Cholestasis induced by sulphated glycolithocholic acid in the rat: protection by endogenous bile acids.

Abstract

Sulphated glycolithocholic acid (SGLC) causes cholestasis in experimental animals, despite its sulphated form. In the present study, the cholestatic potency and the pharmacokinetics of SGLC were investigated in rats under two conditions: (a) in the presence of an intact circulating bile acid pool and (b) after exhaustion of the bile acid pool by 24 h of bile diversion. Intravenous administration of SGLC (8 mumol/100 g body weight) to rats with an intact bile acid pool did not cause cholestasis. However, biliary phospholipid and cholesterol concentrations were reduced by 40% and 29% respectively during the first hour after administration. When the same dose of the bile acid was injected in rats with a 24 h biliary drainage, a complete cessation of bile production was observed within 1 h. Twelve hours after the onset of cholestasis, bile production gradually increased again, showed a marked overshoot, and reached control levels after 3 days. In the recovery phase, biliary phospholipid and cholesterol concentrations were greatly reduced. The absence of endogenous bile acids did not change the hepatic clearance rate of a tracer dose of radiolabelled SGLC, but markedly decreased its biliary excretion rate. It was concluded that the hepatotoxic effect of SGLC is much more pronounced in rats with an exhausted bile acid pool, possibly due to a slower biliary excretion of the toxic compound. This phenomenon may have clinical implications for patients with a contracted bile acid pool.

• Authors: F Kuipers, R Havinga, R J Vonk
• Journal: Clinical science (London, England : 1979) (Clin Sci (Lond)) Vol. 68 Issue 2 Pg. 127-34 (Feb 1985) ISSN: 0143-5221 [Print] England
• PMID: 3967462 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Bile Acids and Salts
• sulfolithocholylglycine
• Glycocholic Acid

Topics

• Animals
• Bile (analysis, metabolism)
• Bile Acids and Salts (blood, physiology)
• Cholestasis (chemically induced)
• Glycocholic Acid (analogs & derivatives, blood, toxicity)
• Kinetics
• Male
• Rats
• Rats, Inbred Strains
• Secretory Rate (drug effects)