Literature DB >> 1578373

Prolactin regulates maternal bile secretory function post partum.

Y Liu1, J F Hyde, M Vore.   

Abstract

The single-pass isolated perfused rat liver was used to assess bile secretory function in pregnancy and the post partum period and to evaluate the regulatory role of prolactin. Nonpregnant controls, post partum rats (48 hr post partum), pregnant rats (19-20 days of pregnancy) and pregnant rats treated with bromocriptine (3 mg/kg/day, s.c.) from day 20 of pregnancy until 48 hr post partum to block prolactin secretion were examined. In a separate set of experiments, ovariectomized rats were implanted with osmotic minipumps containing solvent alone or solvent plus varying concentrations of ovine prolactin (oPRL). Livers were isolated, [3H]taurocholate (TC) was infused at increasing concentrations and bile flow, bile acid secretory rate and hepatic clearance of TC from the perfusate were determined. Maximal bile flow (microliters/min/g liver) in response to infusion of TC was significantly higher in post partum rats (3.4 +/- 0.3) than in pregnant rats (1.4 +/- 0.3) and bromocriptine-treated post partum rats (1.7 +/- 0.3). The maximal bile acid secretory rate (SRm, nmol/min/g liver) in post partum rats was 276 +/- 19 and was significantly greater than SRm in pregnant (103 +/- 26) and bromocriptine-treated post partum rats (142 +/- 25). Hepatic clearance (ml/min) was significantly greater in post partum rats than in pregnant, control and bromocriptine-treated post partum rats at the highest TC concentration. Infusion of oPRL at doses of 100, 250 and 500 micrograms/day significantly increased maximal bile flow and SRm in a dose-dependent manner; these measures were increased to 4.38 +/- 0.21 microliters/min/g liver and 338.2 +/- 16.3 nmol/min/g liver, respectively, in rats treated with 500 micrograms/day oPRL.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1992        PMID: 1578373

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  9 in total

1.  Regulation of the rat liver sodium-dependent bile acid cotransporter gene by prolactin. Mediation of transcriptional activation by Stat5.

Authors:  T C Ganguly; M L O'Brien; S J Karpen; J F Hyde; F J Suchy; M Vore
Journal:  J Clin Invest       Date:  1997-06-15       Impact factor: 14.808

Review 2.  Altered drug metabolism during pregnancy: hormonal regulation of drug-metabolizing enzymes.

Authors:  Hyunyoung Jeong
Journal:  Expert Opin Drug Metab Toxicol       Date:  2010-06       Impact factor: 4.481

3.  Reproductive experience alters prolactin receptor expression in mammary and hepatic tissues in female rats.

Authors:  Robert S Bridges; Victoria F Scanlan; Jong-O Lee; Elizabeth M Byrnes
Journal:  Biol Reprod       Date:  2011-04-20       Impact factor: 4.285

4.  ABCG5/ABCG8-independent biliary cholesterol excretion in lactating rats.

Authors:  Donna J Coy; Clavia R Wooton-Kee; Baoxiang Yan; Nadezhda Sabeva; Kai Su; Gregory Graf; Mary Vore
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2010-04-22       Impact factor: 4.052

5.  Increased cholesterol 7alpha-hydroxylase expression and size of the bile acid pool in the lactating rat.

Authors:  Clavia Ruth Wooton-Kee; David E Cohen; Mary Vore
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2008-02-21       Impact factor: 4.052

6.  Prolactin increases hepatic Na+/taurocholate co-transport activity and messenger RNA post partum.

Authors:  T C Ganguly; Y Liu; J F Hyde; B Hagenbuch; P J Meier; M Vore
Journal:  Biochem J       Date:  1994-10-01       Impact factor: 3.857

7.  Differential gene expression in liver and small intestine from lactating rats compared to age-matched virgin controls detects increased mRNA of cholesterol biosynthetic genes.

Authors:  Antony Athippozhy; Liping Huang; Clavia Ruth Wooton-Kee; Tianyong Zhao; Paiboon Jungsuwadee; Arnold J Stromberg; Mary Vore
Journal:  BMC Genomics       Date:  2011-02-03       Impact factor: 3.969

Review 8.  Phase III elimination: another two-edge sword.

Authors:  M Vore
Journal:  Environ Health Perspect       Date:  1994-05       Impact factor: 9.031

9.  Expression of an epidermal keratin protein in liver of transgenic mice causes structural and functional abnormalities.

Authors:  K M Albers; F E Davis; T N Perrone; E Y Lee; Y Liu; M Vore
Journal:  J Cell Biol       Date:  1995-01       Impact factor: 10.539

  9 in total

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