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胶质细胞反应性降低可能与大麻二酚的抗精神病样作用有关。

Decreased glial reactivity could be involved in the antipsychotic-like effect of cannabidiol.

作者信息

Gomes Felipe V, Llorente Ricardo, Del Bel Elaine A, Viveros Maria-Paz, López-Gallardo Meritxell, Guimarães Francisco S

机构信息

Department of Pharmacology, Medical School of Ribeirão Preto, University of São Paulo, Brazil; Center for Interdisciplinary Research on Applied Neurosciences (NAPNA), University of São Paulo, Brazil.

Department of Physiology, Faculty of Medicine, Complutense University of Madrid, Spain.

出版信息

Schizophr Res. 2015 May;164(1-3):155-63. doi: 10.1016/j.schres.2015.01.015. Epub 2015 Feb 10.

Abstract

NMDA receptor hypofunction could be involved, in addition to the positive, also to the negative symptoms and cognitive deficits found in schizophrenia patients. An increasing number of data has linked schizophrenia with neuroinflammatory conditions and glial cells, such as microglia and astrocytes, have been related to the pathogenesis of schizophrenia. Cannabidiol (CBD), a major non-psychotomimetic constituent of Cannabis sativa with anti-inflammatory and neuroprotective properties induces antipsychotic-like effects. The present study evaluated if repeated treatment with CBD (30 and 60 mg/kg) would attenuate the behavioral and glial changes observed in an animal model of schizophrenia based on the NMDA receptor hypofunction (chronic administration of MK-801, an NMDA receptor antagonist, for 28 days). The behavioral alterations were evaluated in the social interaction and novel object recognition (NOR) tests. These tests have been widely used to study changes related to negative symptoms and cognitive deficits of schizophrenia, respectively. We also evaluated changes in NeuN (a neuronal marker), Iba-1 (a microglia marker) and GFAP (an astrocyte marker) expression in the medial prefrontal cortex (mPFC), dorsal striatum, nucleus accumbens core and shell, and dorsal hippocampus by immunohistochemistry. CBD effects were compared to those induced by the atypical antipsychotic clozapine. Repeated MK-801 administration impaired performance in the social interaction and NOR tests. It also increased the number of GFAP-positive astrocytes in the mPFC and the percentage of Iba-1-positive microglia cells with a reactive phenotype in the mPFC and dorsal hippocampus without changing the number of Iba-1-positive cells. No change in the number of NeuN-positive cells was observed. Both the behavioral disruptions and the changes in expression of glial markers induced by MK-801 treatment were attenuated by repeated treatment with CBD or clozapine. These data reinforces the proposal that CBD may induce antipsychotic-like effects. Although the possible mechanism of action of these effects is still unknown, it may involve CBD anti-inflammatory and neuroprotective properties. Furthermore, our data support the view that inhibition of microglial activation may improve schizophrenia symptoms.

摘要

除了与精神分裂症患者的阳性症状有关外,N-甲基-D-天冬氨酸(NMDA)受体功能减退可能还与阴性症状和认知缺陷有关。越来越多的数据将精神分裂症与神经炎症状态联系起来,并且神经胶质细胞,如小胶质细胞和星形胶质细胞,已被认为与精神分裂症的发病机制有关。大麻二酚(CBD)是大麻的一种主要非致幻成分,具有抗炎和神经保护特性,可诱导产生类抗精神病作用。本研究评估了重复给予CBD(30和60mg/kg)是否会减轻在基于NMDA受体功能减退的精神分裂症动物模型(连续28天给予NMDA受体拮抗剂MK-801)中观察到的行为和神经胶质细胞变化。在社交互动和新物体识别(NOR)测试中评估行为改变。这些测试已分别广泛用于研究与精神分裂症阴性症状和认知缺陷相关的变化。我们还通过免疫组织化学评估了内侧前额叶皮质(mPFC)、背侧纹状体、伏隔核核心和壳以及背侧海马中神经元核抗原(NeuN,一种神经元标志物)、离子钙接头蛋白1(Iba-1,一种小胶质细胞标志物)和胶质纤维酸性蛋白(GFAP,一种星形胶质细胞标志物)表达的变化。将CBD的作用与非典型抗精神病药物氯氮平诱导的作用进行比较。重复给予MK-801会损害社交互动和NOR测试中的表现。它还增加了mPFC中GFAP阳性星形胶质细胞的数量以及mPFC和背侧海马中具有反应性表型的Iba-1阳性小胶质细胞的百分比,而Iba-1阳性细胞的数量没有变化。未观察到NeuN阳性细胞数量的变化。MK-801治疗诱导的行为破坏和神经胶质细胞标志物表达变化均通过重复给予CBD或氯氮平得到减轻。这些数据强化了CBD可能诱导类抗精神病作用的观点。尽管这些作用的可能作用机制仍然未知,但可能涉及CBD的抗炎和神经保护特性。此外,我们的数据支持抑制小胶质细胞激活可能改善精神分裂症症状的观点。

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