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一种胆汁盐类似物:甘氨二氢fusidate的肝脏摄取和胆汁排泄。

Hepatic uptake and biliary excretion of a bile salt analog : glycodihydrofusidate.

作者信息

Montet J C, Gerolami A, Durbec J P, Crotte C, Montet A M, Hauton J C

出版信息

Biomedicine. 1977 Feb;26(1):60-4.

PMID:861346
Abstract

Glyco-24, 25-dihydrofusidate is efficiently excreted in the bile by the liver. This compound partially inhibits hepatobiliary transport of bile salts and bilirubin. In order to determine if bile salts and glycodihydrofusidate share common pathways at the hepatocyte level, we studied the effect of sodium dehydrocholate on the blood clearance of glycodihydrofusidate. Two groups of rats were perfused, controls with 0.15M NaCl, and test animals with 10 micronmol + min-(1) + kg(1) of dehydrocholate; both groups received 1 micronCi of 14C-glycodihydrofusidate intravenously. Carotid blood was removed every minute and the disappearance of radioactivity from the blood was monitored. The results are consisgent with a theoretical model of two compartments. The experimental curves were fit to the sum of exponentials.

摘要

甘氨-24,25-二氢梭链孢酸钠可被肝脏有效地排泄到胆汁中。该化合物可部分抑制胆汁盐和胆红素的肝胆转运。为了确定胆汁盐和甘氨二氢梭链孢酸钠在肝细胞水平上是否共享共同途径,我们研究了去氢胆酸钠对甘氨二氢梭链孢酸钠血液清除率的影响。对两组大鼠进行灌注,对照组用0.15M氯化钠,试验动物用10微摩尔·分钟⁻¹·千克⁻¹的去氢胆酸钠;两组均静脉注射1微居里的¹⁴C-甘氨二氢梭链孢酸钠。每分钟采集颈动脉血,并监测血液中放射性的消失情况。结果与两室理论模型一致。将实验曲线拟合为指数之和。

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