Stoff J S, Rosa R M, Silva P, Epstein F H
Am J Physiol. 1981 Sep;241(3):F231-7. doi: 10.1152/ajprenal.1981.241.3.F231.
The mechanisms by which endogenous renal prostaglandins regulate water excretion were investigated in these studies. Inhibition of prostaglandin synthesis slowed water diuresis in water-loaded unanesthetized Sprague-Dawley rats and in Brattleboro rats with hereditary diabetes insipidus owing to absence of endogenous vasopressin. In both strains, treatment with indomethacin or meclofenamate increased the osmolality of the renal papilla by raising sodium and urea content, and also increased the osmolality of the urine. Endogenous creatinine clearance and solute excretion were unchanged. The data are consistent with an effect of prostaglandins on solute transport by renal tubules and demonstrate that endogenous prostaglandins influence water excretion by a mechanism independent of the presence of antidiuretic hormone.
在这些研究中,对内源性肾前列腺素调节水排泄的机制进行了研究。在水负荷的未麻醉斯普拉格-道利大鼠和因缺乏内源性血管加压素而患有遗传性尿崩症的布拉特洛伐大鼠中,前列腺素合成的抑制减缓了水利尿。在这两种品系中,用吲哚美辛或甲氯芬那酸治疗可通过提高钠和尿素含量来增加肾乳头的渗透压,同时也增加尿的渗透压。内源性肌酐清除率和溶质排泄未改变。这些数据与前列腺素对肾小管溶质转运的作用一致,并表明内源性前列腺素通过一种独立于抗利尿激素存在的机制影响水排泄。