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首页> 外文期刊>Canadian Journal of Physiology and Pharmacology >Cooperative mechanisms of acute antidiuretic response to bendroflumethiazide in rats with lithium-induced nephrogenic diabetes insipidus.
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Cooperative mechanisms of acute antidiuretic response to bendroflumethiazide in rats with lithium-induced nephrogenic diabetes insipidus.

机译:锂诱导的肾病性尿崩症大鼠对苯达氟甲肼急性抗利尿反应的合作机制。

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摘要

The exact mechanism underlying thiazides-induced paradoxical antidiuresis in diabetes insipidus is still elusive, but it has been hypothesized that it is exerted either via Na+-depletion activating volume-homeostatic reflexes to decrease distal delivery, or direct stimulation of distal water reabsorption. This study examined how these two proposed mechanisms actually cooperate to induce an acute bendroflumethiazide (BFTZ)-antidiuretic effect in nephrogenic diabetes insipidus (NDI). Anaesthetized rats with lithium (Li)-induced NDI were prepared in order to measure their renal functional parameters, and in some of them, bilateral renal denervation (DNX) was induced. After a 30 min control clearance period, we infused either BFTZ into 2 groups, NDI+BFTZ and NDI/DNX+BFTZ, or its vehicle into a NDI+V group, and six 30 min experimental clearance periods were taken. During BFTZ infusion in the NDI+BFTZ group, transiently elevated Na+ excretion was associated with rapidly increased urinary osmolality and decreased free water clearance, but Li clearance and urine flow declined in the later periods. However, in the NDI/DNX+BFTZ group, there was persistently elevated Na+ excretion with unchanged Li clearance and urine flow during the experimental period, while alterations in free water clearance and urinary osmolality resembled those in the NDI+BFTZ group. In conclusion, BFTZ initially exerted two direct effects of natriuresis-diuresis and stimulating free water reabsorption at the distal nephron in NDI, which together elevated Na+ excretion and urinary osmolality but kept the urine volume unchanged in the first hour. Thereafter, the resultant sodium depletion led to the activation of neural reflexes that reduced distal fluid delivery to compensate for BFTZ-induced natriuresis-diuresis which, in cooperation with the direct distal BFTZ-antidiuretic effect, resulted in excretion of urine with a low volume, high osmolality, and normal sodium.
机译:噻嗪类药物在尿崩症中引起的悖论抗利尿的确切机制仍不清楚,但是据推测,其作用是通过耗竭Na +的活动量体内稳态反射来减少远端输送,或直接刺激远端水吸收。这项研究检查了这两种提议的机制实际上如何协同作用,以在肾源性尿崩症(NDI)中诱导急性苯达氟甲酰肼(BFTZ)抗利尿作用。制备了麻醉的锂(Li)诱导的NDI大鼠,以测量其肾功能参数,其中一些大鼠诱发了双侧肾去神经支配(DNX)。在30分钟的对照清除期后,我们将BFTZ注入NDI + BFTZ和NDI / DNX + BFTZ两组,或将其媒介物注入NDI + V组,并进行了六个30分钟的实验清除期。在NDI + BFTZ组中进行BFTZ输注期间,Na +排泄的短暂升高与尿渗透压的迅速增加和游离水清除率的降低有关,但后期的Li清除率和尿流减少了。然而,在NDI / DNX + BFTZ组中,在实验期间Na +排泄持续增加,而Li清除率和尿液流量不变,而自由水清除率和尿渗透压的变化类似于NDI + BFTZ组。总之,BFTZ最初发挥了利尿利尿的两个直接作用,并刺激了NDI远端肾单位的自由水重吸收,这共同提高了Na +排泄量和尿渗透压,但在第一小时内尿液量保持不变。此后,钠的减少导致神经反射的激活,减少了远端流体的输送,从而补偿了BFTZ引起的利钠利尿作用,再加上远端的BFTZ抗利尿作用,排泄了少量尿液,渗透压高,钠含量正常。

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