Article citationsMore>>
Gaita, L., Manzi, B., Sacco, R., Lintas, C., Altieri, L., Lombardi, F., Pawlowski, T.L., Redman, M., Craig, D.W., Huentelman, M.J., Ober-Reynolds, S., Brautigam, S., Melmed, R., Smith, C.J., Marsillach, J., Camps, J., Curatolo, P. and Persico, A.M. (2010) Decreased Serum Arylesterase Activity in Autism Spectrum Disorders. Psychiatry Research, 180, 105-113.
http://dx.doi.org/10.1016/j.psychres.2010.04.010
has been cited by the following article:
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TITLE:
Nuclear Factor-Kappa B and Other Oxidative Stress Biomarkers in Serum of Autistic Children
AUTHORS:
Omar M. E. Abdel-Salam, Eman R. Youness, Nadia A. Mohammed, Walaa A. Abu Elhamed
KEYWORDS:
Autism Spectrum Disorder, Oxidative Stress, Redox-Sensing Transcription Factor
JOURNAL NAME:
Open Journal of Molecular and Integrative Physiology,
Vol.5 No.1,
February
16,
2015
ABSTRACT: The aim of the present study was to investigate the status of oxidative stress in the serum of children affected with autism spectrum disorder. Twenty autistic children aged 3 to 12 years, were gender and age-matched with 20 typically developing children. Changes in the levels of the redox-sensing transcription factor nuclear factor-kappa B (NF-κB) was measured in serum of autistic children and controls. Other oxidative stress biomarkers such as malondialdehyde, reduced glutathione, total antioxidant capacity, catalase activity, and paraoxonase 1 activity were determined in serum as well. Significant increase was observed in serum NF-κB of autistic children compared to that in controls (by 138.6%). There was also marked increase in malondialdehyde level by 87.3% in autistic patients. Meanwhile, there were significant decreases in reduced glutathione (by 24%), catalase activity (by 40.8%), paraoxonase 1 activity (by 36.6%), and total antioxidant capacity (by 36.5%) compared to the control group. These data clearly demonstrate increased oxidative stress in serum of autistic children and suggest that the NF-κB signaling pathway is activated in autism, possibly due to increased oxidative burden.
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