相似文献
1
Effect of cyclodextrins and undigested starch on the loss of chenodeoxycholate in the faeces.
Biochem J. 1994 May 1;299 ( Pt 3)(Pt 3):725-30. doi: 10.1042/bj2990725.
2
Impact of beta-cyclodextrin and resistant starch on bile acid metabolism and fecal steroid excretion in regard to their hypolipidemic action in hamsters.
Biochim Biophys Acta. 1999 Jan 29;1437(1):1-12. doi: 10.1016/s0005-2760(98)00174-x.
3
Antilithiasic effect of beta-cyclodextrin in LPN hamster: comparison with cholestyramine.
J Lipid Res. 1999 Apr;40(4):726-34.
4
The effects of cholecystectomy on the bile salt pool of the syrian hamster.
Digestion. 1977;15(4):338-47. doi: 10.1159/000198020.
5
Metabolism of chenodeoxycholate by intestinal mucosa.
Gastroenterology. 1976 Jul;71(1):82-6.
6
Nutritional significance of cyclodextrins: indigestibility and hypolipemic effect of alpha-cyclodextrin.
J Nutr Sci Vitaminol (Tokyo). 1985 Apr;31(2):209-23. doi: 10.3177/jnsv.31.209.
7
Increased fecal bile acid excretion and changes in the circulating bile acid pool are involved in the hypocholesterolemic and gallstone-preventive actions of psyllium in hamsters.
J Nutr. 1999 Apr;129(4):896-902. doi: 10.1093/jn/129.4.896.
8
Specific inhibition by cyclodextrins of raw starch digestion by fungal glucoamylase.
Biosci Biotechnol Biochem. 1992 Apr;56(4):556-9. doi: 10.1271/bbb.56.556.
9
Increased sulfation of lithocholate in patients with cholesterol gallstones during chenodeoxycholate treatment.
Digestion. 1975;12(2):105-10. doi: 10.1159/000197660.
10
Inhibition of buckwheat starch digestion by the formation of starch/bile salt complexes: possibility of its occurrence in the intestine.
J Agric Food Chem. 2011 Jun 8;59(11):6277-83. doi: 10.1021/jf2006326. Epub 2011 May 13.
引用本文的文献
1
Dietary resistant starch supplementation increases gut luminal deoxycholic acid abundance in mice.
Gut Microbes. 2024 Jan-Dec;16(1):2315632. doi: 10.1080/19490976.2024.2315632. Epub 2024 Feb 20.
2
Formation of Intermediate Amylose Rice Starch-Lipid Complex Assisted by Ultrasonication.
Foods. 2022 Aug 12;11(16):2430. doi: 10.3390/foods11162430.
3
Gut Microbiota-A Future Therapeutic Target for People with Non-Alcoholic Fatty Liver Disease: A Systematic Review.
Int J Mol Sci. 2022 Jul 27;23(15):8307. doi: 10.3390/ijms23158307.
4
Zwitterionic near infrared fluorescent agents for noninvasive real-time transcutaneous assessment of kidney function.
Chem Sci. 2017 Apr 1;8(4):2652-2660. doi: 10.1039/c6sc05059j. Epub 2017 Jan 11.
5
In vitro and in vivo evaluation of novel cross-linked saccharide based polymers as bile acid sequestrants.
Molecules. 2015 Feb 24;20(3):3716-29. doi: 10.3390/molecules20033716.
6
A study on the inhibitory mechanism for cholesterol absorption by α-cyclodextrin administration.
Beilstein J Org Chem. 2014 Dec 2;10:2827-35. doi: 10.3762/bjoc.10.300. eCollection 2014.
7
The mechanism of enterohepatic circulation in the formation of gallstone disease.
J Membr Biol. 2014 Nov;247(11):1067-82. doi: 10.1007/s00232-014-9715-3. Epub 2014 Aug 9.
8
New pathophysiological concepts underlying pathogenesis of pigment gallstones.
Clin Res Hepatol Gastroenterol. 2012 Apr;36(2):122-9. doi: 10.1016/j.clinre.2011.08.010. Epub 2011 Oct 5.
9
Effectiveness of resistant starch, compared to guar gum, in depressing plasma cholesterol and enhancing fecal steroid excretion.
Lipids. 1996 Oct;31(10):1069-75. doi: 10.1007/BF02522464.
10
Resistant starch is more effective than cholestyramine as a lipid-lowering agent in the rat.
Lipids. 1995 Sep;30(9):847-53. doi: 10.1007/BF02533961.
本文引用的文献
1
An amylose antiparallel double helix at atomic resolution.
Science. 1987 Oct 9;238(4824):205-8. doi: 10.1126/science.238.4824.205.
2
The action of some alpha-amylases on starch granules.
Biochem J. 1963 Mar;86(3):452-62. doi: 10.1042/bj0860452.
3
Hypolipidemic effects of beta-cyclodextrin in the hamster and in the genetically hypercholesterolemic Rico rat.
Lipids. 1993 Mar;28(3):181-8. doi: 10.1007/BF02536637.
4
Intestinal absorption of 14C-labelled beta-cyclodextrin in rats.
Arzneimittelforschung. 1980;30(5):808-10.
5
A simple reverse-phase high pressure liquid chromatographic determination of conjugated bile acids in serum and bile using a novel radial compression separation system.
Clin Chim Acta. 1982 Feb 26;119(1-2):41-50. doi: 10.1016/0009-8981(82)90403-x.
6
Physical factors influencing postprandial glucose and insulin responses to starch.
Am J Clin Nutr. 1980 Apr;33(4):760-5. doi: 10.1093/ajcn/33.4.760.
7
New alpha-amylase inhibitor, trestatins. II. Structure determination of trestatins A, B and C.
J Antibiot (Tokyo). 1983 Sep;36(9):1166-75. doi: 10.7164/antibiotics.36.1166.
8
New alpha-amylase inhibitor, trestatins. I. Isolation, characterization and biological activities of trestatins A, B and C.
J Antibiot (Tokyo). 1983 Sep;36(9):1157-65. doi: 10.7164/antibiotics.36.1157.
9
Physicochemical properties of bile acids and their relationship to biological properties: an overview of the problem.
J Lipid Res. 1984 Dec 15;25(13):1477-89.
10
The effect of a new specific alpha-amylase inhibitor on post-prandial glucose and insulin excursions in normal subjects and Type 2 (non-insulin-dependent) diabetic patients.
Diabetologia. 1984 Apr;26(4):278-81. doi: 10.1007/BF00283650.
Zotero 插件