Swales J D
Department of Medicine, University of Leicester, United Kingdom.
Cardiovasc Drugs Ther. 1990 Mar;4 Suppl 2:367-72. doi: 10.1007/BF02603178.
A variety of disturbances in transmembrane monovalent and divalent cation fluxes has been described in blood cells from hypertensive patients. Other membrane properties, such as fluidity and calcium binding, are also altered. It is now abundantly clear that some of the inconsistencies in this field are due to poor matching of patients and controls. However, even when careful matching is carried out, differences in membrane functions are still seen. It is suggested that these are due to a disturbance in the physicochemical properties of the cell membrane, related to changes in cell membrane phospholipid fluidity. This change could maintain peripheral resistance either by directly or indirectly increasing tone or by predisposing to resistance vessel hypertrophy. Recent evidence emphasizes the role of the latter rather than the former in experimental hypertension. It is postulated that overactivity of the phosphoinositide second messenger system as a result of alteration in all membrane properties predisposes genetically susceptible individuals to resistance-vessel hypertrophy and hypertension.
高血压患者血细胞中已发现多种跨膜单价和二价阳离子通量紊乱的情况。其他膜特性,如流动性和钙结合能力也发生了改变。现在很清楚,该领域的一些不一致之处是由于患者与对照匹配不佳所致。然而,即使进行了仔细匹配,仍能观察到膜功能的差异。有人认为,这些差异是由于细胞膜物理化学性质的紊乱,这与细胞膜磷脂流动性的变化有关。这种变化可能通过直接或间接增加张力或使阻力血管肥大,从而维持外周阻力。最近的证据强调了后者而非前者在实验性高血压中的作用。据推测,由于所有膜特性的改变导致磷酸肌醇第二信使系统过度活跃,使遗传易感个体易患阻力血管肥大和高血压。