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Yıl 2024, Cilt: 17 Sayı: 3, 811 - 825, 31.12.2024
https://doi.org/10.18185/erzifbed.1555393

Öz

Kaynakça

  • [1] https://www.who.int/news-room/fact-sheets/detail/the-top-10-causes-of-death, 16.09.2024
  • [2] Pilleron, S., Sarfati, D., Janssen‐Heijnen, M., Vignat, J., Ferlay, J., Bray, F., & Soerjomataram, I. (2019) Global cancer incidence in older adults, 2012 and 2035: a population‐based study. International Journal of Cancer, 144(1), 49-58.
  • [3] Simcock, R., Fallowfield, L., Monson, K., Solis-Trapala, I., Parlour, L., Langridge, C., Jenkins, V. Arix. (2013) A Randomised Trial of Acupuncture V Oral Care Sessions in Patients with Chronic Xerostomia Following Treatment of Head and Neck Cancer. Annual Oncology, 24 (3), 776–783.
  • [4] Konak, M., Cincik, H., Erkul, E., Kucukodaci, Z., Gungor, A., Ozdemir, S., Cekin, E., Arisan, V., Mutluoglu, M., Salihoglu, M. (2016) The Protective Effects of Different Treatments on Rat SalivaryGlands after Radiotherapy. European Archives of Oto-Rhino-Laryngology, 273 (12), 4501–4506.
  • [5] Huang, Y., Zhang, W., Yu, F., Gao F. (2017) The Cellular and Molecular Mechanism of Radiation-Induced Lung Injury. Medical Science Monitor,15(23), 3446-3450.
  • [6] Azmoonfar, R., Khosravi, H., Rafieemehr, H., Mirzaei, F., Dastan, D., Ghiasvand, M. R., Khorshidi, L., Pashaki, A. S. (2023) Radioprotective effect of Malva sylvestris L. against radiation-induced liver, kidney and intestine damages in rat: A histopathological study. Biochemistry and Biophysics Reports, 34, 101455.
  • [7] Aras, S., Efendioğlu, M., Wulamujiang, A., Ozkanli, S. S., Keleş, M. S., Tanzer, İ.O. (2021) Radioprotective effect of melatonin against radiotherapy-induced cerebral cortex and cerebellum damage in rat. International Journal of Radiation Biology, 97(3), 348-355.
  • [8] Kaplan, M., Demir, E., Yavuz, F., Kaplan, G. I., Taysi, M. R., Taysi, S., Sucu, M.M. (2022) Radioprotective effect of nigella sativa oil on heart tissues of rats exposed to irradition. International Journal of Cardiovascular Sciences, 35(2), 214-219.
  • [9] Zhang, J., He, X., Bai, X., Sun, Y., Jiang, P., Wang, X., Li, W., Zhang, Y. (2020) Protective effect of trimetazidine in radiation-induced cardiac fibrosis in mice. Journal of Radiation Research, 61(5), 657-665.
  • [10] Adaramoye, O., Okiti, O., Farombi, E. (2011) Dried fruit extract from Xylopiaaethiopica (Annonaceae) protects Wistar albino rats from adverse effects of whole body radiation. Experimental and Toxicologic Pathology, 63 (7-8), 635-39.
  • [11] Şener, G., Kabasakal, L., Atasoy, B.M., Erzik, C., Velioğlu-Öğünç, A, Çetinel, Ş., Contuk, G., Gedik, N., Yeğen, B.Ç. (2006) Propylthiouracil-induced hypothyroidism protects ionizing radiation-induced multiple organ damage in rats. Journal of Endocrinology, 189 (2), 257-62.
  • [12] Benzie, I.F. (2000) Evolution of antioxidant defence mechanisms. European Journal of Nutrition, 39, 53-61. [13] McCord, J.M. (2000) The evolution of free radicals and oxidative stress. The American Journal of Medicine, 108(8), 652-659.
  • [14] Ames, B.N. (2001) DNA damage from micronutrient deficiencies is likely to be a major cause of cancer. Mutation Research/Fundamental And Molecular Mechanisms Of Mutagenesis, 475(1-2), 7-20.
  • [15] Kasaian, J., Mohammadi, A. (2018) Biological activities of farnesiferol C: a review. Journal of Asian Natural Products Research, 20 (1), 27-35.
  • [16] Garg, S.S., Gupta, J., Sharma, S., Sahu, D. (2020) An insight into the therapeutic applications of coumarin compounds and their mechanisms of action. European Journal of Pharmaceutical Sciences, 152, 105424.
