Wilson A N, Broadley K J
Department of Pharmacology, Welsh School of Pharmacy, University of Wales College of Cardiff, U.K.
Can J Physiol Pharmacol. 1989 Apr;67(4):294-303. doi: 10.1139/y89-048.
The effects of adenosine were examined upon the tension developed by isolated paced left atria, left ventricular papillary muscles, and right ventricular strips, and upon the spontaneous rate of contraction of right atria of guinea pigs. Three aspects of the direct and indirect actions were examined: the direct effects upon resting developed tension and rate, the indirect activity when added to tissues prestimulated by isoprenaline, and the indirect activity upon isoprenaline concentration--response curves when added prior to exposure to isoprenaline. The direct effects on the atria were decreases in left atrial tension and right atrial rate. These responses were antagonized by 8-phenyltheophylline (8-PT) and therefore were due to stimulation of cell surface P1 purinoceptors. This antagonism was greater in the left atria than the right. The direct ventricular effects were, in contrast, increases in force of contraction, which were not antagonized by 8-PT. This positive inotropy was also unaffected by reserpine pretreatment of the guinea pigs and therefore not due to release of endogenous catecholamines. A possible intracellular effect of adenosine is discussed. Adenosine reduced the isoprenaline-prestimulated tension or rate in both atrial and ventricular tissues, and this indirect effect was susceptible to antagonism by 8-PT. In the presence of adenosine, concentration-response curves of the left and right atria for isoprenaline were displaced to the right, and the maxima were reduced. In contrast, there was no antagonism of the papillary muscle curves to isoprenaline, but the maximum developed tension was elevated. The minimal inhibitory effects of adenosine in ventricular muscles and the high concentrations required are discussed in the context of a physiological role for endogenous adenosine in attenuating cardiac overstimulation by the sympathetic nervous system or endogenously released catecholamines.
研究了腺苷对豚鼠离体起搏左心房、左心室乳头肌和右心室条带所产生张力的影响,以及对右心房自发收缩频率的影响。研究了直接和间接作用的三个方面:对静息时产生的张力和频率的直接影响;加入经异丙肾上腺素预刺激的组织时的间接活性;在暴露于异丙肾上腺素之前加入时对异丙肾上腺素浓度 - 反应曲线的间接活性。腺苷对心房的直接作用是降低左心房张力和右心房频率。这些反应被8 - 苯基茶碱(8 - PT)拮抗,因此是由于细胞表面P1嘌呤受体的刺激。这种拮抗作用在左心房比右心房更强。相比之下,腺苷对心室的直接作用是增加收缩力,这不受8 - PT拮抗。这种正性肌力作用也不受豚鼠利血平预处理的影响,因此不是由于内源性儿茶酚胺的释放。讨论了腺苷可能的细胞内作用。腺苷降低了心房和心室组织中经异丙肾上腺素预刺激后的张力或频率,并且这种间接作用易被8 - PT拮抗。在有腺苷存在的情况下,左、右心房对异丙肾上腺素的浓度 - 反应曲线向右移位,且最大值降低。相比之下,乳头肌曲线对异丙肾上腺素没有拮抗作用,但最大产生的张力升高。在讨论内源性腺苷在减弱交感神经系统或内源性释放儿茶酚胺引起的心脏过度刺激中的生理作用时,探讨了腺苷在心室肌中的最小抑制作用及其所需的高浓度。