Henrich W L, McAllister E A, Smith P B, Campbell W B
Department of Medicine, Dallas Veterans Administration Medical Center 75216.
Am J Physiol. 1988 Sep;255(3 Pt 2):F474-8. doi: 10.1152/ajprenal.1988.255.3.F474.
The role of guanosine 3',5'-cyclic monophosphate (cGMP) as an inhibitory mediator of tissue renin release was examined in two different in vitro preparations. In rat superficial cortical slices, renin release stimulated by isoproterenol (10(-5) M) was ablated by atriopeptin III (ANP, 2.1 x 10(-8) M), nitroprusside (NP, 10(-3) M), and 8-bromoguanosine 3',5'-cyclic monophosphate (8-BrcGMP, 10(-3) and 10(-6) M). Arachidonic acid (10(-3) M)-stimulated renin release was also inhibited by ANP and 8-BrcGMP (10(-3) and 10(-6) M). Both ANP and NP increased tissue cGMP concentrations significantly (P less than 0.05), but neither had an effect on adenosine 3',5'-cyclic monophosphate (cAMP) concentrations. When methylene blue (10(-5) M), an inhibitor of guanylate cyclase, was added to slices incubated with isoproterenol and ANP, the inhibition of renin release by ANP was abolished. These results were confirmed in a preparation of isolated cultured rat juxtaglomerular cells. In these cells, isoproterenol induced a significant increase (58%, P less than 0.01) in renin release, which was inhibited by the addition of 8-BrcGMP (10(-6) M). These data demonstrate a direct inhibitory effect of ANP on isoproterenol- and arachidonic acid-induced renin release. The results with NP, 8-BrcGMP, and methylene blue suggest that cGMP is an intracellular mediator of this inhibition.
在两种不同的体外制备物中研究了3',5'-环磷酸鸟苷(cGMP)作为组织肾素释放抑制介质的作用。在大鼠浅表皮质切片中,异丙肾上腺素(10⁻⁵ M)刺激的肾素释放被心房肽III(ANP,2.1×10⁻⁸ M)、硝普钠(NP,10⁻³ M)和8-溴-3',5'-环磷酸鸟苷(8-BrcGMP,10⁻³和10⁻⁶ M)消除。花生四烯酸(10⁻³ M)刺激的肾素释放也被ANP和8-BrcGMP(10⁻³和10⁻⁶ M)抑制。ANP和NP均显著增加组织cGMP浓度(P<0.05),但两者对3',5'-环磷酸腺苷(cAMP)浓度均无影响。当将鸟苷酸环化酶抑制剂亚甲蓝(10⁻⁵ M)添加到与异丙肾上腺素和ANP一起孵育的切片中时,ANP对肾素释放的抑制作用被消除。这些结果在分离培养的大鼠肾小球旁细胞制备物中得到证实。在这些细胞中,异丙肾上腺素诱导肾素释放显著增加(58%,P<0.01),添加8-BrcGMP(10⁻⁶ M)可抑制这种增加。这些数据表明ANP对异丙肾上腺素和花生四烯酸诱导的肾素释放具有直接抑制作用。NP、8-BrcGMP和亚甲蓝的结果表明cGMP是这种抑制作用的细胞内介质。