Surapisitchat James, Beavo Joseph A
Department of Pharmacology, University of Washington School of Medicine, 1959 NE Pacific St., 357280, Seattle, WA 98195-7280, USA.
Handb Exp Pharmacol. 2011(204):193-210. doi: 10.1007/978-3-642-17969-3_8.
The endothelium plays an important role in maintaining normal vascular function. Endothelial barrier dysfunction leading to increased permeability and vascular leakage is associated with several pathological conditions such as edema and sepsis. Thus, the development of drugs that improve endothelial barrier function is an active area of research. In this chapter, the current knowledge concerning the signaling pathways regulating endothelial barrier function is discussed with a focus on cyclic nucleotide second messengers (cAMP and cGMP) and cyclic nucleotide phosphodiesterases (PDEs). Both cAMP and cGMP have been shown to have differential effects on endothelial permeability in part due to the various effector molecules, crosstalk, and compartmentalization of cyclic nucleotide signaling. PDEs, by controlling the amplitude, duration, and localization of cyclic nucleotides, have been shown to play a critical role in regulating endothelial barrier function. Thus, PDEs are attractive drug targets for the treatment of disease states involving endothelial barrier dysfunction.
内皮细胞在维持正常血管功能中发挥着重要作用。导致通透性增加和血管渗漏的内皮屏障功能障碍与多种病理状况相关,如水肿和脓毒症。因此,开发改善内皮屏障功能的药物是一个活跃的研究领域。在本章中,将讨论目前关于调节内皮屏障功能的信号通路的知识,重点是环核苷酸第二信使(cAMP和cGMP)和环核苷酸磷酸二酯酶(PDEs)。cAMP和cGMP均已显示出对内皮通透性有不同影响,部分原因是各种效应分子、环核苷酸信号的相互作用和区室化。通过控制环核苷酸的幅度、持续时间和定位,PDEs已被证明在调节内皮屏障功能中起关键作用。因此,PDEs是治疗涉及内皮屏障功能障碍疾病状态的有吸引力的药物靶点。