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Antioxidant Effect of O 3 The first O 3 antioxidant effects were explored by the studies of Boccis group showing that, by using doses below the threshold of the O 2 -O 3 therapeutic window, i.e., below the concentration of 80 g/ml, whole blood was protected from hemolysis and its reactivity was controlled for about 20%40% by the antioxidant system of the plasma, avoiding the toxic effects observed at higher concentrations, such as those detected in erythrocytes (lipid peroxidation, methemoglobin levels, hemolysis
Poly (I:C) MIA offspring exhibit behaviors similar to the core symptoms of autismdeficits in social interaction and communication (USVs) and increased repetitive/stereotyped motor behaviors [32]
This yields a more bioavailable and effective formula
Systemic inhibition of the SSP may induce potential toxicities and narrow the therapeutic window
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