Department of Nephrology, Renal Pathophysiology Laboratory, Instituto Nacional de Cardiología "Ignacio Chávez", Juan Badiano No.1, 14080, Mexico City, DF, Mexico.
Department Molecular Biology, Instituto Nacional de Cardiología "Ignacio Chávez", Mexico City, Mexico.
Purinergic Signal. 2019 Jun;15(2):277-285. doi: 10.1007/s11302-019-09662-5. Epub 2019 Jun 11.
Glomerular arteriolar vasoconstriction and tubulointerstitial injury are observed before glomerular damage occurs in models of hypertension. High interstitial ATP concentrations, caused by the increase in arterial pressure, alter renal mechanisms involved in the long-term control of blood pressure, autoregulation of glomerular filtration rate and blood flow, tubuloglomerular feedback (TGF) responses, and sodium excretion. Elevated ATP concentrations and augmented expression of P2X receptors have been demonstrated under a genetic background or induction of hypertension with vasoconstrictor peptides. In addition to the alterations of the microcirculation in the hypertensive kidney, the vascular actions of elevated intrarenal angiotensin II levels may be mitigated by the administration of broad purinergic P2 antagonists or specific P2Y12, P2X1, and P2X7 receptor antagonists. Furthermore, the prevention of tubulointerstitial infiltration with immunosuppressor compounds reduces the development of salt-sensitive hypertension, indicating that tubulointerstitial inflammation is essential for the development and maintenance of hypertension. Inflammatory cells also express abundant purinergic receptors, and their activation by ATP induces cytokine and growth factor release that in turn contributes to augment tubulointerstitial inflammation. Collectively, the evidence suggests a pathophysiological activation of purinergic P2 receptors in angiotensin-dependent hypertension. Coexistent increases in intrarenal angiotensin II and activates Ang II AT1 receptors, which interacts with over-activated purinergic receptors in a complex manner, suggesting convergence of their post-receptor signaling processes.
在高血压模型中,肾小球血管收缩和肾小管间质损伤先于肾小球损伤发生。由于动脉压升高导致的间质 ATP 浓度升高,改变了参与血压长期控制、肾小球滤过率和血流自动调节、管球反馈(TGF)反应以及钠排泄的肾脏机制。在遗传背景或血管收缩肽诱导的高血压下,已经证明了 ATP 浓度升高和 P2X 受体表达增强。除了高血压肾脏中小血管的改变外,升高的肾内血管紧张素 II 水平的血管作用可以通过施用广泛的嘌呤能 P2 拮抗剂或特定的 P2Y12、P2X1 和 P2X7 受体拮抗剂来减轻。此外,用免疫抑制剂化合物预防肾小管间质浸润可减少盐敏感性高血压的发展,表明肾小管间质炎症是高血压发生和维持所必需的。炎症细胞也表达丰富的嘌呤能受体,其被 ATP 激活诱导细胞因子和生长因子释放,进而有助于增加肾小管间质炎症。总之,这些证据表明嘌呤能 P2 受体在血管紧张素依赖性高血压中存在病理生理激活。肾内血管紧张素 II 和激活的 Ang II AT1 受体同时增加,以复杂的方式相互作用,表明它们的受体后信号转导过程存在会聚。