritici insoluble dietary fiber powder.
4. Preparation method of composite dietary fiber nutrition powder for regulating blood glucose metabolism
(1) Firstly, uniformly mixing insoluble dietary fibers and soluble dietary fibers of wheat bran, and then adding the insoluble dietary fibers and the soluble dietary fibers and the functional oligosaccharides into a three-dimensional mixer for fully and uniformly mixing to obtain composite nutrition powder;
(2) Packaging the composite nutrition powder by adopting an aluminum-plastic composite bag, and storing at normal temperature.
The test design is as follows:
blank group: 1mL of ultrapure water+1 mL of IGF solution+9 mL of medium;
control group: 4.05g of wheat bran insoluble dietary fiber was taken and 1mL of IGF solution and 9mL of medium were added thereto.
Experimental group (1): 3g of wheat bran insoluble dietary fiber was taken, and 1g of inulin, 0.01g of resistant dextrin, 0.02g of fructo-oligosaccharide, and 0.02g of stachyose were added, respectively, to which 1mL of IGF solution and 9mL of medium were added.
Experimental group (2): 3g of wheat bran insoluble dietary fiber was taken, 1g of resistant dextrin, 0.01g of fructo-oligosaccharide, 0.02g of stachyose and 0.02g of inulin were added respectively, and 1mL of IGF solution and 9mL of medium were added thereto.
Experimental group (3): 3g of wheat bran insoluble dietary fiber was taken, 1g of fructooligosaccharide, 0.01g of stachyose, 0.02g of inulin, 0.02g of resistant dextrin were added respectively, and 1mL of IGF solution and 9mL of medium were added thereto.
Experimental group (4): 3g of wheat bran insoluble dietary fiber was taken, and 1g of stachyose, 0.01g of inulin, 0.02g of resistant dextrin, and 0.02g of fructo-oligosaccharide were added, respectively, to which 1mL of IGF solution and 9mL of medium were added.
And (3) filling nitrogen into the control group and the experimental group to achieve an anaerobic environment, fermenting for 24 hours at the constant temperature of 37 ℃, and exploring the generation condition of each group of short chain fatty acid.
Screening was performed using acetic acid and propionic acid in SCFAs as the main factors, and the results are shown in fig. 1. As a result, it was found that the effect of promoting the production of short-chain fatty acids was optimal in the case where the wheat bran insoluble dietary fiber and the soluble dietary fiber inulin were added as the main raw materials in the experimental group (1), and thus the experiment was continued using the wheat bran insoluble dietary fiber powder and the soluble dietary fiber inulin as the main raw materials in the following example 2.
Example 2
In order to explore whether inulin with different molecular weights of soluble dietary fibers can influence blood sugar regulation or not, inulin with insoluble dietary fibers and inulin with soluble dietary fibers of wheat bran are used as main raw material components, inulin with different molecular weights is detected, intestinal microorganism effect is simulated in an in vitro fermentation mode, and the experimental design is as follows:
blank group: 1mL of ultrapure water+1 mL of IGF solution+9 mL of medium;
control group: using non-screened molecular weight inulin raw sugar;
test group: m (molecular weight) is less than 1kDa, 1kDa is less than m and less than 5kDa, 5kDa is less than m and less than 10kDa, 10kDa is less than m, four groups of inulin with different molecular weights;
to the control and experimental groups, 1mL of IGF solution and 9mL of medium were added, respectively, and fermentation experiments were performed in accordance with the method of example 1.
Screening was performed using acetic acid and propionic acid in SCFAs as major factors, and the screening results are shown in fig. 2.
The results in FIG. 2 show that inulin of the molecular weight range 5-10kDa has a stronger ability to promote the production of short-chain fatty acids (acetic acid, propionic acid) than those of other ranges.
Example 3
The wheat bran dietary fiber powder and the soluble dietary fiber inulin are used as main raw material components, other raw materials are the same as the experimental group (1) in the embodiment 1, and the influence of the proportion of the wheat bran dietary fiber powder and the soluble dietary fiber inulin on the short-chain fatty acid generation capacity of intestinal flora is explored;
and (3) test design:
blank group: 1mL of ultrapure water+1 mL of IGF solution+9 mL of medium;
experimental group: mixing wheat bran insoluble dietary fiber and 5-10kDa inulin according to a ratio of 1: 1. 2: 1. 3: mixing in proportion of 1; the remaining components were the same as in experimental group 1 of example 1.
