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钠耗竭在去垂体尿崩症Brattleboro大鼠中氢氯噻嗪诱导的抗利尿作用中的作用。

The role of sodium depletion in hydrochlorothiazide-induced antidiuresis in Brattleboro rats with diabetes insipidus.

作者信息

Shirley D G, Walter S J, Laycock J F

出版信息

Clin Sci Mol Med. 1978 Mar;54(3):209-15. doi: 10.1042/cs0540209.

Abstract
  1. The mechanism of the antidiuretic effect of hydrochlorothiazide in diabetes insipidus was studied in anaesthetized Brattleboro rats with the hereditary hypothalamic form of the disease. 2. The antidiuresis caused by acute administration of hydrochlorothiazide followed an increase in sodium excretion and was associated with a significant fall in the plasma sodium concentration. There were concomitant falls in effective renal plasma flow and glomerular filtration rate. 3. When sodium depletion was prevented by adjusting the infusion of sodium chloride, the falls in plasma sodium concentration, effective renal plasma flow and glomerular filtration rate were abolished. Under these circumstances there was an increase in urine volume, which suggests that hydrochlorothiazide may inhibit fractional fluid reabsorption in the proximal convoluted tubule. 4. The results indicate that the antidiuresis caused by hydrochlorothiazide in diabetes insipidus results, at least in part, from falls in effective renal plasma flow and glomerular filtration rate. These in turn seem to be entirely secondary to the drug-induced sodium depletion.
摘要
  1. 在患有遗传性下丘脑型尿崩症的麻醉Brattleboro大鼠中,研究了氢氯噻嗪对尿崩症的抗利尿作用机制。2. 急性给予氢氯噻嗪引起的抗利尿作用伴随着钠排泄增加,并与血浆钠浓度显著下降相关。同时,有效肾血浆流量和肾小球滤过率下降。3. 通过调整氯化钠输注量防止钠耗竭时,血浆钠浓度、有效肾血浆流量和肾小球滤过率的下降被消除。在这些情况下,尿量增加,这表明氢氯噻嗪可能抑制近端曲管的液体重吸收分数。4. 结果表明,氢氯噻嗪在尿崩症中引起的抗利尿作用至少部分是由于有效肾血浆流量和肾小球滤过率下降所致。而这些下降似乎完全继发于药物引起的钠耗竭。

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