Miao L, Qiu Z, Morgan J P
Charles A. Dana Research Institute, Boston, Massachusetts, USA.
Am J Physiol. 1996 Feb;270(2 Pt 2):H678-84. doi: 10.1152/ajpheart.1996.270.2.H678.
We tested the hypothesis that the negative inotropic effect (NIE) of cocaine is mediated, at least in part, by cholinergic stimulation and can be correlated with the degree of adenosine 3',5'-cyclic monophosphate (cAMP) dependency of the inotropic state. Cardiac myocytes were isolated from left ventricles of ferrets and loaded with the fluorescent Ca2+ indicator indo 1. Cells were placed in physiological solution containing 2.0 mM Ca2+ and stimulated at 0.5 Hz and 30 degrees C. Cocaine decreased peak cell shortening and peak intracellular Ca2+ in a concentration-dependent manner (10(-8)-10(-4) M). The concentration-response curve of cocaine was shifted significantly downward compared with those of lidocaine and procaine in the same range of concentrations. Atropine (10(-6) M) shifted the concentration-response curve of cocaine, but not those of lidocaine and procaine, rightward, with a pA2 value (7.66) similar to that obtained with carbachol (7.99). With prior addition of isoproterenol (ISO, 10(-8) M) or increased Ca2+ (4.0 mM) to increase cell shortening to the same degree (approximately 60%), cocaine and carbachol decreased contractility to a significantly greater extent in ISO-stimulated myocytes. To clarify whether these treatments changed responsiveness of the contractile elements to Ca2+, the effect of 2,3-butanedione monoxime, an agent that interferes with the interaction of myosin and actin, was tested with previous addition of ISO or increased Ca2+, and no differential effect occurred. Therefore, we postulate that 1) the NIE of cocaine on myocytes is caused by decreased Ca2+ availability; 2) this effect is due to specific stimulation of cholinergic receptors in addition to other direct myocardial (probably local anesthetic) effects; and 3) the NIE correlates with the level of cAMP dependence of the inotropic state.
可卡因的负性肌力作用(NIE)至少部分是由胆碱能刺激介导的,并且可能与肌力状态对3',5'-环磷酸腺苷(cAMP)的依赖程度相关。从雪貂的左心室分离出心肌细胞,并加载荧光Ca2+指示剂indo 1。将细胞置于含有2.0 mM Ca2+的生理溶液中,在0.5 Hz和30℃下进行刺激。可卡因以浓度依赖性方式(10(-8)-10(-4) M)降低细胞缩短峰值和细胞内Ca2+峰值。在相同浓度范围内,与利多卡因和普鲁卡因相比,可卡因的浓度-反应曲线显著下移。阿托品(10(-6) M)使可卡因的浓度-反应曲线右移,但未使利多卡因和普鲁卡因的浓度-反应曲线右移,其pA2值(7.66)与卡巴胆碱(7.99)相似。预先加入异丙肾上腺素(ISO,10(-8) M)或增加Ca2+(4.0 mM)以使细胞缩短程度增加到相同水平(约60%)后,可卡因和卡巴胆碱在ISO刺激的心肌细胞中使收缩性降低的程度显著更大。为了阐明这些处理是否改变了收缩元件对Ca2+的反应性,在预先加入ISO或增加Ca2+的情况下测试了2,3-丁二酮单肟(一种干扰肌球蛋白和肌动蛋白相互作用的药物)的作用,未出现差异效应。因此,我们推测:1)可卡因对心肌细胞的NIE是由Ca2+可用性降低引起的;2)这种效应除了其他直接的心肌(可能是局部麻醉)作用外,还归因于胆碱能受体的特异性刺激;3)NIE与肌力状态对cAMP的依赖水平相关。