The specific addition amounts are shown in Table 1 below:
proportion of | Wheat bran insoluble dietary fiber/g | 5-10kDa inulin/g |
1:1 | 1 | 1 |
2:1 | 2 | 1 |
3:1 | 3 | 1 |
In addition, the wheat bran insoluble dietary fiber with the same weight is taken as a control, and the rest components are the same as the experimental group 1 of the example 1;
the control and experimental groups were each supplemented with 1mL IGF solution and 9mL medium, and fermentation experiments were performed as in example 1, screening was performed using acetic acid and propionic acid in SCFAs as the main factors under investigation, and the screening results are shown in FIG. 3.
The results of fig. 3 found that the insoluble dietary fiber and soluble dietary fiber inulin ratio was 3:1, the effect of promoting the generation of short-chain fatty acid is optimal, so insoluble dietary fiber and soluble dietary fiber inulin are selected for compounding, and the proportion is 3:1.
EXAMPLE 4 therapeutic Effect experiment on blood glucose Regulation
1. Experimental materials
1.1 test animals: 40 male diabetic db/db mice and 10C 57BL/6J mice (5 weeks old, no specific pathogen grade) were obtained from hangzhou child source laboratory animal technologies limited and maintained at controlled light (12 h light-dark cycle) and temperature (25±3 ℃) in specific pathogen barrier facilities. In addition, standard food and distilled water were provided throughout the experiment.
1.2 instrument: the electronic blood glucose meter, the electronic balance and the enzyme label meter are all commonly and commercially available.
2. Test procedure
After 7 days of adaptation, db/db mice were randomized into four groups (n=10 per group), including diabetes model control (MD), IDF wheat bran, inulin, and idf+inulin (example 3 best screening), with 10C 57BL/6J mice as Normal Control (NC), euglycemic.
Throughout the course of the experiment, NC and MD groups were given a normal AIN-93G diet, and the other 3 groups were added with respective experimental group products on the basis of the normal AIN-93G diet in an amount of 1 bag (about 3G) each time after breakfast and supper each for 13 consecutive weeks, blood glucose was measured every 2 weeks on an empty stomach, and body weight was weighed every 1 week, and changes were observed.
3. Results
(1) Product efficacy detection
From fig. 4-5, it can be seen that the IDF wheat bran and Inulin group of the present invention has good blood glucose regulating effect. The IDF wheat bran and Inulin group mice show obvious weight gain phenomenon compared with diabetic mice. Therefore, the nutrition powder prepared by the invention can be applied to preparing blood sugar control products, such as sugar control medicines, health care foods and common foods, and can be taken together with meals.
(2) Product stability and odor evaluation
The product of the invention is subjected to evaluation of the nourishing, smell and stability after being stored for 6 months, and the result is as follows:
table 3 evaluation results
According to the evaluation results of the table, the state of the powder body of the nutritional powder prepared by the invention is kept stable after packaging for 6 months, the conditions of agglomeration and poor fluidity are avoided, and no peculiar smell is generated; no lump appears after brewing.
Claims (8)
1. The composite dietary fiber nutrition powder for regulating blood glucose metabolism is characterized by comprising the following raw materials in parts by weight: 3-9 parts of insoluble dietary fiber; 1-3 parts of soluble dietary fiber; 0.05-1 part of functional oligosaccharide;
the insoluble dietary fiber is wheat bran dietary fiber powder;
the soluble dietary fiber is inulin with molecular weight of 5-10kDa;
the composite dietary fiber nutrition powder realizes the regulation effect on sugar metabolism by regulating intestinal flora and host metabolites.
2. The composite dietary fiber nutritional powder of claim 1, wherein the functional oligosaccharide is at least one of isomaltooligosaccharide, resistant dextrin, stachyose, fructooligosaccharide, galactooligosaccharide, and arabinose.
3. The composite dietary fiber nutritional powder of claim 1, wherein the wheat bran dietary fiber powder is prepared by the following method:
(1) Wheat bran powder was mixed with 1: mixing 7-10 mass-volume ratio with distilled water to form a mixture A;
(2) Adding 1-3% of heat-resistant alpha-amylase into the mixture A, and performing enzymolysis for 10-30 minutes at 90-95 ℃; adding 0.5-1.5% of amyloglucosidase by weight of the mixture A, and reacting for 30 minutes at 40-60 ℃; adding alkaline protease accounting for 2-4% of the weight of the mixture A, and reacting for 1.5-2 hours at 45-55 ℃ to obtain an enzymolysis material;
(3) Adding pH regulator into the enzymolysis material to regulate pH to 7+ -0.5, inactivating enzyme in boiling water bath for 10-20min;
(4) Centrifuging the material subjected to enzyme deactivation for 10-30 minutes at 6000-10000 Xg, and collecting solid precipitate;
(5) Freeze drying the solid precipitate at-60 to-80 ℃, grinding, and sieving with a 80-mesh sieve to obtain the wheat bran insoluble dietary fiber powder.
