Division of Nephrology, Rochester General Hospital, University of Rochester School of Medicine and Dentistry, Rochester, NY 14621, USA.
Semin Nephrol. 2011 Nov;31(6):475-82. doi: 10.1016/j.semnephrol.2011.09.002.
The clinical use of diuretics almost uniformly predated the localization of their site of action. The consequence of diuretic specificity predicts clinical application and side effect, and the proximity of the sodium transporters, one to the next, often dictates potency or diuretic efficiency. All diuretics function by inhibiting the normal transport of sodium from the filtrate into the renal tubular cells. This movement of sodium into the renal epithelial cells on the apical side is facilitated by a series of transporters whose function is, in turn, dependent on the adenosine triphosphate (ATP)-dependent Na-K cotransporter on the basolateral side of the cell. Our growing understanding of the physiology of sodium transport has spawned new possibilities for diuretic development.
利尿剂的临床应用几乎普遍早于其作用部位的定位。利尿剂的特异性决定了其临床应用和副作用,而钠离子转运体彼此相邻,通常决定了其效力或利尿效率。所有利尿剂的作用机制都是通过抑制正常的钠从滤液向肾小管细胞的转运。钠离子进入肾上皮细胞的顶端侧是由一系列转运体促进的,其功能又依赖于细胞基底外侧的三磷酸腺苷(ATP)依赖性钠-钾共转运体。我们对钠转运生理的认识不断加深,为利尿剂的发展带来了新的可能性。