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部分流出道阻塞或鬼笔环肽中毒后,从灌注大鼠肝脏制备的微粒体的葡萄糖-6-磷酸酶(EC 3.1.3.9)和酯酶(EC 3.1.1.1)活性。

Glucose-6-phosphatase (EC 3.1.3.9) and esterase (EC 3.1.1.1) activities of microsomes prepared from perfused rat livers after partial outflow block or phalloidin poisoning.

作者信息

Homann J, Frimmer M

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1975;288(1):87-96. doi: 10.1007/BF00501816.

Abstract

Microsomes were prepared from perfused rat livers after different perfusion procedures. The yield of microsomal protein and the kinetic data (Km, Vmax) of glucose-6-phosphatase (3.1.3.9) and esterase (3.1.1.1) activities were analysed in each preparation. No marked differences were detected between conventionally prepared liver microsomes and those from livers perfused 1 hr with an erythrocytes-free medium under the conditions of open outflow. If the outflow pressure was increased artificially, the yield of microsomal protein decreased. The Vmax of both enzymes was markedly increased, whereas the Km values remained unchanged. The same microsomal alterations occurred when perfused rat livers were poisoned with phalloidin in vitro under the condition of open outflow. Our findings indicate that microsomal alterations in livers from poisoned animals might be due to microcirculatory disturbances, and not primary effects of the toxin on the endoplasmatic reticulum.

摘要

在不同的灌注程序后,从灌注的大鼠肝脏中制备微粒体。分析了每种制剂中微粒体蛋白的产量以及葡萄糖-6-磷酸酶(3.1.3.9)和酯酶(3.1.1.1)活性的动力学数据(Km,Vmax)。在开放流出条件下,常规制备的肝脏微粒体与用无红细胞培养基灌注1小时的肝脏微粒体之间未检测到明显差异。如果人为增加流出压力,微粒体蛋白的产量会降低。两种酶的Vmax明显增加,而Km值保持不变。在开放流出条件下,当体外灌注的大鼠肝脏用鬼笔环肽中毒时,会出现相同的微粒体改变。我们的研究结果表明,中毒动物肝脏中的微粒体改变可能是由于微循环紊乱,而不是毒素对内质网的直接作用。

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