Bile Acids in the Assessment of Hepatocellular Function
Open Access
- 1 January 1996
- journal article
- other
- Published by SAGE Publications in Toxicologic Pathology
- Vol. 24 (1) , 62-71
- https://doi.org/10.1177/019262339602400109
Abstract
Bile acids, which are synthesized in the liver from cholesterol, are important in the production of bile flow, excretion of cholesterol, and intestinal digestion and absorption of fats and fat-soluble vitamins. Increases and/or alterations in concentrations of bile acids in serum are specific and sensitive indicators of hepatobiliary disorders. Synthesis of bile acids in hepatocytes involves steps in endoplasmic reticulum, cytosol, mitochondria, and peroxisomes. Other important hepatocellular processes involving bile acids include active uptake by the basolateral membrane, intracellular transport, P-450-mediated conjugations and hydroxylations, and canalicular secretion. Hydrophobic bile acids produce hepatotoxicity in vivo and in vitro. In experimental and epidemiologic studies, some of these forms have been identified as causative agents in the development of colon and liver (experimental only) cancer. Conversely, several hydrophilic forms, primarily ursodeoxycholic acid, have demonstrated cytoprotective properties in a variety of clinical and experimental hepatobiliary diseases and disorders. Because bile acids can have dramatically different properties and effects, determination of mechanisms of action of these compounds has become an active area of research. Primary isolated hepatocytes provide an opportunity to investigate bile acid-related functions and effects in well-designed, carefully controlled studies. Short-term cultures have been used to study a variety of issues related to bile acids, including cytotoxicity, synthesis, and hepatocellular processing. With these systems, however, many functions of mature hepatocytes, including those pertaining to bile acids, can be lost when cultures are maintained for more than several days. Recent developments in culture techniques permit long-term maintenance of functionally stable, differentiated cells. Pertaining to bile acid research, these systems remain to be fully characterized but, in appropriate situations, they should provide important alternatives to in vivo studies and short-term in vitro assays.Keywords
This publication has 107 references indexed in Scilit:
- Improvement of cyclosporin A-induced cholestasis by tauroursodeoxycholate in a long-term study in the ratDigestive Diseases and Sciences, 1994
- Effects of Bile Acids and Steroid/Thyroid Hormones on the Expression of Cholesterol 7α-Hydroxylase mRNA and the CYP7 Gene in HepG2 CellsBiochemical and Biophysical Research Communications, 1994
- Effect of Collagen Gel Configuration on the Cytoskeleton in Cultured Rat HepatocytesExperimental Cell Research, 1993
- Chenodeoxycholic Acid-Dependent Induction of Major Histocompatibility Complex Class 1 mRNA Expression in a Human Hepatoma Cell LineBiochemical and Biophysical Research Communications, 1993
- Effect of ursodeoxycholic acid administration on bile duct proliferation and cholestasis in bile duct ligated ratDigestive Diseases and Sciences, 1993
- A Correlative Study on Serum Cholylglycine Levels in Hepatobiliary DiseaseHormone and Metabolic Research, 1992
- Microtubule functionsLife Sciences, 1992
- Effect of indomethacin on the uptake, metabolism and excretion of 3-oxocholic acid: Studies in isolated hepatocytes and perfused rat liverBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1991
- Potential bile acid precursors in plasma—Possible indicators of biosynthetic pathways to cholic and chenodeoxycholic acids in manThe Journal of Steroid Biochemistry and Molecular Biology, 1990
- The order of hepatic cytotoxicity of bile salts in vitro does not agree with that examined in vivo in ratsLife Sciences, 1990