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活性氧物质在甲基[5-[[4-(2-吡啶基)-1-哌嗪基]羰基]-1H-苯并咪唑-2-基]氨基甲酸酯对仓鼠抗锡兰钩虫的化学预防作用中的作用

Role of reactive oxygen species in the chemoprophylactic action of methyl [5-[[4-(2-pyridinyl)-1-piperazinyl]-carbonyl]-1H-benzimidazol-2 yl] carbamate in hamster against Ancylostoma ceylanicum.

作者信息

Singh S P, Srivastava J K, Katiyar J C, Srivastava V M

机构信息

Division of Biochemistry, Central Drug Research Institute, Lucknow, India.

出版信息

Biochem Pharmacol. 1994 Jun 15;47(12):2253-7. doi: 10.1016/0006-2952(94)90263-1.

Abstract

To delineate mechanisms involved in the prophylactic action of methyl [5-[[4-(2-pyridinyl)-1-piperazinyl]-carbonyl]-1H-benzimidazol-2 yl] carbamate (compound 81/470) in hamster against Ancylostoma ceylanicum infection, plasma level of the compound and status of reactive oxygen metabolites in jejunum at different periods of the drug treatment were examined. The compound was found to enhance the generation of both O2- and H2O2 by the jejunum possibly by activating xanthine oxidase. This stimulation was found to be both time and dose dependent. At 100 mg/kg dose the increase in O2- production could be recorded at least upto 50 days, whereas at 25 mg/kg the stimulation remained effective upto 20 days only, and at 5 mg/kg there was no change in the activity. This correlated well with the reported prophylactic pattern of the compound i.e. upto 45 and 7 days by 100 and 25 mg/kg doses, respectively. Plasma level of the compound also exhibited dose dependent variation. The compound given at 100 mg/kg dose could be detected in significant concentration upto at least 42 days while that given in 25 and 5 mg/kg doses was present in equivalent concentration upto 14 days and 1 day, respectively. It is concluded that the activation of respiratory burst in the jejunum induced by the persistent presence of compound 81/470 may represent one of the important mechanisms for the chemoprophylactic activity of this anthelmintic.

摘要

为了阐明甲基[5-[[4-(2-吡啶基)-1-哌嗪基]羰基]-1H-苯并咪唑-2-基]氨基甲酸酯(化合物81/470)对仓鼠预防锡兰钩虫感染的作用机制,检测了药物治疗不同时期该化合物的血浆水平以及空肠中活性氧代谢产物的状态。发现该化合物可能通过激活黄嘌呤氧化酶增强空肠中O2-和H2O2的生成。这种刺激具有时间和剂量依赖性。在100mg/kg剂量下,O2-生成的增加至少可记录到50天,而在25mg/kg剂量下,刺激仅在20天内有效,在5mg/kg剂量下活性没有变化。这与该化合物报道的预防模式很好地相关,即100mg/kg和25mg/kg剂量分别可达45天和7天。该化合物的血浆水平也呈现剂量依赖性变化。100mg/kg剂量给予的化合物在至少42天内可检测到显著浓度,而25mg/kg和5mg/kg剂量给予的化合物分别在14天和1天内以等效浓度存在。结论是,化合物81/470的持续存在诱导空肠呼吸爆发的激活可能是这种驱虫药化学预防活性的重要机制之一。

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