Endoh M, Brodde O E, Schümann H J
Naunyn Schmiedebergs Arch Pharmacol. 1976 Nov;295(2):109-15. doi: 10.1007/BF00499441.
The time course of changes of the level of 3',5'-cyclic AMP (cAMP) and of the tension developed under stimulation of alpha- and beta-adrenoceptors by phenylephrine was investigated in the isolated rabbit papillary muscle. Furthermore the dose-response relationships for increases of cAMP and of developed tension elicited by phenylephrine were determined. 1. A submaximally effective concentration of phenylephrine (10(-5) M) increased significantly the level of cAMP of the papillary muscle at 15 and 30 s by 45 and 36% respectively; the level of cAMP returned to the control value at 60 s after the administration. The developed tension increased significantly not before 45 s and reached its maximal level at 180 s. 2. When alpha-adrenoceptors were blocked by phentolamine (10(-6) M), the positive inotropic effect of phenylephrine was decreased significantly but the increase of cAMP induced by phenylephrine was not reduced. In the presence of phentolamine the increase of cAMP induced by phenylephrine lasted longer than in the control experiments. 3. The effects of phenylephrine (10(-5) M) both on the level of cAMP and the developed tension mediated via stimulation of beta-adrenoceptors in the presence of phentolamine were enhanced by the phosphodiesterase inhibitor papaverine throughout the course of responses. 4. Phenylephrine produced an increase in developed tension as well as in cAMP. The corresponding dose-response curves run parallel to each other but differed by about 1.5 log units whereby the developed tension was evoked by lower concentrations. Phentolamine (10(-6) M) shifted the curve for the positive inotropic action by about 1.5 log units but did not affect that for increase in cAMP. Therefore, in the presence of the alpha-adrenolytic drug phentolamine the difference between both curves became smaller so that both curves were superimposed. Papaverine (10(-5) M) shifted the whole curve for cAMP upwards and enhanced the maximal contractile response to phenylephrine mediated by stimulation of beta-adrenoceptors. 5. The present results indicate that the positive inotropic action of phenylephrine in lower concentrations (less than 10(-5) M) induced by stimulation of alpha-adrenoceptors is independent of the level of cAMP. The positive inotropic action of the higher concentrations of phenylephrine induced via stimulation of beta-adrenoceptors was preceded by an accumulation of cAMP; the inhibition of the cAMP phosphodiesterase activity by papaverine enhanced the actions of phenylephrine both on the level of cAMP and on the contractile force.
在离体兔乳头肌中研究了3',5'-环磷酸腺苷(cAMP)水平的变化时间进程以及去氧肾上腺素刺激α和β肾上腺素能受体时所产生的张力变化。此外,还确定了去氧肾上腺素引起的cAMP增加和张力增加的剂量-反应关系。1. 次最大有效浓度的去氧肾上腺素(10⁻⁵ M)在给药后15秒和30秒时分别使乳头肌的cAMP水平显著升高45%和36%;给药后60秒时cAMP水平恢复到对照值。所产生的张力在45秒之前没有显著增加,在180秒时达到最大水平。2. 当用酚妥拉明(10⁻⁶ M)阻断α肾上腺素能受体时,去氧肾上腺素的正性肌力作用显著降低,但去氧肾上腺素诱导的cAMP增加并未减少。在酚妥拉明存在的情况下,去氧肾上腺素诱导的cAMP增加持续的时间比对照实验中更长。3. 在整个反应过程中,磷酸二酯酶抑制剂罂粟碱增强了去氧肾上腺素(10⁻⁵ M)在酚妥拉明存在时对cAMP水平和通过刺激β肾上腺素能受体介导的所产生张力的作用。4. 去氧肾上腺素使所产生的张力以及cAMP增加。相应的剂量-反应曲线相互平行,但相差约1.5个对数单位,其中较低浓度即可引起所产生的张力。酚妥拉明(10⁻⁶ M)使正性肌力作用的曲线右移约1.5个对数单位,但不影响cAMP增加的曲线。因此,在α肾上腺素能阻断药酚妥拉明存在时,两条曲线之间的差异变小,从而两条曲线相互重叠。罂粟碱(10⁻⁵ M)使cAMP的整个曲线向上移动,并增强了由刺激β肾上腺素能受体介导的对去氧肾上腺素的最大收缩反应。5. 目前的结果表明,低浓度(低于10⁻⁵ M)的去氧肾上腺素通过刺激α肾上腺素能受体诱导的正性肌力作用与cAMP水平无关。高浓度的去氧肾上腺素通过刺激β肾上腺素能受体诱导的正性肌力作用之前有cAMP的积累;罂粟碱对cAMP磷酸二酯酶活性的抑制增强了去氧肾上腺素对cAMP水平和收缩力的作用。