Guccione Manuela, Ettari Roberta, Taliani Sabrina, Da Settimo Federico, Zappalà Maria, Grasso Silvana
Dipartimento di Scienze Chimiche, Biologiche, Farmaceutiche ed Ambientali, Università degli Studi di Messina , Viale Annunziata, 98168 Messina, Italy.
Dipartimento di Farmacia, Università di Pisa , Via Bonanno Pisano 6, 56126 Pisa, Italy.
J Med Chem. 2016 Oct 27;59(20):9277-9294. doi: 10.1021/acs.jmedchem.5b01939. Epub 2016 Jul 8.
G-protein-coupled receptor kinase 2 (GRK2) is a G-protein-coupled receptor kinase that is ubiquitously expressed in many tissues and regulates various intracellular mechanisms. The up- or down-regulation of GRK2 correlates with several pathological disorders. GRK2 plays an important role in the maintenance of heart structure and function; thus, this kinase is involved in many cardiovascular diseases. GRK2 up-regulation can worsen cardiac ischemia; furthermore, increased kinase levels occur during the early stages of heart failure and in hypertensive subjects. GRK2 up-regulation can lead to changes in the insulin signaling cascade, which can translate to insulin resistance. Increased GRK2 levels also correlate with the degree of cognitive impairment that is typically observed in Alzheimer's disease. This article reviews the most potent and selective GRK2 inhibitors that have been developed. We focus on their mechanism of action, inhibition profile, and structure-activity relationships to provide insight into the further development of GRK2 inhibitors as drug candidates.
G蛋白偶联受体激酶2(GRK2)是一种G蛋白偶联受体激酶,在许多组织中广泛表达,并调节各种细胞内机制。GRK2的上调或下调与多种病理疾病相关。GRK2在维持心脏结构和功能方面发挥着重要作用;因此,这种激酶参与了许多心血管疾病。GRK2的上调会加重心脏缺血;此外,在心力衰竭早期和高血压患者中激酶水平会升高。GRK2的上调会导致胰岛素信号级联反应的变化,进而导致胰岛素抵抗。GRK2水平的升高也与阿尔茨海默病中常见的认知障碍程度相关。本文综述了已开发出的最有效和选择性最强的GRK2抑制剂。我们重点关注它们的作用机制、抑制谱以及构效关系,以便深入了解GRK2抑制剂作为候选药物的进一步开发情况。