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Bile acid transporters: structure, function, regulation and pathophysiological implications.

Bile acid transporters: structure, function, regulation and pathophysiological implications. Research Abstract Details 

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  • Bile acid transporters: structure, function, regulation and pathophysiological implications. Abstract Text:

    waddah a alrefaiWaddah A Alrefai,ravinder k gillRavinder K Gill,

    Specific transporters expressed in the liver and the intestine, play a critical role in driving the enterohepatic circulation of bile acids. By preserving a circulating pool of bile acids, an important factor influencing bile flow, these transporters are involved in maintaining bile acid and cholesterol homeostasis. Enterohepatic circulation of bile acids is fundamentally composed of two major processes: secretion from the liver and absorption from the intestine. In the hepatocytes, the vectorial transport of bile acids from blood to bile is ensured by Na+ taurocholate co-transporting peptide (NTCP) and organic anion transport polypeptides (OATPs). After binding to a cytosolic bile acid binding protein, bile acids are secreted into the canaliculus via ATP-dependent bile salt excretory pump (BSEP) and multi drug resistant proteins (MRPs). Bile acids are then delivered to the intestinal lumen through bile ducts where they emulsify dietary lipids and cholesterol to facilitate their absorption. Intestinal epithelial cells reabsorb the majority of the secreted bile acids through the apical sodium dependent bile acid transporter (ASBT) and sodium independent organic anion transporting peptide (OATPs). Cytosolic ileal bile acid binding protein (IBABP) mediates the transcellular movement of bile acids to the basolateral membrane across which they exit the cells via organic solute transporters (OST). An essential role of bile acid transporters is evident from the pathology associated with their genetic disruption or dysregulation of their function. Malfunctioning of hepatic and intestinal bile acid transporters is implicated in the pathophysiology of cholestatic liver disease and the depletion of circulating pool of bile acids, respectively. Extensive efforts have been recently made to enhance our understanding of the structure, function and regulation of the bile acid transporters and exploring new potential therapeutics to treat bile acid or cholesterol related diseases. This review will highlight current knowledge about structure, function and molecular characterization of bile acid transporters and discuss the implications of their defects in various hepatic and intestinal disorders.

    Bile acid transporters: structure, function, regulation and pathophysiological implications. Publishing Authors By Initials

    wa alrefaiWA Alrefai,rk gillRK Gill,

    For similar proteins: carrier proteins: membrane transport proteins: ion pumps: symporters research abstracts see: proteins: carrier proteins: membrane transport proteins: ion pumps: symporters research

    PUBMED ID PMID:

    MEDLINE DATE:

    Bile acid transporters: structure, function, regulation and pathophysiological implications. Journal Published:

    PUBLICATION TYPE: Review

    Journal: Pharmaceutical research

    VOLUME: 24

    Page Numbers: 1803-23

    Journal Abbreviation: Pharm. Res.

    ISSN: 0724-8741

    DAY: 3

    MONTH: 04

    YEAR: 2007

    Bile acid transporters: structure, function, regulation and pathophysiological implications. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8406521

    Bile acid transporters: structure, function, regulation and pathophysiological implications. Keywords Mesh Terms:

    KEYWORDS: Symporters

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Bile acid transporters: structure, function, regulation and pathophysiological implications. Information

    Substance Name: sodium-bile acid cotransporter

    Registry Number: 145420-23-1

    Grant and Affiliation Information for Bile acid transporters: structure, function, regulation and pathophysiological implications.

    AFFILIATION: Section of Digestive Diseases and Nutrition, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois 60612, USA. walrefai@uic.edu

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIDDK

    GRANT: DK71596

    ACRONYM: DK

    MEDLINETA: Pharm Res

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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