Proceedings of the National Academy of Sciences · 1997 · 327 citations · 25 references
MedicineNeurobiologyNeuroscienceCellular NeuroscienceMolecular NeuroscienceNeuropharmacologyNerve RegenerationNervous TissueNeural RegenerationNeuroprotectionNeurotransmissionNeurotrophic FactorsDopaminergic NeuronsImmunosuppressive CompoundsImmunosuppressive FunctionNeurite Outgrowth InhibitionNeurodegenerative ToxicityNigrostriatal Dopamine PathwayNigrostriatal Dopamine SystemSomatosensory Cortex Physiology
Although immunosuppressant immunophilin ligands promote neurite outgrowth in vitro, their neurotrophic activities are clearly independent of their immunosuppressive activity. In the present report, a novel nonimmunosuppressive immunophilin ligand, GPI-1046 (3-(3-pyridyl)-1-propyl (2S)-1-(3,3-dimethyl-1,2-dioxopentyl)-2-pyrrolidinecarboxylate+ ++) is described. In vitro, GPI-1046 bound to FK506 binding protein-12 and elicited neurite outgrowth from sensory neuronal cultures with picomolar potency with maximal effects comparable to nerve growth factor. In vivo, GPI-1046 stimulated the regeneration of lesioned sciatic nerve axons and myelin levels. In the central nervous system, GPI-1046 promoted protection and/or sprouting of serotonin-containing nerve fibers in somatosensory cortex following parachloroamphetamine treatment. GPI-1046 also induced regenerative sprouting from spared nigrostriatal dopaminergic neurons following 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine toxicity in mice or 6-hydroxydopamine (6-OHDA) toxicity in rats. The rotational abnormality in 6-OHDA treated rats was alleviated by GPI-1046. These neurotrophic actions in multiple models suggest therapeutic utility for GPI-1046 in neurodegenerative diseases.
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