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丙磺舒增强氯噻嗪的利尿作用。

Increase in diuretic effect of chlorothiazide by probenecid.

作者信息

Brater D C

出版信息

Clin Pharmacol Ther. 1978 Mar;23(3):259-65. doi: 10.1002/cpt1978233259.

Abstract

Thiazide diuretics reach their presumed intraluminal site of action by active transport at the organic acid secretory site of the proximal tubule. Probenecid competes for this transport and might therefore affect the diuresis induced by thiazide at that site. Doses of 500 mg and 1 gm of chlorothiazide (CTZ) intravenously to 5 volunteers with probenecid pretreatment increased 8-hr rates of excretion of sodium and urine over that without probenecid. Eight-hour excretion of sodium after administering 500 mg of CTZ was 147 +/- 7.5 mEq and 257.9 +/- 16.4 mEq after CTZ with probenecid (p less than 0.0005). The volume of urine after CTZ was 728 +/- 37 ml and 1,886 +/- 301 ml after CTZ with probenecid (p less than 0.001). This increase was associated with prolongation of CTZ diuresis rather than increase in intensity. These results are consistent with CTZ reaching its site of action from the peritubular side or that prolonged exposure of the lumen to lesser amounts of filtered CTZ causes a greater overall effect.

摘要

噻嗪类利尿剂通过近端小管有机酸分泌部位的主动转运到达其假定的管腔内作用部位。丙磺舒竞争这种转运,因此可能影响噻嗪类在该部位诱导的利尿作用。对5名预先用丙磺舒治疗的志愿者静脉注射500毫克和1克氯噻嗪(CTZ),与未用丙磺舒相比,钠和尿的8小时排泄率增加。注射500毫克CTZ后钠的8小时排泄量为147±7.5毫当量,注射CTZ并用丙磺舒后为257.9±16.4毫当量(p小于0.0005)。CTZ后的尿量为728±37毫升,CTZ并用丙磺舒后为1886±301毫升(p小于0.001)。这种增加与CTZ利尿作用的延长有关,而不是强度增加。这些结果与CTZ从肾小管周围侧到达其作用部位一致,或者管腔长时间暴露于较少滤过量的CTZ会产生更大的总体效应。

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