Cerebrospinal Fluid -Aminobutyric Acid Variations in Neurological Disorders
- 1 November 1977
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 34 (11) , 683-685
- https://doi.org/10.1001/archneur.1977.00500230053008
Abstract
• Neuropathologically, Huntington's disease is characterized by a profound reduction in neuronal cells originating in the corpus striatum and globus pallidus. Since one of these cell types utilizes γ-aminobutyric acid (GABA) as a neurotransmitter, it may be possible to differentially diagnose this disorder on the basis of the CSF content of this amino acid. In order to determine the validity of this hypothesis, cerebrospinal fluid GABA was analyzed, using a recently developed radioreceptor assay procedure and was found to be significantly reduced in patients diagnosed as having Huntington's disease and also lower in patients with Alzheimer's disease, though no difference was noted between Parkinson patients and control subjects. The results suggest that analysis of cerebrospinal fluid GABA may have diagnostic, and perhaps predictive, value in certain neurological disorders.This publication has 5 references indexed in Scilit:
- γ‐Aminobutyric acid (GABA) in human cerebrospinal fluid: radioreceptor assayJournal of Neurochemistry, 1977
- Neurobiology and pharmacology of Huntington's diseaseLife Sciences, 1977
- Is GABA detectable in human CSF?Journal of Neurochemistry, 1976
- A simple. sensitive and specific radioreceptor assay for endogenous GABA in brain tissueJournal of Neurochemistry, 1976
- Measurement of GABA in human cerebrospinal fluidBiochemical Medicine, 1975