Literature DB >> 12149508

Analysis of the effect of intestinal resection on rat ileal bile Acid transporter expression and on bile Acid and cholesterol homeostasis.

Namir Al-Ansari1, Guorong Xu, Katie Kollman-Bauerly, Chris Coppola, Sarah Shefer, Peter Ujhazy, Daniel Ortiz, Lin Ma, Steven Yang, Richard Tsai, Gerald Salen, Jon Vanderhoof, Benjamin L Shneider.   

Abstract

Ileal reclamation of bile salts is mediated in large part by an apical sodium-dependent bile acid transporter (ASBT) located in the terminal ileum. The following studies were performed to elucidate the adaptive response of ASBT to intestinal resection. Two separate series of intestinal resections were performed: 1) limited (25%) ileal and 2) massive (70%) intestinal resection. The boundaries of the resections were varied to examine differences in compensation when variable amounts of endogenous transporter activity were resected. Previously demonstrated supraphysiologic expression of ASBT, which was seen after proximal ileal resection, led to a contraction in the bile acid pool size and a paradoxical reduction in bile acid (cholesterol 7alpha-hydroxylase and sterol 27-hydroxylase) and cholesterol (hydroxymethylglutaryl coenzyme A reductase) biosynthetic enzyme activities. Massive intestinal resection resulted in ileal hypertrophy and an apparently maladaptive specific down-regulation in ASBT protein expression. In this model bile acid pool size correlated with the amount of residual ASBT-expressing terminal ileum. Cholesterol and bile acid biosynthetic enzyme activities were inversely related to bile acid pool size. Adaptive changes in ASBT expression and alterations in bile acid and cholesterol homeostasis are dependent on the type and location of intestinal resection.

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Year:  2002        PMID: 12149508     DOI: 10.1203/00006450-200208000-00023

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  5 in total

1.  Conditional Gata4 deletion in mice induces bile acid absorption in the proximal small intestine.

Authors:  Eva Beuling; Ilona M Kerkhof; Grace A Nicksa; Michael J Giuffrida; Jamie Haywood; Daniel J aan de Kerk; Christina M Piaseckyj; William T Pu; Terry L Buchmiller; Paul A Dawson; Stephen D Krasinski
Journal:  Gut       Date:  2010-07       Impact factor: 23.059

2.  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

3.  Mutation screening of apical sodium-dependent bile acid transporter (SLC10A2): novel haplotype block including six newly identified variants linked to reduced expression.

Authors:  Olga Renner; Simone Harsch; Elke Schaeffeler; Matthias Schwab; Dietmar M Klass; Wolfgang Kratzer; Eduard F Stange
Journal:  Hum Genet       Date:  2009-01-30       Impact factor: 4.132

Review 4.  Bile acid transporters.

Authors:  Paul A Dawson; Tian Lan; Anuradha Rao
Journal:  J Lipid Res       Date:  2009-06-04       Impact factor: 5.922

5.  Human bile acid transporter ASBT (SLC10A2) forms functional non-covalent homodimers and higher order oligomers.

Authors:  Paresh P Chothe; Lindsay C Czuba; Robyn H Moore; Peter W Swaan
Journal:  Biochim Biophys Acta Biomembr       Date:  2017-12-01       Impact factor: 3.747

  5 in total

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