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L-精氨酸对1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导的Balb/c小鼠黑质神经元变性的有益作用。

Beneficial effects of L-arginine on 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neuronal degeneration in substantia nigra of Balb/c mice.

作者信息

Hami Javad, Hosseini Mehran, Nezhad Saeed Vafaei, Shahi Sekineh, Lotfi Nassim, Ehsani Hossein, Sadeghi Akram

机构信息

Department of Anatomical Sciences, School of Medicine, Birjand University of Medical Sciences, Birjand, Iran.

Department of Public Health, Research Centre of Experimental Medicine, Deputy of Research and Technology, Birjand University of Medical Sciences, Birjand, Iran.

出版信息

Adv Biomed Res. 2016 Aug 30;5:140. doi: 10.4103/2277-9175.187374. eCollection 2016.

Abstract

BACKGROUND

L-arginine has been recently investigated and proposed to reduce neurological damage after various experimental models of neuronal cellular damage. In this study, we aim to evaluate the beneficial effects of L-arginine administration on the numerical density of dark neurons (DNs) in the substantia nigra pars compacta (SNc) of Balb/c mice subjected to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) administration.

MATERIALS AND METHODS

Male Balb/c mice were randomly divided into 4 groups (n = 7 each): MPTP only; saline only (control); MPTP + L-arginine; and L-arginine only. The animals were infused intranasally with a single intranasal administration of the proneurotoxin MPTP (1 mg/nostril). L-arginine (300 mg/kg) was administrated intraperitoneally once daily for 1-week starting from 3 days after MPTP administration. Cavalieri principle method was used to estimate the numerical density of DNs in the SNc of different studied groups.

RESULTS

Twenty days following MPTP administration, the number of DNs was significantly increased when compared to sham-control and L-arginine-control groups (P < 0.05). Nevertheless, our results showed that L-arginine administration significantly decreased the numerical density of DNs in SNc of mice.

CONCLUSION

This investigation provides new insights in experimental models of Parkinson's disease, indicating that L-arginine represents a potential treatment agent for dopaminergic neuron degeneration in SNc observed in Parkinson's disease patients.

摘要

背景

最近对L-精氨酸进行了研究,并提出其可减轻各种神经元细胞损伤实验模型后的神经损伤。在本研究中,我们旨在评估给予L-精氨酸对接受1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)的Balb/c小鼠黑质致密部(SNc)中暗神经元(DNs)数量密度的有益作用。

材料与方法

雄性Balb/c小鼠随机分为4组(每组n = 7):仅MPTP组;仅生理盐水组(对照组);MPTP + L-精氨酸组;仅L-精氨酸组。动物经鼻内单次给予亲神经毒素MPTP(1 mg/鼻孔)。从MPTP给药后3天开始,每天腹腔注射一次L-精氨酸(300 mg/kg),持续1周。采用卡瓦列里原理方法估计不同研究组SNc中DNs的数量密度。

结果

MPTP给药20天后,与假手术对照组和L-精氨酸对照组相比,DNs数量显著增加(P < 0.05)。然而,我们的结果表明,给予L-精氨酸可显著降低小鼠SNc中DNs的数量密度。

结论

本研究为帕金森病实验模型提供了新的见解,表明L-精氨酸是帕金森病患者中观察到的SNc多巴胺能神经元变性的潜在治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89c1/5025923/4635587ff014/ABR-5-140-g003.jpg

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