Melatonin Attenuates Alcohol-Induced Oxidative Stress and Duodenal Injury in Wistar Rats
DOI:
https://doi.org/10.47743/jemb-2026-265Keywords:
Alcohol-induced injury, Antioxidant enzymes, Duodenum, Melatonin, Oxidative stress.Abstract
Long-term alcohol intake can damage the lining of the small intestine by increasing harmful oxidative processes. Melatonin is a naturally produced substance in the body known for its strong protective and antioxidant properties. This study examined whether melatonin could protect the duodenum against alcohol-induced injury in adult rats. Sixteen female Wistar rats were divided into four groups and treated for twenty-eight days with 1 ml/kg of 50% alcohol, 5 mg/kg of melatonin, both substances together, or neither. Changes in body weight, antioxidant activity, lipid damage, and duodenal tissue structure were assessed. Alcohol exposure reduced weight gain, weakened antioxidant defenses, increased lipid damage, and caused marked injury to the duodenal lining. Treatment with melatonin significantly improved weight gain, restored antioxidant balance, reduced tissue damage, and preserved normal duodenal structure. Melatonin alone produced no harmful effects. These findings suggest that melatonin protects the duodenum against alcohol-induced damage, possibly through attenuation of oxidative stress.
References
Akinci, A., Esrefoglu, M., Cetin, A., & Ates, B. (2015). Melatonin is more effective than ascorbic acid and β-carotene in improvement of gastric mucosal damage induced by intensive stress. Archives of Medical Science, 11(5), 1129-1136. https://doi.org/10.5114/aoms.2015.54870
Akinrinde, A., & Ajibade, T. (2024). Evaluation of the Effects of Alpha-Tocopherol, Quercetin and their Combination on Ethanol-Induced Pancreatic and Duodenal Mucosal injuries: An Experimental Study. International Journal of Biochemistry Research & Review, 33(3), 14-26. https://doi.org/10.9734/ijbcrr/2024/v33i3860
Albano, E. (2006). Alcohol, oxidative stress and free radical damage. Proceedings of the Nutrition society, 65(3), 278-290. https://doi.org/10.1079/PNS2006496
Beck, I. T. (2017). Small bowel injury by ethanol. In Alcohol and the Gastrointestinal Tract (pp. 163-202). CRC Press. https://www.taylorfrancis.com/chapters/edit/10.4324/9781315149844-10/small-bowel-injury-ethanol-ivan-beck
Brzozowska, I., Strzalka, M., Drozdowicz, D., J. Konturek, S., & Brzozowski, T. (2014). Mechanisms of esophageal protection, gastroprotection and ulcer healing by melatonin. Implications for the therapeutic use of melatonin in gastroesophageal reflux disease (GERD) and peptic ulcer disease. Current Pharmaceutical Design, 20(30), 4807-4815. https://doi.org/10.2174/1381612819666131119110258
Buege, J. A., & Aust, S. D. (1978). [30] Microsomal lipid peroxidation. Methods in Enzymology (Vol. 52, pp. 302-310). Academic press. https://doi.org/10.1016/S0076-6879(78)52032-6
Butts, M., Sundaram, V. L., Murughiyan, U., Borthakur, A., & Singh, S. (2023). The influence of alcohol consumption on intestinal nutrient absorption: a comprehensive review. Nutrients, 15(7), 1571. https://doi.org/10.3390/nu15071571
Chen, G., & Haber, P. S. (2021). Gastrointestinal disorders related to alcohol and other drug use. In Textbook of Addiction Treatment: International Perspectives (pp. 1077-1097). Cham: Springer International Publishing. https://doi.org/10.1007/978-3-030-36391-8_76
Chung, B. S., Yang, K., Park, C., & Ryu, T. (2025). Prolonged Intestinal Ethanol Absorption and Oxidative Stress: Revisiting the Gut–Liver Axis in Alcohol-Associated Disease. International Journal of Molecular Sciences, 26(12), 5442. https://www.mdpi.com/1422-0067/26/12/5442#
