7692009

pubmed:Citation

10

An impairment of energy metabolism may underlie slow excitotoxic neuronal death in neurodegenerative diseases. We therefore examined the effects of intrastriatal, subacute systemic, or chronic systemic administration of the mitochondrial toxin 3-nitropropionic acid (3-NP) in rats. Following intrastriatal injection 3-NP produced dose-dependent striatal lesions. Neurochemical and histologic evaluation showed that markers of both spiny projection neurons (GABA, substance P, calbindin) and aspiny interneurons (somatostatin, neuropeptide Y, NADPH-diaphorase) were equally affected. Subacute systemic administration of 3-NP produced age-dependent bilateral striatal lesions with a similar neurochemical profile. However, in contrast to the intrastriatal injections, striatal dopaminergic afferent projections were spared. Both freeze-clamp measurements and chemical shift magnetic resonance spectroscopy showed that 3-NP impairs energy metabolism in the striatum in vivo. Microdialysis showed no increase in extracellular glutamate concentrations after systemic administration of 3-NP. The lesions produced by intrastriatal injection or systemic administration of 3-NP were blocked by prior decortication. However, the NMDA antagonist MK-801 did not block the effects of intrastriatal 3-NP, consistent with a non-NMDA excitotoxic mechanism. In contrast to subacute systemic administration of 3-NP, chronic (1 month) administration produced lesions confined to the striatum in which there was relative sparing of NADPH-diaphorase interneurons, consistent with an NMDA excitotoxic process. Chronic administration showed growth-related proliferative changes in dendrites of spiny neurons similar to changes in Huntington's disease (HD). These results are consistent with in vitro studies showing that mild metabolic compromise can selectively activate NMDA receptors while more severe compromise activates both NMDA and non-NMDA receptors. Chronic administration of 3-NP over 1 month produces selective striatal lesions that replicate many of the characteristic histologic and neurochemical features of HD.

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0270-6474

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4181-92

pubmed-meshheading:7692009-3,4-Dihydroxyphenylacetic Acid, pubmed-meshheading:7692009-Animals, pubmed-meshheading:7692009-Calcium-Binding Protein, Vitamin D-Dependent, pubmed-meshheading:7692009-Cell Adhesion Molecules, Neuronal, pubmed-meshheading:7692009-Corpus Striatum, pubmed-meshheading:7692009-Dopamine, pubmed-meshheading:7692009-Energy Metabolism, pubmed-meshheading:7692009-Glial Fibrillary Acidic Protein, pubmed-meshheading:7692009-Homovanillic Acid, pubmed-meshheading:7692009-Interneurons, pubmed-meshheading:7692009-Male, pubmed-meshheading:7692009-Mitochondria, pubmed-meshheading:7692009-NADPH Dehydrogenase, pubmed-meshheading:7692009-Neurons, pubmed-meshheading:7692009-Neuropeptide Y, pubmed-meshheading:7692009-Neurotoxins, pubmed-meshheading:7692009-Nitro Compounds, pubmed-meshheading:7692009-Propionic Acids, pubmed-meshheading:7692009-Rats, pubmed-meshheading:7692009-Rats, Sprague-Dawley, pubmed-meshheading:7692009-Reference Values, pubmed-meshheading:7692009-Somatostatin, pubmed-meshheading:7692009-Substance P, pubmed-meshheading:7692009-gamma-Aminobutyric Acid

Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid.

Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't