  • [17] Küpeli Akkol, E., Genç, Y., Karpuz, B., Sobarzo-Sánchez, E., & Capasso, R. (2020) Coumarins and coumarin-related compounds in pharmacotherapy of cancer. Cancers, 12 (7), 1959.
  • [18] Mazimba, O. (2017) Umbelliferone: Sources, chemistry and bioactivities review. Bulletin of Faculty of Pharmacy, Cairo University, 55 (2), 223-232.
  • [19] Althunibat, O. Y., Abduh, M. S., Abukhalil, M. H., Aladaileh, S. H., Hanieh, H., & Mahmoud, A. M. (2022) Umbelliferone prevents isoproterenol-induced myocardial injury by upregulating Nrf2/HO-1 signaling, and attenuating oxidative stress, inflammation, and cell death in rats. Biomedicine & Pharmacotherapy, 149, 112900.
  • [20] Dikmen, M. (2016) Antiproliferative and apoptotic effects of aprepitant on human glioblastoma U87MG cells. Marmara Pharmaceutical Journal, 21(1), 156-164.
  • [21] Mahmoud, A. M., Hozayen, W. G., Hasan, I. H., Shaban, E., & Bin-Jumah, M. (2019) Umbelliferone ameliorates CCl 4-induced liver fibrosis in rats by upregulating PPARγ and attenuating oxidative stress, inflammation, and TGF-β1/Smad3 signaling. Inflammation, 42, 1103-1116.
  • [22] Alotaibi, M. F., Al-Joufi, F., Abou Seif, H. S., Alzoghaibi, M. A., Djouhri, L., Ahmeda, A. F., Mahmoud, A. M. (2023) Umbelliferone Inhibits Spermatogenic Defects and Testicular Injury in Lead-Intoxicated Rats by Suppressing Oxidative Stress and Inflammation, and Improving Nrf2/HO-1 Signaling [Retraction]. Drug Design, Development and Therapy, 17, 1153-1154.
  • [23] Wang, H.Q., Wang, S.S., Chiufai, K., Wang, Q., Cheng, X.L. (2019) Umbelliferone ameliorates renal function in diabetic nephropathy rats through regulating inflammation and TLR/NF-kappaB pathway. Chinise Journal of Natural Medicine, 17(5), 346-354.
  • [24] Council, N.R. (2011) National Institutes of Health guide for the care and use of laboratory animals.
  • [25] Cruz, L. F., De-Figueiredo, G.F., Pedro, L.P., Amorin, Y.M., Andrade, J.T., Passos, T. F., Rodrigues, F. F., Souza, I.LA., Gonçalves, T.P.R., Dos Santos Lima, L.A.R., Ferreira, J.M.S., Freitas Araújo, M. G. (2020) Umbelliferone (7-hydroxycoumarin): A non-toxic antidiarrheal and antiulcerogenic coumarin. Biomedicine & Pharmacotherapy, 129, 110432.
  • [26] Sproull, M., Kramp, T., Tandle, A., Shankavaram, U., Camphausen, K. (2017) Multivariate analysis of radiation responsive proteins to predict radiation exposure in total-body irradiation and partial-body irradiation models. Radiation Research, 187 (2), 251-258.
  • [27] Jacobs, E. R., Narayanan, J., Fish, B. L., Gao, F., Harmann, L. M., Bergom, C., Tracy, G., Jennifer, S., Medhora, M. (2019) Cardiac remodeling and reversible pulmonary hypertension during pneumonitis in rats after 13-Gy partial-body irradiation with minimal bone marrow sparing: effect of lisinopril. Health physics, 116 (4), 558-565.
  • [28] Erel, O. (2004) A novel automated method to measure total antioxidant response against potent free radical reactions. Clinical Biochemistry, 37 (2), 112-119.
  • [29] Erel, O. (2005) A new automated colorimetric method for measuring total oxidant status. Clinical Biochemistry, 38 (12), 1103-1111.
  • [30] Akyazi, I., Eraslan, E., Gülçubuk, A., Ekiz, E. E., Çırakli, Z. L., Haktanir, D., Bala D.A., Özkurt, M., Matur, E., Özcan, M. (2013) Long-term aspirin pretreatment in the prevention of cerulein-induced acute pancreatitis in rats. World Journal of Gastroenterology, 19 (19), 2894-2903.
