Cerebrospinal fluid hypoxanthine, xanthine and uric acid levels may reflect glutamate-mediated excitotoxicity in different neurological diseases

• Published in: Neuroscience letters Vol. 238; no. 1; pp. 25 - 28
• Main Authors: Stover, John F, Lowitzsch, Klaus, Kempski, Oliver S
• Format: Journal Article
• Language: English
• Published: Shannon Elsevier Ireland Ltd 28.11.1997; Elsevier
• Subjects: Adenosine triphosphate; Adult; Albumins - cerebrospinal fluid; Biological and medical sciences; Central Nervous System Diseases - metabolism; Cerebrospinal fluid; Cerebrovascular Disorders - metabolism; Chromatography, High Pressure Liquid; Epilepsy - metabolism; Female; Glutamate; Glutamic Acid - cerebrospinal fluid; Humans; Hypoxanthine; Hypoxanthine - cerebrospinal fluid; L-Lactate Dehydrogenase - cerebrospinal fluid; Lactate; Lactic Acid - cerebrospinal fluid; Male; Medical sciences; Meningitis, Viral - metabolism; Middle Aged; Multiple Sclerosis - metabolism; Nervous system involvement in other diseases. Miscellaneous; Neurology; Oxygen free radicals; Serum Albumin - analysis; Spinal Cord Diseases - metabolism; Uric acid; Uric Acid - cerebrospinal fluid; Xanthine; Xanthine - cerebrospinal fluid; Lactate; Oxygen free radicals; Hypoxanthine; Xanthine; Uric acid; Cerebrospinal fluid; Glutamate; Adenosine triphosphate; Human; Nervous system diseases; Oxygen; Toxicity; Excitatory aminoacid; Neurotransmitter; Free radical
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/S0304-3940(97)00840-9

Glutamate-mediated excitotoxicity is associated with adenosine triphosphate (ATP) degradation and generation of oxygen radicals. Hypoxanthine and lactate depict energetic impairment, while xanthine and uric acid reflect activity of radical producing xanthine oxidase. Cerebrospinal fluid (CSF) glutamate, hypoxanthine, lactate, xanthine, and uric acid were investigated in neurological patients. In multiple sclerosis, myelopathy, stroke, epilepsy and viral meningitis glutamate, hypoxanthine, xanthine, and uric acid are increased 2–3-fold compared to controls. Lactate is only elevated in meningitis. Normal lactate dehydrogenase (LDH) levels and absent correlation between the albumin ratio and neurochemical parameters exclude an artificial increase due to cell lysis and barrier damage. Absent correlation between neurochemical parameters within each patient group is most likely related to preserved glial and neuronal uptake mechanisms. CSF hypoxanthine, xanthine, and uric acid levels appear superior to lactate in reflecting glutamate-mediated excitotoxicity in neurological patients.