Beck J S, Burgess W J, Balment R J
School of Biological Sciences, University of Manchester, UK.
Ren Physiol Biochem. 1995 Sep-Oct;18(5):231-6. doi: 10.1159/000173920.
Using a micro-radioimmunoassay, cAMP was measured in single, isolated S2 proximal straight tubules dissected from rabbit kidneys to investigate the effects of adrenergic agonists on adenylate cyclase activity. The baseline activity of adenylate cyclase was low and unaffected by either the alpha 2 agonist clonidine, the beta agonist isoprenaline (in the absence or presence of 1 microM forskolin) or 1 microM forskolin. Adenylate cyclase activity was markedly stimulated by 20 microM forskolin, an effect which was inhibited by 1 microM clonidine. The inhibition by clonidine was not apparent in the presence of the alpha 2 antagonist yohimbine. These results confirm the inability of isoprenaline to stimulate adenylate cyclase in the rabbit proximal tubule and demonstrate the coupling of alpha 2 receptors, in an inhibitory fashion, to adenylate cyclase. The inhibitory action of the alpha 2-receptor agonist was independent of other hormone activity in the renal proximal tubule.
采用微量放射免疫分析法,测定从兔肾分离出的单个孤立S2近端直管中的环磷酸腺苷(cAMP),以研究肾上腺素能激动剂对腺苷酸环化酶活性的影响。腺苷酸环化酶的基础活性较低,且不受α2激动剂可乐定、β激动剂异丙肾上腺素(无论有无1微摩尔的福斯高林)或1微摩尔福斯高林的影响。20微摩尔的福斯高林可显著刺激腺苷酸环化酶活性,而1微摩尔的可乐定可抑制这一作用。在存在α2拮抗剂育亨宾的情况下,可乐定的抑制作用不明显。这些结果证实了异丙肾上腺素无法刺激兔近端小管中的腺苷酸环化酶,并表明α2受体以抑制方式与腺苷酸环化酶偶联。α2受体激动剂的抑制作用独立于肾近端小管中的其他激素活性。