Protective effect of melatonin on antioxidative system in experimental ischemia-reperfusion of rat small intestine

• Published in: Cellular physiology and biochemistry Vol. 10; no. 4; p. 229
• Main Authors: Ustundag, B, Kazez, A, Demirbag, M, Canatan, H, Halifeoglu, I, Ozercan, I H
• Format: Journal Article
• Language: English
• Published: Germany 01.01.2000
• Subjects: Animals; Antioxidants - metabolism; Antioxidants - pharmacology; Antioxidants - therapeutic use; Copper - blood; Erythrocytes - drug effects; Erythrocytes - enzymology; Erythrocytes - metabolism; Glutathione Peroxidase - metabolism; Histocytochemistry; Intestine, Small - drug effects; Intestine, Small - enzymology; Intestine, Small - metabolism; Intestine, Small - pathology; Melatonin - metabolism; Melatonin - pharmacology; Melatonin - therapeutic use; Rats; Reperfusion Injury - drug therapy; Reperfusion Injury - enzymology; Reperfusion Injury - metabolism; Reperfusion Injury - pathology; Selenium - analysis; Selenium - metabolism; Superoxide Dismutase - metabolism; Zinc - blood
• ISSN: 1015-8987
• DOI: 10.1159/000016354

Effect of exogenously administered melatonin (N-acetyl 5-methoxytryptamine) on antioxidant systems in experimental Ischemia-Reperfusion (I-R) of rat gastrointestinal system (GIS) was examined. A total of 40 rats were divided into 4 groups: Group 1 (Sham), Group 2 (I-R), Group 3 (I-R + 10 mg/kg melatonin) and Group 4 (I-R + 20 mg/kg melatonin). Activity levels of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) were determined in small intestines. There was a significant (p<0.05) reduction in GSH-Px levels in Group 2 (64.16+/-7.02 U/mg protein) compared to Group 1 (80.15+/-9.32 U/mg protein). We observed a meaningful increase in GSH-Px levels in melatonin applied groups (Group 3: 75.94+/-9.83 U/mg protein, Group 4: 78.55+/-9.11 U/mg protein) compared to Group 2. Correspondingly, SOD activity levels were significantly reduced (p<0.001) in Group 2 (24.14+/-4.35 U/mg protein) compared to controls (52.91+/-6.13 U/mg protein). A stronger effect (p<0.001) of melatonin was observed on SOD levels compared to GSH-Px levels in both doses (Group 3: 38.96+/-6.39 U/mg protein, Group 4: 43.07+/-7.76 U/mg protein). Levels of selenium were reduced significantly in Group 2 (1.11+/-0.31 microg/g tissue) compared to Group 1 (2.01+/-0.19 microg/g tissue). Melatonin application in Group 3 (1.13+/-0.28 microg/g tissue) and Group 4 (1.89+/-0.48 microg/g tissue) caused an increase in selenium levels. There was a strong correlation between increases in selenium and GSH-Px levels in Group 4 (r:0.651 p<0.01). Melatonin seems to exert its antioxidant effect in GIS tract by stimulating SOD and GSH-Px. Selenium also seems to have an antioxidant contribution on protecting rat gastrointestinal tract I-R injury.