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Brain neurotransmitters in glycine encephalopathy.
Kish, S J; Dixon, L M; Burnham, W M; Perry, T L; Becker, L; Cheng, J; Chang, L J; Rebbetoy, M.
Affiliation
  • Kish SJ; Clarke Institute of Psychiatry, Human Brain Laboratory, Toronto, Ontario, Canada.
Ann Neurol ; 24(3): 458-61, 1988 Sep.
Article de En | MEDLINE | ID: mdl-2906530
ABSTRACT
We measured neurotransmitter markers in autopsied brain of infants with glycine encephalopathy (GE). Because patients with GE develop intractable seizures, special attention was devoted to those neurotransmitter systems implicated in human epilepsy. Mean levels of glycine in the frontal cortex of GE patients were three times higher than control values. No abnormalities were observed for concentrations of gamma-aminobutyric acid (and related receptors), other major neurotransmitter amino compounds, or activities of cholineacetyltransferase and aspartate aminotransferase. Mean acetylcholinesterase activity was significantly elevated by 46%. As experimental data suggest, glycine markedly potentiates the action of the excitatory neurotransmitter glutamic acid. To the extent that the brain seizures in patients with GE can be explained by this mechanism, pharmacotherapy with excitatory amino acid antagonists may represent a new approach to the treatment of GE.
Sujet(s)
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Sujet principal: Encéphalopathies métaboliques / Cortex cérébral / Agents neuromédiateurs / Aminoacidopathies congénitales / Acides aminés / Glycine Limites: Humans / Infant Langue: En Journal: Ann Neurol Année: 1988 Type de document: Article Pays d'affiliation: Canada
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Sujet principal: Encéphalopathies métaboliques / Cortex cérébral / Agents neuromédiateurs / Aminoacidopathies congénitales / Acides aminés / Glycine Limites: Humans / Infant Langue: En Journal: Ann Neurol Année: 1988 Type de document: Article Pays d'affiliation: Canada