Wagner J, Schümann H J, Knorr A, Rohm N, Reidemeister J C
Naunyn Schmiedebergs Arch Pharmacol. 1980 May;312(1):99-102. doi: 10.1007/BF00502581.
In isolated electrically driven right auricular strips of human hearts (1 Hz at 37 degrees C) the ability of the endogenous catecholamines noradrenaline, adrenaline, and dopamine to mediate positive inotropic effects by stimulation of myocardial alpha-adrenoceptors was investigated. 1. The concentration-response curve for the positive inotropic effect of noradrenaline was shifted to the right by pindolol, 10(-8)M, whereas the additional blockade by phentolamine, 3 x 10(-6)M, was without further effect; therefore, the positive inotropic effect of noradrenaline is mediated by beta-adrenoceptors only. 2. In contrast, the positive inotropic effects of adrenaline as well as of dopamine are caused by stimulation of both, beta- and alpha-adrenoceptors. 3. These results are discussed with respect to the possible physiological and pathophysiological function of myocardial alpha-adrenoceptors.
在离体的人心脏电驱动右心房条带(37℃下1Hz)中,研究了内源性儿茶酚胺去甲肾上腺素、肾上腺素和多巴胺通过刺激心肌α-肾上腺素能受体介导正性肌力作用的能力。1. 对于去甲肾上腺素的正性肌力作用,其浓度-反应曲线被10(-8)M的吲哚洛尔向右移动,而3×10(-6)M的酚妥拉明进一步阻断没有额外作用;因此,去甲肾上腺素的正性肌力作用仅由β-肾上腺素能受体介导。2. 相比之下,肾上腺素和多巴胺的正性肌力作用是由β-和α-肾上腺素能受体的刺激共同引起的。3. 就心肌α-肾上腺素能受体可能的生理和病理生理功能对这些结果进行了讨论。