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用胶质细胞源性神经营养因子治疗的帕金森病猴的功能恢复

Functional recovery in parkinsonian monkeys treated with GDNF.

作者信息

Gash D M, Zhang Z, Ovadia A, Cass W A, Yi A, Simmerman L, Russell D, Martin D, Lapchak P A, Collins F, Hoffer B J, Gerhardt G A

机构信息

Department of Anatomy and Neurobiology, University of Kentucky, College of Medicine, Lexington, Kentucky 40536, USA.

出版信息

Nature. 1996 Mar 21;380(6571):252-5. doi: 10.1038/380252a0.

Abstract

Parkinson's disease results from the progressive degeneration of dopamine neurons that innervate the striatum. In rodents, glial-cell-line-derived neurotrophic factor (GDNF) stimulates an increase in midbrain dopamine levels, protects dopamine neurons from some neurotoxins, and maintains injured dopamine neurons. Here we extend the rodent studies to an animal closer to the human in brain organization and function, by evaluating the effects of GDNF injected intracerebrally in rhesus monkeys that have had the symptomatology and pathophysiological features of Parkinson's disease induced by the neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). The recipients of GDNF displayed significant improvements in three of the cardinal symptoms of parkinsonism: bradykinesia, rigidity and postural instability. GDNF administered every four weeks maintained functional recovery. On the lesioned side of GDNF-treated animals, dopamine levels in the midbrain and globus pallidus were twice as high, and nigral dopamine neurons were, on average, 20% larger, with an increased fibre density. The results indicate that GDNF may be of benefit in the treatment of Parkinson's disease.

摘要

帕金森病是由支配纹状体的多巴胺能神经元进行性退变所致。在啮齿动物中,胶质细胞源性神经营养因子(GDNF)可刺激中脑多巴胺水平升高,保护多巴胺能神经元免受某些神经毒素的侵害,并维持受损的多巴胺能神经元。在此,我们通过评估向患有由神经毒素1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的帕金森病症状和病理生理特征的恒河猴脑内注射GDNF的效果,将啮齿动物研究扩展至脑组织结构和功能更接近人类的动物。接受GDNF治疗的动物在帕金森病的三个主要症状方面有显著改善:运动迟缓、僵硬和姿势不稳。每四周给予一次GDNF可维持功能恢复。在接受GDNF治疗的动物的损伤侧,中脑和苍白球的多巴胺水平高出两倍,黑质多巴胺能神经元平均大20%,纤维密度增加。结果表明,GDNF可能对帕金森病的治疗有益。

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