锰致神经毒性的神经保护和治疗策略。

Clinical pharmacology and translational medicine Pub Date : 2017-01-01 Epub Date: 2017-05-26
A P Marreilha Dos Santos, V Andrade, M Aschner
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引用次数: 0

摘要

锰(Mn)是生长、发育和一般健康维持所必需的基本元素。然而,长期或高度的职业和环境暴露于过量的锰水平,长期以来被认为会导致类似帕金森病的进行性神经系统疾病。锰中毒患者表现出多种症状,包括精神、认知和行为障碍,以及与基底神经节功能障碍相关的运动功能障碍。考虑到药代动力学和锰相关的毒性机制,研究人员研究了几种神经保护化合物和治疗方法,以评估其减轻其神经毒性的功效。在这里,我们将简要介绍锰的一些毒性机制,然后是旨在减少或治疗锰诱导的神经毒性的神经保护策略和治疗方法。介绍了天然和合成抗氧化剂、抗炎化合物、ATP/ADP比值保护剂和谷氨酸保护剂,以期降低锰诱导的神经毒性。此外,一些治疗干预措施,如左旋多巴,乙二胺-四乙酸(EDTA)和对氨基水杨酸(PAS),旨在改善人类锰神经毒性症状的疗效和机制,将进行审查。
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Neuroprotective and Therapeutic Strategies for Manganese-Induced Neurotoxicity.

Manganese (Mn) is an essential element required for growth, development and general maintenance of health. However, chronic or high occupational and environmental exposure to excessive levels of Mn has long been known to lead to a progressive neurological disorder similar to Parkinsonism. Manganism patients display a variety of symptoms, including mental, cognitive and behavioural impediments, as well as motor dysfunctions that are associated with basal ganglia dysfunction. Taking into account the pharmacokinetics and Mn-related toxicity mechanisms, several neuroprotective compounds and therapeutic approaches have been investigated to assess their efficacy in mitigating its neurotoxicity. Here, we will briefly address some of the toxic mechanisms of Mn, followed by neuroprotective strategies and therapeutic approaches aiming to reduce or treat Mn induced neurotoxicity. Natural and synthetic antioxidants, anti-inflammatory compounds, ATP/ADP ratio protectors and glutamate protectors have been introduced in view of decreasing Mn-induced neurotoxicity. In addition, the efficacy and mechanisms of several therapeutic interventions such as levodopa, ethylene-diamine-tetraacetic acid (EDTA) and para-aminosalicylic acid (PAS), aimed at ameliorating Mn neurotoxic symptoms in humans, will be reviewed.

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