Rawani Neha S, Chan Allen W, Todd Kathryn G, Baker Glen B, Dursun Serdar M
Neurochemical Research Unit and Bebensee Schizophrenia Research Unit, Department of Psychiatry and Neuroscience and Mental Health Institute, University of Alberta, Edmonton, AB T6G 2G3, Canada.
Biomolecules. 2024 Dec 25;15(1):10. doi: 10.3390/biom15010010.
Schizophrenia is a complex heterogenous disorder thought to be caused by interactions between genetic and environmental factors. The theories developed to explain the etiology of schizophrenia have focused largely on the dysfunction of neurotransmitters such as dopamine, serotonin and glutamate with their receptors, although research in the past several decades has indicated strongly that other factors are also involved and that the role of neuroglial cells in psychotic disorders including schizophrenia should be given more attention. Although glia were originally thought to be present in the brain only to support neurons in a physical, metabolic and nutritional capacity, it has become apparent that these cells have a variety of important physiological roles and that abnormalities in their function may make significant contributions to the symptoms of schizophrenia. In the present paper, we review the interactions of brain microglia, astrocytes and oligodendroglia with aspects such as transmitter dysregulation, neuro-inflammation, oxidative stress, synaptic function, the gut microbiome, myelination and the blood-brain barrier that appear to affect the cause, development and treatment of schizophrenia. We also review crosstalk between microglia, astrocytes and oligodendrocytes and the effects of antipsychotics on neuroglia. Problems associated with studies on specific biomarkers for glia in schizophrenia are discussed.
精神分裂症是一种复杂的异质性疾病,被认为是由遗传和环境因素相互作用引起的。为解释精神分裂症病因所提出的理论主要集中在多巴胺、血清素和谷氨酸等神经递质及其受体的功能障碍上,尽管过去几十年的研究强烈表明其他因素也参与其中,并且神经胶质细胞在包括精神分裂症在内的精神障碍中的作用应得到更多关注。尽管神经胶质细胞最初被认为仅以物理、代谢和营养能力存在于大脑中以支持神经元,但很明显这些细胞具有多种重要的生理作用,并且其功能异常可能对精神分裂症的症状产生重大影响。在本文中,我们综述了脑小胶质细胞、星形胶质细胞和少突胶质细胞与递质失调、神经炎症、氧化应激、突触功能、肠道微生物群、髓鞘形成和血脑屏障等方面的相互作用,这些似乎会影响精神分裂症的病因、发展和治疗。我们还综述了小胶质细胞、星形胶质细胞和少突胶质细胞之间的相互作用以及抗精神病药物对神经胶质细胞的影响。讨论了与精神分裂症中神经胶质细胞特异性生物标志物研究相关的问题。