  • [31] Ping, Z., Peng, Y., Lang, H., Xinyong, C., Zhiyi, Z., Xiaocheng, W., Hong, Z., Liang, S. (2020) Oxidative stress in radiation‐induced cardiotoxicity. Oxidative Medicine and Cellular Longevity, 2020(1), 3579143.
  • [32] Armanious, M.A., Mohammadi, H., Khodor, S., Oliver, D.E., Johnstone, P.A., Fradley, M.G. (2018) Cardiovascular effects of radiation therapy. Current Problems in Cancer, 42 (4), 433–442.
  • [33] Puukila, S., Lemon, J. A., Lees, S. J., Tai, T.C., Boreham, D.R., Khaper, N. (2017) Impact of ionizing radiation on the cardiovascular system: a review. Radiation Research, 188 (4.2), 539–546.
  • [34] Vona, R., Gambardella, L., Cittadini, C., Straface, E., Pietraforte, D. (2019) Biomarkers of oxidative stress in metabolicsyndrome and associated diseases. Oxidative Medicine and Cellular Longevity, 1, 8267234,
  • [35] Karslioglu, I., Ertekin, M. V., Kocer, I., Taysi, S., Sezen, O., Gepdiremen, A., & Balci, E. (2004) Protective role of intramuscularly administered vitamin E on the levels of lipid peroxidation and the activities of antioxidant enzymes in the lens of rats made cataractous with gamma-irradiation. European Journal of Ophthalmology, 14(6), 478-485.
  • [36] Dilber, B., Akbulut, U. E., Alver, A., Menteşe, A., Kolaylı, C. C., & Cansu, A. (2021) Plasma and erytrocyte oxidative stress markers in children with frequent breath-holding spells. Klinische Pädiatrie, 233 (04), 173-180.
  • [37] Elahi, M.M., Kong, Y.X., Matata, B.M. (2009) Oxidative stress as a mediator of cardiovascular disease. Oxidative Medicine and Cellular Longevity, 2(5), 259-269.
  • [38] Zhang, C., Chen, H., Xie, H. H., Shu, H., Yuan, W. J., & Su, D. F. (2003) Inflammation is involved in the organ damage induced by sinoaortic denervation in rats. Journal of Hypertension, 21(11), 2141-2148.
  • [39] Luo, N., Zhu, W., Li, X., Fu, M., Peng, X., Yang, F., Zhang, Y., Yin, H., Yang, C., Zhao, J., Yuan, X., Hu, G. (2022) Impact of Gut Microbiota on Radiation-Associated Cognitive Dysfunction and Neuroinflammation in Mice. Radiation Research, 197 (4), 350-364.
  • [40] Guo, D.B., Zhu, X.Q., Li, Q.Q., Li, G.M., Ruan, G.P., Pang, R.Q., Chen, Y.H., Wang, Q., Wang, J.X., Liu, J.F., Chen, Q., Pan, X.H. (2018) Efficacy and mechanisms underlying the effects of allogeneic umbilical cord mesenchymal stem cell transplantation on acute radiation injury in tree shrews. Cytotechnology, 70 (5), 1447-1468.
  • [41] Brasier, A. R. (2010) The nuclear factor-κB–interleukin-6 signalling pathway mediating vascular inflammation. Cardiovascular Research, 86 (2), 211-218.
  • [42] Gan, J., Qian, W., Lin, S. (2018) Umbelliferone alleviates myocardial ischemia: the role of inflammation and apoptosis. Inflammation, 41, 464-473.
  • [43] Danborno, A.M., Monnet, P. L., Orr, A.J. (2020) TxA2 Receptor Antagonist (SQ29548) attenuates Endothelium-Independent recovery from Thromboxane A2 Contraction of Isolated Rabbit Aorta. Journal of African Association of Physiological Sciences, 8(1), 8-15.
  • [44] El-Benhawy, S. A., Morsi, M. I., El-Tahan, R. A., Matar, N. A., & Ehmaida, H. M. (2021) Radioprotective effect of thymoquinone in X-irradiated rats. Asian Pacific Journal of Cancer Prevention, 22(9), 3005.
  • [45] Sarhan, H., Naoum, L. (2020) Protective role of royal jelly against gamma radiation induced oxidative stress, cardio-toxicity and organ dysfunctions in male rats. The Egyptian Journal of Hospital Medicine, 78(1), 62-67.
  • [46] Hemnani, T., Parihar, M.S. (1998) Reactive oxygen species and oxidative DNA damage. Indian Journal of Physiology and Pharmacology, 42, 440-452.

