Keely S L, Lincoln T M, Corbin J D
Am J Physiol. 1978 Apr;234(4):H432-8. doi: 10.1152/ajpheart.1978.234.4.H432.
In the isolated perfused rat heart, epinephrine produced a rapid, concentration-dependent increase in cyclic adenosine 3',5'-monophosphate (cAMP), activation of cAMP-dependent protein kinase, activation of phosphorylase, and increase in contractile force. At epinephrine concentrations of 1 micron or less, acetylcholine antagonized all these beta-adrenergic effects and also increased cyclic guanosine 3',5'-monophosphate (cGMP) levels. When used alone, acetylcholine produced a rapid elevation of cGMP and markedly diminished contractile force but did not significantly lower basal cAMP levels or cAMP-dependent protein kinase activity. The data suggest that changes in cAMP-dependent protein kinase activity can explain the antagonism of epinephrine-induced activation of phosphorylase by acetylcholine, but cannot completely account for the inhibitory effect of the cholinergic agent on contractile force.
在离体灌注大鼠心脏中,肾上腺素可使环磷酸腺苷(cAMP)迅速产生浓度依赖性增加,激活依赖cAMP的蛋白激酶,激活磷酸化酶,并增强收缩力。在肾上腺素浓度为1微摩尔或更低时,乙酰胆碱可拮抗所有这些β-肾上腺素能效应,还可提高环磷酸鸟苷(cGMP)水平。单独使用时,乙酰胆碱可使cGMP迅速升高,并显著减弱收缩力,但不会显著降低基础cAMP水平或依赖cAMP的蛋白激酶活性。数据表明,依赖cAMP的蛋白激酶活性变化可以解释乙酰胆碱对肾上腺素诱导的磷酸化酶激活的拮抗作用,但不能完全解释胆碱能药物对收缩力的抑制作用。