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大鼠苍白球损伤后丘脑底核对多巴胺系统损伤的影响。

The influence of the subthalamic nucleus upon the damage to the dopamine system following lesions of globus pallidus in rats.

作者信息

Wright A K, Arbuthnott G W

机构信息

Division of Neuroscience, University of Edinburgh, EH9 1QH, Scotland, UK.

出版信息

Eur J Neurosci. 2007 Aug;26(3):642-8. doi: 10.1111/j.1460-9568.2007.05706.x. Epub 2007 Jul 18.

Abstract

Lesioning or stimulating the subthalamic nucleus (STN) in patients with Parkinson's disease, or in animal models of parkinsonism, alleviates many of the symptoms and so it is tempting to think of the STN as a part of the cause of Parkinson's disease. The globus pallidus (GP) is thought to have a tonic inhibitory action on the STN. An ibotenic acid injection into the GP in rats removes the cells of the GP and, over the following 6 weeks, a progressive loss of dopamine cells (counted stereologically in sections stained for tyrosine hydroxylase) develops in substantia nigra (SN). In this investigation we show that, when animals have the STN cells destroyed by very small ibotenic acid injections, their dopamine neurons are not damaged. Furthermore, if a lesion to the GP follows a lesion of STN then the dopamine cells also survive this double insult, at least for the first 3 weeks following the lesion. The experiments provide good reason to suspect that, at least in the short term, increased activity in the STN is a contributory cause of the loss of dopamine cells which follows the lesion of the GP in rats. Whether or not this is part of the mechanism of cell loss in Parkinson's disease, the rats with GP lesions at least provide an opportunity to test strategies that might protect dopamine cells from slowly developing damage. Removing the STN seems to be neuroprotective in this new model of dopamine degeneration.

摘要

在帕金森病患者或帕金森病动物模型中,损毁或刺激底丘脑核(STN)可缓解许多症状,因此人们很容易认为STN是帕金森病病因的一部分。苍白球(GP)被认为对STN具有持续性抑制作用。向大鼠的GP注射鹅膏蕈氨酸可去除GP的细胞,在接下来的6周内,黑质(SN)中的多巴胺能细胞(通过对酪氨酸羟化酶染色切片进行体视学计数)逐渐减少。在本研究中,我们发现,当通过非常小剂量的鹅膏蕈氨酸注射破坏动物的STN细胞时,其多巴胺神经元并未受损。此外,如果在STN损伤后再对GP进行损伤,那么多巴胺能细胞在这种双重损伤下也能存活,至少在损伤后的前3周如此。这些实验提供了充分的理由怀疑,至少在短期内,STN活性增加是大鼠GP损伤后多巴胺能细胞丢失的一个促成因素。无论这是否是帕金森病细胞丢失机制的一部分,患有GP损伤的大鼠至少提供了一个机会来测试可能保护多巴胺能细胞免受缓慢发展损伤的策略。在这个新的多巴胺变性模型中,去除STN似乎具有神经保护作用。

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