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Thirst Driving and Suppressing Signals Encoded by Distinct Neural Populations in the Brain

机译:大脑中不同神经种群编码的干裂驱动信号和抑制信号

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摘要

Thirst is the basic instinct to drink water. Previously, it was shown that neurons in several circumventricular organs (CVO) of the hypothalamus are activated by thirst-inducing conditions . Here, we identify two distinct, genetically-separable neural populations in the subfornical organ (SFO) that trigger or suppress thirst. We show that optogenetic activation of SFO excitatory neurons, marked by the expression of the transcription factor ETV-1, evokes intense drinking behavior, and does so even in fully water-satiated animals. The light-induced response is highly specific for water, immediate, and strictly locked to the laser stimulus. In contrast, activation of a second population of SFO neurons, marked by expression of the vesicular GABA transporter VGAT, drastically suppressed drinking, even in water-craving thirsty animals. These results reveal an innate brain circuit that can turn on and off an animal’s water-drinking behavior, and likely functions as a center for thirst control in the mammalian brain.
机译:口渴是喝水的基本本能。以前的研究表明,诱发口渴的条件 激活了下丘脑的几个室室器官(CVO)中的神经元。在这里,我们确定了触发或抑制口渴的子下器官(SFO)中两个不同的,基因上可分离的神经种群。我们显示SFO兴奋性神经元的光遗传学激活,以转录因子ETV-1的表达为标志,唤起强烈的饮酒行为,甚至在完全喝水的动物中也是如此。光诱导的响应对水具有高度的特异性,立即且严格锁定于激光刺激。相反,以水泡GABA转运蛋白VGAT的表达为特征的第二个SFO神经元的激活,甚至在渴望水的口渴动物中,也大大抑制了饮酒。这些结果揭示了一种先天性大脑回路,可以开启和关闭动物的饮水行为,并可能充当哺乳动物大脑中口渴控制的中心。

著录项

  • 期刊名称 other
  • 作者单位
  • 年(卷),期 -1(520),7547
  • 年度 -1
  • 页码 349–352
  • 总页数 19
  • 原文格式 PDF
  • 正文语种
  • 中图分类
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  • 入库时间 2022-08-21 11:16:41

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