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去氧肾上腺素在普萘洛尔存在时的正性肌力作用。峰值力出现时间和舒张时间增加,而环磷酸腺苷(c-AMP)不增加。

The positive inotropic effect of phenylephrine in the presence of propranolol. Increase in time to peak force and in relaxation time without increase in c-AMP.

作者信息

Brückner R, Hackbarth I, Meinertz T, Schmelzle B, Scholz H

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1978 Jul;303(3):205-11. doi: 10.1007/BF00498045.

Abstract

The effects of phenylephrine on the shape of the contraction curve and on the cyclic adenosine 3',5'-monophosphate (c-AMP) content were studied in electrically driven (frequency 0.2 Hz) cat papillary muscles. All experiments were done in the presence of 1 micron propranolol in order to minimize interference from beta-adrenoceptors. 1. Phenylephrine increased the force of contraction in a concentration-dependent manner. Maximal effects (about 200% of control) occurred at 30 micron phenylephrine. 2. The positive inotropic effect (PIE) of phenylephrine was antagonized by phentolamine. Phentolamine, 5 micron, produced a parallel shift of the concentration-response curve for the PIE of phenylephrine by about two log units to the right. 3. The PIE of 30 micron phenylephrine occurred without any detectable increase in the c-AMP levels of the preparations. 4. The PIE of 30 micron phenylephrine developed about three times more slowly than the PIE of an equieffective concentration of isoprenaline. 5. The PIE of phenylephrine was accompanied by significant, concentration-dependent increases in both time to peak force and relaxation time. 6. It is concluded that the PIE of phenylephrine in the presence of propranolol is mediated mainly by a stimulation of alpha-adrenoceptors. It is unlikely to be related to an increase in c-AMP. With respect to time course and influence on the shape of the contraction curve it is qualitatively different from the effects of beta-adrenoceptor stimulation. These data are taken to support the hypothesis that the mechanical effects of alpha- and beta-adrenoceptor stimulating agents on the heart are produced by different mechanisms.

摘要

在电驱动(频率0.2Hz)的猫乳头肌中研究了去氧肾上腺素对收缩曲线形状和环磷酸腺苷(c-AMP)含量的影响。所有实验均在1微摩尔普萘洛尔存在的情况下进行,以尽量减少β-肾上腺素受体的干扰。1. 去氧肾上腺素以浓度依赖的方式增加收缩力。在30微摩尔去氧肾上腺素时出现最大效应(约为对照的200%)。2. 酚妥拉明拮抗去氧肾上腺素的正性肌力作用(PIE)。5微摩尔酚妥拉明使去氧肾上腺素PIE的浓度-反应曲线平行右移约两个对数单位。3. 30微摩尔去氧肾上腺素的PIE出现时,制剂的c-AMP水平没有任何可检测到的增加。4. 30微摩尔去氧肾上腺素的PIE发展速度比等效应浓度的异丙肾上腺素的PIE慢约三倍。5. 去氧肾上腺素的PIE伴随着达峰力时间和舒张时间显著的、浓度依赖性的增加。6. 得出结论,在普萘洛尔存在的情况下,去氧肾上腺素的PIE主要由α-肾上腺素受体的刺激介导。它不太可能与c-AMP的增加有关。就时间进程和对收缩曲线形状的影响而言,它在性质上与β-肾上腺素受体刺激的效应不同。这些数据支持以下假设,即α-和β-肾上腺素受体激动剂对心脏的机械效应是由不同机制产生的。

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