Literature DB >> 9225240

Altered bile acid metabolism related to atherosclerosis in alloxan diabetic rats.

K Uchida1, T Satoh, H Takase, Y Nomura, N Takasu, H Kurihara, N Takeuchi.   

Abstract

Normal and alloxan diabetic rats were kept on a 0.25% cholesterol diet for 12 months and the changes in serum cholesterol levels, and fecal excretion of sterols and bile acids were examined to elucidate the influence of changes in bile acid metabolism on manifestations of hypercholesterolemia and development of atheromatous lesions. Diabetic rats fed the cholesterol diet showed increases in bile acid synthesis and in the cholic acid group/chenodeoxycholic acid group (CA/CDCA) ratio, and developed significant hypercholesterolemia and atheromatous lesions. In contrast, normal rats showed increased bile acids synthesis but a decreased CA/CDCA ratio after feeding with the cholesterol diet, and developed neither hypercholesterolemia nor atheromatous lesions. Fecal sterol excretion and the cholesterol/sitosterol ratio decreased in diabetic rats. Positive correlations were found between the cumulative serum cholesterol level and the atheromatous lesion area, and between the fecal CA/CDCA ratio and the serum cholesterol level, in the latter of which the correlation was higher in rats on the cholesterol diet than in those on the standard diet. These findings suggest that alteration of bile acid metabolism with increases in cholic acid synthesis and CA/CDCA ratio in diabetic rats enhances cholesterol absorption to produce significant hypercholesterolemia, which in turn leads to development of atheromatous lesions.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 9225240     DOI: 10.5551/jat1994.3.52

Source DB:  PubMed          Journal:  J Atheroscler Thromb        ISSN: 1340-3478            Impact factor:   4.928


  8 in total

1.  N-glycosylation is essential for ileal ASBT function and protection against proteases.

Authors:  Saminathan Muthusamy; Pooja Malhotra; Mobashir Hosameddin; Amish K Dudeja; Sujata Borthakur; Seema Saksena; Ravinder K Gill; Pradeep K Dudeja; Waddah A Alrefai
Journal:  Am J Physiol Cell Physiol       Date:  2015-04-08       Impact factor: 4.249

2.  Impaired generation of 12-hydroxylated bile acids links hepatic insulin signaling with dyslipidemia.

Authors:  Rebecca A Haeusler; Matthew Pratt-Hyatt; Carrie L Welch; Curtis D Klaassen; Domenico Accili
Journal:  Cell Metab       Date:  2011-12-22       Impact factor: 27.287

3.  Cyp8b1 ablation prevents Western diet-induced weight gain and hepatic steatosis because of impaired fat absorption.

Authors:  Enrico Bertaggia; Kristian K Jensen; Jose Castro-Perez; Yimeng Xu; Gilbert Di Paolo; Robin B Chan; Liangsu Wang; Rebecca A Haeusler
Journal:  Am J Physiol Endocrinol Metab       Date:  2017-04-04       Impact factor: 4.310

4.  Adaptation of Intestinal and Bile Acid Physiology Accompany the Metabolic Benefits Following Ileal Interposition in the Rat.

Authors:  Ping Zhao; Donna Wendt; Sean Z Goodin; Shwetha Ravichandran; Tara E Chouinard; April D Strader
Journal:  Obes Surg       Date:  2018-03       Impact factor: 4.129

5.  All-trans retinoic acid regulates hepatic bile acid homeostasis.

Authors:  Fan Yang; Yuqi He; Hui-Xin Liu; Jessica Tsuei; Xiaoyue Jiang; Li Yang; Zheng-Tao Wang; Yu-Jui Yvonne Wan
Journal:  Biochem Pharmacol       Date:  2014-08-28       Impact factor: 5.858

6.  Human insulin resistance is associated with increased plasma levels of 12α-hydroxylated bile acids.

Authors:  Rebecca A Haeusler; Brenno Astiarraga; Stefania Camastra; Domenico Accili; Ele Ferrannini
Journal:  Diabetes       Date:  2013-07-24       Impact factor: 9.461

7.  Circulating bile acids concentration is predictive of coronary artery disease in human.

Authors:  Caroline Chong Nguyen; Denis Duboc; Dominique Rainteau; Harry Sokol; Lydie Humbert; Philippe Seksik; Adèle Bellino; Hendy Abdoul; Naïm Bouazza; Jean-Marc Treluyer; Malika Saadi; Karim Wahbi; Heithem Soliman; Benoit Coffin; André Bado; Maude Le Gall; Olivier Varenne; Henri Duboc
Journal:  Sci Rep       Date:  2021-11-22       Impact factor: 4.379

8.  Gut microbiota-bile acid crosstalk contributes to the rebound weight gain after calorie restriction in mice.

Authors:  Mengci Li; Shouli Wang; Yitao Li; Mingliang Zhao; Junliang Kuang; Dandan Liang; Jieyi Wang; Meilin Wei; Cynthia Rajani; Xinran Ma; Yajun Tang; Zhenxing Ren; Tianlu Chen; Aihua Zhao; Cheng Hu; Chengxing Shen; Weiping Jia; Ping Liu; Xiaojiao Zheng; Wei Jia
Journal:  Nat Commun       Date:  2022-04-19       Impact factor: 17.694

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.