Salicylate as an in vivo free radical trap: Studies on ischemic insult to the rat intestine

Ischemia of rat intestine was induced in vivo by occlusion of the superior mesenteric artery (SMA) for 15 min. Sodium salicylate, 100 mg/kg, given IP, 30 min prior to the ischemic event served as a specific trap for hydroxyl radicals. Portions of the bowel were sequentially isolatd and removed - 2 min prior to ischemia, 2 min prior to declamping of the SMA, and 10 min following reperfusion. The bowel segments were homogenized in 3% TCA. The homogenate was centrifuged and filtrated through a 0.22 μ filter. The hydroxylation products of salicylate, dihydroxybenzoic acid (DHBA) derivatives, were isolated, identified, and quantified by HPLC coupled with electrochemical detection (ECD). The level of 2,5-DHBA (M ± SE, ng/g tissue) in the preischemic bowel (N = 21) was 241.8 ± 10.0. In the ischemic specimen the level of 2.5-DHBA increased significantly to 313.3 ± 15.5 (p = 0.0129), and remained unchanged in the reperfusion period (322.8 ± 15.5). The histological examination correlated well with these levels; mild villi damage in the ischemic period with no further exacerbation during the reperfusion period. This study in an in vivo animal model of intestinal ischemia-reperfusion provides direct evidence for the involvement of free radicals during the ischemic result.