Anand-Srivastava M B
Department of Physiology, Faculty of Medicine, University of Montréal, Québec, Canada.
Am J Hypertens. 1993 Jun;6(6 Pt 1):538-41. doi: 10.1093/ajh/6.6.538.
We have recently shown that ANF-R2 receptors are coupled to the adenylyl cyclase/cAMP system through inhibitory guanine nucleotide regulatory protein (Gi). The present studies were undertaken to investigate the regulation of ANF-R2 receptor-mediated inhibition of adenylyl cyclase in spontaneously hypertensive rats (SHR) which have been reported to have high plasma ANF levels. ANF99-126 inhibited adenylyl cyclase activity in a concentration dependent manner in both aorta and heart sarcolemma from SHR and age-matched Wistar-Kyoto (WKY) rats, however, the extent of inhibition was greater in SHR as compared to WKY. On the other hand, ANF99-126 also inhibited the adenylyl cyclase activity in rat platelets from WKY rats in a concentration dependent manner, however, the inhibition in SHR was completely attenuated. In addition GTP gamma S stimulated adenylyl cyclase activity by about 600% in aorta from WKY rats and about 300% in SHR. On the other hand, the GTP gamma S-stimulated adenylyl cyclase activity was higher in platelets from SHR as compared to WKY. The observed difference may be attributed to the differential alterations in ANF-R2 receptor number or postreceptor events or both. Nonetheless, these results indicate that ANF-R2 receptors in platelets from SHR are differentially regulated than those in heart and aorta.
我们最近发现,心钠素受体2(ANF-R2)通过抑制性鸟嘌呤核苷酸调节蛋白(Gi)与腺苷酸环化酶/cAMP系统偶联。本研究旨在探讨在自发性高血压大鼠(SHR)中,ANF-R2受体介导的腺苷酸环化酶抑制作用的调节情况,据报道,SHR的血浆心钠素水平较高。心钠素99-126(ANF99-126)以浓度依赖性方式抑制SHR和年龄匹配的Wistar-Kyoto(WKY)大鼠主动脉和心肌细胞膜中的腺苷酸环化酶活性,然而,与WKY大鼠相比,SHR中的抑制程度更大。另一方面,ANF99-126也以浓度依赖性方式抑制WKY大鼠血小板中的腺苷酸环化酶活性,然而,SHR中的抑制作用完全减弱。此外,GTPγS使WKY大鼠主动脉中的腺苷酸环化酶活性提高约600%,使SHR中的提高约300%。另一方面,与WKY大鼠相比,SHR血小板中GTPγS刺激的腺苷酸环化酶活性更高。观察到的差异可能归因于ANF-R2受体数量或受体后事件或两者的差异改变。尽管如此,这些结果表明,SHR血小板中的ANF-R2受体与心脏和主动脉中的受体受到不同的调节。