Reichen J, Le M
Department of Clinical Pharmacology, University of Berne, Switzerland.
Experientia. 1989 Feb 15;45(2):135-7. doi: 10.1007/BF01954847.
We investigated whether acinar differences in taurocholate transport are responsible for the increased maximal secretory rate observed after expansion of the bile acid pool. The bile acid pool was expanded by cholate feeding for four days. Periportal and centrizonal hepatocytes were then probed by ante- and retrograde liver perfusion, respectively. In control animals, secretory rate constant (alpha 1) averaged 0.439 +/- 0.123 and 0.104 +/- 0.035 min-1 during ante- and retrograde perfusion, respectively, in the absence of exogenous taurocholate. These values did not significantly change when taurocholate was infused. In cholate-fed animals, alpha 1 was comparable during antegrade perfusion but was significantly reduced (0.038 +/- 0.035, p less than 0.05) during retrograde perfusion in the absence of exogenous taurocholate, presumably owing to induction of cytosolic bile acid binding proteins. During loading with exogenous taurocholate, by contrast, alpha 1 was significantly accelerated (0.252 +/- 0.026; p less than 0.01) in centrizonal hepatocytes from bile-acid fed rats. Expansion of the bile acid pool is able to change the bile salt secretory characteristics of centrizonal hepatocytes toward those of periportal ones.
我们研究了牛磺胆酸盐转运的腺泡差异是否是胆汁酸池扩张后观察到的最大分泌率增加的原因。通过喂食胆酸盐四天来扩张胆汁酸池。然后分别通过顺行和逆行肝脏灌注对门静脉周围和中央带肝细胞进行检测。在对照动物中,在没有外源性牛磺胆酸盐的情况下,顺行和逆行灌注期间的分泌率常数(α1)分别平均为0.439±0.123和0.104±0.035 min-1。当输注牛磺胆酸盐时,这些值没有显著变化。在喂食胆酸盐的动物中,在没有外源性牛磺胆酸盐的情况下,顺行灌注期间α1相当,但在逆行灌注期间显著降低(0.038±0.035,p<0.05),这可能是由于细胞溶质胆汁酸结合蛋白的诱导。相比之下,在加载外源性牛磺胆酸盐时,来自喂食胆汁酸大鼠的中央带肝细胞中的α1显著加快(0.252±0.026;p<0.01)。胆汁酸池的扩张能够使中央带肝细胞的胆盐分泌特性向门静脉周围肝细胞的特性转变。