Radioprotective effect of Umbelliferon Against Radiation-Induced Myocardial Damages

Yıl 2024, Cilt: 17 Sayı: 3, 811 - 825, 31.12.2024
https://doi.org/10.18185/erzifbed.1555393

Öz

Radiation at a high dose may attenuate myocardial functions while presenting the therapeutic effect on cancer cells and thus can be life-threatening. Today, many studies reveal that supportive treatments provide important protective effects against acute radiation damage in vital organs including the heart. To our knowledge, the role of umbelliferone in the prevention of radiation damage to the heart has not yet been clarified. Therefore, the current study was planned to evaluate the role of umbelliferone radiation-induced cardiac injury using biochemical and histological data. Rats will be divided into eight different groups as control, radiation and treatment groups. No application was made to the control group. The second group animals were exposed to a single dose (12Gy) radiation throughout the body. Groups 3, 4 and 5 were orally given umbelliferone (25, 50 and 100 mg/kg) single dose for 3 days. Groups 6, 7 and 8 received umbelliferone and then radiation was applied. After the experiments, the myocardial tissues of the rats were removed and the protection of the substance against radiation was investigated. Radiation exposure to the rats induced oxidative stress, inflammation, pathological changes and vascular dysfunction in cardiac tissue. Whereas umbelliferone in high dose (100 mg/kg) pretreatment supported the anti-oxidant activity and also reduced the inflammatory response on heart tissue against radiation-associated toxicity. Besides, radiation-induced histopathological changes significantly ameliorated in umbelliferone-treated rat groups. Umbelliferone (100 mg/kg) pretreatment reduced radiation-induced heart damage, which was thought to provide the greatest opportunity for umbelliferone's efficacy as a new drug against the side effects of radiotherapy

