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Autism Studies and Related Medical Conditions, January 2009 - TACA

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tissue. Mean cerebellar 3-NT was elevated in autism by 68.9% <strong>and</strong> the increase<br />

was statistically significant (p=0.045). Cerebellar Hg, measured by atomic<br />

absorption spectrometry ranged from 0.9 to 35 pmol g¯1 tissue in controls<br />

(n=10) <strong>and</strong> from 3.2 to 80.7 pmol g¯1 tissue in autistic cases (n=9); the 68.2%<br />

increase in cerebellar Hg was not statistically significant. However, there was a<br />

positive correlation between cerebellar 3-NT <strong>and</strong> Hg levels (r=0.7961,<br />

p=0.0001). A small decrease in cerebellar Se levels in autism, measured by<br />

atomic absorption spectroscopy, was not statistically significant but was<br />

accompanied by a 42.9% reduction in the molar ratio of Se to Hg in the autistic<br />

cerebellum. While preliminary, the results of the present study add elevated<br />

oxidative stress markers in brain to the growing body of data reflecting greater<br />

oxidative stress in autism.<br />

Sierra, C., M. A. Vilaseca, et al. (2001). "Oxidative stress in Rett syndrome." Brain Dev<br />

23 Suppl 1: S236-9.<br />

The investigation of parameters that might influence the neurological evolution<br />

of Rett syndrome might also yield new information about its pathogenic<br />

mechanisms. Oxidative stress caused by oxygen free radicals is involved in the<br />

neuropathology of several neurodegenerative disorders, as well as in stroke <strong>and</strong><br />

seizures. To evaluate the free radical metabolism in Rett syndrome, we<br />

measured red blood cell antioxidant enzyme activities (superoxide dismutase,<br />

glutathione peroxidase, glutathione reductase <strong>and</strong> catalase) <strong>and</strong> plasma<br />

malondialdehyde, as lipid peroxidation marker in a group of patients with Rett<br />

syndrome. No significant differences were observed in erythrocyte glutathione<br />

peroxidase, glutathione reductase <strong>and</strong> catalase activities, between the Rett<br />

syndrome patients <strong>and</strong> the control group. Erythrocyte superoxide dismutase<br />

activities were significantly decreased in Rett syndrome patients (P

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