Korean J Physiol Pharmacol.  1999 Dec;3(6):565-570.

Glycochenodeoxycholic acid induces cell death in primary cultured rat hepatocyte: Apoptosis and necrosis

Affiliations
  • 1Department of Pharmacology, College of Medicine, Ewha Womans University, Seoul, Korea.

Abstract

Intracellular accumulation of bile acids in the hepatocytes during cholestasis is thought to be pathogenic in cholestatic liver injury. Due to the detergent-like effect of the hydrophobic bile acids, hepatocellular injury has been attributed to direct membrane damage. However histological findings of cholestatic liver diseases suggest apoptosis can be a mechanism of cell death during cholestatic liver diseases instead of necrosis. To determine the pattern of hepatocellular toxicity induced by bile acid, we incubated primary cultured rat hepatocytes with a hydrophobic bile acid, Glycochenodeoxycholate (GCDC), up to 5 hours. After 5 hours incubation with 400 muM GCDC, lactate dehydrogenase released significantly. Cell viability, quantitated in propidium iodide stained cells concomitant with fluoresceindiacetate was decreased time-and dose-dependently. Most nuclei with condensed chromatin and shrunk cytoplasm were heavily labelled time- and dose-dependently by a positive TUNEL reaction. These findings suggest that both apoptosis and necrosis are involved in hepatocytes injury caused by GCDC.

Keyword

Hepatocyte; GCDC; Apoptosis; Necrosis

MeSH Terms

Animals
Apoptosis*
Bile
Bile Acids and Salts
Cell Death*
Cell Survival
Cholestasis
Chromatin
Cytoplasm
Glycochenodeoxycholic Acid*
Hepatocytes*
In Situ Nick-End Labeling
L-Lactate Dehydrogenase
Liver
Liver Diseases
Membranes
Necrosis*
Propidium
Rats*
Bile Acids and Salts
Chromatin
Glycochenodeoxycholic Acid
L-Lactate Dehydrogenase
Propidium
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