Department of Pharmaceutical Sciences, Nova Southeastern University College of Pharmacy, Fort Lauderdale, Florida, USA.
Prog Mol Biol Transl Sci. 2013;118:297-334. doi: 10.1016/B978-0-12-394440-5.00012-7.
Of the four mammalian arrestins, only the β-arrestins (βarrs; Arrestin2 and -3) are expressed throughout the cardiovascular system, where they regulate, as either desensitizers/internalizers or signal transducers, several G-protein-coupled receptors (GPCRs) critical for cardiovascular homeostasis. The cardiovascular roles of βarrs have been delineated at an accelerated pace via a variety of techniques and tools, such as knockout mice, siRNA knockdown, artificial or naturally occurring polymorphic GPCRs, and availability of new βarr "biased" GPCR ligands. This chapter summarizes the current knowledge of cardiovascular arrestin physiology and pharmacology, addressing the individual cardiovascular receptors affected by βarrs in vivo, as well as the individual cell types, tissues, and organs of the cardiovascular system in which βarr effects are exerted; for example, cardiac myocyte or fibroblast, vascular smooth muscle, adrenal gland and platelet. In the broader scope of cardiovascular βarr pharmacology, a discussion of the βarr "bias" of certain cardiovascular GPCR ligands is also included.
在四种哺乳动物的 arrestin 中,只有β-arrestin(βarrs;Arrestin2 和 -3)在整个心血管系统中表达,在那里它们作为脱敏剂/内吞体或信号转导物调节几种对心血管稳态至关重要的 G 蛋白偶联受体 (GPCR)。通过各种技术和工具,如敲除小鼠、siRNA 敲低、人工或天然存在的多态性 GPCR 以及新型βarr“偏向”GPCR 配体,βarrs 的心血管作用得到了快速阐明。本章总结了心血管 arrestin 生理学和药理学的最新知识,讨论了体内受βarrs 影响的个别心血管受体,以及心血管系统中发挥βarr 作用的个别细胞类型、组织和器官;例如,心肌细胞或成纤维细胞、血管平滑肌、肾上腺和血小板。在更广泛的心血管βarr 药理学范围内,还讨论了某些心血管 GPCR 配体的βarr“偏向性”。