Ohta Yoshiji, Kobayashi Takashi, Inui Kazuo, Yoshino Junji, Nakazawa Saburo
Department of Chemistry, School of Medicine, Fujita Health University, Toyoake, Aichi, Japan.
Jpn J Pharmacol. 2002 Dec;90(4):295-303. doi: 10.1254/jjp.90.295.
The protective effect of ebselen, which possesses glutathione peroxidase-like activity and antioxidative and anti-inflammatory properties, against the progression of acute gastric mucosal lesions was examined in rats with a single intraperitoneal injection of compound 48/80 (0.75 mg/kg). Ebselen (50, 100 or 200 mg/kg) was orally administered 0.5 h after compound 48/80 treatment, at which time gastric mucosal lesions appeared. Post-administered ebselen suppressed gastric mucosal lesion progression at 3 h after compound 48/80 treatment dose-dependently, although no dose of ebselen affected the decreased gastric mucosal blood flow and increased serum serotonin and histamine concentrations found at 3 h after the treatment. A decrease in Se-glutathione peroxidase activity and increases in myeloperoxidase and xanthine oxidase activities and the concentration of thiobarbituric acid reactive substances were found in gastric mucosal tissues at 0.5 h after compound 48/80 treatment, and these changes were further enhanced at 3 h. Post-administered ebselen attenuated all these changes found at 3 h after compound 48/80 treatment dose-dependently. The present results indicate that ebselen exerts a protective effect against the progression of compound 48/80-induced acute gastric mucosal lesions in rats, and they suggest that this protective effect of ebselen could be due to its glutathione peroxidase-like activity and its antioxidative and anti-inflammatory properties.
依布硒啉具有谷胱甘肽过氧化物酶样活性以及抗氧化和抗炎特性,本研究通过对大鼠单次腹腔注射化合物48/80(0.75毫克/千克),考察了依布硒啉对急性胃黏膜损伤进展的保护作用。在化合物48/80处理0.5小时后口服给予依布硒啉(50、100或200毫克/千克),此时胃黏膜损伤已经出现。给药后的依布硒啉在化合物48/80处理后3小时剂量依赖性地抑制胃黏膜损伤进展,尽管任何剂量的依布硒啉均未影响处理后3小时出现的胃黏膜血流量降低以及血清5-羟色胺和组胺浓度升高。在化合物48/80处理后0.5小时,胃黏膜组织中硒-谷胱甘肽过氧化物酶活性降低,髓过氧化物酶和黄嘌呤氧化酶活性以及硫代巴比妥酸反应性物质浓度升高,并且这些变化在3小时时进一步增强。给药后的依布硒啉剂量依赖性地减轻了化合物48/80处理后3小时出现的所有这些变化。本研究结果表明,依布硒啉对化合物48/80诱导的大鼠急性胃黏膜损伤进展具有保护作用,并且提示依布硒啉的这种保护作用可能归因于其谷胱甘肽过氧化物酶样活性以及抗氧化和抗炎特性。