Biliary excretion of bile acids and organic anions in zone 1- and zone 3-injured rats

Liver. 2000 Feb;20(1):38-44. doi: 10.1034/j.1600-0676.2000.020001038.x.

Abstract

Aims: Hepatocytes in zone 1 of the hepatic lobule play a role in the uptake and biliary excretion of bile acids and organic anions under physiological conditions, and those in zone 3 may play a role only with a high-dose load. To further elucidate the role of hepatic zonation on the handling of bile acids and organic anions, biliary excretion of these compounds was studied in zone 1- and zone 3-injured rats.

Methods: Biliary excretion of bile acids and organic anions was studied in zone 1- and zone 3-injured rats, caused by allyl alcohol and bromobenzene, respectively.

Results: Biliary excretion of a tracer dose of taurocholate was unchanged in the injury in both zones, but that of leukotriene C4 was decreased in zone 1 injury. The excretory maximum of taurocholate was decreased with zone 1 and the zone 3 injuries. Biliary excretion of deoxycholate metabolites was decreased in zone 3 injury, although the profile of metabolites in the bile was unchanged. Sulfobromophthalein excretion was decreased in zone 1 injury, but unchanged in zone 3 injury.

Conclusions: These findings indicate that zone 1 is very important for biliary excretion of both organic anions and bile acids. In contrast, zone 3 is considered not to have a role in biliary excretion of organic anions, but to play a role in the excretion of bile acids.

MeSH terms

  • Alanine Transaminase / blood
  • Alkaline Phosphatase / blood
  • Animals
  • Bile Ducts / metabolism*
  • Bromobenzenes / toxicity
  • Leukotriene C4 / metabolism*
  • Liver / drug effects
  • Liver / metabolism*
  • Liver / pathology
  • Male
  • Propanols / toxicity
  • Rats
  • Rats, Sprague-Dawley
  • Sulfobromophthalein / metabolism
  • Taurocholic Acid / metabolism*

Substances

  • Bromobenzenes
  • Propanols
  • Sulfobromophthalein
  • Leukotriene C4
  • allyl alcohol
  • Taurocholic Acid
  • bromobenzene
  • Alanine Transaminase
  • Alkaline Phosphatase