Genotoxicity of Streptozotocin versus High Fat Diet-Induced Hyperglycemia in Adult Albino Rat Myocardium
DOI:
https://doi.org/10.59573/emsj.7(5).2023.18Ключевые слова:
streptozotocin, high-fat diet, hyperglycemia, myocardium, genotoxicityАннотация
Background: Hyperglycemia has detrimental systemic and cardiac effects by increasing oxidative stress and advanced glycation end products (AGE). Prolonged hyperglycemia-induced DNA damage in various tissues. Aim: To compare the hyperglycemia-induced genotoxicity of STZ versus a high-fat diet (HFD) on rat myocardial tissue. Methods: Sixty-six adult male rats were allocated randomly into 3 groups of 22 rats each; Group I was maintained on a standard chow diet, Group II where rats were injected with STZ (40 mg/kg, intraperitoneally) for 5 consecutive days, and Group III where rats were fed HFD for 15 weeks. After reaching the hyperglycemic level (> 150 mg/dl), all rats were kept for 5 weeks on HFD to ensure the occurrence of DNA damage. Rats were euthanized and sacrificed at the end of the experiment. Blood samples were collected from the tail vein. The heart was excised carefully and processed for histological (Hematoxylin & eosin) and immunohistochemical staining (?H2AX). Results: The HFD group's serum levels were significantly higher for NO and MDA than the STZ group's serum levels, whereas GSH levels were lower. On histopathological examination, congested blood vessels, inflammatory cells, and spacing between cardiac muscle fibers were seen in Groups II and III. Regarding ?H2AX immunostaining, the reaction was marked in Group III as compared with Group II. Conclusion: Hyperglycemia induced deteriorative changes in the myocardial tissue. HFD-induced hyperglycemia produced much genotoxic damage to the myocardium. This could be related to its dramatic oxidative damage.
Библиографические ссылки
Ahmed, H. H., Abd El-Maksoud, M. D., Abdel Moneim, A. E., & Aglan, H. A. (2017). Pre-Clinical Study for the Antidiabetic Potential of Selenium Nanoparticles. Biol Trace Elem Res, 177(2), 267-280. doi:10.1007/s12011-016-0876-z
Akkoc, R., Ogeturk, M., Aydin, S., Kuloglu, T., & Aydin, S. (2021). Effects of carnosine on apoptosis, transient receptor potential melastatin 2, and betatrophin in rats exposed to formaldehyde. Biotechnic & Histochemistry, 96(3), 223-229. doi:10.1080/10520295.2020.1783571
Amin, K. A., & Nagy, M. A. (2009). Effect of Carnitine and herbal mixture extract on obesity induced by high fat diet in rats. Diabetology & metabolic syndrome, 1(1), 1-14. doi:10.1186/1758-5996-1-17
Ataie, Z., Dastjerdi, M., Farrokhfall, K., & Ghiravani, Z. (2021). The Effect of Cinnamaldehyde on iNOS Activity and NO-Induced Islet Insulin Secretion in High-Fat-Diet Rats. Evid Based Complement Alternat Med, 2021, 9970678. doi:10.1155/2021/9970678
Aydın, S., Bacanlı, M., Anlar, H. G., Çal, T., Arı, N., Bucurgat, Ü. Ü., . . . Başaran, N. (2019). Preventive role of Pycnogenol® against the hyperglycemia-induced oxidative stress and DNA damage in diabetic rats. Food and Chemical Toxicology, 124, 54-63. doi:https://doi.org/10.1016/j.fct.2018.11.038
Azzarà, A., Chiaramonte, A., Filomeni, E., Pinto, B., Mazzoni, S., Piaggi, S., . . . Scarpato, R. (2017). Increased level of DNA damage in some organs of obese Zucker rats by γ‐H2AX analysis. Environmental and Molecular Mutagenesis, 58(7), 477-484. doi:https://doi.org/10.1002/em.22115
Barrientos, C., Perez, A., & Vazquez, J. (2021). Ameliorative Effects of Oral Glucosamine on Insulin Resistance and Pancreatic Tissue Damage in Experimental Wistar rats on a High-fat Diet. Comp Med, 71(3), 215-221. doi:10.30802/AALAS-CM-21-000009
Battiprolu, P. K., Hojayev, B., Jiang, N., Wang, Z. V., Luo, X., Iglewski, M., . . . Gillette, T. G. (2012). Metabolic stress–induced activation of FoxO1 triggers diabetic cardiomyopathy in mice. The Journal of clinical investigation, 122(3), 1109-1118. doi:https://doi.org/10.1172/JCI60329
Bjelland, S., & Seeberg, E. (2003). Mutagenicity, toxicity and repair of DNA base damage induced by oxidation. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 531(1-2), 37-80. doi:10.1016/j.mrfmmm.2003.07.002
Booth, F. W., Roberts, C. K., & Laye, M. J. (2012). Lack of exercise is a major cause of chronic diseases. Comprehensive physiology, 2(2), 1143. doi:https://doi.org/10.1002%2Fcphy.c110025
Boudina, S., & Abel, E. D. (2007). Diabetic cardiomyopathy revisited. Circulation, 115(25), 3213-3223. doi:10.1161/CIRCULATIONAHA.106.679597
Cadet, J., Douki, T., & Ravanat, J.-L. (2004). The human genome as a target of oxidative modification: damage to nucleic acids. Oxidative Stress and Disease, 10, 145-192.
