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二乙氨基二硫代甲酸盐诱导大鼠胃窦溃疡发病机制中涉及的超氧自由基来源。

Sources of superoxide radicals involved in the pathogenesis of diethyldithiocarbamate-induced gastric antral ulcer in rats.

作者信息

Chen S H, Pan S

机构信息

Department of Internal Medicine, Taipei Medical College, Taiwan.

出版信息

J Formos Med Assoc. 1998 Feb;97(2):131-4.

PMID:9509850
Abstract

The production of superoxide radicals as a result of decreased Cu,Zn-superoxide dismutase activity is considered to be the most important factor in the pathogenesis of diethyldithiocarbamate (DDC)-induced gastric antral ulcers in rats. The aim of the present study was to identify possible sources of superoxide radicals and the role of platelet-activating factor (PAF) in DDC-induced ulcer formation. Groups of rats were pretreated with a drug or antiserum before DDC (800 mg/kg) administration. The size of the DDC-induced gastric antral ulcers was measured. Pretreatment with anti-rat polymorphonuclear leukocyte serum or CV-3988 (a specific antagonist of PAF) 20 mg/kg significantly reduced the size of DDC-induced gastric antral ulcers. The results confirmed that superoxide radicals play an important role in the pathogenesis of DDC-induced gastric ulcer in rats and suggested that NADPH (reduced nicotinamide-adenine dinucleotide phosphate) oxidase in PAF-activated polymorphonuclear leukocytes may be involved in the generation of these radicals.

摘要

由于铜锌超氧化物歧化酶活性降低而产生超氧自由基,被认为是二乙基二硫代氨基甲酸盐(DDC)诱导的大鼠胃窦溃疡发病机制中最重要的因素。本研究的目的是确定超氧自由基的可能来源以及血小板活化因子(PAF)在DDC诱导的溃疡形成中的作用。在给予DDC(800mg/kg)之前,用药物或抗血清对大鼠进行预处理。测量DDC诱导的胃窦溃疡的大小。用抗大鼠多形核白细胞血清或20mg/kg的CV-3988(PAF的特异性拮抗剂)预处理可显著减小DDC诱导的胃窦溃疡的大小。结果证实超氧自由基在DDC诱导的大鼠胃溃疡发病机制中起重要作用,并提示PAF激活的多形核白细胞中的NADPH(还原型烟酰胺腺嘌呤二核苷酸磷酸)氧化酶可能参与这些自由基的产生。

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