Luo Yuchong, Chen Xiao, Wei Chunren, Zhang Hongyang, Zhang Lingyi, Han Lu, Sun Ke, Li Boxing, Wen Shenglin
Department of Psychology, The Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, China.
Guangdong Provincial Key Laboratory of Brain Function and Disease, Neuroscience Program, Zhongshan School of Medicine and the Fifth Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Front Mol Neurosci. 2022 Jul 12;15:926572. doi: 10.3389/fnmol.2022.926572. eCollection 2022.
Obsessive-compulsive disorder (OCD) is a severe mental illness characterized by obsessions and compulsions. However, its underlying mechanisms remain to be elucidated. Recent studies have suggested that neuroimmune dysregulation is involved in the pathogenesis of OCD. To investigate the role of microglia in this disorder, we established a pharmacological mouse model by using the serotonin (5-HT) 1A/1B receptor agonist RU24969 to mimic monoamine dysregulation in OCD, and we examined the morphological and functional alterations of microglia in this model. We found that RU24969 treatment led to compulsive circling behavior in mice. Strikingly, we found that the density and mobility of microglia in the prelimbic cortex were much lower in RU24969-treated mice than in control mice. Moreover, the expression of cytokines and chemokines, including BDNF, IL-1β, IL-6, TNFα, CD80, CD86, MHC-I, and MHC-II, also decreased in RU24969-treated mice. Importantly, we found that injection of BDNF or induction of BDNF expression by trehalose completely reversed microglial dysfunction and reduced stereotypic behavior. These results indicate that microglial dysfunction is closely related to stereotypic behaviors in our mouse model of OCD and that BDNF could be an effective treatment for stereotypic behaviors.
强迫症(OCD)是一种以强迫观念和强迫行为为特征的严重精神疾病。然而,其潜在机制仍有待阐明。最近的研究表明,神经免疫失调参与了强迫症的发病机制。为了研究小胶质细胞在这种疾病中的作用,我们通过使用血清素(5-HT)1A/1B受体激动剂RU24969建立了一种药理学小鼠模型,以模拟强迫症中的单胺失调,并在该模型中检测了小胶质细胞的形态和功能变化。我们发现,RU24969处理导致小鼠出现强迫性转圈行为。令人惊讶的是,我们发现,与对照小鼠相比,接受RU24969处理的小鼠前边缘皮层中小胶质细胞的密度和迁移率要低得多。此外,在接受RU24969处理的小鼠中,包括脑源性神经营养因子(BDNF)、白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNFα)、CD80、CD86、主要组织相容性复合体-I(MHC-I)和主要组织相容性复合体-II(MHC-II)在内的细胞因子和趋化因子的表达也降低了。重要的是,我们发现注射BDNF或用海藻糖诱导BDNF表达可完全逆转小胶质细胞功能障碍并减少刻板行为。这些结果表明,在我们的强迫症小鼠模型中,小胶质细胞功能障碍与刻板行为密切相关,并且BDNF可能是治疗刻板行为的有效药物。