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生理浓度的抗利尿激素(AVP)和醛固酮对大鼠皮质集合管(CCD)中的钠离子转运具有协同作用。

AVP and aldosterone at physiological concentrations have synergistic effects on Na+ transport in rat CCD.

作者信息

Hawk C T, Li L, Schafer J A

机构信息

Department of Comparative Medicine, University of Alabama at Birmingham, USA.

出版信息

Kidney Int Suppl. 1996 Dec;57:S35-41.

PMID:8941920
Abstract

These studies examined whether the previously reported synergism between pharmacological doses of deoxycorticosterone (DOC) and arginine vasopressin (AVP) also occur at physiological concentrations of aldosterone and AVP. We examined the dose-response of salt transport, as measured by the lumen-to-bath 22Na+ flux (J1 --> b) and transepithelial voltage (VT), and of osmotic water permeability (Pf), to AVP in isolated perfused cortical collecting ducts (CCDs) from three groups of rats: (1) implanted with a 1 mg d-aldosterone pellet, which produced a moderately elevated, but physiologically relevant, plasma aldosterone concentration of 18.4 +/- 2.6 ng/dl; (2) implanted with a 2.5 mg DOC pellet (a high pharmacological dose); and (3) untreated rats, Pf reached the same maximal value in all three groups, and the concentration of AVP producing one-half the maximal Pf response (K0.5) was not significantly different among the three groups, ranging from 5 to 10 pM. There was a significantly greater increase in J1 --> b and hyperpolarization of VT with increasing AVP in both groups of treated rats than in the untreated group. The maximum values of J1 --> b and VT achieved at high AVP concentrations were not significantly different in CCDs from the aldosterone-treated and DOC-treated groups, but they were significantly higher than in the CCDs from untreated rats. Although maximal VT values achieved with DOC and aldosterone treatment were the same, the AVP K0.5 for VT were significantly lower in the DOC-treated than in the aldosterone-treated group. Although not statistically significant, the same trend was observed for J1 --> b. We conclude that AVP and aldosterone synergistically stimulate Na+ reabsorption at physiological concentrations of both hormones; however, VT (and probably Na+ reabsorption, which is generally proportional to VT) reaches maximum values at lower AVP concentrations when pharmacological doses of DOC are employed.

摘要

这些研究考察了先前报道的脱氧皮质酮(DOC)药理剂量与精氨酸加压素(AVP)之间的协同作用在醛固酮和AVP生理浓度时是否也会出现。我们检测了三组大鼠分离灌注的皮质集合管(CCD)中,通过管腔到浴液的22Na+通量(J1→b)和跨上皮电压(VT)所测量的盐转运以及渗透水通透性(Pf)对AVP的剂量反应:(1)植入1mg d-醛固酮丸剂,其产生了适度升高但生理相关的血浆醛固酮浓度18.4±2.6ng/dl;(2)植入2.5mg DOC丸剂(高药理剂量);(3)未处理的大鼠。在所有三组中Pf达到相同的最大值,且产生最大Pf反应一半(K0.5)的AVP浓度在三组之间无显著差异,范围为5至10pM。与未处理组相比,两组处理过的大鼠中随着AVP增加,J1→b有显著更大的增加以及VT超极化。在高AVP浓度下醛固酮处理组和DOC处理组的CCD中J1→b和VT的最大值无显著差异,但它们显著高于未处理大鼠的CCD中的值。尽管DOC和醛固酮处理所达到的最大VT值相同,但DOC处理组中VT的AVP K0.5显著低于醛固酮处理组。对于J1→b观察到相同趋势,尽管无统计学意义。我们得出结论,在两种激素的生理浓度下,AVP和醛固酮协同刺激Na+重吸收;然而,当使用DOC药理剂量时,VT(以及可能与VT大致成比例的Na+重吸收)在较低AVP浓度时达到最大值。

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