Suppr超能文献

抗疟药青蒿素对离体豚鼠心脏标本的抗胆碱能作用。

Anticholinergic effects of artemisinin, an antimalarial drug, in isolated guinea pig heart preparations.

作者信息

Hara Yukio, Yamawaki Hideyuki, Shimada Masami, Okada Kiyohiro, Tanai Toshiki, Ichikawa Daiki, Miyake Kimihito, Kizaki Keiichiro

机构信息

Laboratory of Veterinary Pharmacology, School of Veterinary Medicine and Animal Sciences, Kitasato University, Towada, Aomori 034-8628, Japan.

出版信息

J Vet Med Sci. 2007 Jul;69(7):697-702. doi: 10.1292/jvms.69.697.

Abstract

Concern has been growing about the cardiac toxicity of antimalarial drugs. Artemisinin, a unique type of antimalarial drug originating from a Chinese medicinal plant, has minimal adverse effects, but it has been reported to inhibit delayed rectifier potassium current, a voltage-gated potassium current. However, no studies have been published concerning the effect of artemisinin on ligand-gated potassium currents. Therefore, in the present study, we examined the influence of artemisinin on the acetylcholine receptor-operated potassium current (IK.ACh), a ligand-gated potassium current, in guinea pig atrial myocytes using a patch clamp technique. Artemisinin (1 to 300 microM) inhibited I(K.ACh) induced by extracellular application of both carbachol (1 microM) and adenosine (10 microM) and that induced by intracellular loading of GTPgammaS (100 microM) in a concentration-dependent manner. Artemisinin inhibited carbachol-induced, adenosine-induced, and GTPgammaS-activated IK.ACh within almost the same concentration range. In left atria, artemisinin (1 to 100 microM) partially reversed the shortening of action potential duration induced by carbachol in a concentration-dependent manner. Carbachol-induced negative inotropic action in left atria was also inhibited by artemisinin (10 to 300 microM). In conclusion, we suggest that the anticholinergic action of artemisinin is mediated through inhibition of IK.ACh via inhibition of the muscarinic potassium channel and/or associated GTP-binding proteins.

摘要

人们对抗疟药物的心脏毒性越来越担忧。青蒿素是一种源自中国药用植物的独特抗疟药物,副作用极小,但据报道它能抑制延迟整流钾电流,一种电压门控钾电流。然而,尚未有关于青蒿素对配体门控钾电流影响的研究发表。因此,在本研究中,我们使用膜片钳技术研究了青蒿素对豚鼠心房肌细胞中乙酰胆碱受体介导的钾电流(IK.ACh),一种配体门控钾电流的影响。青蒿素(1至300微摩尔)以浓度依赖性方式抑制细胞外应用卡巴胆碱(1微摩尔)和腺苷(10微摩尔)诱导的IK.ACh以及细胞内加载GTPγS(100微摩尔)诱导的IK.ACh。青蒿素在几乎相同的浓度范围内抑制卡巴胆碱诱导的、腺苷诱导的和GTPγS激活的IK.ACh。在左心房中,青蒿素(1至100微摩尔)以浓度依赖性方式部分逆转了卡巴胆碱诱导的动作电位时程缩短。青蒿素(10至300微摩尔)也抑制了卡巴胆碱在左心房中诱导的负性肌力作用。总之,我们认为青蒿素的抗胆碱能作用是通过抑制毒蕈碱钾通道和/或相关GTP结合蛋白来抑制IK.ACh介导的。

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