Brain Function and Disease Laboratory, Shantou University Medical College, Shantou, Guangdong, China.
Department of Neurobiology, Barrow Neurological Institute and St. Joseph's Hospital and Medical Center, Phoenix, Arizona, USA.
Cannabis Cannabinoid Res. 2024 Oct;9(5):1267-1276. doi: 10.1089/can.2023.0186. Epub 2024 Jan 22.
The cannabinoid receptor 2 (CB2R), a cannabinoid receptor primarily expressed in immune cells, has been found in the brain, particularly in the hippocampus, where it plays crucial roles in modulating various neural functions, including synaptic plasticity, neuroprotection, neurogenesis, anxiety and stress responses, and neuroinflammation. Despite this growing understanding, the intricate electrophysiological characteristics of hippocampal neurons in CB2R knockout (CB2R KO) mice remain elusive. This study aimed to comprehensively assess the electrophysiological traits of hippocampal synaptic and network functions in CB2R KO mice. The focus was on aspects such as synaptic transmission, short- and long-term synaptic plasticity, and neural network synchrony (theta oscillations). Our findings unveiled multiple functional traits in these CB2R KO mice, notably elevated synaptic transmission in hippocampal CA1 neurons, decreased both synaptic short-term plasticity (paired-pulse facilitation) and long-term potentiation (LTP), and impaired neural network synchronization. In essence, this study yields insightful revelations about the influence of CB2Rs on hippocampal neural functions. By illuminating the electrophysiological modifications in CB2R KO mice, our research enriches the comprehension of CB2R involvement in hippocampal function. Such insights could hold implications for advancing our understanding of the neural mechanisms under the influence of CB2Rs within the brain.
大麻素受体 2(CB2R)是一种主要在免疫细胞中表达的大麻素受体,已在大脑中发现,特别是在海马体中,它在调节各种神经功能方面发挥着关键作用,包括突触可塑性、神经保护、神经发生、焦虑和应激反应以及神经炎症。尽管人们对此有了更多的了解,但 CB2R 敲除(CB2R KO)小鼠海马神经元的复杂电生理特征仍然难以捉摸。本研究旨在全面评估 CB2R KO 小鼠海马突触和网络功能的电生理特征。重点是突触传递、短期和长期突触可塑性以及神经网络同步(θ 振荡)等方面。我们的发现揭示了这些 CB2R KO 小鼠的多种功能特征,特别是海马 CA1 神经元中突触传递的增加、突触短期可塑性(成对脉冲易化)和长期增强(LTP)的减少以及神经网络同步的受损。本质上,这项研究揭示了 CB2R 对海马神经功能的影响。通过阐明 CB2R KO 小鼠的电生理变化,我们的研究丰富了对 CB2R 参与海马功能的理解。这些见解可能对深入了解大脑中 CB2R 影响下的神经机制具有重要意义。