Disruption of redox homeostasis in cerebral cortex of developing rats by acylcarnitines accumulating in medium-chain acyl-CoA dehydrogenase deficiency

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• 作者：Anelise M. Tonin^a ; Mateus Grings^a ; Lisiane A. Knebel^a ; Â ; ngela Zanatta^a ; Alana P. Moura^a ; Cé ; sar A.J. Ribeiro^a ; Guilhian Leipnitz^a ; Moacir Wajner^a ; ^b ; ^{mwajner@ufrgs.br}
• 关键词：HA ; hexanoic acid ; HC ; hexanoylcarnitine ; HG ; hexanoylglycine ; OC ; octanoylcarnitine ; DC ; decanoylcarnitine ; cDC ; cis-4-decenoylcarnitine ; MCAC ; medium-chain acylcarnitines
• 刊名：International Journal of Developmental Neuroscience
• 出版年：2012
• 出版时间：August, 2012
• 年：2012
• 卷：30
• 期：5
• 页码：383-390
• 全文大小：985 K

文摘

Medium-chain fatty acids and acylcarnitines accumulate in medium-chain acyl-CoA dehydrogenase deficiency (MCADD), the most frequent fatty acid oxidation defect clinically characterized by episodic crises with vomiting, seizures and coma. Considering that the pathophysiology of the neurological symptoms observed in MCADD is poorly known and, to our knowledge, there is no report on the involvement of acylcarnitines in the brain damage presented by the affected patients, the objective of the present study was to investigate the in vitro effects of hexanoylcarnitine (HC), octanoylcarnitine, decanoylcarnitine (DC) and cis-4-decenoylcarnitine (cDC) at concentrations varying from 0.01 to 1.0 mM on important oxidative stress parameters in cerebral cortex of young rats. HC, DC and cDC significantly induced lipid peroxidation, as determined by increased thiobarbituric acid-reactive substances (TBA-RS) values. In addition, carbonyl formation was significantly augmented and sulfhydryl content diminished by DC, reflecting induction of protein oxidative damage. HC, DC and cDC also decreased glutathione (GSH) levels, the most important brain antioxidant defense. Furthermore, DC-induced elevation of TBA-RS values and decrease of GSH levels were prevented by the free radical scavengers melatonin and ¦Á-tocopherol, indicating the involvement of reactive oxygen species in these effects. We also found that l-carnitine itself did not induce lipid and protein oxidative damage, neither reduced the antioxidant defenses. Our present data show that the major medium-chain acylcarnitines accumulating in MCADD elicit oxidative stress in rat brain. It is therefore presumed that these compounds may be involved to a certain extent in the pathogenesis of the neurologic dysfunction of MCADD.