Comparison the Effects of Vitamin E and Propolis on Interleukin-5 and STAT1 Gene Expression in Wistar Rats with Non-alcoholic Fatty Liver Disease
Subject Areas :
Journal of Animal Biology
Saeede Baarforoush
1
,
Maryam Bananaj
2
,
Ramin Hajikhani
3
,
Hengameh Alibeik
4
1 - Department of Biology, North Tehran Branch, Islamic Azad University, Tehran, Iran
2 - Department of Biology, North Tehran Branch, Islamic Azad University, Tehran, Iran
3 - Department of Biology, North Tehran Branch, Islamic Azad University, Tehran, Iran
4 - Department of Biology, North Tehran Branch, Islamic Azad University, Tehran, Iran
Received: 2022-03-02
Accepted : 2022-10-15
Published : 2023-02-20
Keywords:
Propolis,
vitamin E,
IL-5,
Nonalcoholic fatty liver disease,
STAT1 Gene,
Abstract :
Nonalcoholic fatty liver disease (NAFLD) is a growing health concern worldwide. Unfortunately, scientists have not succeeded in finding a suitable treatment method for this disease, and more research is needed. Studies have shown that treatment with antioxidants is effective in this disease. In this study, the effect of two different antioxidants on NAFLD induced in male Wistar rats was evaluated. This study was conducted on 32 male Wistar rats weighing 200 grams, which were randomly divided into four groups of eight. Mice were fed by gavage with high-fat emulsion at the rate of 2 mg/kg for 40 days. After suffering from fatty liver, the level of interleukin-5 (IL-5) in the serum was measured and also the expression level of STAT1 gene was determined using real-time PCR. The results showed that the level of serum IL-5 in the patient group significantly increased compared to the control group, and the treatment groups with vitamin E and propolis, significantly decreased the level of interleukin-5 compared to the patient group (p < 0.05). In addition, the greatest decrease was related to the propolis group (p < 0.05). On the other hand, the level of STAT1 gene expression in the fatty liver group is significantly increased compared to the control group (p < 0.05); Whereas, after treatment with antioxidants, the expression of this gene decreased (p < 0.05). Based on the obtained results, the use of propolis and also vitamin E as natural antioxidants by reducing the inflammatory interleukin and also reducing the expression of genes effective in the formation of NAFLD, have a promising therapeutic role in non-alcoholic fatty liver disease.
References:
1. Bai J., Wu L., Chen X., Wang L., Li Q., Zhang Y., Wu J., Cai G., Chen X. 2018. Suppressor of Cytokine Signaling-1/STAT1 Regulates Renal Inflammation in Mesangial Proliferative Glomerulonephritis Models. Frontiers in Immunology, 9:1982.
Bellentani S., Scaglioni F., Marino M., Bedogni G. 2010. Epidemiology of non-alcoholic fatty liver disease. Digestive Diseases, 28(1):155-161.
Chung M.Y., Yeung S.F., Park H.J., Volek J.S., Bruno R.S. 2010. Dietary α-and γ-tocopherol supplementation attenuates lipopolysaccharide-induced oxidative stress and inflammatory-related responses in an obese mouse model of nonalcoholic steatohepatitis. The Journal of Nutritional Biochemistry, 21(12):1200-1206.
CotterG., Rinella M. 2020. Nonalcoholic Fatty Liver Disease: The State of the Disease. Gastroenterology, 158(7):1851-1864.
Croker B.A., Kiu H., Nicholson S.E. 2008. SOCS regulation of the JAK/STAT signalling pathway. Seminars in Cell and Developmental Biology, Elsevier.
Daleprane J.B., Abdalla D.S. 2013. Emerging roles of propolis: antioxidant, cardioprotective, and antiangiogenic actions. Evidence-based Complementary and Alternative Medicine, 2013:175135.
El Hadi H., Vettor R., Rossato M. 2018. Congenital vitamin E deficiency. Handbook of Famine, Starvation, and Nutrient Deprivation; Preedy, VR, Patel, VB, Eds. 2018:1-18.
Federico A., Dallio M., Masarone M., Gravina A.G., Di Sarno R., Tuccillo C. 2019 Evaluation of the effect derived from silybin with vitamin D and vitamin E administration on clinical, metabolic, endothelial dysfunction, oxidative stress parameters, and serological worsening markers in nonalcoholic fatty liver disease patients. Oxidative Medicine and Cellular Longevity, 2019: 8742075.
