The relationships between neuroglial and neuronal changes in Alzheimer's disease, and the related controversies II: gliotherapies and multimodal therapy.

IF 2.6 Q2 CLINICAL NEUROLOGY
Journal of Central Nervous System Disease Pub Date : 2022-11-14 eCollection Date: 2022-01-01 DOI:10.1177/11795735221123896
Adolfo Toledano-Díaz, M Isabel Álvarez, Adolfo Toledano
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Abstract

Since the original description of Alzheimer´s disease (AD), research into this condition has mainly focused on assessing the alterations to neurons associated with dementia, and those to the circuits in which they are involved. In most of the studies on human brains and in many models of AD, the glial cells accompanying these neurons undergo concomitant alterations that aggravate the course of neurodegeneration. As a result, these changes to neuroglial cells are now included in all the "pathogenic cascades" described in AD. Accordingly, astrogliosis and microgliosis, the main components of neuroinflammation, have been integrated into all the pathogenic theories of this disease, as discussed in this part of the two-part monograph that follows an accompanying article on gliopathogenesis and glioprotection. This initial reflection verified the implication of alterations to the neuroglia in AD, suggesting that these cells may also represent therapeutic targets to prevent neurodegeneration. In this second part of the monograph, we will analyze the possibilities of acting on glial cells to prevent or treat the neurodegeneration that is the hallmark of AD and other pathologies. Evidence of the potential of different pharmacological, non-pharmacological, cell and gene therapies (widely treated) to prevent or treat this disease is now forthcoming, in most cases as adjuncts to other therapies. A comprehensive AD multimodal therapy is proposed in which neuronal and neuroglial pharmacological treatments are jointly considered, as well as the use of new cell and gene therapies and non-pharmacological therapies that tend to slow down the progress of dementia.

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阿尔茨海默病中神经胶质细胞和神经元变化的关系及相关争议II:胶质治疗和多模式治疗。
自阿尔茨海默病(AD)的最初描述以来,对这种疾病的研究主要集中在评估与痴呆症相关的神经元的改变,以及它们所涉及的回路的改变。在大多数关于人脑和许多阿尔茨海默病模型的研究中,伴随这些神经元的胶质细胞发生了伴随的改变,从而加剧了神经退行性变的过程。因此,神经胶质细胞的这些变化现在包括在阿尔茨海默病中描述的所有“致病级联反应”中。因此,星形胶质细胞增生和小胶质细胞增生是神经炎症的主要组成部分,已被纳入该疾病的所有致病理论,正如在两部分专著的这一部分中所讨论的那样,该专著随后发表了一篇关于胶质病变发生和胶质保护的文章。这一初步反映证实了阿尔茨海默病中神经胶质细胞改变的含义,表明这些细胞也可能代表预防神经变性的治疗靶点。在本专著的第二部分,我们将分析作用于神经胶质细胞的可能性,以预防或治疗神经退行性变,这是阿尔茨海默病和其他病理的标志。目前有证据表明,不同的药理学、非药理学、细胞和基因疗法(广泛治疗)有可能预防或治疗这种疾病,在大多数情况下是作为其他疗法的辅助疗法。提出了一种综合的AD多模式治疗方法,该方法联合考虑神经元和神经胶质药物治疗,以及使用新的细胞和基因治疗以及倾向于减缓痴呆进展的非药物治疗。
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
CiteScore
6.90
自引率
0.00%
发文量
39
审稿时长
8 weeks
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