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Multiple sclerosis: An overview of the disease and current concepts of its pathophysiology

机译:多发性硬化症:疾病概述及其当前病理生理学概念

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The oligodendrocytes, myelin-producing cells in the central nervous system (CNS), have an essential role in “multiple sclerosis”. This disease is of unknown etiology, and thus, of a variable prognosis. The main pathologic feature is the injury to the myelin and loss of oligodendrocytes in the CNS. Studies of animal models, demonstrating that autoreactive T cells (CD4 or CD8) can result in inflammatory demyelination of the central nervous system, support the theory that multiple sclerosis is an immune-mediated disorder involving one or more antigens located in the myelin of central nervous system cells (neurons and glia). About the disorder′s pathology, important findings have been made regarding inflammation, adhesion-molecules, ion-channel alterations and the process of neurodegeneration in the progression of the multiple sclerosis plaque. The progress made so far in the pathogenesis of the disease will allow a better understanding of the mechanisms involved in its progression and so, more specific treatments can be developed to ensure a better quality of life of the affected patients.
机译:少突胶质细胞是中枢神经系统(CNS)中产生髓磷脂的细胞,在“多发性硬化症”中具有重要作用。该病的病因不明,因此预后可变。主要病理特征是中枢神经系统中髓磷脂的损伤和少突胶质细胞的丢失。动物模型研究表明,自身反应性T细胞(CD4或CD8)可导致中枢神经系统发炎性脱髓鞘,支持以下理论:多发性硬化症是一种免疫介导的疾病,涉及一种或多种位于中枢神经系统髓鞘中的抗原系统细胞(神经元和神经胶质细胞)。关于该疾病的病理学,在炎症,粘附分子,离子通道改变以及多发性硬化斑块发展过程中的神经变性过程方面取得了重要发现。迄今为止,该疾病的发病机理方面的进展将使人们更好地了解其发展所涉及的机制,因此,可以开发出更具体的治疗方法以确保受影响患者的生活质量更好。

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