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Neurochemical evidence that lysine inhibits synaptic Na+,K+-ATPase activity and provokes oxidative damage in striatum of young rats in vivo.

Abstract
Lysine (Lys) accumulation in tissues and biological fluids is the biochemical hallmark of patients affected by familial hyperlysinemia (FH) and other inherited metabolic disorders. In the present study we investigated the effects of acute administration of Lys on relevant parameters of energy metabolism and oxidative stress in striatum of young rats. We verified that Lys in vivo intrastriatal injection did not change the citric acid cycle function and creatine kinase activity, but, in contrast, significantly inhibited synaptic Na(+),K(+)-ATPase activity in striatum prepared 2 and 12 h after injection. Moreover, Lys induced lipid peroxidation and diminished the concentrations of glutathione 2 h after injection. These effects were prevented by the antioxidant scavengers melatonin and the combination of α-tocopherol and ascorbic acid. Lys also inhibited glutathione peroxidase activity 12 h after injection. Therefore it is assumed that inhibition of synaptic Na(+),K(+)-ATPase and oxidative damage caused by brain Lys accumulation may possibly contribute to the neurological manifestations of FH and other neurometabolic conditions with high concentrations of this amino acid.
AuthorsBianca Seminotti, Carolina Gonçalves Fernandes, Guilhian Leipnitz, Alexandre Umpierrez Amaral, Angela Zanatta, Moacir Wajner
JournalNeurochemical research (Neurochem Res) Vol. 36 Issue 2 Pg. 205-14 (Feb 2011) ISSN: 1573-6903 [Electronic] United States
PMID20976553 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Thiobarbituric Acid Reactive Substances
  • Sodium-Potassium-Exchanging ATPase
  • Lysine
Topics
  • Animals
  • Corpus Striatum (drug effects, metabolism, pathology)
  • Lysine (pharmacology)
  • Oxidation-Reduction
  • Oxidative Stress (drug effects)
  • Rats
  • Rats, Wistar
  • Sodium-Potassium-Exchanging ATPase (antagonists & inhibitors)
  • Synapses (metabolism)
  • Thiobarbituric Acid Reactive Substances (metabolism)

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