Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117456.
J Am Soc Nephrol. 2010 Jun;21(6):993-1002. doi: 10.1681/ASN.2009090949. Epub 2010 Apr 1.
The development of renovascular hypertension depends on the release of renin from the juxtaglomerular (JG) cells, a process regulated by intracellular cAMP. Hydrogen sulfide (H2S) downregulates cAMP production in some cell types by inhibiting adenylyl cyclase, suggesting the possibility that it may modulate renin release. Here, we investigated the effect of H2S on plasma renin activity and BP in rat models of renovascular hypertension. In the two-kidney-one-clip (2K1C) model of renovascular hypertension, the H2S donor NaHS prevented and treated hypertension. Compared with vehicle, NaHS significantly attenuated the elevation in plasma renin activity and angiotensin II levels but did not affect plasma angiotensin-converting enzyme activity. Furthermore, NaHS inhibited the upregulation of renin mRNA and protein levels in the clipped kidneys of 2K1C rats. In primary cultures of renin-rich kidney cells, NaHS markedly suppressed forskolin-stimulated renin activity in the medium and the intracellular increase in cAMP. In contrast, NaHS did not affect BP or plasma renin activity in normal or one-kidney-one-clip (1K1C) rats, both of which had normal plasma renin activity. In conclusion, these results demonstrate that H2S may inhibit renin activity by decreasing the synthesis and release of renin, suggesting its potential therapeutic value for renovascular hypertension.
肾血管性高血压的发展取决于球旁(JG)细胞中肾素的释放,这一过程受细胞内 cAMP 的调节。在某些细胞类型中,硫化氢(H2S)通过抑制腺苷酸环化酶来下调 cAMP 的产生,这表明它可能调节肾素的释放。在这里,我们研究了 H2S 对肾血管性高血压大鼠模型中血浆肾素活性和血压的影响。在肾血管性高血压的双肾一夹(2K1C)模型中,H2S 供体 NaHS 可预防和治疗高血压。与载体相比,NaHS 显著减弱了血浆肾素活性和血管紧张素 II 水平的升高,但不影响血浆血管紧张素转换酶活性。此外,NaHS 抑制了 2K1C 大鼠夹闭侧肾脏中肾素 mRNA 和蛋白水平的上调。在富含肾素的肾细胞原代培养中,NaHS 明显抑制了福斯可林刺激的培养基中肾素活性和细胞内 cAMP 的增加。相比之下,NaHS 对正常或单侧肾一夹(1K1C)大鼠的血压或血浆肾素活性没有影响,这两种大鼠的血浆肾素活性均正常。总之,这些结果表明 H2S 可能通过减少肾素的合成和释放来抑制肾素活性,这表明其对肾血管性高血压具有潜在的治疗价值。