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实验性慢性肝性卟啉病中的尿卟啉原脱羧酶缺乏症

Uroporphyrinogen decarboxylase deficiency in experimental chronic hepatic porphyria.

作者信息

von Tiepermann R, Koss G, Doss M

出版信息

Hoppe Seylers Z Physiol Chem. 1980 Aug;361(8):1217-22. doi: 10.1515/bchm2.1980.361.2.1217.

Abstract

During hexachlorobenzene feeding of rats the following biochemical signs of a chronic hepatic porphyria developed: porphyrinuria with increase of uro- and hexacarboxyporphyrin, hepatic prophyrin accumulation of uro- and heptacarboxyporphyrin and a diminished activity of uroporphyrinogen decarboxylase in the liver, but nut in the red cells. During the 5.3 days of the intoxication the behaviour of metabolite constellation and enzyme activities was inverse. Hexachlorobenzene porphyria in rats is a pathobiochemical model of chronic hepatic prophyria, which in man becomes clinically manifest as porphyria cutanea tarda.

摘要

在给大鼠喂食六氯苯的过程中,出现了以下慢性肝性卟啉症的生化迹象:卟啉尿,尿卟啉和六羧基卟啉增加;肝脏中尿卟啉和七羧基卟啉的卟啉积累;肝脏中尿卟啉原脱羧酶活性降低,但红细胞中该酶活性未降低。在中毒的5.3天期间,代谢物组成和酶活性的变化情况相反。大鼠的六氯苯卟啉症是慢性肝性卟啉症的病理生化模型,在人类中临床表现为迟发性皮肤卟啉症。

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