Key result
Administration of N-acetylcysteine significantly decreased histopathological lung injury induced by skeletal muscle ischemia-reperfusion in rats compared to control (P=0.005).
Why the study?
Does N-acetylcysteine prevent lung injury induced by skeletal muscle ischemia-reperfusion in a rat model?
RCT (n=20)
randomly divided
Does N-acetylcysteine prevent lung injury induced by skeletal muscle ischemia-reperfusion in a rat model?
p-value: p=0.005
N-acetylcysteine administration before reperfusion significantly attenuates remote lung injury following skeletal muscle ischemia-reperfusion in a rat model.
Should not change clinical practice; hypothesis-generating for antioxidant protection in remote organ injury.
PURPOSE: To investigate whether N-acetylcysteine, a free radicals scavenger has a protective effect against lung injury as a remote organ after skeletal muscle ischemia-reperfusion. METHODS: Twenty Wistar male rats were divided randomly into two experimental groups: group ischemia-reperfusion (group I) and group ischemia-reperfusion +N-acetylcysteine (group II). All animals were undergone two hours of ischemia by occlusion femoral artery and 24h of reperfusion. Before clamped the femoral artery, 250 IU heparin was administered via the jugular vein to prevent clotting. Rats that were treated with N-acetylcysteine given IV at a dose of 150 mgkg(-1), immediately before reperfusion. After 24h of reperfusion, animals were euthanized and left lung harvested for histopathological analysis under light microscopy. RESULTS: In the group I, tissues showed histological changes with intra-alveolar edema, intra-alveolar hemorrhage and neutrophilic infiltration. Histopathologically, there was a significant difference (P = 0.005) between two groups. CONCLUSION: Administration of N-acetylcysteine treatment significantly decreased lung injury induced by skeletal muscle ischemia reperfusion according to histological findings.
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Sotoudeh et al. (2012) conducted an RCT in lung injury induced by skeletal muscle ischemia-reperfusion (n=20). N-acetylcysteine vs. ischemia-reperfusion alone was evaluated on histopathological changes in lung tissue (p=0.005). Administration of N-acetylcysteine significantly decreased histopathological lung injury induced by skeletal muscle ischemia-reperfusion in rats compared to control (P=0.005).
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