Department of Physiology, Hypertension and Renal Center of Excellence, Tulane University School of Medicine, New Orleans, LA 70112, USA.
Chulabhorn International College of Medicine, Thammasat University, Klong Luang 12120, Thailand.
Int J Mol Sci. 2023 Jul 13;24(14):11413. doi: 10.3390/ijms241411413.
In angiotensin II (Ang II)-dependent hypertension, Ang II activates angiotensin II type 1 receptors (AT1R) on renal vascular smooth muscle cells, leading to renal vasoconstriction with eventual glomerular and tubular injury and interstitial inflammation. While afferent arteriolar vasoconstriction is initiated by the increased intrarenal levels of Ang II activating AT1R, the progressive increases in arterial pressure stimulate the paracrine secretion of adenosine triphosphate (ATP), leading to the purinergic P2X receptor (P2XR)-mediated constriction of afferent arterioles. Thus, the afferent arteriolar tone is maintained by two powerful systems eliciting the co-existing activation of P2XR and AT1R. This raises the conundrum of how the AT1R and P2XR can both be responsible for most of the increased renal afferent vascular resistance existing in angiotensin-dependent hypertension. Its resolution implies that AT1R and P2XR share common receptor or post receptor signaling mechanisms which converge to maintain renal vasoconstriction in Ang II-dependent hypertension. In this review, we briefly discuss (1) the regulation of renal afferent arterioles in Ang II-dependent hypertension, (2) the interaction of AT1R and P2XR activation in regulating renal afferent arterioles in a setting of hypertension, (3) mechanisms regulating ATP release and effect of angiotensin II on ATP release, and (4) the possible intracellular pathways involved in AT1R and P2XR interactions. Emerging evidence supports the hypothesis that P2X1R, P2X7R, and AT1R actions converge at receptor or post-receptor signaling pathways but that P2XR exerts a dominant influence abrogating the actions of AT1R on renal afferent arterioles in Ang II-dependent hypertension. This finding raises clinical implications for the design of therapeutic interventions that will prevent the impairment of kidney function and subsequent tissue injury.
在血管紧张素 II(Ang II)依赖性高血压中,Ang II 激活肾脏血管平滑肌细胞上的血管紧张素 II 型 1 受体(AT1R),导致肾血管收缩,最终导致肾小球和肾小管损伤以及间质炎症。虽然入球小动脉收缩是由增加的肾内 Ang II 激活 AT1R 引起的,但动脉压的逐渐升高刺激腺苷三磷酸(ATP)的旁分泌分泌,导致嘌呤能 P2X 受体(P2XR)介导的入球小动脉收缩。因此,入球小动脉张力由两个强大的系统维持,这两个系统引发 P2XR 和 AT1R 的共存激活。这就提出了一个难题,即 AT1R 和 P2XR 如何都能导致血管紧张素依赖性高血压中存在的大部分增加的肾入球血管阻力。其解决办法意味着 AT1R 和 P2XR 共享共同的受体或受体后信号转导机制,这些机制汇聚在一起,以维持 Ang II 依赖性高血压中的肾血管收缩。在这篇综述中,我们简要讨论了(1)Ang II 依赖性高血压中肾入球小动脉的调节,(2)AT1R 和 P2XR 激活在高血压情况下调节肾入球小动脉的相互作用,(3)调节 ATP 释放的机制和血管紧张素 II 对 ATP 释放的影响,以及(4)可能涉及 AT1R 和 P2XR 相互作用的细胞内途径。新出现的证据支持这样一种假设,即 P2X1R、P2X7R 和 AT1R 的作用在受体或受体后信号通路汇聚,但 P2XR 发挥主导作用,削弱了 Ang II 依赖性高血压中 AT1R 对肾入球小动脉的作用。这一发现对设计治疗干预措施具有临床意义,这些措施将防止肾功能受损和随后的组织损伤。