Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Más filtros

Bases de datos
Tipo del documento
Intervalo de año de publicación
1.
Brain Res ; 492(1-2): 385-8, 1989 Jul 17.
Artículo en Inglés | MEDLINE | ID: mdl-2568879

RESUMEN

We examined the ability of the neurotoxin, L-beta-methylaminoalanine (L-BMAA), to inhibit [3H]glutamate binding to rat brain synaptic junctions. In a tris(hydroxymethyl)aminomethane acetate buffer, L-BMAA did not affect [3H]glutamate binding (IC50 greater than 10 mM). However, in the presence of ammonium bicarbonate (20 mM) L-BMAA blocked [3H]glutamate binding with an IC50 of 1 mM. This inhibition was not caused by ammonium ion since other ammonium salts were inactive. Furthermore, identical inhibition was obtained in the presence of potassium bicarbonate. Bicarbonate ion did not alter the ability of N-methyl-D-aspartic acid to block glutamate binding. These results indicate that bicarbonate ion is required for the interaction of L-BMAA with the glutamate receptor and may account for the observation that beta-methylaminoalanine is neurotoxic in vitro only in the presence of bicarbonate.


Asunto(s)
Aminoácidos Diaminos/farmacología , Bicarbonatos/farmacología , Lóbulo Frontal/metabolismo , Glutamatos/metabolismo , Neurotoxinas/farmacología , Receptores de Neurotransmisores/metabolismo , Animales , Toxinas de Cianobacterias , Lóbulo Frontal/efectos de los fármacos , Ácido Glutámico , Técnicas In Vitro , Ratas , Receptores de Glutamato , Receptores de Neurotransmisores/efectos de los fármacos
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA