Wright F S, Brenner B M, Bennett C M, Keimowitz R I, Berliner R W, Schrier R W, Verroust P J, De Wardener H E, Holzgreve H
J Clin Invest. 1969 Jun;48(6):1107-13. doi: 10.1172/JCI106067.
Recently, it has been reported that a humoral inhibitor of proximal sodium reabsorption could be detected in plasma, and dialysates of plasma, of rats and dogs undergoing saline diuresis. We have repeated these studies using similar techniques and protocols. Fractional sodium reabsorption by the proximal tubule (as estimated in free-flow micropuncture studies from tubule fluid-to-plasma inulin ratios) was found not to be lower during infusion of "natriuretic" plasma than during subsequent infusion of "hydropenic" plasma. Similarly, infusion of natriuretic plasma failed to prolong reabsorptive half-time of the shrinking drop beyond that seen during hydropenic plasma infusion. No increase in urine volume or rate of sodium excretion was observed during the period of natriuretic plasma infusion, nor did natriuretic plasma result in an increase in these measures in rats undergoing water diuresis. It also has been reported that dialysates of natriuretic plasma, but not of hydropenic plasma, when placed directly into the tubule lumen, inhibit proximal sodium reabsorption. In double blind studies carried out independently in Bethesda, London, and Cologne, we failed to detect the presence of a dialyzable inhibitor in natriuretic plasma. Finally, in contrast to other recent reports, we were unable to detect inhibitory activity in plasma obtained from dogs during the "escape" phase of chronic deoxycorticosterone acetate administration.
最近,有报道称在进行盐水利尿的大鼠和犬的血浆以及血浆透析液中可检测到一种近端钠重吸收的体液抑制剂。我们使用类似的技术和方案重复了这些研究。通过近端小管的钠分数重吸收(如在自由流微穿刺研究中根据小管液与血浆菊粉比率估算)在输注“利钠”血浆期间并不比随后输注“缺水”血浆期间更低。同样,输注利钠血浆未能使缩滴重吸收半衰期延长至超过缺水血浆输注期间所见。在输注利钠血浆期间未观察到尿量或钠排泄率增加,利钠血浆也未使进行水利尿的大鼠的这些指标增加。也有报道称,利钠血浆的透析液直接注入小管腔时可抑制近端钠重吸收,而缺水血浆的透析液则无此作用。在贝塞斯达、伦敦和科隆独立进行的双盲研究中,我们未能检测到利钠血浆中存在可透析抑制剂。最后,与其他近期报道相反,我们无法在慢性给予醋酸脱氧皮质酮的“逃逸”期从犬获得的血浆中检测到抑制活性。