Thompson M B
Laboratory of Experimental Pathology, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA.
Toxicol Pathol. 1996 Jan-Feb;24(1):62-71. doi: 10.1177/019262339602400109.
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.
胆汁酸由肝脏中的胆固醇合成,在胆汁流动的产生、胆固醇的排泄以及脂肪和脂溶性维生素的肠道消化与吸收过程中发挥着重要作用。血清中胆汁酸浓度的升高和/或改变是肝胆疾病的特异性敏感指标。肝细胞中胆汁酸的合成涉及内质网、细胞质、线粒体和过氧化物酶体中的多个步骤。其他涉及胆汁酸的重要肝细胞过程包括基底外侧膜的主动摄取、细胞内运输、P-450介导的结合与羟化以及胆小管分泌。疏水性胆汁酸在体内和体外均会产生肝毒性。在实验和流行病学研究中,其中一些形式已被确定为结肠癌和肝癌(仅实验性)发生的致病因素。相反,几种亲水性形式,主要是熊去氧胆酸,在多种临床和实验性肝胆疾病及病症中已显示出细胞保护特性。由于胆汁酸可能具有截然不同的性质和作用,确定这些化合物的作用机制已成为一个活跃的研究领域。原代分离肝细胞为在精心设计、严格控制的研究中探究胆汁酸相关功能和作用提供了机会。短期培养已被用于研究与胆汁酸相关的各种问题,包括细胞毒性、合成以及肝细胞处理过程。然而,使用这些系统时,当培养时间超过数天,成熟肝细胞的许多功能,包括与胆汁酸相关的功能,可能会丧失。培养技术的最新进展使得功能稳定、分化的细胞能够长期维持。就胆汁酸研究而言,这些系统仍有待充分表征,但在适当情况下,它们应为体内研究和短期体外试验提供重要的替代方法。