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雌二醇对雌性大鼠摄水量控制的双向影响。

Bidirectional effects of estradiol on the control of water intake in female rats.

机构信息

University of Kentucky, Department of Biology, 675 Rose Street, Lexington, KY 40506, USA.

University of Kentucky, Department of Biology, 675 Rose Street, Lexington, KY 40506, USA.

出版信息

Horm Behav. 2021 Jul;133:104996. doi: 10.1016/j.yhbeh.2021.104996. Epub 2021 May 18.

Abstract

The inhibitory effect of estradiol (E2) on water intake has been recognized for 50 years. Despite a rich literature describing this phenomenon, we report here a previously unidentified dipsogenic effect of E2 during states of low fluid intake. Our initial goal was to test the hypothesis that the anti-dipsogenic effect of E2 on unstimulated water intake is independent of its anorexigenic effect in female rats. In support of this hypothesis, water intake was reduced during estrus, compared to diestrus, when food was present or absent. Water intake was reduced by E2 in ovariectomized rats when food was available, demonstrating a causative role of E2. Surprisingly, however, when food was removed, resulting in a significant reduction in baseline water intake, E2 enhanced drinking. Accordingly, we next tested the effect of E2 on water intake after an acute suppression of intake induced by exendin-4. The initial rebound drinking was greater in E2-treated, compared to Oil-treated, rats. Finally, to reconcile conflicting reports regarding the effect of ovariectomy on water intake, we measured daily water and food intake, and body weight in ovariectomized and sham-operated rats. Predictably, ovariectomy significantly increased food intake and body weight, but only transiently increased water intake. Together these results provide further support for independent effects of E2 on the controls of water and food intake. More importantly, this report of bidirectional effects of E2 on water intake may lead to a paradigm shift, as it challenges the prevailing view that E2 effects on fluid intake are exclusively inhibitory.

摘要

雌二醇(E2)对水摄入的抑制作用已被认识了 50 年。尽管有丰富的文献描述了这一现象,但我们在这里报告了 E2 在低液体摄入状态下以前未被识别的促饮作用。我们的最初目标是检验以下假设:E2 对非刺激性水摄入的抗促饮作用与其在雌性大鼠中的厌食作用无关。支持这一假设,当食物存在或不存在时,发情期的大鼠比发情期的大鼠水摄入量减少。当食物可用时,去卵巢大鼠中的 E2 可减少水的摄入,证明了 E2 的因果作用。然而,令人惊讶的是,当食物被去除时,导致基础水摄入量显著减少时,E2 增强了饮水。因此,我们接下来测试了 E2 在 exendin-4 急性抑制摄入后对水摄入的影响。与 Oil 处理的大鼠相比,E2 处理的大鼠的初始反弹饮水更多。最后,为了调和关于卵巢切除术对水摄入影响的相互矛盾的报告,我们测量了去卵巢和假手术大鼠的每日水和食物摄入量以及体重。可以预见的是,卵巢切除术显著增加了食物摄入量和体重,但仅短暂增加了水摄入量。这些结果进一步支持了 E2 对水和食物摄入控制的独立作用。更重要的是,E2 对水摄入的双向作用的这一报告可能会导致范式转变,因为它挑战了 E2 对液体摄入的影响完全是抑制性的普遍观点。

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