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Background  Increased nerve activity causes hypertension and kidney disease. Recent studies suggest that renal denervation reduces BP in patients with hypertension. Renal NE release is regulated by prejunctional  α 2A-adrenoceptors on sympathetic nerves, and  α 2A-adrenoceptors act as autoreceptors by binding endogenous NE to inhibit its own release. However, the role of  α 2A-adrenoceptors in the pathogenesis of hypertensive kidney disease is unknown.    Methods  We investigated effects of  α 2A-adrenoceptor–regulated renal NE release on the development of angiotensin II–dependent hypertension and kidney disease. In uninephrectomized wild-type and  α 2A-adrenoceptor–knockout mice, we induced hypertensive kidney disease by infusing AngII for 28 days.    Results  Urinary NE excretion and BP did not differ between normotensive  α 2A-adrenoceptor–knockout mice and wild-type mice at baseline. However, NE excretion increased during AngII treatment, with the knockout mice displaying NE levels that were significantly higher than those of wild-type mice. Accordingly, the  α 2A-adrenoceptor–knockout mice exhibited a systolic BP increase, which was about 40 mm Hg higher than that found in wild-type mice, and more extensive kidney damage. In isolated kidneys, AngII-enhanced renal nerve stimulation induced NE release and pressor responses to a greater extent in kidneys from  α 2A-adrenoceptor–knockout mice. Activation of specific sodium transporters accompanied the exaggerated hypertensive BP response in  α 2A-adrenoceptor–deficient kidneys. These effects depend on renal nerves, as demonstrated by reduced severity of AngII-mediated hypertension and improved kidney function observed in  α 2A-adrenoceptor–knockout mice after renal denervation.    Conclusions  Our findings reveal a protective role of prejunctional inhibitory  α 2A-adrenoceptors in pathophysiologic conditions with an activated renin-angiotensin system, such as hypertensive kidney disease, and support the concept of sympatholytic therapy as a treatment.

α2A-Adrenoceptors Modulate Renal Sympathetic Neurotransmission and Protect against Hypertensive Kidney Disease