有机酸尿症患者大脑白质改变与少突胶质细胞脆弱性有关:戊二酸尿症 I 型的启示。

IF 2.9 3区 医学 Q2 NEUROSCIENCES
Eugenia Isasi, Moacir Wajner, Juliana Avila Duarte, Silvia Olivera-Bravo
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引用次数: 0

摘要

白质是中枢神经系统的重要组成部分,包含轴突、少突胶质细胞及其祖细胞、星形胶质细胞和小胶质细胞。少突胶质细胞是髓鞘合成的核心,而髓鞘是保护轴突的绝缘包膜,可实现正常的神经传导。在许多与髓鞘化紊乱有关的神经发育和神经退行性疾病中,少突胶质细胞和髓鞘都极易受到毒性因素的影响。在此,我们回顾了在一些有机酸病/贫血症中观察到的少突胶质细胞和髓鞘的主要变化,这些病症与遗传性神经代谢紊乱相对应,其生物化学特征是潜在神经毒性有机酸及其衍生物的积累。本文特别讨论了戊二酸血症 I 型(最典型的脑有机酸尿症)中的有机酸和/或髓鞘极易受到损伤的机制,但人们对这一机制的理解尚不完全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cerebral White Matter Alterations Associated With Oligodendrocyte Vulnerability in Organic Acidurias: Insights in Glutaric Aciduria Type I.

Cerebral White Matter Alterations Associated With Oligodendrocyte Vulnerability in Organic Acidurias: Insights in Glutaric Aciduria Type I.

The white matter is an important constituent of the central nervous system, containing axons, oligodendrocytes, and its progenitor cells, astrocytes, and microglial cells. Oligodendrocytes are central for myelin synthesis, the insulating envelope that protects axons and allows normal neural conduction. Both, oligodendrocytes and myelin, are highly vulnerable to toxic factors in many neurodevelopmental and neurodegenerative disorders associated with disturbances of myelination. Here we review the main alterations in oligodendrocytes and myelin observed in some organic acidurias/acidemias, which correspond to inherited neurometabolic disorders biochemically characterized by accumulation of potentially neurotoxic organic acids and their derivatives. The yet incompletely understood mechanisms underlying the high vulnerability of OLs and/or myelin in glutaric acidemia type I, the most prototypical cerebral organic aciduria, are particularly discussed.

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来源期刊
Neurotoxicity Research
Neurotoxicity Research 医学-神经科学
CiteScore
7.70
自引率
5.40%
发文量
164
审稿时长
6-12 weeks
期刊介绍: Neurotoxicity Research is an international, interdisciplinary broad-based journal for reporting both basic and clinical research on classical neurotoxicity effects and mechanisms associated with neurodegeneration, necrosis, neuronal apoptosis, nerve regeneration, neurotrophin mechanisms, and topics related to these themes. Published papers have focused on: NEURODEGENERATION and INJURY Neuropathologies Neuronal apoptosis Neuronal necrosis Neural death processes (anatomical, histochemical, neurochemical) Neurodegenerative Disorders Neural Effects of Substances of Abuse NERVE REGENERATION and RESPONSES TO INJURY Neural Adaptations Neurotrophin mechanisms and actions NEURO(CYTO)TOXICITY PROCESSES and NEUROPROTECTION Excitatory amino acids Neurotoxins, endogenous and synthetic Reactive oxygen (nitrogen) species Neuroprotection by endogenous and exogenous agents Papers on related themes are welcome.
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