Tomac A, Lindqvist E, Lin L F, Ogren S O, Young D, Hoffer B J, Olson L
Department of Neuroscience, Karolinska Institute, Stockholm, Sweden.
Nature. 1995 Jan 26;373(6512):335-9. doi: 10.1038/373335a0.
Glial-cell-line-derived neurotrophic factor (GDNF), a recently cloned new member of the transforming growth factor-beta superfamily, promotes survival of cultured fetal mesencephalic dopamine neurons and is expressed in the developing striatum. There have, however, been no reports about effects of GDNF in situ. We have used the dopaminergic neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), which produces parkinsonian symptoms in man, to determine whether GDNF might exert protective or regenerative effects in vivo in the adult nigrostriatal dopamine system in C57/B1 mice. GDNF injected over the substantia nigra or in striatum before MPTP potently protects the dopamine system, as shown by numbers of mesencephalic dopamine nerve cell bodies, dopamine nerve terminal densities and dopamine levels. When GDNF is given after MPTP, dopamine levels and fibre densities are significantly restored. In both cases, motor behaviour is increased above normal levels. We conclude that intracerebral GDNF administration exerts both protective and reparative effects on the nigrostriatal dopamine system, which may have implications for the development of new treatment strategies for Parkinson's disease.
胶质细胞源性神经营养因子(GDNF)是转化生长因子-β超家族中最近克隆出的新成员,它能促进培养的胎儿中脑多巴胺能神经元的存活,并在发育中的纹状体中表达。然而,尚无关于GDNF原位效应的报道。我们使用了能在人类中产生帕金森症状的多巴胺能神经毒素1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP),来确定GDNF是否可能在成年C57/B1小鼠黑质纹状体多巴胺系统中发挥体内保护或再生作用。在MPTP注射前,将GDNF注射到黑质或纹状体内,可有效保护多巴胺系统,这可从中脑多巴胺神经细胞体数量、多巴胺神经终末密度和多巴胺水平得到证明。当在MPTP注射后给予GDNF时,多巴胺水平和纤维密度会显著恢复。在这两种情况下,运动行为均高于正常水平。我们得出结论,脑内给予GDNF对黑质纹状体多巴胺系统具有保护和修复作用,这可能对帕金森病新治疗策略的开发具有重要意义。