Gender-specific reduction of hepatic Mrp2 expression by high-fat diet protects female mice from ANIT toxicity-Reference-Cited by-同舟云学术

Gender-specific reduction of hepatic Mrp2 expression by high-fat diet protects female mice from ANIT toxicity

Published:2012-06 Issue:2 Volume:261 Page:189-195
ISSN:0041-008X
Container-title:Toxicology and Applied Pharmacology
language:en
Short-container-title:Toxicology and Applied Pharmacology

Author:

Kong Bo,Csanaky Iván L.,Aleksunes Lauren M.,Patni Meghan,Chen Qi,Ma Xiaochao,Jaeschke Hartmut,Weir Scott,Broward Melinda,Klaassen Curtis D.,Guo Grace L.

Publisher

Elsevier BV

Subject

Pharmacology,Toxicology

Reference26 articles.

1. Coordinated expression of multidrug resistance-associated proteins (Mrps) in mouse liver during toxicant-induced injury;Aleksunes;Toxicol. Sci.,2006

2. The hepatic metabolism and biliary excretion of benzo[a]pyrene in guinea-pigs fed normal, high-fat or high-cholesterol diets;Bowes;Xenobiotica,1986

3. Drug-metabolizing enzyme and transporter expression in a mouse model of diabetes and obesity;Cheng;Mol. Pharm.,2008

4. Time course gene expression using laser capture microscopy-extracted bile ducts, but not hepatic parenchyma, reveals acute alpha-naphthylisothiocyanate toxicity;Cullen;Toxicol. Pathol.,2010

5. Role of MRP2 and GSH in intrahepatic cycling of toxins;Dietrich;Toxicology,2001

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