4. A method for preparing the composite dietary fiber nutritional powder of claim 1, which is characterized by comprising the following steps:
(1) Firstly, uniformly mixing insoluble dietary fibers and soluble dietary fibers, and then adding the insoluble dietary fibers and the soluble dietary fibers into a three-dimensional mixer together with functional oligosaccharides to fully and uniformly mix to obtain composite nutrition powder;
(2) Packaging the composite nutrition powder by adopting an aluminum-plastic composite bag, and storing at normal temperature.
5. The use of the composite dietary fiber nutritional powder of claim 1 in the preparation of a health product/food having a blood glucose regulating effect.
6. Use of the composite dietary fiber nutritional powder of claim 1 in the preparation of a product that promotes the production of short chain fatty acids SCFAs and alleviates type ii diabetes conditions.
7. Use of the composite dietary fiber nutritional powder of claim 1 for the preparation of a product having the ability to regulate intestinal short chain fatty acid SCFAs metabolism.
8. The use according to claim 7, wherein the use is achieved by improving intestinal ecological disturbances and promoting insulin secretion by increasing the ratio of acetic acid to propionic acid in its short chain fatty acid metabolites.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202310243397.6A CN116195747B (en) | 2023-03-14 | 2023-03-14 | Composite dietary fiber nutrition powder for regulating blood glucose metabolism and preparation method and application thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202310243397.6A CN116195747B (en) | 2023-03-14 | 2023-03-14 | Composite dietary fiber nutrition powder for regulating blood glucose metabolism and preparation method and application thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN116195747A true CN116195747A (en) | 2023-06-02 |
CN116195747B CN116195747B (en) | 2024-09-20 |
Family
ID=86509382
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202310243397.6A Active CN116195747B (en) | 2023-03-14 | 2023-03-14 | Composite dietary fiber nutrition powder for regulating blood glucose metabolism and preparation method and application thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN116195747B (en) |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1840674A (en) * | 2006-01-19 | 2006-10-04 | 江南大学 | Process for preparing xylo-oligosaccharide by enzymolysis of wheat bran |
CN1840673A (en) * | 2006-01-19 | 2006-10-04 | 江南大学 | Process for preparing feruoylated oligosaccharide by enzymolysis of wheat bran |
US20090214511A1 (en) * | 2008-02-21 | 2009-08-27 | Trung Hong Tran | Digestible compositions of inulin for managing blood glucose levels |
CN105296567A (en) * | 2015-09-01 | 2016-02-03 | 运城学院 | Combined preparation method of triticale feruloyl oligosaccharide and Arab xylo-oligosaccharide |
CN107198250A (en) * | 2017-05-23 | 2017-09-26 | 北京瑞千景科技发展有限公司 | Improve intestinal microecology Chronic disease prevention composition and balanced nutritious food and application |
CN107518418A (en) * | 2016-12-19 | 2017-12-29 | 北京康华源科技发展有限公司 | Application of the dietary fiber as metabolism regulators |
CN111480778A (en) * | 2020-04-24 | 2020-08-04 | 金鹏 | Food composite food partner for relaxing bowels, beautifying features, enhancing immunity and delaying senescence |
CN115260330A (en) * | 2022-08-26 | 2022-11-01 | 皖南医学院 | Inulin type fructan extracted from stevia rebaudiana Bertoni root, and its preparation method and application |
-
2023
- 2023-03-14 CN CN202310243397.6A patent/CN116195747B/en active Active
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1840674A (en) * | 2006-01-19 | 2006-10-04 | 江南大学 | Process for preparing xylo-oligosaccharide by enzymolysis of wheat bran |
CN1840673A (en) * | 2006-01-19 | 2006-10-04 | 江南大学 | Process for preparing feruoylated oligosaccharide by enzymolysis of wheat bran |
US20090214511A1 (en) * | 2008-02-21 | 2009-08-27 | Trung Hong Tran | Digestible compositions of inulin for managing blood glucose levels |
