Neuroglia in Tourette syndrome and obsessive-compulsive disorder.

Q2 Medicine
Luciana R Frick
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引用次数: 0

Abstract

In recent years, neuroglia have drawn the attention of researchers in the fields of neurology and psychiatry. Besides their well-known functions providing support to neurons, myelinating axons, and clearing up debris, a constantly growing of evidence indicates that glial cells are key contributors to the pathophysiology of neuropsychiatric disorders. Alterations in microglia, astrocytes, and oligodendrocytes have been described in Tourette syndrome (TS) and obsessive-compulsive disorder (OCD). The sudden onset of tics and OCD-like symptoms after infection in children (Pediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcal Infections) suggests a connection with the immune system; in fact, neuroinflammation has been reported. Many imaging studies revealed abnormal myelination in the brain of TS and OCD patients, highlighting the implication of oligodendroglia in the connectivity alterations. Moreover, animal models have unveiled a cell-autonomous role of microglia and astrocytes in the etiology of pathologic grooming, which links these glial cells to the related disorder trichotillomania. This chapter reviews the state of the art and current gaps in the literature, proposing possible pathomechanisms and future research directions.

图雷特综合症和强迫症中的神经胶质细胞。
近年来,神经胶质细胞引起了神经病学和精神病学研究人员的广泛关注。除了它们众所周知的支持神经元、髓鞘轴突和清除碎片的功能外,越来越多的证据表明,神经胶质细胞是神经精神疾病病理生理学的关键贡献者。小胶质细胞、星形胶质细胞和少突胶质细胞的改变已经在图雷特综合征(TS)和强迫症(OCD)中被描述过。儿童感染后突然出现抽搐和强迫症样症状(与链球菌感染相关的儿童自身免疫性神经精神障碍)表明与免疫系统有关;事实上,已经有神经炎症的报道。许多影像学研究显示,TS和OCD患者的大脑中存在异常的髓鞘形成,强调了少突胶质细胞在连接改变中的意义。此外,动物模型揭示了小胶质细胞和星形胶质细胞在病理性梳理病因学中的细胞自主作用,这将这些胶质细胞与相关的拔毛症联系起来。本章回顾了目前的研究现状和文献空白,提出了可能的病理机制和未来的研究方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Handbook of clinical neurology
Handbook of clinical neurology Medicine-Neurology (clinical)
CiteScore
4.10
自引率
0.00%
发文量
302
期刊介绍: The Handbook of Clinical Neurology (HCN) was originally conceived and edited by Pierre Vinken and George Bruyn as a prestigious, multivolume reference work that would cover all the disorders encountered by clinicians and researchers engaged in neurology and allied fields. The first series of the Handbook (Volumes 1-44) was published between 1968 and 1982 and was followed by a second series (Volumes 45-78), guided by the same editors, which concluded in 2002. By that time, the Handbook had come to represent one of the largest scientific works ever published. In 2002, Professors Michael J. Aminoff, François Boller, and Dick F. Swaab took on the responsibility of supervising the third (current) series, the first volumes of which published in 2003. They have designed this series to encompass both clinical neurology and also the basic and clinical neurosciences that are its underpinning. Given the enormity and complexity of the accumulating literature, it is almost impossible to keep abreast of developments in the field, thus providing the raison d''être for the series. The series will thus appeal to clinicians and investigators alike, providing to each an added dimension. Now, more than 140 volumes after it began, the Handbook of Clinical Neurology series has an unparalleled reputation for providing the latest information on fundamental research on the operation of the nervous system in health and disease, comprehensive clinical information on neurological and related disorders, and up-to-date treatment protocols.
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