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大麻素信号招募星形胶质细胞调节视交叉上核的突触前功能。

Cannabinoid Signaling Recruits Astrocytes to Modulate Presynaptic Function in the Suprachiasmatic Nucleus.

机构信息

Oregon Institute of Occupational Health Sciences, Oregon Health & Science University, Portland, OR 97239.

Department of Behavioral Neuroscience, Oregon Health and Science University, Portland, OR 97239.

出版信息

eNeuro. 2020 Feb 13;7(1). doi: 10.1523/ENEURO.0081-19.2020. Print 2020 Jan/Feb.

Abstract

Circadian rhythms are 24-h cycles in physiology regulated by the suprachiasmatic nucleus (SCN) in the brain, where daily cues act on SCN neurons to alter clock timing. Cannabinoid signaling modulates SCN neuronal activity, although the mechanism remains unclear. We propose that neuronal activity generates endocannabinoid release, activating astrocyte Ca signaling, which releases adenosine and activates adenosine-1 receptors (A1Rs) on the presynaptic axon terminals, decreasing GABA release. We demonstrated, in mice, that activation of cannabinoid-1 receptors (CB1R) with the agonist WIN 55,212-2 (WIN) reduced the miniature GABA receptor-mediated postsynaptic current (mGPSC) frequency by a mechanism that requires astrocytes and A1R. WIN activated an intracellular Ca signaling pathway in astrocytes. Activating this intracellular Ca pathway with designer receptors exclusively activated by designer drugs (DREADDs) also decreased the mGPSC frequency and required A1R activation. The frequency of spontaneous Ca events, including those induced by depolarization of a postsynaptic SCN neuron, was reduced by blocking CB1R activation with AM251, demonstrating neuronal endocannabinoid signaling modulates astrocytic Ca signaling in the SCN. Finally, daytime application of WIN or adenosine phase advanced the molecular circadian clock, indicating that this cannabinoid signaling pathway is vital for the timing of circadian rhythms.

摘要

昼夜节律是由大脑中的视交叉上核 (SCN) 调节的 24 小时生理周期,其中日常提示作用于 SCN 神经元以改变时钟计时。大麻素信号调节 SCN 神经元活动,尽管其机制尚不清楚。我们提出,神经元活动产生内源性大麻素释放,激活星形胶质细胞 Ca 信号,释放腺苷并激活突触前轴突末梢上的腺苷-1 受体 (A1R),减少 GABA 释放。我们在小鼠中证明,用激动剂 WIN 55,212-2 (WIN) 激活大麻素-1 受体 (CB1R) 可通过一种需要星形胶质细胞和 A1R 的机制减少微小 GABA 受体介导的突触后电流 (mGPSC) 频率。WIN 激活星形胶质细胞中的细胞内 Ca 信号通路。用专门被设计药物激活的受体 (DREADDs) 激活这种细胞内 Ca 通路也降低了 mGPSC 频率,并且需要 A1R 激活。包括由 SCN 神经元去极化诱导的 Ca 事件在内的自发 Ca 事件的频率通过用 AM251 阻断 CB1R 激活而降低,表明神经元内源性大麻素信号调节 SCN 中的星形胶质细胞 Ca 信号。最后,白天应用 WIN 或腺苷使分子生物钟提前,表明这种大麻素信号通路对昼夜节律的计时至关重要。

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