血管紧张素Ⅱ受体1型
背景(考古学)
受体
血管紧张素II
信号转导
肾素-血管紧张素系统
血管紧张素受体
药理学
生物
医学
内科学
内分泌学
细胞生物学
血压
古生物学
作者
Robert Eckenstaler,Jana Sandori,Michael Gekle,Ralf A. Benndorf
标识
DOI:10.1016/j.bcp.2021.114673
摘要
The AT1 receptor, a major effector of the renin-angiotensin system, has been extensively studied in the context of cardiovascular and renal disease. Moreover, angiotensin receptor blockers, sartans, are among the most frequently prescribed drugs for the treatment of hypertension, chronic heart failure and chronic kidney disease. However, precise molecular insights into the structure of this important drug target have not been available until recently. In this context, seminal studies have now revealed exciting new insights into the structure and biased signaling of the receptor and may thus foster the development of novel therapeutic approaches to enhance the efficacy of pharmacological angiotensin receptor antagonism or to enable therapeutic induction of biased receptor activity. In this review, we will therefore highlight these and other seminal publications to summarize the current understanding of the tertiary structure, ligand binding properties and downstream signal transduction of the AT1 receptor.
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