Department of Behavioral Neuroscience, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR, 97239, USA.
Department of Behavioral Neuroscience, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR, 97239, USA.
Neuropharmacology. 2021 Dec 1;200:108795. doi: 10.1016/j.neuropharm.2021.108795. Epub 2021 Sep 21.
Previous studies in rodents have repeatedly demonstrated that the centrally-projecting Edinger-Westphal nucleus (EWcp) is highly sensitive to alcohol and is also involved in regulating alcohol intake and body temperature. Historically, the EWcp has been known as the main site of Urocortin 1 (Ucn1) expression, a corticotropin-releasing factor-related peptide, in the brain. However, the EWcp also contains other populations of neurons, including neurons that express the vesicular glutamate transporter 2 (Vglut2). Here we transduced the EWcp with adeno-associated viruses (AAVs) encoding Designer Receptors Exclusively Activated by Designer Drugs (DREADDs) to test the role of the EWcp in alcohol drinking and in the regulation of body temperature. Activation of the EWcp with excitatory DREADDs inhibited alcohol intake in a 2-bottle choice procedure in male C57BL/6J mice, whereas inhibition of the EWcp with DREADDs had no effect. Surprisingly, analysis of DREADD expression indicated Ucn1-containing neurons of the EWcp did not express DREADDs. In contrast, AAVs transduced non-Ucn1-containing EWcp neurons. Subsequent experiments showed that the inhibitory effect of EWcp activation on alcohol intake was also present in male Ucn1 KO mice, suggesting that a Ucn1-devoid population of EWcp regulates alcohol intake. A final set of chemogenetic experiments showed that activation of Vglut2-expressing EWcp neurons inhibited alcohol intake and induced hypothermia in male and female mice. These studies expand on previous literature by indicating that a glutamatergic, Ucn1-devoid subpopulation of the EWcp regulates alcohol consumption and body temperature.
先前在啮齿动物中的研究反复表明,投射到中枢的 Edinger-Westphal 核(EWcp)对酒精高度敏感,并且还参与调节酒精摄入和体温。历史上,EWcp 被认为是脑内 Urocortin 1(Ucn1)表达的主要部位,Ucn1 是一种促肾上腺皮质激素释放因子相关肽。然而,EWcp 还包含其他神经元群体,包括表达囊泡谷氨酸转运体 2(Vglut2)的神经元。在这里,我们用编码 Designer Receptors Exclusively Activated by Designer Drugs(DREADDs)的腺相关病毒(AAV)转导 EWcp,以测试 EWcp 在酒精摄入和体温调节中的作用。在雄性 C57BL/6J 小鼠的 2 瓶选择程序中,用兴奋性 DREADDs 激活 EWcp 抑制了酒精摄入,而用 DREADDs 抑制 EWcp 则没有影响。令人惊讶的是,DREADD 表达的分析表明,EWcp 的 Ucn1 包含神经元不表达 DREADDs。相比之下,AAV 转导了非 Ucn1 包含的 EWcp 神经元。随后的实验表明,EWcp 激活对酒精摄入的抑制作用也存在于雄性 Ucn1 KO 小鼠中,这表明 Ucn1 缺乏的 EWcp 群体调节酒精摄入。最后一组化学遗传实验表明,激活表达 Vglut2 的 EWcp 神经元抑制酒精摄入,并在雄性和雌性小鼠中引起体温过低。这些研究通过表明 EWcp 的谷氨酸能、Ucn1 缺乏亚群调节酒精消耗和体温,扩展了先前的文献。