Kamal Fadia A, Travers Joshua G, Schafer Allison E, Ma Qing, Devarajan Prasad, Blaxall Burns C
The Heart Institute, Molecular Cardiovascular Biology and.
Division of Nephrology and Hypertension, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
J Am Soc Nephrol. 2017 Jan;28(1):197-208. doi: 10.1681/ASN.2015080852. Epub 2016 Jun 13.
Development of CKD secondary to chronic heart failure (CHF), known as cardiorenal syndrome type 2 (CRS2), clinically associates with organ failure and reduced survival. Heart and kidney damage in CRS2 results predominantly from chronic stimulation of G protein-coupled receptors (GPCRs), including adrenergic and endothelin (ET) receptors, after elevated neurohormonal signaling of the sympathetic nervous system and the downstream ET system, respectively. Although we and others have shown that chronic GPCR stimulation and the consequent upregulated interaction between the G-protein βγ-subunit (Gβγ), GPCR-kinase 2, and β-arrestin are central to various cardiovascular diseases, the role of such alterations in kidney diseases remains largely unknown. We investigated the possible salutary effect of renal GPCR-Gβγ inhibition in CKD developed in a clinically relevant murine model of nonischemic hypertrophic CHF, transverse aortic constriction (TAC). By 12 weeks after TAC, mice developed CKD secondary to CHF associated with elevated renal GPCR-Gβγ signaling and ET system expression. Notably, systemic pharmacologic Gβγ inhibition by gallein, which we previously showed alleviates CHF in this model, attenuated these pathologic renal changes. To investigate a direct effect of gallein on the kidney, we used a bilateral ischemia-reperfusion AKI mouse model, in which gallein attenuated renal dysfunction, tissue damage, fibrosis, inflammation, and ET system activation. Furthermore, in vitro studies showed a key role for ET receptor-Gβγ signaling in pathologic fibroblast activation. Overall, our data support a direct role for GPCR-Gβγ in AKI and suggest GPCR-Gβγ inhibition as a novel therapeutic approach for treating CRS2 and AKI.
慢性心力衰竭(CHF)继发的慢性肾脏病(CKD),即2型心肾综合征(CRS2),在临床上与器官功能衰竭和生存率降低相关。CRS2中的心脏和肾脏损伤主要源于G蛋白偶联受体(GPCRs)的慢性刺激,包括肾上腺素能受体和内皮素(ET)受体,分别是在交感神经系统和下游ET系统的神经激素信号升高之后。尽管我们和其他人已经表明,慢性GPCR刺激以及随之而来的G蛋白βγ亚基(Gβγ)、GPCR激酶2和β抑制蛋白之间上调的相互作用是各种心血管疾病的核心,但这种改变在肾脏疾病中的作用仍然很大程度上未知。我们在非缺血性肥厚性CHF的临床相关小鼠模型——横断主动脉缩窄(TAC)中,研究了肾脏GPCR-Gβγ抑制对所发生的CKD的可能有益作用。在TAC后12周,小鼠发生了继发于CHF的CKD,伴有肾脏GPCR-Gβγ信号和ET系统表达升高。值得注意的是,我们之前表明在该模型中能减轻CHF的加仑因对Gβγ的全身药理学抑制作用,减轻了这些病理性肾脏变化。为了研究加仑因对肾脏的直接作用,我们使用了双侧缺血再灌注急性肾损伤(AKI)小鼠模型,其中加仑因减轻了肾功能障碍、组织损伤、纤维化、炎症和ET系统激活。此外,体外研究表明ET受体-Gβγ信号在病理性成纤维细胞激活中起关键作用。总体而言,我们的数据支持GPCR-Gβγ在AKI中的直接作用,并表明GPCR-Gβγ抑制作为治疗CRS2和AKI的一种新的治疗方法。