Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, 210029, Nanjing, China.
Cardiovascular Device and Technique Engineering Laboratory of Jiangsu Province, 210029, Nanjing, China.
Nat Commun. 2022 Jun 6;13(1):3130. doi: 10.1038/s41467-022-30868-6.
Hypertension is a pathological condition of persistent high blood pressure (BP) of which the underlying neural mechanisms remain obscure. Here, we show that the afferent nerves in perirenal adipose tissue (PRAT) contribute to maintain pathological high BP, without affecting physiological BP. Bilateral PRAT ablation or denervation leads to a long-term reduction of high BP in spontaneous hypertensive rats (SHR), but has no effect on normal BP in control rats. Further, gain- and loss-of-function and neuron transcriptomics studies show that augmented activities and remodeling of L1-L2 dorsal root ganglia neurons are responsible for hypertension in SHR. Moreover, we went on to show that calcitonin gene-related peptide (CGRP) is a key endogenous suppressor of hypertension that is sequestered by pro-hypertensive PRAT in SHRs. Taken together, we identify PRAT afferent nerves as a pro-hypertensive node that sustains high BP via suppressing CGRP, thereby providing a therapeutic target to tackle primary hypertension.
高血压是一种持续性血压升高的病理状态,其潜在的神经机制仍不清楚。在这里,我们发现肾周脂肪组织(PRAT)中的传入神经有助于维持病理性高血压,而不影响生理血压。双侧 PRAT 消融或去神经支配可导致自发性高血压大鼠(SHR)的高血压长期降低,但对正常血压无影响。此外,功能获得和丧失以及神经元转录组学研究表明,L1-L2 背根神经节神经元的活动增强和重塑是 SHR 高血压的原因。此外,我们还发现降钙素基因相关肽(CGRP)是一种关键的内源性高血压抑制物,它被 SHR 中的促高血压 PRAT 所隔离。综上所述,我们确定 PRAT 传入神经是一种促高血压的节点,它通过抑制 CGRP 来维持高血压,从而为治疗原发性高血压提供了一个治疗靶点。