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全球大脑 c-Fos 分析揭示了酒精再暴露后主要功能性大脑网络的重新排列。

Global brain c-Fos profiling reveals major functional brain networks rearrangements after alcohol reexposure.

机构信息

Laboratory of Neurobiology, Nencki Institute, BRAINCITY, Warsaw, Poland.

Laboratory of Neurobiology, Nencki Institute, BRAINCITY, Warsaw, Poland; Institute of Experimental Physics, Section of Optics, Warsaw University, Warsaw, Poland.

出版信息

Neurobiol Dis. 2023 Mar;178:106006. doi: 10.1016/j.nbd.2023.106006. Epub 2023 Jan 20.

Abstract

Many fundamental questions on alcohol use disorder (AUD) are frequently difficult to address by examining a single brain structure, but should be viewed from the whole brain perspective. c-Fos is a marker of neuronal activation. Global brain c-Fos profiling in rodents represents a promising platform to study brain functional networks rearrangements in AUD. We used a mouse model of alcohol drinking in IntelliCage. We trained mice to voluntarily drink alcohol, next subjected them to withdrawal and alcohol reexposure. We have developed a dedicated image computational workflow to identify c-Fos-positive cells in three-dimensional images obtained after whole-brain optical clearing and imaging in the light-sheet microscope. We provide a complete list of 169 brain structures with annotated c-Fos expression. We analyzed functional networks, brain modularity and engram index. Brain c-Fos levels in animals reexposed to alcohol were different from both control and binge drinking animals. Structures involved in reward processing, decision making and characteristic for addictive behaviors, such as precommissural nucleus, nucleus Raphe, parts of colliculus and tecta stood out particularly. Alcohol reexposure leads to a massive change of brain modularity including a formation of numerous smaller functional modules grouping structures involved in addiction development. Binge drinking can lead to substantial functional remodeling in the brain. We provide a list of structures that can be used as a target in pharmacotherapy but also point to the networks and modules that can hold therapeutic potential demonstrated by a clinical trial in patients.

摘要

许多关于酒精使用障碍(AUD)的基本问题,通过检查单一的大脑结构往往难以解决,但应该从全脑的角度来看待。c-Fos 是神经元激活的标志物。在啮齿动物中进行全脑 c-Fos 分析代表了研究 AUD 中大脑功能网络重排的有前途的平台。我们使用 IntelliCage 中的酒精饮用小鼠模型。我们训练小鼠自愿饮酒,然后让它们戒断并再次暴露于酒精中。我们开发了一种专用的图像计算工作流程,用于在光片显微镜中对全脑光学清除和成像后获得的三维图像中识别 c-Fos 阳性细胞。我们提供了一份带有注释的 c-Fos 表达的 169 个脑结构的完整列表。我们分析了功能网络、大脑模块性和印痕指数。重新暴露于酒精的动物的大脑 c-Fos 水平与对照组和 binge 饮酒组的动物不同。涉及奖励处理、决策和成瘾行为特征的结构,如前连合核、中缝核、脑丘和顶盖特别突出。酒精再暴露导致大脑模块性的巨大变化,包括形成许多更小的功能模块,将参与成瘾发展的结构分组。 binge 饮酒可导致大脑发生实质性的功能重塑。我们提供了一个可作为药物治疗靶点的结构列表,但也指出了网络和模块,这些靶点可以通过对患者进行临床试验证明具有治疗潜力。

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