Romano F D, Dobson J G
Department of Physiology, Midwestern University, Downers Grove, IL 60515, USA.
Life Sci. 1996;58(6):493-502. doi: 10.1016/0024-3205(95)02314-3.
Interstitial levels and release of adenosine have been shown to be greater for aged adult hearts compared to young adult hearts. Furthermore, blockade of A1 adenosine receptors in the aged adult heart prevents the reduced contractile and metabolic response to isoproterenol. The aim of this study was to determine whether there is an enhanced antiadrenergic effect of adenosine in the aged adult heart. Ventricular membranes from young and aged adult hearts were incubated in the presence of isoproterenol (ISO) and phenylisopropyladenosine (PIA) either alone or in combination. Basal and ISO-enhanced adenylyl cyclase activity were significantly reduced in the membranes from aged rats. PIA alone, at 0.1 nM to 100 microM, had no direct effect on basal adenylyl cyclase activity in membranes from either group. In the presence of either 100 nM or 1 microM ISO, 100 microM PIA significantly attenuated ISO-enhanced adenylyl cyclase activity to a greater extent in the aged adult heart membranes (78 or 48% for the aged vs. 37 or 25% for the young). Moreover, in the presence of 100 nM ISO the IC50 for the PIA concentration response curve was shifted to the left for the aged ventricular membranes as compared to the membranes from young adults (1.62 x 10(-7) M vs 1.5 x 10(-6) M, aged vs young, respectively). The enhanced inhibition of adenylyl cyclase is associated with an increase in adenosine A1 receptor density (23.7 +/- 3.5 vs 14.7 +/- 1.7 fmol/mg, aged vs young) and Kd (6.1 +/- 1.7 vs 2.2 +/- 0.5 nM, aged vs young) in the aged adult heart membranes as determined by [3H]DPCPX binding. These results suggest that the reduced response to catecholamines in the aged adult heart may be due, at least in part, to an enhanced expression of the antiadrenergic effect of adenosine on beta-adrenergic receptor mediated activation of adenylyl cyclase.
与年轻成年心脏相比,老年成年心脏的腺苷间质水平和释放量更高。此外,阻断老年成年心脏中的A1腺苷受体可防止对异丙肾上腺素的收缩和代谢反应降低。本研究的目的是确定老年成年心脏中腺苷的抗肾上腺素能作用是否增强。将年轻和老年成年心脏的心室膜分别单独或联合置于异丙肾上腺素(ISO)和苯异丙基腺苷(PIA)存在的环境中进行孵育。老年大鼠膜中的基础腺苷酸环化酶活性和ISO增强的腺苷酸环化酶活性均显著降低。单独使用PIA,浓度在0.1 nM至100 μM时,对两组膜中的基础腺苷酸环化酶活性均无直接影响。在存在100 nM或1 μM ISO的情况下,100 μM PIA在老年成年心脏膜中对ISO增强的腺苷酸环化酶活性的抑制作用更为显著(老年组分别为78%或48%,年轻组为37%或25%)。此外,在存在100 nM ISO的情况下,与年轻成年心脏膜相比,老年心室膜的PIA浓度反应曲线的IC50向左移动(老年组为1.62×10−7 M,年轻组为1.5×10−6 M)。通过[3H]DPCPX结合测定发现,老年成年心脏膜中腺苷酸环化酶抑制作用的增强与腺苷A1受体密度增加(老年组为23.7±3.5 fmol/mg,年轻组为14.7±1.7 fmol/mg)和Kd增加(老年组为6.1±1.7 nM,年轻组为2.2±0.5 nM)有关。这些结果表明,老年成年心脏对儿茶酚胺反应降低可能至少部分是由于腺苷对β-肾上腺素能受体介导的腺苷酸环化酶激活的抗肾上腺素能作用增强所致。