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胶质细胞源性神经营养因子的神经保护和神经修复特性。

Neuroprotective and neurorestorative properties of GDNF.

作者信息

Gash D M, Zhang Z, Gerhardt G

机构信息

Department of Anatomy and Neurobiology and Center for Magnetic Resonance Imaging and Spectroscopy, University of Kentucky, College of Medicine, Lexington, USA.

出版信息

Ann Neurol. 1998 Sep;44(3 Suppl 1):S121-5. doi: 10.1002/ana.410440718.

Abstract

Glial cell line-derived neurotrophic factor (GDNF) promotes recovery of the injured nigrostriatal dopamine system and improves motor functions in both rodent and nonhuman primate models of Parkinson's disease (PD). The neurorestorative effects of a single administration of GDNF last for at least 1 month and can be maintained in rhesus monkeys by monthly injections. Adult midbrain dopamine neurons stimulated by GDNF show increased cell size, neurite extent, and expression of phenotypic markers. In parkinsonian nonhuman primates, GDNF treatment improves three of the cardinal features of PD: bradykinesia, rigidity, and postural instability. Although intracerebral administration is necessary because of the blood-brain barrier, intraventricular, intrastriatal, and intranigral routes of administration have been found to be efficacious in rodents and nonhuman primates. GDNF also induces neuroprotective changes in dopamine neurons which are active within hours after trophic factor administration. The powerful neuroprotective and neurorestorative properties of GDNF seen in preclinical studies suggest that trophic factors may play an important role in treating PD.

摘要

胶质细胞源性神经营养因子(GDNF)可促进帕金森病(PD)啮齿动物模型和非人类灵长类动物模型中受损黑质纹状体多巴胺系统的恢复,并改善运动功能。单次给予GDNF的神经修复作用可持续至少1个月,在恒河猴中通过每月注射可维持该作用。受GDNF刺激的成年中脑多巴胺神经元表现出细胞大小增加、神经突长度增加以及表型标志物表达增加。在帕金森病非人类灵长类动物中,GDNF治疗可改善PD的三个主要特征:运动迟缓、僵硬和姿势不稳。尽管由于血脑屏障,脑内给药是必要的,但已发现脑室内、纹状体内和黑质内给药途径在啮齿动物和非人类灵长类动物中是有效的。GDNF还会在给予营养因子后数小时内使活跃的多巴胺神经元发生神经保护变化。临床前研究中观察到的GDNF强大的神经保护和神经修复特性表明,营养因子可能在治疗PD中发挥重要作用。

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