Cai, L., & Kang, Y. J. (2001). Oxidative stress and diabetic cardiomyopathy: a brief review. Cardiovasc Toxicol, 1(3), 181-193. doi:10.1385/ct:1:3:181
Carpentier, A. C. (2018). Abnormal Myocardial Dietary Fatty Acid Metabolism and Diabetic Cardiomyopathy. Can J Cardiol, 34(5), 605-614. doi:10.1016/j.cjca.2017.12.029
Chang, X., Luo, F., Jiang, W., Zhu, L., Gao, J., He, H., . . . Yan, T. (2015). Protective activity of salidroside against ethanol-induced gastric ulcer via the MAPK/NF-κB pathway in vivo and in vitro. International Immunopharmacology, 28(1), 604-615. doi:https://doi.org/10.1016/j.intimp.2015.07.031
Collins, A., & Harrington, V. (2002). Repair of oxidative DNA damage: assessing its contribution to cancer prevention. Mutagenesis, 17(6), 489-493. doi:10.1093/mutage/17.6.489
Costantino, S., Paneni, F., Mitchell, K., Mohammed, S. A., Hussain, S., Gkolfos, C., . . . Cosentino, F. (2018). Hyperglycaemia-induced epigenetic changes drive persistent cardiac dysfunction via the adaptor p66(Shc). Int J Cardiol, 268, 179-186. doi:10.1016/j.ijcard.2018.04.082
El-shaer, N. H., & Nofal, A. E. (2019). The enhancing effect of chamomile on histological and immunohistochemical alterations in diabetic rats. Egyptian Academic Journal of Biological Sciences, D. Histology & Histochemistry, 11(1), 15-32. doi:https://doi.org/10.21608/eajbsd.2019.29932
El Hayek, M. S., Ernande, L., Benitah, J. P., Gomez, A. M., & Pereira, L. (2021). The role of hyperglycaemia in the development of diabetic cardiomyopathy. Arch Cardiovasc Dis, 114(11), 748-760. doi:10.1016/j.acvd.2021.08.004
Elhessy, H. M., Habotta, O. A., Eldesoqui, M., Elsaed, W. M., Soliman, M. F. M., Sewilam, H. M., . . . Lashine, N. H. (2023). Comparative neuroprotective effects of Cerebrolysin, dexamethasone, and ascorbic acid on sciatic nerve injury model: Behavioral and histopathological study. Front Neuroanat, 17, 1090738. doi:10.3389/fnana.2023.1090738
Faria, A., & Persaud, S. J. (2017). Cardiac oxidative stress in diabetes: Mechanisms and therapeutic potential. Pharmacol Ther, 172, 50-62. doi:10.1016/j.pharmthera.2016.11.013
Farshid, A. A., Tamaddonfard, E., Moradi-Arzeloo, M., & Mirzakhani, N. (2016). The effects of crocin, insulin and their co-administration on the heart function and pathology in streptozotocin-induced diabetic rats. Avicenna journal of phytomedicine, 6(6), 658. doi:https://doi.org/10.22038/ajp.2016.6775
Fouda, A., El-Aziz, A., & Mabrouk, N. (2019). Effects of Arabic Gum on cardiomyopathy in a rat model of type II diabetes. Al-Azhar Medical Journal, 48(1), 29-42. doi:10.21608/amj.2019.50720
Furman, B. L. (2015). Streptozotocin-Induced Diabetic Models in Mice and Rats. Curr Protoc Pharmacol, 70(1), 5 47 41-45 47 20. doi:10.1002/0471141755.ph0547s70
Hassan, H. M., Elnagar, M. R., Abdelrazik, E., Mahdi, M. R., Hamza, E., Elattar, E. M., . . . Al-Khater, K. M. (2022). Neuroprotective effect of naringin against cerebellar changes in Alzheimer’s disease through modulation of autophagy, oxidative stress and tau expression: An experimental study. Frontiers in Neuroanatomy, 16, 1012422. doi: https://doi.org/10.3389/fnana.2022.1012422
He, H. J., Wang, G. Y., Gao, Y., Ling, W. H., Yu, Z. W., & Jin, T. R. (2012). Curcumin attenuates Nrf2 signaling defect, oxidative stress in muscle and glucose intolerance in high fat diet-fed mice. World J Diabetes, 3(5), 94-104. doi:10.4239/wjd.v3.i5.94
