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Alterations in Antioxidant Status and Erythrocyte Properties in Children with Autism Spectrum Disorder
Tomas Jasenovec1, Dominika Radosinska2, Katarina Jansakova1
1Institute of Physiology, Faculty of Medicine, Comenius University in Bratislava, Sasinkova 2, 811 08 Bratislava, Slovakia.
Insights
Children with autism spectrum disorder (ASD) show increased oxidative damage in erythrocytes, impacting oxygen transport. These erythrocyte abnormalities may contribute to ASD
Area of Science:
- Biochemistry
- Hematology
- Neuroscience
Background:
- Erythrocytes are vital for oxygen transport, especially to nerve tissues.
- Oxidative stress negatively impacts erythrocyte quality and function.
- Autism Spectrum Disorder (ASD) is a neurodevelopmental condition with potential links to oxidative stress.
Purpose of the Study:
- To compare oxidative stress markers and erythrocyte properties between children with ASD and neurotypical controls.
- To investigate the relationship between oxidative status and erythrocyte alterations in ASD.
Main Methods:
- Measurement of oxidative stress markers in plasma and erythrocytes.
- Assessment of erythrocyte deformability, osmotic resistance, Na,K-ATPase activity, nitric oxide, and free radical levels.
- Comparison between children with ASD and control groups.
Main Results:
- Erythrocytes from children with ASD exhibited greater oxidative damage to proteins and lipids than plasma.
- Antioxidant enzyme activity was higher in plasma than in erythrocytes of ASD children.
- Erythrocytes in ASD individuals showed significantly higher nitric oxide levels and Na,K-ATPase activity, with increased echinocyte formation and reduced deformability compared to controls.
Conclusions:
- Oxidative stress and altered erythrocyte properties are significantly associated with ASD.
- These erythrocyte abnormalities may play a role in the pathomechanisms and clinical manifestations of ASD.
- Further research into erythrocyte function could offer insights into ASD.
Abstract:
Erythrocytes are responsible for the transport of oxygen within the organism, which is particularly important for nerve tissues. Erythrocyte quality has been shown to be deteriorated in oxidative stress conditions. In this study, we measured the same series of oxidative stress markers in plasma and erythrocytes to compare the differences between neurotypical children (controls) and children with autism spectrum disorder (ASD). We also focused on erythrocyte properties including their deformability, osmotic resistance, Na,K-ATPase activity, nitric oxide levels and free radical levels in children with ASD and controls. Greater oxidative damage to proteins and lipids was observed in the erythrocytes than in the plasma of ASD subjects. Additionally, antioxidant enzymes were more active in plasma samples from ASD children than in their erythrocytes. Significantly higher nitric oxide level and Na,K-ATPase enzyme activity were detected in erythrocytes of ASD individuals in comparison with the controls. Changes in oxidative status could at least partially contribute to the deterioration of erythrocyte morphology, as more frequent echinocyte formation was detected in ASD individuals. These alterations are most probably responsible for worsening the erythrocyte deformability observed in children with ASD. We can conclude that abnormalities in antioxidant status and erythrocyte properties could be involved in the pathomechanisms of ASD and eventually contribute to its clinical manifestations.
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