Journal of Neuroscience · 1997 · 130 citations · 21 references
MedicineNeurobiologyNeuroscienceMolecular NeurobiologyMolecular NeuroscienceNeuropharmacologyDopaminergic PharmacologyNeurodegenerative DiseasesNeurodegenerative DisordersNeuromodulationNeuroprotectionNeuroprotective PharmacologyBrain ToxicityDopaminergic NeuroprotectionN-methyl-d-aspartate Receptor-mediated ExcitotoxicityNeuroprotective AgentsNeuroprotective MechanismsNeuroprotective SignalingParkinsonian NeuroprotectionPretreatment
Glial cell line-derived neurotrophic factor (GDNF) injected intranigrally protects midbrain dopamine neurons against 6-hydroxydopamine (6-OHDA) toxicity. The timing between GDNF administration and exposure to 6-OHDA is critical in achieving optimal protection. When injected 6 hr before an intranigral injection of 6-OHDA, GDNF provides complete protection as measured by the number of surviving neurons in the substantia nigra of adult rats. The surviving neuronal population decreases by approximately 50% with 12 and 24 hr separating GDNF and 6-OHDA administrations. In controls with 6-OHDA lesions, there is <10% survival of nigral dopamine neurons. No significant increase in survival is seen with either concurrent injections of GDNF and 6-OHDA or 1 hr GDNF pretreatment. Based on HPLC measurements, striatal and midbrain dopamine levels are at least twofold higher on the lesioned side in animals receiving GDNF 6 hr before a 6-OHDA lesion compared with vehicle recipients. Protein synthesis is necessary for GDNF-induced neuroprotective effects because cycloheximide pretreatment that inhibits protein synthesis also blocks neuroprotection.
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Protection and repair of the nigrostriatal dopaminergic system by GDNF in vivo
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Don M. Gash, Zhiming Zhang, Aliza Ovadia et al. · Nature · 1996 · 964 citations
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Gerald Cohen, Richard E. Heikkila, With the technical assistance of Dana MacNamee · Journal of Biological Chemistry · 1974 · 896 citations · Full text