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锰诱导神经毒性的神经保护及治疗策略

Neuroprotective and Therapeutic Strategies for Manganese-Induced Neurotoxicity.

作者信息

Marreilha Dos Santos A P, Andrade V, Aschner M

机构信息

Institute of Medicine Research (iMed.ULisboa), Faculty of Pharmacy, University of Lisbon, Lisbon. Portugal.

Department of Molecular Pharmacology, Albert Einstein College of Medicine, USA.

出版信息

Clin Pharmacol Transl Med. 2017;1(2):54-62. Epub 2017 May 26.

Abstract

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.

摘要

锰(Mn)是生长、发育和维持身体健康所必需的元素。然而,长期以来人们都知道,职业和环境中长期或大量接触过量的锰会导致一种类似于帕金森氏症的进行性神经疾病。锰中毒患者会出现多种症状,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。考虑到锰的药代动力学和相关毒性机制,人们研究了几种神经保护化合物和治疗方法,以评估它们减轻锰神经毒性的功效。在此,我们将简要阐述锰的一些毒性机制,随后介绍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。为了降低锰诱导的神经毒性,人们引入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。此外,还将综述几种旨在改善人类锰神经毒性症状的治疗干预措施,如左旋多巴、乙二胺四乙酸(EDTA)和对氨基水杨酸(PAS)的疗效和作用机制。

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