δ -9-四氢大麻酚对狨猴帕金森模型的神经保护作用

Sanneke A. M. van Vliet, R. Vanwersch, M. Jongsma, J. Gugten, B. Olivier, I. Philippens
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引用次数: 2

摘要

目前治疗帕金森氏症(PD)的药物不能阻止或减缓疾病的进展。因此,在神经细胞死亡过程的关键阶段进行药物干预将是一种更好的策略。大麻素在氧化应激和兴奋性毒性模型中是有效的神经保护化合物,并在PD模型中提供潜在的保护。因此,本研究确定了- 9 -四氢大麻酚(- 9 - thc)在绒猴1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)模型中的神经保护作用。12只狨猴在9天内接受总累积剂量为6 mg/kg的MPTP治疗。其中7只动物同时接受每日口服剂量- 9 -四氢大麻酚(4mg /kg), 5只动物同时接受27天的载药。在实验期间,每天观察帕金森症状,每周检测一次运动活动和手眼协调能力。死后分析纹状体多巴胺水平,应用酪氨酸羟化酶免疫组化法测定黑质中活的多巴胺能神经元。9 -THC对任何参数都没有保护作用。这些阴性结果可能与MPTP诱导细胞死亡的严重程度有关,这与该帕金森模型中使用的低剂量- 9 -四氢大麻酚有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuroprotective Effects of Delta-9-Tetrahydrocannabinol in a Marmoset Parkinson Model
The present medication in Parkinson's disease (PD) is unable to stop or slow down the progression of the dis- ease. Therefore pharmacological intervention at crucial steps in the neuronal cell death processes would be a better stra- tegy. Cannabinoids are potent neuroprotective compounds in models of oxidative stress and excitotoxicity and offer po- tential protection in models of PD. Therefore the present study determines the neuroprotective effects of � 9 - tetrahydrocannabinol (� 9 -THC) in the marmoset 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) model on beha- vior and pathology. Twelve marmoset monkeys were treated with a total cumulative dose of 6 mg/kg MPTP in 9 days. Seven of these animals received simultaneously a daily oral dose of � 9 -THC (4 mg/kg) and five animals received simulta- neously vehicle for 27 days. The parkinsonian symptoms were observed daily and locomotor activity and hand-eye coor- dination were tested once a week during the experimental period. Postmortem, dopamine levels in the striatum were ana- lyzed and tyrosine hydroxylase immunohistochemistry was applied to determine viable dopaminergic neurons in the sub- stantia nigra. � 9 -THC has no protective effects on any parameter. These negative results might be related to the severity of the cell death induction by MPTP in relation to the low dose of � 9 -THC used in this Parkinson model.
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