Hadi H.E., Vettor R., Rossato M. 2018. Vitamin E as a treatment for nonalcoholic fatty liver disease: reality or myth? Antioxidants, 7(1):12.
Haghighatfard A., Andalib S., Amini Faskhodi M., Sadeghi S., Ghaderi A.H., Moradkhani S. 2018. Gene expression study of mitochondrial complex I in schizophrenia and paranoid personality disorder. The World Journal of Biological Psychiatry, 19(sup3):S133-S146.
Ji H.F., Sun Y., Shen L. 2014. Effect of vitamin E supplementation on aminotransferase levels in patients with NAFLD, NASH, and CHC: results from a meta-analysis. Nutrition, 30(9):986-991.
Jin X.L, Wang K., Li Q.Q., Tian W.L., Xue X.F., Wu L.M. 2017. Antioxidant and anti-inflammatory effects of Chinese propolis during palmitic acid-induced lipotoxicity in cultured hepatocytes. Journal of Functional Foods, 34:216-223.
Kismet K., Ozcan C., Kuru S., Celemli O.G., Celepli P., Senes M. 2017. Does propolis have any effect on non-alcoholic fatty liver disease? Biomedicine and Pharmacotherapy, 90:863-871.
Lirussi F., Azzalini L., Orando S., Orlando R., Angelico F. 2007. Antioxidant supplements for non‐alcoholic fatty liver disease and/or steatohepatitis. Cochrane Database of Systematic Reviews, 2007(1): CD004996.
Loguercio C., Andreone P., Brisc C., Brisc M.C., Bugianesi E., Chiaramonte M. 2012. Silybin combined with phosphatidylcholine and vitamin E in patients with nonalcoholic fatty liver disease: a randomized controlled trial. Free Radical Biology and Medicine, 52(9):1658-1665.
Mohamed E.H., Baiomy A.A., Ibrahim Z.S., Soliman M.M. 2016. Modulatory effects of levamisole and garlic oil on the immune response of Wistar rats: Biochemical, immunohistochemical, molecular and immunological study. Molecular Medicine Reports, 14(3):2755-2763.
Mujica V., Orrego R., Pérez J., Romero P., Ovalle P., Zúñiga-Hernández J. 2017. The role of propolis in oxidative stress and lipid metabolism: a randomized controlled trial. Evidence-Based Complementary and Alternative Medicine, 2017:4272940.
Murphy S.K., Yang H., Moylan C.A., Pang H., Dellinger A., Abdelmalek F. 2013. Relationship between methylome and transcriptome in patients with nonalcoholic fatty liver disease. Gastroenterology, 145(5):1076-1087.
Musso G., Gambino R., Cassader M., Pagano G. 2010. A meta‐analysis of randomized trials for the treatment of nonalcoholic fatty liver disease. Hepatology, 52(1):79-104.
Nagashimada M., Ota T. 2019. Role of vitamin E in nonalcoholic fatty liver disease. Iubmb Life, 71(4):516-522.
Nan Y.M., Wu W.J., Fu N., Liang B.L., Wang R.Q., Li L.X. 2009. Antioxidants vitamin E and 1-aminobenzotriazole prevent experimental non-alcoholic steatohepatitis in mice. Scandinavian Journal of Gastroenterology, 44(9):1121-1131.
Nobili V., Manco M., Devito R., Ciampalini P, Piemonte F., Marcellini M. 2006. Effect of vitamin E on aminotransferase levels and insulin resistance in children with non‐alcoholic fatty liver disease. Alimentary Pharmacology and Therapeutics, 24(11‐12):1553-1561.
Oliveira C.P., da Costa Gayotto L..C, Tatai C., Della Nina B.I., Lima S., Abdalla D.S., 2003. Vitamin C and vitamin E in prevention of nonalcoholic fatty liver disease (NAFLD) in choline deficient diet fed rats. Nutrition Journal, 2(1):1-5.
Perdomo C.M., Frühbeck G., Escalada J. 2019. Impact of nutritional changes on nonalcoholic fatty liver disease. Nutrients, 11(3):677.
Phung N, Farrell G, Robertson G, George J, editors. Vitamin E but not glutathione precursors inhibit hepatic fibrosis in experimental NASH exhibiting oxidative stress and mitochondrial abnormalities. Hepatology; 2001: WB Saunders Co Independence Square West Curtis Center, STE 300, Philadelphia.
