Schölmerich J, Baumgartner U, Miyai K, Gerok W
Department of Internal Medicine, University of Freiburg, Federal Republic of Germany.
J Hepatol. 1990 May;10(3):280-3. doi: 10.1016/0168-8278(90)90133-c.
Ursodeoxycholate has been advocated for the treatment of cholestatic liver diseases. The coinfusion of tauroursodeoxycholate with taurolithocholate in the perfused rat liver completely prevented the decrease of bile flow and the increase of oxygen uptake found with taurolithocholate only. Bile flow and bile salt secretion were increased with the coinfusion of both bile acids as compared with the infusion of tauroursodeoxycholate only (+4.30 microliters/g liver per 30 min) with 16 and 32 mumol/l tauroursodeoxycholate (+1.55 microliters/g liver per 30 min with 80 and 160 mumol/l). Morphological examination revealed a 50% decrease of the number of necrotic cells in the periportal area. Tauroursodeoxycholate did not inhibit the uptake of taurolithocholate, but increased its transcellular passage and biotransformation. Thus, tauroursodeoxycholate prevents taurolithocholate-induced cholestasis and liver cell toxicity probably by an intracellular mechanism.
熊去氧胆酸已被推荐用于治疗胆汁淤积性肝病。在灌注大鼠肝脏中,将牛磺熊去氧胆酸与牛磺石胆酸共同输注,完全防止了仅使用牛磺石胆酸时所发现的胆汁流量减少和氧摄取增加。与仅输注牛磺熊去氧胆酸(16和32微摩尔/升牛磺熊去氧胆酸时为每30分钟+4.30微升/克肝脏,80和160微摩尔/升时为每30分钟+1.55微升/克肝脏)相比,两种胆汁酸共同输注时胆汁流量和胆汁盐分泌增加。形态学检查显示门周区域坏死细胞数量减少了50%。牛磺熊去氧胆酸不抑制牛磺石胆酸的摄取,但增加其跨细胞转运和生物转化。因此,牛磺熊去氧胆酸可能通过细胞内机制预防牛磺石胆酸诱导的胆汁淤积和肝细胞毒性。