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Neurotransmitters in cerebrospinal fluid reflect pathological activity
- Source :
- European Journal of Clinical Investigation. 27:1038-1043
- Publication Year :
- 1997
- Publisher :
- Wiley, 1997.
-
Abstract
- The excitatory transmitters glutamate and aspartate become toxic whenever their extracellular levels are increased because of neuronal, glial and endothelial impairment. Taurine, a volume-regulating amino acid, is released upon excitotoxin-induced cell swelling. Our aim was to investigate if glutamate and aspartate in cerebrospinal fluid (CSF) reveal neuropathology in neurological patients, and if taurine unmasks glutamate-mediated toxicity. Glutamate and aspartate are doubled in viral meningitis, acute multiple sclerosis (MS) and myelopathy compared with control subjects and patients with peripheral facial nerve palsy. These levels do not coincide with a disturbed blood-brain barrier, as estimated by the albumin ratio, are independent of their precursors (glutamine, asparagine) and are not associated with cell lysis. Taurine is significantly increased in meningitis, acute MS, and myelopathy, suggesting glutamate-mediated toxicity. Analysis of transmitters in lumbar CSF can be used to identify patients with cerebral and spinal pathology who might benefit from specific receptor-modulating agents.
- Subjects :
- Adult
Male
medicine.medical_specialty
Taurine
Pathology
Glutamine
Clinical Biochemistry
Glycine
Glutamic Acid
Blood–brain barrier
Biochemistry
Myelopathy
chemistry.chemical_compound
Cerebrospinal fluid
Central Nervous System Diseases
Internal medicine
Serine
medicine
Viral meningitis
Humans
Aged
Aspartic Acid
Neurotransmitter Agents
L-Lactate Dehydrogenase
business.industry
Multiple sclerosis
Glutamate receptor
General Medicine
Middle Aged
medicine.disease
medicine.anatomical_structure
Endocrinology
chemistry
Blood-Brain Barrier
Female
Asparagine
business
Subjects
Details
- ISSN :
- 13652362 and 00142972
- Volume :
- 27
- Database :
- OpenAIRE
- Journal :
- European Journal of Clinical Investigation
- Accession number :
- edsair.doi.dedup.....2da4d8f703555d2f9e362a2612ebcde4