Literature DB >> 7951853

Bile flow in a mutant Sprague-Dawley rat with defective biliary excretion of glutathione.

H Yoshida1, K Okano, T Tamano, Y Kuronuma, M Iijima, T Harada.   

Abstract

The Eisai hyperbilirubinemic rat is a mutant strain of Sprague-Dawley origin with hereditary defects in the biliary excretion of bilirubin glucuronide, glutathione, and several other organic anions. The correlation between bile flow and bile acid excretion rates during taurocholate infusion revealed that bile acid-independent flow was smaller in the mutant than in intact Sprague-Dawley rats (19.3 vs 56.0 microliters/kg per min), while bile acid-dependent flow was similar. The correlation between bile flow and glutathione excretion rates in Sprague-Dawley rats with modified hepatic glutathione levels revealed that a certain portion of bile flow was proportional to the biliary excretion of glutathione, with a coefficient of 551 bile per 1 mol glutathione. One-third of bile acid-independent bile flow in intact Sprague-Dawley rats was accounted for by glutathione osmosis, which feature was absent in the mutant rats.

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Year:  1994        PMID: 7951853     DOI: 10.1007/BF02361240

Source DB:  PubMed          Journal:  J Gastroenterol        ISSN: 0944-1174            Impact factor:   7.527


  12 in total

1.  Relation between biliary glutathione excretion and bile acid-independent bile flow.

Authors:  N Ballatori; A T Truong
Journal:  Am J Physiol       Date:  1989-01

2.  Sinusoidal efflux of glutathione in the perfused rat liver. Evidence for a carrier-mediated process.

Authors:  M Ookhtens; K Hobdy; M C Corvasce; T Y Aw; N Kaplowitz
Journal:  J Clin Invest       Date:  1985-01       Impact factor: 14.808

3.  Factors influencing the efflux of hepatic glutathione into bile in rats.

Authors:  N Kaplowitz; D E Eberle; J Petrini; J Touloukian; M C Corvasce; J Kuhlenkamp
Journal:  J Pharmacol Exp Ther       Date:  1983-01       Impact factor: 4.030

4.  Hereditary chronic conjugated hyperbilirubinemia in mutant rats caused by defective hepatic anion transport.

Authors:  P L Jansen; W H Peters; W H Lamers
Journal:  Hepatology       Date:  1985 Jul-Aug       Impact factor: 17.425

5.  The influence of bile salt structure on self-association in aqueous solutions.

Authors:  A Roda; A F Hofmann; K J Mysels
Journal:  J Biol Chem       Date:  1983-05-25       Impact factor: 5.157

6.  Canalicular transport of reduced glutathione in normal and mutant Eisai hyperbilirubinemic rats.

Authors:  J C Fernández-Checa; H Takikawa; T Horie; M Ookhtens; N Kaplowitz
Journal:  J Biol Chem       Date:  1992-01-25       Impact factor: 5.157

7.  Biliary excretion of bile acid conjugates in a hyperbilirubinemic mutant Sprague-Dawley rat.

Authors:  H Takikawa; N Sano; T Narita; Y Uchida; M Yamanaka; T Horie; T Mikami; O Tagaya
Journal:  Hepatology       Date:  1991-08       Impact factor: 17.425

8.  Glutathione as a primary osmotic driving force in hepatic bile formation.

Authors:  N Ballatori; A T Truong
Journal:  Am J Physiol       Date:  1992-11

9.  Intrabiliary glutathione hydrolysis. A source of glutamate in bile.

Authors:  N Ballatori; R Jacob; J L Boyer
Journal:  J Biol Chem       Date:  1986-06-15       Impact factor: 5.157

10.  Mechanism of biliary lipid secretion in the rat: a role for bile acid-independent bile flow?

Authors:  H J Verkade; H Wolters; A Gerding; R Havinga; V Fidler; R J Vonk; F Kuipers
Journal:  Hepatology       Date:  1993-06       Impact factor: 17.425

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