Kaynakça

  • [1] https://www.who.int/news-room/fact-sheets/detail/the-top-10-causes-of-death, 16.09.2024
  • [2] Pilleron, S., Sarfati, D., Janssen‐Heijnen, M., Vignat, J., Ferlay, J., Bray, F., & Soerjomataram, I. (2019) Global cancer incidence in older adults, 2012 and 2035: a population‐based study. International Journal of Cancer, 144(1), 49-58.
  • [3] Simcock, R., Fallowfield, L., Monson, K., Solis-Trapala, I., Parlour, L., Langridge, C., Jenkins, V. Arix. (2013) A Randomised Trial of Acupuncture V Oral Care Sessions in Patients with Chronic Xerostomia Following Treatment of Head and Neck Cancer. Annual Oncology, 24 (3), 776–783.
  • [4] Konak, M., Cincik, H., Erkul, E., Kucukodaci, Z., Gungor, A., Ozdemir, S., Cekin, E., Arisan, V., Mutluoglu, M., Salihoglu, M. (2016) The Protective Effects of Different Treatments on Rat SalivaryGlands after Radiotherapy. European Archives of Oto-Rhino-Laryngology, 273 (12), 4501–4506.
  • [5] Huang, Y., Zhang, W., Yu, F., Gao F. (2017) The Cellular and Molecular Mechanism of Radiation-Induced Lung Injury. Medical Science Monitor,15(23), 3446-3450.
  • [6] Azmoonfar, R., Khosravi, H., Rafieemehr, H., Mirzaei, F., Dastan, D., Ghiasvand, M. R., Khorshidi, L., Pashaki, A. S. (2023) Radioprotective effect of Malva sylvestris L. against radiation-induced liver, kidney and intestine damages in rat: A histopathological study. Biochemistry and Biophysics Reports, 34, 101455.
  • [7] Aras, S., Efendioğlu, M., Wulamujiang, A., Ozkanli, S. S., Keleş, M. S., Tanzer, İ.O. (2021) Radioprotective effect of melatonin against radiotherapy-induced cerebral cortex and cerebellum damage in rat. International Journal of Radiation Biology, 97(3), 348-355.
  • [8] Kaplan, M., Demir, E., Yavuz, F., Kaplan, G. I., Taysi, M. R., Taysi, S., Sucu, M.M. (2022) Radioprotective effect of nigella sativa oil on heart tissues of rats exposed to irradition. International Journal of Cardiovascular Sciences, 35(2), 214-219.
  • [9] Zhang, J., He, X., Bai, X., Sun, Y., Jiang, P., Wang, X., Li, W., Zhang, Y. (2020) Protective effect of trimetazidine in radiation-induced cardiac fibrosis in mice. Journal of Radiation Research, 61(5), 657-665.
  • [10] Adaramoye, O., Okiti, O., Farombi, E. (2011) Dried fruit extract from Xylopiaaethiopica (Annonaceae) protects Wistar albino rats from adverse effects of whole body radiation. Experimental and Toxicologic Pathology, 63 (7-8), 635-39.
  • [11] Şener, G., Kabasakal, L., Atasoy, B.M., Erzik, C., Velioğlu-Öğünç, A, Çetinel, Ş., Contuk, G., Gedik, N., Yeğen, B.Ç. (2006) Propylthiouracil-induced hypothyroidism protects ionizing radiation-induced multiple organ damage in rats. Journal of Endocrinology, 189 (2), 257-62.
  • [12] Benzie, I.F. (2000) Evolution of antioxidant defence mechanisms. European Journal of Nutrition, 39, 53-61. [13] McCord, J.M. (2000) The evolution of free radicals and oxidative stress. The American Journal of Medicine, 108(8), 652-659.
  • [14] Ames, B.N. (2001) DNA damage from micronutrient deficiencies is likely to be a major cause of cancer. Mutation Research/Fundamental And Molecular Mechanisms Of Mutagenesis, 475(1-2), 7-20.
  • [15] Kasaian, J., Mohammadi, A. (2018) Biological activities of farnesiferol C: a review. Journal of Asian Natural Products Research, 20 (1), 27-35.
  • [16] Garg, S.S., Gupta, J., Sharma, S., Sahu, D. (2020) An insight into the therapeutic applications of coumarin compounds and their mechanisms of action. European Journal of Pharmaceutical Sciences, 152, 105424.
  • [17] Küpeli Akkol, E., Genç, Y., Karpuz, B., Sobarzo-Sánchez, E., & Capasso, R. (2020) Coumarins and coumarin-related compounds in pharmacotherapy of cancer. Cancers, 12 (7), 1959.