Ishii, N., Patel, K. P., Lane, P. H., Taylor, T., Bian, K., Murad, F., . . . Carmines, P. K. (2001). Nitric oxide synthesis and oxidative stress in the renal cortex of rats with diabetes mellitus. Journal of the American Society of Nephrology, 12(8), 1630-1639. doi:10.1681/ASN.V1281630
Ivanović-Matić, S., Bogojević, D., Martinović, V., Petrović, A., Jovanović-Stojanov, S., Poznanović, G., & Grigorov, I. (2014). Catalase inhibition in diabetic rats potentiates DNA damage and apoptotic cell death setting the stage for cardiomyopathy. Journal of Physiology and Biochemistry, 70, 947-959. doi:https://doi.org/10.1007/s13105-014-0363-y
Jia, G., DeMarco, V. G., & Sowers, J. R. (2016). Insulin resistance and hyperinsulinaemia in diabetic cardiomyopathy. Nat Rev Endocrinol, 12(3), 144-153. doi:10.1038/nrendo.2015.216
Korany, R., Ahmed, K. S., Halawany, H., & Ahmed, K. A. (2019). Effect of long-term arsenic exposure on female Albino rats with special reference to the protective role of Spirulina platensis. Explor Anim Med Res, 9(2), 125-136. Retrieved from Website: www.animalmedicalresearch.org
Kuwabara, W. M. T., Panveloski-Costa, A. C., Yokota, C. N. F., Pereira, J. N. B., Filho, J. M., Torres, R. P., . . . Alba-Loureiro, T. C. (2017). Comparison of Goto-Kakizaki rats and high fat diet-induced obese rats: Are they reliable models to study Type 2 Diabetes mellitus? PloS one, 12(12), e0189622. doi:https://doi.org/10.1371/journal.pone.0189622
Lee, H. G., Choi, J. H., Jang, Y. S., Kim, U. K., Kim, G. C., & Hwang, D. S. (2020). Non-thermal plasma accelerates the healing process of peripheral nerve crush injury in rats. Int J Med Sci, 17(8), 1112-1120. doi:10.7150/ijms.44041
Luc, K., Schramm-Luc, A., Guzik, T. J., & Mikolajczyk, T. P. (2019). Oxidative stress and inflammatory markers in prediabetes and diabetes. J Physiol Pharmacol, 70(6). doi:10.26402/jpp.2019.6.01
Marino, F., Scalise, M., Salerno, N., Salerno, L., Molinaro, C., Cappetta, D., . . . Cianflone, E. (2022). Diabetes-Induced Cellular Senescence and Senescence-Associated Secretory Phenotype Impair Cardiac Regeneration and Function Independently of Age. Diabetes, 71(5), 1081-1098. doi:10.2337/db21-0536
Marnett, L. J. (2000). Oxyradicals and DNA damage. carcinogenesis, 21(3), 361-370. doi:10.1093/carcin/21.3.361
Mattapally, S., & Banerjee, S. K. (2011). Nitric oxide: Redox balance, protein modification and therapeutic potential in cardiovascular system. IIOAB J, 2(6), 29-38. doi:https://experts.umn.edu/en/organisations/genetics-cell-biology-and-development-tmed
Mellor, K. M., Ritchie, R. H., & Delbridge, L. M. (2010). Reactive oxygen species and insulin-resistant cardiomyopathy. Clin Exp Pharmacol Physiol, 37(2), 222-228. doi:10.1111/j.1440-1681.2009.05274.x
Mittler, R. (2002). Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci, 7(9), 405-410. doi:10.1016/s1360-1385(02)02312-9
Pappachan, J. M., Varughese, G. I., Sriraman, R., & Arunagirinathan, G. (2013). Diabetic cardiomyopathy: Pathophysiology, diagnostic evaluation and management. World J Diabetes, 4(5), 177-189. doi:10.4239/wjd.v4.i5.177
Rostoka, E., Isajevs, S., Sokolovska, J., Duburs, G., & Sjakste, N. (2023). Antimutagenic 1, 4-Dihydropyridine AV-153 Normalizes Expression of GLUT1, GLUT4, INOS, PARP1, and Gamma H2AX Histone in Myocardium of Rats with Streptozotocin Model of Diabetes Mellitus. Paper presented at the Proceedings of the Latvian Academy of Sciences.