CN105296567A (en) * | 2015-09-01 | 2016-02-03 | 运城学院 | Combined preparation method of triticale feruloyl oligosaccharide and Arab xylo-oligosaccharide |
CN107518418A (en) * | 2016-12-19 | 2017-12-29 | 北京康华源科技发展有限公司 | Application of the dietary fiber as metabolism regulators |
CN107198250A (en) * | 2017-05-23 | 2017-09-26 | 北京瑞千景科技发展有限公司 | Improve intestinal microecology Chronic disease prevention composition and balanced nutritious food and application |
CN111480778A (en) * | 2020-04-24 | 2020-08-04 | 金鹏 | Food composite food partner for relaxing bowels, beautifying features, enhancing immunity and delaying senescence |
CN115260330A (en) * | 2022-08-26 | 2022-11-01 | 皖南医学院 | Inulin type fructan extracted from stevia rebaudiana Bertoni root, and its preparation method and application |
Non-Patent Citations (4)
Title |
---|
刘丽娜等: "糖尿病及肥胖人群专用菊芋多糖功能食品制备技术", 工程科技Ⅰ辑, 8 December 2022 (2022-12-08), pages 2 * |
王亚伟等: "麦麸制备膳食纤维的工艺研究", 粮油加工与食品机械, no. 2002, 15 September 2002 (2002-09-15), pages 36 * |
纵伟等: "食品科学概论(第2版)", 中国纺织出版社有限公司, pages: 75 * |
闫俊江等: "营养学基础与常见疾病的营养治疗研究", 30 June 2020, 中国纺织出版社有限公司, pages: 52 * |
Also Published As
Publication number | Publication date |
---|---|
CN116195747B (en) | 2024-09-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Tester et al. | Glucomannans and nutrition | |
Qiang et al. | Health benefit application of functional oligosaccharides | |
Topping | Cereal complex carbohydrates and their contribution to human health | |
CN102657262B (en) | Use of polydextrose for simulating the functional attributes of human milk oligosaccharides in formula-fed infants | |
Kaczmarczyk et al. | The health benefits of dietary fiber: beyond the usual suspects of type 2 diabetes mellitus, cardiovascular disease and colon cancer | |
Shen et al. | Effects of oat β-glucan and barley β-glucan on fecal characteristics, intestinal microflora, and intestinal bacterial metabolites in rats | |
Cummings et al. | Gastrointestinal effects of food carbohydrate | |
KR102080562B1 (en) | Hypoglycemic hyper-branched maltodextrins | |
CN102439048B (en) | Compositions and methods for making alpha-(1,2)-branched alpha-(1,6) oligodextrans | |
CN106619743A (en) | Probiotic solid drink with hypoglycaemic effect and preparation method of probiotic solid drink | |
Moraes et al. | Resistant starch for modulation of gut microbiota: Promising adjuvant therapy for chronic kidney disease patients? | |
Sivieri et al. | Insights on β-glucan as a prebiotic coadjuvant in the treatment of diabetes mellitus: A review | |
Cardoso et al. | Novel and emerging prebiotics: Advances and opportunities | |
CN111903766A (en) | Infant formula milk powder and preparation method thereof | |
Adams et al. | Interactions of dietary fibre with nutritional components on gut microbial composition, function and health in monogastrics | |
Paturi et al. | Evaluation of gastrointestinal transit in rats fed dietary fibres differing in their susceptibility to large intestine fermentation | |
CN112931883A (en) | Prebiotic composition and preparation method and application thereof | |
Han et al. | In vitro fermentation potential of the residue of Korean red ginseng root in a mixed culture of swine faecal bacteria | |
CN116195747B (en) | Composite dietary fiber nutrition powder for regulating blood glucose metabolism and preparation method and application thereof | |
CN116831288A (en) | Prebiotic composition, preparation method thereof and uric acid reducing method | |
Dahiya et al. | Inclusion of dietary-fibers in nutrition provides prebiotic substrates to probiotics for the synthesis of beneficial metabolites SCFA to sustain gut health minimizing risk of IBS, IBD, CRC | |
Li et al. | Effect of polysaccharide extracted from Gynostemma pentaphyllum on the body weight and gut microbiota of mice | |
Liang et al. | Study on supplementary food with beneficial effects on the gut microbiota of infants | |
Schneeman | Food factors and gastrointestinal function: a critical interface | |
Akhtar et al. | Neutraceutical properties of resistant starch |
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 |