Choleretic effect of valproic acid in the rat

John B. Watkins, Curtis D. Klaassen

Research output: Contribution to journalArticle

20 Scopus citations

Abstract

Valproic acid (VPA) is an anticonvulsant agent which produced marked choleresis in the rat. Bile flow rate increased from 50 to 60 μl per min per kg to 120 to 145 μl per min per kg immediately after i.v. injection of VPA (37.5 to 150 mg per kg; 2 ml per kg) in male Sprague‐Dawley rats. The duration of maximal bile flow was dose‐dependent and increased from 30 min (37.5 mg VPA per kg) to approximately 2 hr (150 mg VPA per kg). Choleresis diluted the biliary concentrations of bile acids, Cl, cholesterol, and phospholipids. VPA did not change the bile/plasma ratio for erythritol suggesting that the increased bile flow is of canalicular origin. VPA did not influence the excretion of bile acids or their osmotic activity, whereas bile salt‐independent flow doubled in rats treated with 150 mg VPA per kg. The bile/plasma, bile/liver, and liver/plasma concentration ratios for VPA were 11.7, 1.6, and 7.3, respectively. Approximately 90% of VPA appearing in bile was biotransformed, primarily as a glucuronide. Bile flow correlated with VPA excretion; 16 μl of bile was produced per μmole VPA which suggests that choleresis is primarily due to the osmotic activity of VPA metabolites in bile. VPA enhanced the excretion of inorganic ions which may also contribute to choleresis. Biliary excretion of phenol‐3,6‐dibromophthalein disulfonate and ouabain was unaffected. Thus, VPA is an effective choleretic which stimulates bile salt‐independent flow of canalicular origin largely as a consequence of the osmotic properties of VPA conjugates in bile.

Original languageEnglish (US)
Pages (from-to)341-347
Number of pages7
JournalHepatology
Volume1
Issue number4
DOIs
StatePublished - Jan 1 1981

ASJC Scopus subject areas

  • Hepatology

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