Savi, M., Bocchi, L., Sala, R., Frati, C., Lagrasta, C., Madeddu, D., . . . Miragoli, M. (2016). Parenchymal and stromal cells contribute to pro-inflammatory myocardial environment at early stages of diabetes: protective role of resveratrol. Nutrients, 8(11), 729. doi:https://doi.org/10.3390/nu8110729
Shi, W., Yuan, R., Chen, X., Xin, Q., Wang, Y., Shang, X., . . . Chen, K. (2019). Puerarin Reduces Blood Pressure in Spontaneously Hypertensive Rats by Targeting eNOS. Am J Chin Med, 47(1), 19-38. doi:10.1142/S0192415X19500022
Suryawanshi, N. P., Bhutey, A. K., Nagdeote, A. N., Jadhav, A. A., & Manoorkar, G. S. (2006). Study of lipid peroxide and lipid profile in diabetes mellitus. Indian J Clin Biochem, 21(1), 126-130. doi:10.1007/BF02913080
Teshima, Y., Takahashi, N., Nishio, S., Saito, S., Kondo, H., Fukui, A., . . . Saikawa, T. (2014). Production of Reactive Oxygen Species in the Diabetic Heart–Roles of Mitochondria and NADPH Oxidase–. Circulation Journal, 78(2), 300-306. doi:https://doi.org/10.1253/circj.CJ-13-1187
Tripathi, U. N., & Chandra, D. (2009). The plant extracts of Momordica charantia and Trigonella foenum graecum have antioxidant and anti-hyperglycemic properties for cardiac tissue during diabetes mellitus. Oxidative Medicine and Cellular Longevity, 2, 290-296. doi:https://doi.org/10.4161/oxim.2.5.9529
Tsao, C. W., Aday, A. W., Almarzooq, Z. I., Alonso, A., Beaton, A. Z., Bittencourt, M. S., . . . Commodore-Mensah, Y. (2022). Heart disease and stroke statistics—2022 update: a report from the American Heart Association. Circulation, 145(8), e153-e639. doi:https://doi.org/10.1161/CIR.0000000000001052
Tsutsui, H., Kinugawa, S., & Matsushima, S. (2011). Oxidative stress and heart failure. Am J Physiol Heart Circ Physiol, 301(6), H2181-2190. doi:10.1152/ajpheart.00554.2011
Vatandoust, N., Rami, F., Salehi, A. R., Khosravi, S., Dashti, G., Eslami, G., . . . Salehi, R. (2018). Novel High-Fat Diet Formulation and Streptozotocin Treatment for Induction of Prediabetes and Type 2 Diabetes in Rats. Adv Biomed Res, 7, 107. doi:10.4103/abr.abr_8_17
Vlassara, H., & Striker, G. E. (2011). AGE restriction in diabetes mellitus: a paradigm shift. Nat Rev Endocrinol, 7(9), 526-539. doi:10.1038/nrendo.2011.74
Wang, Y., Sun, H., Zhang, J., Xia, Z., & Chen, W. (2020). Streptozotocin-induced diabetic cardiomyopathy in rats: ameliorative effect of PIPERINE via Bcl2, Bax/Bcl2, and caspase-3 pathways. Biosci Biotechnol Biochem, 84(12), 2533-2544. doi:10.1080/09168451.2020.1815170
Winzell, M. S., & Ahrén, B. (2004). The high-fat diet–fed mouse: a model for studying mechanisms and treatment of impaired glucose tolerance and type 2 diabetes. Diabetes, 53(suppl_3), S215-S219. doi:https://doi.org/10.2337/diabetes.53.suppl_3.S215
Wu, Y., Li, Y., Liao, X., Wang, Z., Li, R., Zou, S., . . . Xiao, J. (2017). Diabetes Induces Abnormal Ovarian Function via Triggering Apoptosis of Granulosa Cells and Suppressing Ovarian Angiogenesis. Int J Biol Sci, 13(10), 1297-1308. doi:10.7150/ijbs.21172
Yan, J., Young, M. E., Cui, L., Lopaschuk, G. D., Liao, R., & Tian, R. (2009). Increased glucose uptake and oxidation in mouse hearts prevent high fatty acid oxidation but cause cardiac dysfunction in diet-induced obesity. Circulation, 119(21), 2818-2828. doi:10.1161/CIRCULATIONAHA.108.832915
Yang, H., Jin, X., Kei Lam, C. W., & Yan, S. K. (2011). Oxidative stress and diabetes mellitus. Clin Chem Lab Med, 49(11), 1773-1782. doi:10.1515/CCLM.2011.250
Zhang, X., Fu, Y., Xu, X., Li, M., Du, L., Han, Y., & Ge, Y. (2014). PERK pathway are involved in NO-induced apoptosis in endothelial cells cocultured with RPE under high glucose conditions. Nitric Oxide, 40, 10-16. doi:10.1016/j.niox.2014.05.001
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