Contreras-Zentella, M. L., Villalobos-García, D., & Hernández-Muñoz, R. (2022). Ethanol metabolism in the liver, the induction of oxidant stress, and the antioxidant defense system. Antioxidants, 11(7), 1258. https://doi.org/10.3390/antiox11071258
Das, S. K., & Vasudevan, D. M. (2007). Alcohol-induced oxidative stress. Life Sciences, 81(3), 177-187. https://doi.org/10.1016/j.lfs.2007.05.005
de Talamoni, N. T., Areco, V., Rodríguez, V., Marchionatti, A., & Pérez, A. (2017). Melatonin, Gastrointestinal Protection, and Oxidative Stress. In Gastrointestinal Tissue (pp. 317-325). Academic Press. https://doi.org/10.1016/B978-0-12-805377-5.00025-4
Favero, G., Franceschetti, L., Bonomini, F., Rodella, L. F., & Rezzani, R. (2017). Melatonin as an anti‐inflammatory agent modulating inflammasome activation. International Journal of Endocrinology, 2017(1), 1835195. https://doi.org/10.1155/2017/1835195
García, J.J., López‐Pingarrón, L., Almeida‐Souza, P., Tres, A., Escudero, P., García‐Gil, F.A., Tan, D.X., Reiter, R.J., Ramírez, J.M. and Bernal‐Pérez, M.. (2014). Protective effects of melatonin in reducing oxidative stress and in preserving the fluidity of biological membranes: a review. Journal of Pineal Research, 56(3), 225-237. https://doi.org/10.1111/jpi.12128
Haber, P. S., & Kortt, N. C. (2021). Alcohol use disorder and the gut. Addiction, 116(3), 658-667. https://doi.org/10.1111/add.15147
Hacışevki, A., & Baba, B. (2018). An overview of melatonin as an antioxidant molecule: A Biochemical Approach. IntechOpen. DOI: 10.5772/intechopen.79421
Halliwell, B. (2012). Free radicals and antioxidants: updating a personal view. Nutrition Reviews, 70(5), 257-265. https://doi.org/10.1111/j.1753-4887.2012.00476.x
Hu, S., Yin, S., Jiang, X., Huang, D., & Shen, G. (2009). Melatonin protects against alcoholic liver injury by attenuating oxidative stress, inflammatory response, and apoptosis. European Journal of Pharmacology, 616(1-3), 287-292. https://doi.org/10.1016/j.ejphar.2009.06.044
Karaaslan, C., & Suzen, S. (2015). Antioxidant properties of melatonin and its potential action in diseases. Current Topics in Medicinal Chemistry, 15(9), 894-903. https://doi.org/10.2174/1568026615666150220120946
Keshavarzian, A., & Fields, J. Z. (2017). Gastrointestinal motility disorders induced by ethanol. In Alcohol and the Gastrointestinal Tract (pp. 235-253). CRC Press. https://doi.org/10.4324/9781315149844
Kolli, V. K., Abraham, P., Isaac, B., & Kasthuri, N. (2013). Preclinical efficacy of melatonin to reduce methotrexate-induced oxidative stress and small intestinal damage in rats. Digestive Diseases and Sciences, 58(4), 959-969. https://doi.org/10.1007/s10620-012-2437-4
Misra, H. P., & Fridovich, I. (1972). The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. Journal of Biological Chemistry, 247(10), 3170-3175. https://doi.org/10.1016/S0021-9258(19)45228-9
Montoro-Huguet, M. A., Belloc, B., & Domínguez-Cajal, M. (2021). Small and large intestine (I): malabsorption of nutrients. Nutrients, 13(4), 1254. https://doi.org/10.3390/nu13041254
Obayuwana, E., & Okereke, J. N. (2024). Evaluating the ameliorative effect of aqueous Azadirachta indica leaf extract on alcohol-induced liver damage in adult Wistar rats. Journal of Experimental and Clinical Anatomy, 21(1), 59-65. https://doi.org/10.4314/jeca.v21i1.9
Reiter, R. J., Mayo, J. C., Tan, D. X., Sainz, R. M., Alatorre‐Jimenez, M., & Qin, L. (2016). Melatonin as an antioxidant: under promises but over delivers. Journal of Pineal Research, 61(3), 253-278. https://doi.org/10.1111/jpi.12360
Paglia, D. E., & Valentine, W. N. (1967). Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. The Journal of laboratory and clinical medicine, 70(1), 158-169.
Sinha, A. K. (1972). Colorimetric assay of catalase. Analytical Biochemistry, 47(2), 389-394. https://doi.org/10.1016/0003-2697(72)90132-7
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