Hepatobiliary excretion of biliverdin isomers and C10-substituted biliverdins in Mrp2-deficient (TR(-)) rats.

Abstract:

:Multidrug resistance protein 2 (Mrp2) is considered the major mammalian membrane transporter of non-bile salt organic anions from liver to bile. Using Mrp2-deficient rats, we show that the protein is not essential for biliary excretion of biliverdin, its IIIalpha and XIIIalpha isomers, mesobiliverdin XIIIalpha or biliverdins bearing bulky lipophilic groups that are not reduced by biliverdin reductase in vivo. Yet, Mrp2 deficiency does retard the biliary excretion of these verdins to different degrees. The data indicate that there are Mrp2-independent mechanisms in the rat for biliary excretion of dicarboxylate organic anions related to biliverdin.

authors

McDonagh AF,Lightner DA,Kar AK,Norona WS

doi

10.1016/S0006-291X(02)00325-X

subject

Has Abstract

pub_date

2002-05-10 00:00:00

pages

1077-83

issue

3

eissn

0006-291X

issn

1090-2104

pii

S0006-291X(02)00325-X

journal_volume

293

pub_type

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