Literature DB >> 19683047

Evidence that the major metabolites accumulating in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome induce oxidative stress in brain of young rats.

Alexandre Umpierrez Amaral1, Guilhian Leipnitz, Carolina Gonçalves Fernandes, Bianca Seminotti, Angela Zanatta, Carolina Maso Viegas, Carlos Severo Dutra-Filho, Moacir Wajner.   

Abstract

Ornithine and homocitrulline are the major metabolites accumulating in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome, a genetic disorder characterized by neurological regression whose pathogenesis is still not understood. The present work investigated the in vitro effects of ornithine and homocitrulline on important parameters of oxidative stress in cerebral cortex from young rats. Ornithine significantly increased chemiluminescence and thiobarbituric acid-reactive substances levels, indicators of lipid peroxidation, while homocitrulline only augmented chemiluminescence values. Furthermore, ornithine-induced increase of thiobarbituric acid-reactive substances levels was attenuated (melatonin and reduced glutathione) or totally prevented (alpha-tocopherol) by free radical scavengers, suggesting that reactive species were involved in the lipid oxidative damage. We also observed that ornithine and homocitrulline significantly decreased the tissue antioxidant defenses, determined by reduced glutathione concentrations, the major non-enzymatic antioxidant defense found in the brain. Homocitrulline reduction of glutathione levels was completely prevented by melatonin and alpha-tocopherol, whereas ornithine-induced decrease of glutathione levels was only attenuated by these free radical scavengers. Ornithine and homocitrulline also induced protein oxidative damage, increasing carbonyl formation and sulfhydryl oxidation. In contrast, these amino acids did not affect nitric oxide production, indicating that nitrogen reactive species were not implicated in the lipid and oxidative damage provoked by ornithine and homocitrulline. Therefore, it is presumed that the major metabolites accumulating in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome elicit oxidative stress and that this pathomechanism may possibly be involved in the brain damage found in patients affected by this disorder.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19683047     DOI: 10.1016/j.ijdevneu.2009.08.004

Source DB:  PubMed          Journal:  Int J Dev Neurosci        ISSN: 0736-5748            Impact factor:   2.457


  4 in total

1.  Ornithine and Homocitrulline Impair Mitochondrial Function, Decrease Antioxidant Defenses and Induce Cell Death in Menadione-Stressed Rat Cortical Astrocytes: Potential Mechanisms of Neurological Dysfunction in HHH Syndrome.

Authors:  Ângela Zanatta; Marília Danyelle Nunes Rodrigues; Alexandre Umpierrez Amaral; Débora Guerini Souza; André Quincozes-Santos; Moacir Wajner
Journal:  Neurochem Res       Date:  2016-05-09       Impact factor: 3.996

2.  Chronic postnatal ornithine administration to rats provokes learning deficit in the open field task.

Authors:  Carolina Maso Viegas; Estela Natacha Brandt Busanello; Anelise Miotti Tonin; Mateus Grings; Alana Pimentel Moura; Luciana Ritter; Angela Zanatta; Lisiane Aurélio Knebel; Vannessa Araujo Lobato; Letícia Ferreira Pettenuzzo; Carmen Regla Vargas; Guilhian Leipnitz; Moacir Wajner
Journal:  Metab Brain Dis       Date:  2012-06-16       Impact factor: 3.584

3.  Ornithine In Vivo Administration Disrupts Redox Homeostasis and Decreases Synaptic Na(+), K (+)-ATPase Activity in Cerebellum of Adolescent Rats: Implications for the Pathogenesis of Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) Syndrome.

Authors:  Ângela Zanatta; Carolina Maso Viegas; Fernanda Hermes Hickmann; Wagner de Oliveira Monteiro; Angela Sitta; Daniela de Moura Coelho; Carmen Regla Vargas; Guilhian Leipnitz; Moacir Wajner
Journal:  Cell Mol Neurobiol       Date:  2015-03-13       Impact factor: 5.046

4.  Impairment of brain redox homeostasis caused by the major metabolites accumulating in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in vivo.

Authors:  Carolina Maso Viegas; Anelise Miotti Tonin; Angela Zanatta; Bianca Seminotti; Estela Natacha Brandt Busanello; Carolina Gonçalves Fernandes; Alana Pimentel Moura; Guilhian Leipnitz; Moacir Wajner
Journal:  Metab Brain Dis       Date:  2012-07-15       Impact factor: 3.584

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.