Corder D W, Heyliger C E, Beamish R E, Dhalla N S
Am Heart J. 1984 Mar;107(3):537-42. doi: 10.1016/0002-8703(84)90097-8.
We have investigated alterations in adrenergic receptors and adenylate cyclase activity in cardiac membranes from rats injected with 40 mg/kg intraperitoneal isoproterenol. Reduction in the number of beta-adrenergic and alpha-adrenergic receptors, as assessed by changes in specific binding of 3H-dihydroalprenolol (DHA) and 3H-dihydroergocryptine (DHE), was observed only at 9 and 24 hours after isoproterenol injection, respectively. On the other hand, epinephrine-stimulated, NaF-stimulated, and Gpp (NH)p-stimulated adenylate cyclase activity was decreased as early as 3 hours after isoproterenol treatment without changes in the basal adenylate cyclase activity. These results demonstrate a defect in the adrenergic receptor-adenylate cyclase system during the development of catecholamine-induced cardiomyopathy and may partly explain the attenuated inotropic adrenergic response of the heart under stressful situations.
我们研究了腹腔注射40mg/kg异丙肾上腺素的大鼠心脏膜中肾上腺素能受体和腺苷酸环化酶活性的变化。通过3H-二氢阿普洛尔(DHA)和3H-二氢麦角隐亭(DHE)特异性结合的变化评估,β-肾上腺素能受体和α-肾上腺素能受体数量的减少分别仅在异丙肾上腺素注射后9小时和24小时观察到。另一方面,早在异丙肾上腺素治疗后3小时,肾上腺素刺激、NaF刺激和Gpp(NH)p刺激的腺苷酸环化酶活性就降低了,而基础腺苷酸环化酶活性没有变化。这些结果表明在儿茶酚胺诱导的心肌病发展过程中,肾上腺素能受体-腺苷酸环化酶系统存在缺陷,并且可能部分解释了在应激情况下心脏变力性肾上腺素能反应减弱的原因。