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脱水刺激的饮水量减少与雌激素受体α有关,GLP-1 可能发挥作用。

The estrogenic reduction in water intake stimulated by dehydration involves estrogen receptor alpha and a potential role for GLP-1.

机构信息

Department of Biology, University of Kentucky, Lexington, KY 40506, USA.

Department of Biology, University of Kentucky, Lexington, KY 40506, USA.

出版信息

Physiol Behav. 2024 Mar 15;276:114484. doi: 10.1016/j.physbeh.2024.114484. Epub 2024 Feb 6.

Abstract

It is well documented that estrogens inhibit fluid intake. Most of this research, however, has focused on fluid intake in response to dipsogenic hormone and/or drug treatments in euhydrated rats. Additional research is needed to fully characterize the fluid intake effects of estradiol in response to true hypovolemia. As such, the goals of this series of experiments were to provide a detailed analysis of water intake in response to water deprivation in ovariectomized female rats treated with estradiol. In addition, these experiments also tested if activation of estrogen receptor alpha is sufficient to reduce water intake stimulated by water deprivation and tested for a role of glucagon like peptide-1 in the estrogenic control of water intake. As expected, estradiol reduced water intake in response to 24 and 48 h of water deprivation. The reduction in water intake was associated with a reduction in drinking burst number, with no change in drinking burst size. Pharmacological activation of estrogen receptor alpha reduced intake. Finally, estradiol-treatment caused a leftward shift in the behavioral dose response curve of exendin-4, the glucagon like peptide-1 agonist. While the highest dose of exendin-4 reduced 10 min intake in both oil and estradiol-treated rats, the intermediate dose only reduced intake in rats treated with estradiol. Together, this series of experiments extends previous research by providing a more thorough behavioral analysis of the anti-dipsogenic effect of estradiol in dehydrated rats, in addition to identifying the glucagon like peptide-1 system as a potential bioregulator involved in the underlying mechanisms by which estradiol reduces water intake in the female rat.

摘要

有大量文献记载雌激素可抑制液体摄入。然而,这些研究大多集中在水合状态的大鼠对血管升压素和/或药物处理的液体摄入反应上。需要进一步的研究来充分描述雌二醇对真正低血容量的液体摄入的影响。因此,这一系列实验的目的是提供对去卵巢雌性大鼠在接受雌二醇处理后因脱水而产生的水摄入的详细分析。此外,这些实验还测试了雌激素受体 α 的激活是否足以减少因脱水而刺激的水摄入,并测试了胰高血糖素样肽-1 在雌激素对水摄入的控制中的作用。正如预期的那样,雌二醇减少了对 24 和 48 小时的水剥夺的水摄入。水摄入的减少与饮水爆发次数的减少有关,而与饮水爆发大小无关。雌激素受体 α 的药理学激活减少了摄入。最后,雌二醇处理导致外啡肽-4(一种胰高血糖素样肽-1 激动剂)的行为剂量反应曲线向左移位。虽然外啡肽-4 的最高剂量降低了油和雌二醇处理大鼠的 10 分钟摄入量,但中间剂量仅降低了雌二醇处理大鼠的摄入量。总的来说,这一系列实验通过提供对脱水大鼠中雌二醇抗脱水作用的更全面的行为分析,扩展了以前的研究,此外还确定了胰高血糖素样肽-1 系统作为一种潜在的生物调节剂,参与了雌二醇降低雌性大鼠水摄入的潜在机制。

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本文引用的文献

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Estrogen Receptor Beta Mediates the Dipsogenic Effect of Estradiol in Ovariectomized Female Rats.
Neuroendocrinology. 2023;113(9):930-942. doi: 10.1159/000530962. Epub 2023 May 12.
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The role of glucagon-like peptide-1 (GLP-1) in fluid and food intakes in vasopressin-deficient Brattleboro rats.
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