  • [18] Mazimba, O. (2017) Umbelliferone: Sources, chemistry and bioactivities review. Bulletin of Faculty of Pharmacy, Cairo University, 55 (2), 223-232.
  • [19] Althunibat, O. Y., Abduh, M. S., Abukhalil, M. H., Aladaileh, S. H., Hanieh, H., & Mahmoud, A. M. (2022) Umbelliferone prevents isoproterenol-induced myocardial injury by upregulating Nrf2/HO-1 signaling, and attenuating oxidative stress, inflammation, and cell death in rats. Biomedicine & Pharmacotherapy, 149, 112900.
  • [20] Dikmen, M. (2016) Antiproliferative and apoptotic effects of aprepitant on human glioblastoma U87MG cells. Marmara Pharmaceutical Journal, 21(1), 156-164.
  • [21] Mahmoud, A. M., Hozayen, W. G., Hasan, I. H., Shaban, E., & Bin-Jumah, M. (2019) Umbelliferone ameliorates CCl 4-induced liver fibrosis in rats by upregulating PPARγ and attenuating oxidative stress, inflammation, and TGF-β1/Smad3 signaling. Inflammation, 42, 1103-1116.
  • [22] Alotaibi, M. F., Al-Joufi, F., Abou Seif, H. S., Alzoghaibi, M. A., Djouhri, L., Ahmeda, A. F., Mahmoud, A. M. (2023) Umbelliferone Inhibits Spermatogenic Defects and Testicular Injury in Lead-Intoxicated Rats by Suppressing Oxidative Stress and Inflammation, and Improving Nrf2/HO-1 Signaling [Retraction]. Drug Design, Development and Therapy, 17, 1153-1154.
  • [23] Wang, H.Q., Wang, S.S., Chiufai, K., Wang, Q., Cheng, X.L. (2019) Umbelliferone ameliorates renal function in diabetic nephropathy rats through regulating inflammation and TLR/NF-kappaB pathway. Chinise Journal of Natural Medicine, 17(5), 346-354.
  • [24] Council, N.R. (2011) National Institutes of Health guide for the care and use of laboratory animals.
  • [25] Cruz, L. F., De-Figueiredo, G.F., Pedro, L.P., Amorin, Y.M., Andrade, J.T., Passos, T. F., Rodrigues, F. F., Souza, I.LA., Gonçalves, T.P.R., Dos Santos Lima, L.A.R., Ferreira, J.M.S., Freitas Araújo, M. G. (2020) Umbelliferone (7-hydroxycoumarin): A non-toxic antidiarrheal and antiulcerogenic coumarin. Biomedicine & Pharmacotherapy, 129, 110432.
  • [26] Sproull, M., Kramp, T., Tandle, A., Shankavaram, U., Camphausen, K. (2017) Multivariate analysis of radiation responsive proteins to predict radiation exposure in total-body irradiation and partial-body irradiation models. Radiation Research, 187 (2), 251-258.
  • [27] Jacobs, E. R., Narayanan, J., Fish, B. L., Gao, F., Harmann, L. M., Bergom, C., Tracy, G., Jennifer, S., Medhora, M. (2019) Cardiac remodeling and reversible pulmonary hypertension during pneumonitis in rats after 13-Gy partial-body irradiation with minimal bone marrow sparing: effect of lisinopril. Health physics, 116 (4), 558-565.
  • [28] Erel, O. (2004) A novel automated method to measure total antioxidant response against potent free radical reactions. Clinical Biochemistry, 37 (2), 112-119.
  • [29] Erel, O. (2005) A new automated colorimetric method for measuring total oxidant status. Clinical Biochemistry, 38 (12), 1103-1111.
  • [30] Akyazi, I., Eraslan, E., Gülçubuk, A., Ekiz, E. E., Çırakli, Z. L., Haktanir, D., Bala D.A., Özkurt, M., Matur, E., Özcan, M. (2013) Long-term aspirin pretreatment in the prevention of cerulein-induced acute pancreatitis in rats. World Journal of Gastroenterology, 19 (19), 2894-2903.
  • [31] Ping, Z., Peng, Y., Lang, H., Xinyong, C., Zhiyi, Z., Xiaocheng, W., Hong, Z., Liang, S. (2020) Oxidative stress in radiation‐induced cardiotoxicity. Oxidative Medicine and Cellular Longevity, 2020(1), 3579143.
  • [32] Armanious, M.A., Mohammadi, H., Khodor, S., Oliver, D.E., Johnstone, P.A., Fradley, M.G. (2018) Cardiovascular effects of radiation therapy. Current Problems in Cancer, 42 (4), 433–442.
