Article date: 1990/11/1
PubMed ID: 2237972
Journal name: Stroke (ISSN: 0039-2499)
Recent morphologic and behavioral studies of the effects of gamma-aminobutyric acid agents on transsynaptic degeneration after cortical and striatal damage are reviewed and discussed. Following unilateral lesions of the anteromedial cortex, mild atrophy appears in the ipsilateral striatum and substantia nigra pars reticulata. Long-term diazepam administration greatly enhances this degeneration, extends the degeneration into the thalamus, and severely disrupts recovery from somatosensory asymmetries. Following unilateral excitotoxic lesions of the striatum, progressive degeneration of neurons occurs in the substantia nigra pars reticulata and efferent targets in the thalamus. This degeneration can be prevented by chronic infusion of muscimol, a gamma-aminobutyric acid agonist. Unexpectedly, this treatment did not facilitate recovery from somatosensory asymmetries. Recovery in muscimol-treated animals was impaired relative to saline-treated controls. Thus, gamma-aminobutyric acid agonists either may enhance or prevent neural atrophy secondary to brain damage, but the behavioral outcome appears to depend importantly on the excitatory and inhibitory characteristics of the affected networks.
Author List: Schallert T, Jones T A, Lindner M D
Publication Types: Journal Article; Research Support, U.S. Gov't, P.H.S.; Review
Substances mentioned in the article: Muscimol; gamma-Aminobutyric Acid; Diazepam;
Mesh terms: Animals; Atrophy; Behavior, Animal/drug effects; Cerebrovascular Disorders/drug therapy; Corpus Striatum/metabolism; Diazepam/pharmacology; Muscimol/pharmacology; Neural Pathways; Neurons/drug effects; Rats; Substantia Nigra/drug effects; Thalamus/drug effects; gamma-Aminobutyric Acid/metabolism;