Suppr超能文献

缓激肽可抑制酒精摄入,并在血管紧张素转换酶抑制剂产生的抑制作用中发挥作用。

Bradykinin suppresses alcohol intake and plays a role in the suppression produced by an ACE inhibitor.

作者信息

Robertson J M, Harding S, Grupp L A

机构信息

Department of Pharmacology, University of Toronto, Ontario, Canada.

出版信息

Pharmacol Biochem Behav. 1993 Dec;46(4):751-8. doi: 10.1016/0091-3057(93)90197-2.

Abstract

The possible role of the endogenous kinins in the control of alcohol intake was assessed in two experiments. In Experiment 1, naive rats, maintained on ad lib food and water, were given daily 40-min access to a 6% (w/v) alcohol solution and water. Daily intraperitoneal (IP) injections of captopril (20 mg/kg) significantly reduced alcohol intake, while pretreatment with subcutaneous (SC) injections of the bradykinin antagonist [D-Phe7]-bradykinin (100-300 micrograms/kg) attenuated the suppressive effect of captopril on alcohol intake. The saline vehicle or the bradykinin antagonist alone did not alter alcohol intake. In Experiment 2, bradykinin was administered daily at 100, 200, and 400 micrograms/kg doses SC either alone or in combination with captopril 10 mg/kg IP. Neither bradykinin nor captopril by themselves changed alcohol or water intake. Bradykinin combined with captopril stimulated water intake and reduced alcohol intake by up to 70%. This effect was not due to drug-induced changes in the pharmacokinetics of alcohol. The angiotensin II receptor antagonist [Sar1,Thr8]-angiotensin II at 250 and 500 micrograms/kg SC attenuated the stimulation of water intake but not the reduction in alcohol intake. It is suggested that by inhibiting kininase II, ACE inhibitors extend the duration of action of bradykinin and thereby unmask a potent inhibition of alcohol intake mediated by kinins--an effect that is dissociable from the accompanying stimulation of water intake. Taken together, these results point to an involvement of the kinin system in the regulation of alcohol intake and in particular to a role of bradykinin in the suppressive effect of ACE inhibitors on alcohol intake.

摘要

通过两个实验评估了内源性激肽在控制酒精摄入方面的可能作用。在实验1中,给自由摄取食物和水的未接触过酒精的大鼠每天提供40分钟饮用6%(w/v)酒精溶液和水的机会。每天腹腔注射卡托普利(20毫克/千克)可显著减少酒精摄入量,而预先皮下注射缓激肽拮抗剂[D - Phe7] - 缓激肽(100 - 300微克/千克)可减弱卡托普利对酒精摄入的抑制作用。单独使用生理盐水或缓激肽拮抗剂不会改变酒精摄入量。在实验2中,每天皮下注射剂量为100、200和400微克/千克的缓激肽,单独使用或与10毫克/千克腹腔注射的卡托普利联合使用。缓激肽和卡托普利单独使用时均未改变酒精或水的摄入量。缓激肽与卡托普利联合使用可刺激水的摄入并使酒精摄入量减少多达70%。这种作用并非由于药物引起的酒精药代动力学变化。皮下注射250和500微克/千克的血管紧张素II受体拮抗剂[Sar1, Thr8] - 血管紧张素II可减弱对水摄入的刺激,但不会减弱酒精摄入量的减少。提示通过抑制激肽酶II,血管紧张素转换酶抑制剂延长了缓激肽的作用持续时间,从而揭示了由激肽介导的对酒精摄入的有效抑制作用——这种作用与伴随的水摄入刺激可分离。综上所述,这些结果表明激肽系统参与了酒精摄入的调节,特别是缓激肽在血管紧张素转换酶抑制剂对酒精摄入的抑制作用中发挥了作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验