Podszun M.C., Alawad A.S., Lingala S., Morris N., Huang W.C.A., Yang S. 2020. Vitamin E treatment in NAFLD patients demonstrates that oxidative stress drives steatosis through upregulation of de-novo lipogenesis. Redox Biology, 37:101710.
Phung N., Pera N., Farrell G., Leclercq I., Hou J.Y., George J. 2009. Pro-oxidant-mediated hepatic fibrosis and effects of antioxidant intervention in murine dietary steatohepatitis. International Journal of Molecular Medicine, 24(2):171-180.
Ramachandran S., Singh M.K., Mobeen A., Chandra A., Joshi S. 2021. A Meta-analysis of comorbidities in COVID-19: Which diseases increase the susceptibility of SARS-CoV-2 infection. Computers in Biology and Medicine, 130:104219.
RenningerL., Seymour R.E., Whiteley L.O., Sundberg J.P., HogenEsch H. 2010. Anti-IL5 decreases the number of eosinophils but not the severity of dermatitis in SHARPIN-deficient mice. Experimental Dermatology, 19(3):252-258.
Romeo S., Sanyal A., Valenti L. 2020. Leveraging human genetics to identify potential new treatments for fatty liver disease. Cell Metabolism, 31(1):35-45.
Sato K., Gosho M., Yamamoto T., Kobayashi Y., Ishii N., Ohashi T. 2015. Vitamin E has a beneficial effect on nonalcoholic fatty liver disease: a meta-analysis of randomized controlled trials. Nutrition, 31(7-8):923-930.
Sepidarkish M., Akbari-Fakhrabadi M., Daneshzad E., Yavari M., Rezaeinejad M., Morvaridzadeh M. 2020. Effect of omega-3 fatty acid plus vitamin E Co-Supplementation on oxidative stress parameters: A systematic review and meta-analysis. Clinical Nutrition, 39(4):1019-1025.
Shen X.H., Tang Q.Y., Huang J., Cai W. 2010. Vitamin E regulates adipocytokine expression in a rat model of dietary-induced obesity. Experimental Biology and Medicine, 235(1):47-51.
Socha P., Horvath A., Vajro P., Dziechciarz P., Dhawan A., Szajewska H. 2009. Pharmacological interventions for nonalcoholic fatty liver disease in adults and in children: a systematic review. Journal of Pediatric Gastroenterology and Nutrition, 48(5):587-596.
Soden J.S., Devereaux M.W., Haas J.E., Gumpricht E., Dahl R., Gralla J. 2007. Subcutaneous vitamin E ameliorates liver injury in an in vivo model of steatocholestasis. Hepatology, 46(2):485-495.
Soleimani D., Rezaie M., Rajabzadeh F., Gholizadeh Navashenaq J., Abbaspour M., Miryan M. 2021. Protective effects of propolis on hepatic steatosis and fibrosis among patients with nonalcoholic fatty liver disease (NAFLD) evaluated by real‐time two‐dimensional shear wave elastography: A randomized clinical trial. Phytotherapy Research, 35(3):1669-1679.
Studio del Fegato, Società Italiana di Diabetologia, Società Italiana dell’Obesità Members of the guidelines panel. Non-alcoholic fatty liver disease in adults 2021: A clinical practice guideline of the Italian Association for the Study of the Liver (AISF), the Italian Society of Diabetology (SID) and the Italian Society of Obesity (SIO). Nutrition, Metabolism and Cardiovascular Diseases, 32(1):1-16.
Türkez H., Yousef M.I., Geyikoglu F. 2010. Propolis prevents aluminium-induced genetic and hepatic damages in rat liver. Food and Chemical Toxicology, 48(10):2741-2746.
Willebrords J., Pereira I.V.A, Maes M., Yanguas S.C., Colle I., Van Den Bossche B. 2015. Strategies, models and biomarkers in experimental non-alcoholic fatty liver disease research. Progress in Lipid Research, 59:106-25.
Yang J., Fernández-Galilea M., Martínez-Fernández L., González-Muniesa P., Pérez-Chávez A., Martínez J.A. 2019. Oxidative stress and non-alcoholic fatty liver disease: effects of omega-3 fatty acid supplementation. Nutrients, 11(4):872.
Zou Y., Li J., Lu C., Wang J., Ge J., Huang Y., 2006. High-fat emulsion-induced rat model of nonalcoholic steatohepatitis. Life Sciences, 79(11):1100-1107.
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