Protective Effect of Monoisoamyl-2, 3-Dimercaptosuccinic Acid against Manganese-induced Neurotoxicity in Rats.

Awanish Mishra, Anjali Dahia, Amit Jaiswal
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Abstract

Background: Apart from being an essential heavy metal, Manganese (Mn) serves as an important component of the antioxidant enzyme system in humans. Overexposure to manganese leads to the development of manganism, which is characterized by motor dysfunction along with neurodegeneration. The management of manganism often utilizes chelation therapy. In this regard, Monoisoamyl-2, 3-Dimercaptosuccinic Acid (MiADMSA) has been reported as a novel arsenic chelator, due to the presence of vicinal sulfhydril group. MiADMSA has been reported to reduce the level in divalent ions (like copper) therefore, it may be hypothesized that MiADMSA would be helpful in Mn-induced neurotoxicity.

Objective: This study is envisaged to explore the protective effect of MiADMSA on Mn-induced neurotoxicity.

Methods: Mn exposure was carried out by intraperitoneal administration of Mn (as manganese chloride, 10 mg/kg; i.p.). The animals were treated with MiADMSA (50 mg/kg; p.o.) either alone or in combination with Mn. The effect of different treatments on neurobehavioral functions was observed by assessing spontaneous locomotor activity, motor rotarod test, and depression-like behavior in the forced swim test. After behavioral evaluations, all the animals were sacrificed and the brain and liver were isolated for metal estimations.

Results: Mn exposure leads to loss of motor coordination as observed in spontaneous locomotor activity and rotarod test. However, treatment with MiADMSA significantly improved motor impairments as compared to Mn exposed animals. Accumulation of Mn in the liver and brain has been recorded with Mn exposure; however, MiADMSA treatment significantly reduced the Mn content from the liver and brain.

Conclusion: The outcome of the study suggests that treatment with MiADMSA reversed Mn-induced neurotoxicity by reducing Mn load. Therefore, the use of MiADMSA may be suggested in manganese toxicity, after careful investigation.

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单异戊基2,3 -二巯基琥珀酸对锰致大鼠神经毒性的保护作用。
背景:锰(Mn)除了是人体必需的重金属外,还是人体抗氧化酶系统的重要组成部分。过量接触锰可导致锰中毒,其特征是运动功能障碍伴神经退行性变。锰中毒的治疗通常采用螯合治疗。在这方面,单异戊酯- 2,3 -二巯基琥珀酸(MiADMSA)由于其邻近巯基的存在而被报道为一种新型的砷螯合剂。据报道,MiADMSA可以降低二价离子(如铜)的水平,因此,可以假设MiADMSA可能有助于锰诱导的神经毒性。目的:探讨MiADMSA对锰致神经毒性的保护作用。方法:通过腹腔注射锰(以氯化锰的形式,10 mg/kg;i.p)。用MiADMSA (50 mg/kg;(名词)单独或与Mn结合。通过自主运动活动、运动轮轮测试和强迫游泳测试中的抑郁样行为,观察不同处理对神经行为功能的影响。行为评价结束后,处死所有动物,分离脑和肝进行金属评价。结果:在自发运动活动和旋转杆试验中观察到,锰暴露导致运动协调性丧失。然而,与Mn暴露的动物相比,MiADMSA治疗显著改善了运动损伤。锰暴露记录了肝脏和大脑中锰的积累;然而,MiADMSA处理显著降低了肝脏和脑中的Mn含量。结论:研究结果表明,MiADMSA治疗可通过降低Mn负荷逆转Mn诱导的神经毒性。因此,在仔细研究锰毒性后,可能建议使用MiADMSA。
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来源期刊
Central nervous system agents in medicinal chemistry
Central nervous system agents in medicinal chemistry Psychology-Neuropsychology and Physiological Psychology
CiteScore
2.10
自引率
0.00%
发文量
21
期刊介绍: Central Nervous System Agents in Medicinal Chemistry aims to cover all the latest and outstanding developments in medicinal chemistry and rational drug design for the discovery of new central nervous system agents. Containing a series of timely in-depth reviews written by leaders in the field covering a range of current topics, Central Nervous System Agents in Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments in the field.
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