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Inflammatory bowel disease (IBD) can be considered multifactorial in genetic background and with regard to neuro-endocrine regulation of immune reactivity to antigens of alimentary and bacterial origin (1). The roles of free radicals and the antioxidant defense mechanisms of the intestine are also well documented (2)(3). Aminosalicylates such as 5-aminosalicylic acid (5-ASA), when used in therapy, exhibit superoxide and hydroxyl-radical scavenger properties (4). This medication can partially restore the depleted mucosal antioxidant protective function that develops in IBD. We used a simple luminol-dependent chemiluminescence method to study the antioxidant protective mechanisms in patients with IBD. Luminol-dependent chemiluminescence, as an indicator of a free radicals, is suitable for detection of the antioxidant status of tissue. The H2O2/·OH-microperoxidase-luminol system can be used to measure the total scavenger capacity (TSC) of the plasma and erythrocytes. We also determined the H+-donor activity and reducing power in the plasma. 1,1-Diphenyl-2-picryl-hydrazyl, stable radical; 5,5′-dithiobis-2-nitrobenzoic acid; luminol; and microperoxidase were obtained from Sigma. All other reagents were purchased from Reanal.
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Blázovics et al. (1999) studied this question.
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