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人体肝脏血流与酶诱导作用

Liver blood flow and enzyme induction in man.

作者信息

Ohnhaus E E, Noelpp U B, Ramos M R

出版信息

Hepatogastroenterology. 1985 Apr;32(2):61-4.

PMID:4007764
Abstract

An increased liver blood flow in rats and monkeys found following induction of the liver microsomal enzyme system by antipyrine and phenobarbitone, formed the basis of the present study in 7 volunteers. The total body clearance of antipyrine, gamma GT, and the urinary excretion of d-glucaric acid and 6-beta-hydroxycortisol were measured. Liver blood flow was estimated after an overnight fast under basal conditions using the 133Xenon inhalation technique. In addition, liver volume was determined by 7 independent investigations using a 99mTechnetium-sulfur-colloid scan of the liver. Afterwards, each volunteer received 1,000 mg antipyrine daily for 14 days and all measurements were repeated. After antipyrine administration the antipyrine half-life decreased significantly from 12.5 to 7.7 hours with an increase of the antipyrine clearance from 34.1 to 50.8 ml/min. In addition, glucaric acid, gamma-GT and 6-beta-hydroxycortisol were significantly increased. Liver blood flow increased from 36.8 ml/min/100 g to 50.9 ml/min/100 g liver (p less than 0.02). The liver volume showed a tendency to increase but was significantly higher in only three of the seven volunteers investigated. The mean liver volumes of 1483 g before and 1585 g after antipyrine administration were not significantly different. In contrast, total liver blood flow increased significantly from 590 ml/min before to 809 ml/min after enzyme induction (p less than 0.02).

摘要

通过安替比林和苯巴比妥诱导大鼠和猴子的肝脏微粒体酶系统后,发现其肝脏血流量增加,这构成了本项针对7名志愿者研究的基础。测量了安替比林的全身清除率、γ-谷氨酰转移酶(gamma GT)以及d-葡萄糖醛酸和6-β-羟基皮质醇的尿排泄量。在基础条件下禁食过夜后,使用氙-133吸入技术估计肝脏血流量。此外,通过对肝脏进行99m锝-硫胶体扫描的7项独立研究来确定肝脏体积。之后,每位志愿者每天服用1000毫克安替比林,持续14天,然后重复所有测量。服用安替比林后,安替比林的半衰期从12.5小时显著降至7.7小时,安替比林清除率从34.1毫升/分钟增至50.8毫升/分钟。此外,葡萄糖醛酸、γ-谷氨酰转移酶和6-β-羟基皮质醇显著增加。肝脏血流量从36.8毫升/分钟/100克肝脏增至50.9毫升/分钟/100克肝脏(p<0.02)。肝脏体积有增加的趋势,但在所研究的7名志愿者中只有3人的肝脏体积显著增大。服用安替比林前肝脏平均体积为1483克,服用后为1585克,差异不显著。相比之下,肝脏总血流量从酶诱导前的590毫升/分钟显著增至809毫升/分钟(p<0.02)。

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