Artigo Revisado por pares

N-Acetylaspartylglutamate (NAAG) protects against rat striatal quinolinic acid lesions in vivo

1997; Elsevier BV; Volume: 236; Issue: 2 Linguagem: Inglês

10.1016/s0304-3940(97)00769-6

ISSN

1872-7972

Autores

Lianna Orlando, Ruth Luthi‐Carter, David G. Standaert, Joseph T. Coyle, John B. Penney, Anne B. Young,

Tópico(s)

Amino Acid Enzymes and Metabolism

Resumo

We examined the effects of N-acetylaspartylglutamate (NAAG), an endogenous peptide thought to be involved in neurotransmission and neuromodulation, on striatal quinolinate lesions, a rodent model of Huntington's disease. We found that NAAG (500 and 1000 nmol) co-injected with quinolinic acid significantly reduced lesion volumes (by 50% and 65%, respectively). A 1000 nmol dose of the non-hydrolyzable analogue, β-NAAG, also reduced quinolinic acid lesion volumes by 78.4%, indicating that the protection observed was not secondary to cleavage of NAAG into N-acetyl-aspartate (NAA) and glutamate. Likewise, co-injection of both NAA and glutamate (1000 nmol each) with quinolinic acid did not significantly alter the size of lesions. NAAG's protective effect may be mediated through actions on N-methyl-d-aspartate receptors or metabotropic glutamate receptors.

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