Department of Psychiatry, University of Pittsburgh Medical Center, Pittsburgh, USA.
Sci Rep. 2022 Jun 10;12(1):9605. doi: 10.1038/s41598-022-13724-x.
Alterations in cannabinoid CB1 receptor (CB1R) are implicated in various psychiatric disorders. CB1R participates in both depolarization induced suppression of inhibition (DSI) and depolarization induced suppression of excitation (DSE), suggesting its involvement in regulating excitatory and inhibitory (E/I) balance. Prior studies examining neuronal cell type specific CB1R distribution have been conducted near exclusively within rodents. Identification of these distribution patterns within the human and non-human primate cortex is essential to increase our insight into its function. Using co-labeling immunohistochemistry and fluorescent microscopy, we examined CB1R protein levels within excitatory and inhibitory boutons of male human and non-human primate prefrontal cortex and auditory cortices, regions involved in the behavioral effects of exogenous cannabinoid exposures. We found that CB1R was present in both bouton populations within all brain regions examined in both species. Significantly higher CB1R levels were found within inhibitory than within excitatory boutons across all regions in both species, although the cell type by brain region interactions differed between the two species. Our results support the importance of conducting more in-depth CB1R examinations to understand how cell type and brain region dependent differences contribute to regional E/I balance regulation, and how aberrations in CB1R distribution may contribute to pathology.
大麻素 CB1 受体 (CB1R) 的改变与各种精神疾病有关。CB1R 参与去极化诱导的抑制 (DSI) 和去极化诱导的兴奋抑制 (DSE),表明其参与调节兴奋和抑制 (E/I) 平衡。先前研究神经元细胞类型特异性 CB1R 分布的研究几乎仅在啮齿动物中进行。在人类和非人类灵长类动物皮层中鉴定这些分布模式对于增加我们对其功能的了解至关重要。使用共标记免疫组织化学和荧光显微镜,我们检查了雄性人类和非人类灵长类动物前额叶皮层和听觉皮层兴奋性和抑制性末梢中 CB1R 蛋白水平,这些区域参与外源性大麻素暴露的行为效应。我们发现,在两种物种的所有研究脑区的两种末梢群体中都存在 CB1R。尽管两种物种之间的细胞类型与脑区的相互作用不同,但在所有脑区中,抑制性末梢中的 CB1R 水平明显高于兴奋性末梢。我们的研究结果支持进行更深入的 CB1R 检查的重要性,以了解细胞类型和脑区依赖性差异如何有助于区域 E/I 平衡调节,以及 CB1R 分布的异常如何导致病理学。