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PMID: 23750858 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Evaluation of the contribution of the ATP binding cassette transporter, P-glycoprotein, to in vivo cholesterol homeostasis.

Molecular pharmaceutics ·Vol. 10 ·No. 8 ·2013-08-05 ·页码 3203-12

Lee SD, Thornton SJ, Sachs-Barrable K, Kim JH, Wasan KM

Abstract

P-glycoprotein (Pgp, encoded by ABCB1, commonly known as MDR1), an ATP-dependent transporter with a broad range of hydrophobic drug substrates, has been associated with the in vitro intracellular transport of cholesterol; however, these findings have not been confirmed in vivo. In this manuscript we tested the contributions of Pgp to in vivo cholesterol homeostasis by comparing the cholesterol phenotype of wild type mice with mice lacking both murine isoforms of Pgp (Abcb1a(-/-)/1b(-/-)) by measuring cholesterol absorption, circulating cholesterol, and lipoprotein cholesterol profiles. The mice were fed diets containing normal or high levels of dietary fat (25% vs 45% kcal from fat) and cholesterol (0.02% vs 0.20% w/w) for 8 weeks to challenge their capacity to maintain homeostasis. There were no significant differences in cholesterol absorption, circulating cholesterol levels, and lipoprotein profiles between Pgp knockout and wild type mice fed matching diets. Compensatory shifts were observed in the activation of two key transcription factors involved in maintaining cholesterol balance, the Liver X Receptor and SREBP-2, which may have maintained the wild type phenotype in the knockout mice. Deletion of Pgp affected the molar composition of gallbladder bile, when the mice were fed diets containing high levels of dietary fat, cholesterol, or both. The mole fraction of bile salts was reduced in the gallbladder bile of Pgp knockout mice, while the mole fraction of cholesterol was increased. In this paper, we provide evidence that Pgp knockout mice maintain cholesterol homeostasis, even when challenged with high cholesterol diets. We suggest that the specific shifts in cholesterol regulatory networks identified in the jejunum and liver of the knockout mice may have compensated for the lack of Pgp. Our finding that Pgp knockout mice were unable to maintain gallbladder bile composition when challenged with high dietary fat and/or cholesterol compliments recent reports that Pgp may be a secondary bile salt export pump.

MeSH 主题词
ATP Binding Cassette Transporter, Subfamily B/genetics,metabolism ATP-Binding Cassette Transporters/genetics,metabolism Animals Cholesterol/metabolism Homeostasis/genetics,physiology Lipid Metabolism/genetics,physiology Male Mice
化学物质
ATP Binding Cassette Transporter, Subfamily B ATP-Binding Cassette Transporters Cholesterol
作者与单位
共 5 位作者,点击展开单位 / ORCID
Lee Stephen D
Faculty of Pharmaceutical Sciences, University of British Columbia , 2405 Wesbrook Mall, Vancouver, BC, Canada V6T 1Z3.
Thornton Sheila J
Sachs-Barrable Kristina
Kim Jenny H
Wasan Kishor M
Article Info
Journal
Molecular pharmaceutics
Abbr.
Mol Pharm
ISSN
1543-8392
Published
2013-08-05
电子出版
2013-00-24
页码
3203-12
Language
English
Country/Region
United States
NLM ID
101197791
基金资助
Canadian Institutes of Health Research · 104543-1 · Canada
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