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新型正性肌力药物维纳利酮对离体犬心室乳头肌细胞内电位的影响 被引量:4

Effect of a New Positive Inotropic Agent(OPC-8212) on Intracellular Potential of Isolated Canine Ventricular Papillary Muscle
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摘要 作者采用微机化的智能仪记录及处理资料,研究了我校新合成药维纳利酮(又名OPC—8212)对14例犬心肌细胞内电位的影响。结果:静息电位(RP)、动作电位振幅(APA)和0期去极最大速度(V_(max))在维纳利酮作用前后均无显著差异,而动作电位全程(APT)、动作电位复极至1/3时程(APD1/3)及复极至2/3时程(APD 2/3)均有明显增加。平台期有所抬高。提示维纳利酮并不影响心肌细胞膜静息时的K^+通透性,也不影响快Na^+通道的激活和开放数目。而有可能增加Ca^(2+)通道的开放时间、增加Ca^(2+)内流;也可能同时具有减弱延迟外向钾电流(Ik)和内向整流钾电流(Ik_1)的作用。因此维纳利酮有可能成为一种很有希望的非甙、非儿茶酚胺类的新型正性肌力药物。 Tnis Andy Med intraCellularatro-eleotrode techniO to ob8erve the effat OfOPC-8212 (Vesnarinon6on 1niracel1ular PO-tentisl Of hotaled Canine ventriCUl8r paPil-lary mWe. The record and data proces-aing were eq16ted by comPUerbed1nt6lled1te 1ndroent designed byOllme1ves.The results of intracellar sord in l4canine veniriodl8r PaP1llary muscle shOwednO slgallleaat thenge ln the resting PO-tenita1 (RP), amPlitude of atiOn poeatta1(APA) and matrim dePOlarbe velocityof 0 Pwt (Vm..). Bu ~chatly ln-oreaSed wbD1e wtton of at1On poteottal(APT). The dundiOn of rePOl8rhatiOnto 1/3 (APD 1 /a) and to 2/3 (APD2/8)steniftoantly increased too. The plateauptw rais6d. These results suggeSt thatK+ permeab1llty at reSt1ng myMrdiac cel1membrane may the nOt been effeCted byOPC--a212. ACt1Vatw Of the fast sodiilmcwte1 may have nO been effected tOO.The reanlts of our Andle8 also SUgge thattwtd flOw of Ca'+ inOMd. Th6delayed ootward K+ (Ik) and th9 inwardredfwt K+ current (Ik, ) POssible de-creased. ThUs, the OPC-8212 mgh become aWtwside and boeOhOlamine newpebo thetrOPic drUg.
出处 《华西医科大学学报》 CSCD 1990年第2期159-162,共4页 Journal of West China University of Medical Sciences
基金 国家攻关资助
关键词 维纳利酮 心室乳头肌 细胞内电位 Vesnarinone Ventricular papillary muscle Intracellular potential
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  • 1林代平,蓝庭剑.维那利酮对离体家兔心室乳头肌动作电位和乳头肌张力影响的同步观察[J].华西医科大学学报,1993,24(2):156-159. 被引量:1
  • 2韩五成,秦韵,张尊仪,周素珍,杨正菀.国产新型强心药维司力农正性肌力作用的研究─—离体试验[J].华西医科大学学报,1994,25(3):316-320. 被引量:5
  • 3郭祖超,医用数理统计方法,1965年
  • 4Yue D T,Biophys J,1989年,55卷,2期,37页
  • 5Lathrop DA, Nanasi PP, Schwartz A et al. Ionic basis for OPC- 8212- induced increase in action potential duration in isolated rabbit, guinea pig and human ventricular myocytes [J]. Eur - J - Pharmacol, 1993 Aug 24; 240 (2 - 3): 127
  • 6Vaughan Williams EM: Classification of antiarrhythmic drugs,in Sandoe E, Flendsted - Jensen E, Olsen K (eds): Sympos- ium on Cardiac Arrhythmias [ M ]. Sodertclje, Sweden AB Astra, 1970; 449 ~ 453
  • 7Zhang ZH, Follmer CH, Sarma JSM, et al. Effect of ambasil- ide, a new class Ⅲ agent, on plateau currents in isolated guinea pig ventricular myocytes: block of delayed outward potassium current [J]. J Pharmacol Exp Ther 1992; 263:40-45
  • 8Colatsky TJ, Argentierri TM. Potassium channel blockers as antiarrhythmic drugs [J]. Drug Develop Res 1994; 33:235
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