Shuangtao Li, Yongchang He, Dharshaun Turner, Naili Wei, Luyao Ma, Devin H Taylor, Danielle T Taylor, Xiaoyu Ji, Jie Wu
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The focus was on aspects such as synaptic transmission, short- and long-term synaptic plasticity, and neural network synchrony (theta oscillations). <b>Results:</b> 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. <b>Conclusion:</b> 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.</p>","PeriodicalId":9386,"journal":{"name":"Cannabis and Cannabinoid Research","volume":" ","pages":"1267-1276"},"PeriodicalIF":3.1000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electrophysiological Phenotypes of Hippocampal Synaptic and Network Functions in Cannabinoid Receptor 2 Knockout Mice.\",\"authors\":\"Shuangtao Li, Yongchang He, Dharshaun Turner, Naili Wei, Luyao Ma, Devin H Taylor, Danielle T Taylor, Xiaoyu Ji, Jie Wu\",\"doi\":\"10.1089/can.2023.0186\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Background:</b> 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. 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引用次数: 0
摘要
背景: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,现已在大脑中发现,尤其是在海马中,它在调节各种神经功能方面发挥着至关重要的作用,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。尽管人们对它的了解越来越多,但对 CB2R 基因敲除(CB2R KO)小鼠海马神经元错综复杂的电生理特征仍然一无所知。目的和方法: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性(θ振荡)等方面。研究结果我们的研究结果揭示了这些 CB2R KO 小鼠的多种功能特征,尤其是海马 CA1 神经元的突触传递升高、突触短期可塑性(配对脉冲促进)和长期电位(LTP)降低以及神经网络同步性受损。结论从本质上讲,这项研究对 CB2Rs 对海马神经功能的影响有深刻的启示。通过阐明 CB2R KO 小鼠的电生理变化,我们的研究丰富了人们对 CB2R 参与海马功能的理解。这些见解将有助于我们进一步了解大脑中受 CB2R 影响的神经机制。
Electrophysiological Phenotypes of Hippocampal Synaptic and Network Functions in Cannabinoid Receptor 2 Knockout Mice.
Background: 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. Aim and Methods: 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). Results: 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. Conclusion: 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.