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肝硬化时肝脏的清除率。I. 大鼠体外普萘洛尔代谢与其经灌注肝脏摄取之间的关系。

Clearance by the liver in cirrhosis. I. Relationship between propranolol metabolism in vitro and its extraction by the perfused liver in the rat.

作者信息

Fenyves D, Gariépy L, Villeneuve J P

机构信息

Department of Medicine, Hôpital Saint-Luc, Montreal, Canada.

出版信息

Hepatology. 1993 Feb;17(2):301-6.

PMID:8428728
Abstract

To delineate the factors responsible for impaired clearance in cirrhosis, we examined propranolol disposition in rats with carbon tetrachloride-induced cirrhosis and compared it with that in control animals, rats treated with chlorpromazine (an inhibitor of propranolol metabolism) and rats with acute liver injury. We measured the extraction ratio of propranolol by the isolated perfused liver and related it to estimates of propranolol drug-metabolizing enzyme activity in homogenates of the same livers. In control animals, drug-metabolizing enzyme activity (measured as the ratio Vmax/Km) averaged 5,319 +/- 1,193 ml/min; the extraction ratio in the perfused liver was close to 1.0 (0.97 +/- 0.01). Important decreases of microsomal enzyme activity were observed in rats treated with chlorpromazine (30 +/- 27 ml/min, p < 0.001) and in rats with acute liver injury (724 +/- 401 ml/min, p < 0.001), accounting for the decrease in the hepatic extraction ratio by the perfused liver (0.33 +/- 0.09 and 0.71 +/- 0.04, respectively, p < 0.01). In cirrhotic livers, enzyme activity was not significantly different from that of controls (3,592 +/- 1,857 ml/min) and could not account for the observed decrease in extraction (0.66 +/- 0.14, p < 0.01). The extraction of antipyrine by the isolated perfused liver was also measured as an index of microsomal enzyme activity and related to propranolol extraction. Antipyrine extraction was decreased by 90% in acute liver injury, compared with 33% in cirrhosis, suggesting a much greater reduction of microsomal enzyme activity in the former group.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为了明确肝硬化患者清除功能受损的相关因素,我们研究了四氯化碳诱导的肝硬化大鼠体内普萘洛尔的处置情况,并将其与对照动物、接受氯丙嗪治疗的大鼠(氯丙嗪为普萘洛尔代谢抑制剂)以及急性肝损伤大鼠进行比较。我们测定了离体灌注肝脏对普萘洛尔的摄取率,并将其与相同肝脏匀浆中普萘洛尔药物代谢酶活性的估计值相关联。在对照动物中,药物代谢酶活性(以Vmax/Km比值衡量)平均为5319±1193 ml/min;灌注肝脏中的摄取率接近1.0(0.97±0.01)。在接受氯丙嗪治疗的大鼠(30±27 ml/min,p<0.001)和急性肝损伤大鼠(724±401 ml/min,p<0.001)中,观察到微粒体酶活性显著降低,这解释了灌注肝脏中肝摄取率的下降(分别为0.33±0.09和0.71±0.04,p<0.01)。在肝硬化肝脏中,酶活性与对照组无显著差异(3592±1857 ml/min),无法解释观察到的摄取率下降(0.66±0.14,p<0.01)。还测定了离体灌注肝脏对安替比林的摄取,作为微粒体酶活性的指标,并与普萘洛尔摄取相关联。与肝硬化中下降33%相比,急性肝损伤中安替比林摄取下降了90%,表明前一组微粒体酶活性降低幅度更大。(摘要截短于250字)

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