Cellular and Molecular Physiology Laboratory (CMPL), Division of Obstetrics and Gynaecology, School of Medicine, Faculty of Medicine, Pontificia Universidad Católica de Chile, Santiago 8330024, Chile; Departamento de Fisiología, Facultad de Farmacia, Universidad de Sevilla, Seville E-41012, Spain.
Cellular and Molecular Physiology Laboratory (CMPL), Division of Obstetrics and Gynaecology, School of Medicine, Faculty of Medicine, Pontificia Universidad Católica de Chile, Santiago 8330024, Chile.
Mol Aspects Med. 2017 Jun;55:126-139. doi: 10.1016/j.mam.2016.12.003. Epub 2017 Jan 12.
Adenosine is an endogenous nucleoside with pleiotropic effects in different physiological processes including circulation, renal blood flow, immune function, or glucose homeostasis. Changes in adenosine membrane transporters, adenosine receptors, and corresponding intracellular signalling network associate with development of pathologies of pregnancy, including preeclampsia. Preeclampsia is a cause of maternal and perinatal morbidity and mortality affecting 3-5% of pregnancies. Since the proposed mechanisms of preeclampsia development include adenosine-dependent biological effects, adenosine membrane transporters and receptors, and the associated signalling mechanisms might play a role in the pathophysiology of preeclampsia. Preeclampsia associates with increased adenosine concentration in the maternal blood and placental tissue, likely due to local hypoxia and ischemia (although not directly demonstrated), microthrombosis, increased catecholamine release, and platelet activation. In addition, abnormal expression and function of equilibrative nucleoside transporters is described in foetoplacental tissues from preeclampsia; however, the role of adenosine receptors in the aetiology of this disease is not well understood. Adenosine receptors activation may be related to abnormal trophoblast invasion, angiogenesis, and ischemia/reperfusion mechanisms in the placenta from preeclampsia. These mechanisms may explain only a low fraction of the associated abnormal transformation of spiral arteries in preeclampsia, triggering cellular stress and inflammatory mediators release from the placenta to the maternal circulation. Although increased adenosine concentration in preeclampsia may be a compensatory or adaptive mechanism favouring placental angiogenesis, a poor angiogenic state is found in preeclampsia. Thus, preeclampsia-associated complications might affect the cell response to adenosine due to altered expression and activity of adenosine receptors, membrane transporters, or cell signalling mechanisms. This review summarizes the evidence available on the potential involvement of the adenosine in the clinical, pathophysiology, and therapeutic features of preeclampsia.
腺苷是一种内源性核苷,在不同的生理过程中具有多种效应,包括循环、肾血流量、免疫功能或葡萄糖稳态。腺苷膜转运体、腺苷受体和相应的细胞内信号网络的变化与妊娠相关疾病的发展有关,包括子痫前期。子痫前期是一种导致孕产妇和围产儿发病率和死亡率的疾病,影响 3-5%的妊娠。由于子痫前期发展的机制包括依赖于腺苷的生物学效应、腺苷膜转运体和受体以及相关的信号机制,因此可能在子痫前期的病理生理学中发挥作用。子痫前期与母体血液和胎盘组织中腺苷浓度的增加有关,这可能是由于局部缺氧和缺血(尽管尚未直接证明)、微血管血栓形成、儿茶酚胺释放增加和血小板激活所致。此外,在子痫前期的胎儿胎盘组织中描述了平衡核苷转运体的异常表达和功能;然而,腺苷受体在这种疾病的病因学中的作用尚不清楚。腺苷受体的激活可能与子痫前期胎盘异常的滋养细胞浸润、血管生成和缺血/再灌注机制有关。这些机制可能只能解释子痫前期螺旋动脉相关异常转化的一小部分,从而触发胎盘向母体循环释放细胞应激和炎症介质。尽管子痫前期中腺苷浓度的增加可能是有利于胎盘血管生成的补偿或适应性机制,但子痫前期中存在血管生成不良的状态。因此,由于腺苷受体、膜转运体或细胞信号机制的表达和活性改变,子痫前期相关并发症可能会影响细胞对腺苷的反应。本综述总结了有关腺苷在子痫前期的临床、病理生理学和治疗特征中的潜在作用的现有证据。