  • [33] Puukila, S., Lemon, J. A., Lees, S. J., Tai, T.C., Boreham, D.R., Khaper, N. (2017) Impact of ionizing radiation on the cardiovascular system: a review. Radiation Research, 188 (4.2), 539–546.
  • [34] Vona, R., Gambardella, L., Cittadini, C., Straface, E., Pietraforte, D. (2019) Biomarkers of oxidative stress in metabolicsyndrome and associated diseases. Oxidative Medicine and Cellular Longevity, 1, 8267234,
  • [35] Karslioglu, I., Ertekin, M. V., Kocer, I., Taysi, S., Sezen, O., Gepdiremen, A., & Balci, E. (2004) Protective role of intramuscularly administered vitamin E on the levels of lipid peroxidation and the activities of antioxidant enzymes in the lens of rats made cataractous with gamma-irradiation. European Journal of Ophthalmology, 14(6), 478-485.
  • [36] Dilber, B., Akbulut, U. E., Alver, A., Menteşe, A., Kolaylı, C. C., & Cansu, A. (2021) Plasma and erytrocyte oxidative stress markers in children with frequent breath-holding spells. Klinische Pädiatrie, 233 (04), 173-180.
  • [37] Elahi, M.M., Kong, Y.X., Matata, B.M. (2009) Oxidative stress as a mediator of cardiovascular disease. Oxidative Medicine and Cellular Longevity, 2(5), 259-269.
  • [38] Zhang, C., Chen, H., Xie, H. H., Shu, H., Yuan, W. J., & Su, D. F. (2003) Inflammation is involved in the organ damage induced by sinoaortic denervation in rats. Journal of Hypertension, 21(11), 2141-2148.
  • [39] Luo, N., Zhu, W., Li, X., Fu, M., Peng, X., Yang, F., Zhang, Y., Yin, H., Yang, C., Zhao, J., Yuan, X., Hu, G. (2022) Impact of Gut Microbiota on Radiation-Associated Cognitive Dysfunction and Neuroinflammation in Mice. Radiation Research, 197 (4), 350-364.
  • [40] Guo, D.B., Zhu, X.Q., Li, Q.Q., Li, G.M., Ruan, G.P., Pang, R.Q., Chen, Y.H., Wang, Q., Wang, J.X., Liu, J.F., Chen, Q., Pan, X.H. (2018) Efficacy and mechanisms underlying the effects of allogeneic umbilical cord mesenchymal stem cell transplantation on acute radiation injury in tree shrews. Cytotechnology, 70 (5), 1447-1468.
  • [41] Brasier, A. R. (2010) The nuclear factor-κB–interleukin-6 signalling pathway mediating vascular inflammation. Cardiovascular Research, 86 (2), 211-218.
  • [42] Gan, J., Qian, W., Lin, S. (2018) Umbelliferone alleviates myocardial ischemia: the role of inflammation and apoptosis. Inflammation, 41, 464-473.
  • [43] Danborno, A.M., Monnet, P. L., Orr, A.J. (2020) TxA2 Receptor Antagonist (SQ29548) attenuates Endothelium-Independent recovery from Thromboxane A2 Contraction of Isolated Rabbit Aorta. Journal of African Association of Physiological Sciences, 8(1), 8-15.
  • [44] El-Benhawy, S. A., Morsi, M. I., El-Tahan, R. A., Matar, N. A., & Ehmaida, H. M. (2021) Radioprotective effect of thymoquinone in X-irradiated rats. Asian Pacific Journal of Cancer Prevention, 22(9), 3005.
  • [45] Sarhan, H., Naoum, L. (2020) Protective role of royal jelly against gamma radiation induced oxidative stress, cardio-toxicity and organ dysfunctions in male rats. The Egyptian Journal of Hospital Medicine, 78(1), 62-67.
  • [46] Hemnani, T., Parihar, M.S. (1998) Reactive oxygen species and oxidative DNA damage. Indian Journal of Physiology and Pharmacology, 42, 440-452.
Toplam 45 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Eczacılık Biyokimyası
Bölüm Makaleler
Yazarlar

Nurdan Dumlu 0009-0009-1658-6484

Fatime Geyikoğlu 0000-0003-2488-1757

Suat Çolak 0000-0001-8320-3038

Erken Görünüm Tarihi 27 Aralık 2024
Yayımlanma Tarihi 31 Aralık 2024
Gönderilme Tarihi 24 Eylül 2024
Kabul Tarihi 1 Kasım 2024
Yayımlandığı Sayı Yıl 2024 Cilt: 17 Sayı: 3

Kaynak Göster

APA Dumlu, N., Geyikoğlu, F., & Çolak, S. (2024). Radioprotective effect of Umbelliferon Against Radiation-Induced Myocardial Damages. Erzincan University Journal of Science and Technology, 17(3), 811-825. https://doi.org/10.18185/erzifbed.1555393