Montet J C, Gerolami A
Can J Physiol Pharmacol. 1978 Apr;56(2):163-7. doi: 10.1139/y78-022.
The biliary elimination of glycodihydrofusidate (GDHF), a structural analogue of bile salts, was studied in bile fistula rats. GDHF was excreted in bile with a maximal excretory rate (Tm = 0.80 mumol min-1 kg-1) which is much lower than bile salts Tm. The effects of dehydrocholate and taurocholate on GDHF biliary secretion suggest a stimulatory effect of bile salts on canalicular excretion of the drug. (a) When a bolus intravenous injection of 3 mumol of GDHF was followed after 2 min by a continuous dehydrocholate perfusion (10 mumol min-1 kg-1), biliary excretion of GDHF was increased in comparison with control rats. (b) Upon attaining the biliary Tm by continuous perfusion of GDHF at a rate of 1.35 mumol min-1 kg-1, infusion with either taurocholate or dehydrocholate increased its Tm to a similar degree. These results are similar to those previously obtained with the effects of bile salt infusions on the Tm of bromosulfophthalein. They suggest therefore that hepatic transport of GDHF and bile salts occurs by routes which are distinct for canalicular transport in spite of the striking structural similarities between GDHF and bile salts.
在胆瘘大鼠中研究了胆汁盐结构类似物甘氨二氢fusidate(GDHF)的胆汁排泄情况。GDHF经胆汁排泄,其最大排泄率(Tm = 0.80 μmol min⁻¹ kg⁻¹)远低于胆汁盐的Tm。脱氢胆酸盐和牛磺胆酸盐对GDHF胆汁分泌的影响表明胆汁盐对药物的胆小管排泄有刺激作用。(a)静脉推注3 μmol的GDHF,2分钟后持续灌注脱氢胆酸盐(10 μmol min⁻¹ kg⁻¹),与对照大鼠相比,GDHF的胆汁排泄增加。(b)以1.35 μmol min⁻¹ kg⁻¹的速率持续灌注GDHF达到胆汁Tm时,输注牛磺胆酸盐或脱氢胆酸盐均可使其Tm升高至相似程度。这些结果与先前关于胆汁盐输注对溴磺酞钠Tm影响的结果相似。因此,它们表明尽管GDHF与胆汁盐在结构上有显著相似性,但GDHF和胆汁盐的肝脏转运通过胆小管转运的不同途径进行。