Barth A, Bergmann R, Zaumseil J, Klinger W
Arch Toxicol Suppl. 1978(1):359-61. doi: 10.1007/978-3-642-66896-8_78.
The hydroxylation of bile acids in rat liver microsomes in cyt P-450 dependent (Björkhem et al., 1975). To find out possible interactions between drugs and bile acid hydroxylation and/or active transport mechanisms we investigated the influence of the microsomal inhibitor metyrapon, the microsomal inducer phenobarbital and the intrahepatic cholestasis producing agents chlorpromazine, phenylbutazone and progesteron on bile flow and bile acid excretion. The excretion in monohydroxy (MBA), dihydroxy (DBA) and trihydroxy (TBA) bile acids were estimated in bile-fistula rats in three one hour periods. MBA, DBA and TBA were separated with thinlayer-chromatography and estimated fluorimetrically. Bile flow, bile acid excretion and relation TBA/DBA were influenced by acute and subchronic administration of the above mentioned drugs in different ways.
胆汁酸在大鼠肝微粒体中的羟基化作用依赖于细胞色素P - 450(比约克姆等人,1975年)。为了探究药物与胆汁酸羟基化和/或主动转运机制之间可能存在的相互作用,我们研究了微粒体抑制剂甲吡酮、微粒体诱导剂苯巴比妥以及可导致肝内胆汁淤积的药物氯丙嗪、保泰松和孕酮对胆汁流量和胆汁酸排泄的影响。在三个一小时时间段内,对胆汁瘘管大鼠单羟基胆汁酸(MBA)、二羟基胆汁酸(DBA)和三羟基胆汁酸(TBA)的排泄情况进行了评估。通过薄层色谱法分离MBA、DBA和TBA,并采用荧光法进行测定。上述药物的急性和亚慢性给药以不同方式影响胆汁流量、胆汁酸排泄以及TBA/DBA比值。