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Year 2023, Volume: 53 Issue: 1, 73 - 79, 28.04.2023

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References

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  • Abdel-Raheem, I.T. (2010). Gastroprotective effect of rutin against indomethacin-induced ulcers in rats. Basic & Clinical Pharmacol- ogy & Toxicology, 107(3), 742-750. https://doi.org/10.1111/j.1742- 7843.2010.00568.x
  • Aebi, H. (1984). Catalase in vitro. Methods in Enzymology, 105, 121- 126. https://doi.org/10.1016/S0076-6879(84)05016-3
  • Ali, S.S., Ahsan, H., Zia, M.K., Siddiqui, T., & Khan, F.H. (2020). Un- derstanding oxidants and antioxidants: Classical team with new players. Journal of Food Biochemistry, 44:e13145. https://doi. org/10.1111/jfbc.13145
  • Atalay, F., Odabasoglu, F., Halici, M., Cadirci, E., Aydin, O., Halici, Z., & Cakir, A. (2016). N-acetyl cysteine has both gastro-protective and anti-inflammatory effects in experimental rat models: Its gastro-protective effect is related to its in vivo and in vitro antioxidant properties. Journal of Cellular Biochemistry, 117(2), 308-319. https://doi.org/10.1002/jcb.25193
  • Assi, M. (2017). The differential role of reactive oxygen species in early and late stages of cancer. American Journal of Physiology- Regulatory, Integrative and Comparative Physiology, 313, R646- R653. https://doi.org/10.1152/ajpregu.00247.2017
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  • Banerjee, D., Maity, B., Nag, S.K., Bandyopadhyay, S.K., & Chatto- padhyay, S. (2008). Healing potential of Picrorhiza kurroa (Scrofu- lariaceae) rhizomes against indomethacin-induced gastric ulcer- ation: a mechanistic exploration. BMC Complementary Medicine and Therapies, 8:3. https://doi.org/10.1186/1472-6882-8-3
  • Basivireddy, J., Jacob, M., & Balasubramanian, K.A. (2005). Indo- methacin induces free radical-mediated changes in renal brush border membranes. Archives of Toxicology, 79, 441-450. https:// doi.org/10.1007/s00204-005-0658-4
  • Bayrak, B.B., Arda-Pirincci, P., Bolkent, S., & Yanardag, R. (2021). Zinc prevents ethanol-induced oxidative damage in tongue tissues of rats. Biological Trace Element Research, https://doi.org/10.1007/ s12011-021-02682-6
  • Ben Amara, I., Soudani, N., Troudi, A., Bouaziz, H., Boudawara, T., & Zeghal, N. (2011). Antioxidant effect of vitamin E and selenium on hepatotoxicity induced by dimethoate in female adult rats. Ecotoxicology and Environmental Safety, 74, 811-819. https://doi. org/10.1016/j.ecoenv.2010.11.007
  • Beutler, E. (1975). Glutathione in Red Cell Metabolism, A Manual of Bio- chemical Methods, 2nd ed., Grune and Stratton, New York, p 112.
  • Bindu, S., Mazumder, S., & Bandyopadhyay, U. (2020). Non-steroi- dal anti-inflammatory drugs (NSAIDs) and organ damage: A cur- rent perspective. Biochemical Pharmacology, 180, 114147. https:// doi.org/10.1016/j.bcp.2020.114147
  • Cai, Z., Zhang, J., & Li, H. (2019). Selenium, aging and aging-related diseases. Aging Clinical and Experimental Research, 31, 1035-1047. https://doi.org/10.1007/s40520-018-1086-7
  • Chattopadhyay, I., Bandyopadhyay, U., Biswas, K., Maity, P., & Ba- nerjee, R.K. (2006). Indomethacin inactivates gastric peroxidase to induce reactive-oxygen-mediated gastric mucosal injury and curcumin protects it by preventing peroxidase inactivation and scavenging reactive oxygen. Free Radical Biology and Medicine, 40, 1397–1408. https://doi.org/10.1016/j.freeradbiomed.2005.12.01678
  • Ching, T.L., Haenen, G.R., & Bast, A. (1993). Cimetidine and other H2 receptor antagonists as powerful hydroxyl radical scaven- gers. Chemico-Biological Interactions, 86, 119–127. https://doi. org/10.1016/0009-2797(93)90116-G
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  • Dragnev, K.H., Rigas, J.R., & Dmitrovsky, E. (2000). The retinoids and cancer prevention mechanisms. The Oncologist, 5, 361-368. https://doi.org/10.1634/theoncologist.5-5-361
  • Eraslan, E., Tanyeli, A., Güler, M.C., Kurt, N., & Yetim, Z. (2020). Agomelatine prevents indomethacin-induced gastric ul- cer in rats. Pharmacological Reports, 72, 984-991. https://doi. org/10.1007/s43440-019-00049-2
  • Gill, M., Sanyal, S.N., & Sareen, M.L. (1991). Interaction of H2-re- ceptor antagonists, cimetidine and ranitidine with microsomal drug metabolizing and other systems in liver. Indian Journal of Experimental Biology, 9, 852-856. https://pubmed.ncbi.nlm.nih. gov/1794870/
  • Guillin, O.M., Vindry, C., Ohlmann, T., & Chavatte, L. (2019). Seleni- um, selenoproteins and viral infection. Nutrients, 11, 2101. https:// doi.org/10.3390/nu11092101
  • Habig, W.H., & Jakoby, W.B. (1981). Assays of differentiation of glutathione S-transferases. Methods in Enzymology, 77, 398-405. https://doi.org/10.1016/S0076-6879(81)77053-8
  • Hariharan, S., & Dharmaraj, S. (2020). Selenium and selenopro- teins: it’s role in regulation of inflammation. Inflammopharmacol- ogy, 28, 667-695. https://doi.org/10.1007/s10787-020-00690-x
  • Jomova, K., & Valko, M. (2011). Advances in metal-induced oxida- tive stress and human disease. Toxicology, 283, 65-87. https://doi. org/10.1016/j.tox.2011.03.001
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Antioxidants prevent indomethacin-induced oxidative damage in tongue tissues of rats

Year 2023, Volume: 53 Issue: 1, 73 - 79, 28.04.2023

Abstract

Background and Aims: Indomethacin (Indo) is an important nonsteroidal anti-inflammatory drug that has beneficial effects as a pain killer, but also has side effects. In this study, the protective effects of vitamins, selenium and ranitidine (Ran) against the side effects of Indo on tongue tissue were investigated.
Methods: Rats were divided into six groups: the control group as group I; the group given a vitamin-selenium (Vitamin C, 100 mg/kg; Vitamin E, 100 mg/kg, beta carotene, 15 mg/kg, selenium, 0.2 mg/kg) combination as group II; the group treated with Indo as group III; the group administered vitamins-selenium and Indo (25 mg/kg, single dose) as group IV; the group given Ran (150 mg/kg) as group V; and the group given Ran and Indo as group VI. The experiments were done for 3 days. Animals received vitamins-selenium and Ran for 3 days, 2 h before the Indo administration (in same dose and time). Tongue tissues were taken and homogenized.
Results: In the supernatants, glutathione levels, superoxide dismutase, catalase and glutathione-dependent enzyme activi- ties were reduced. Protein carbonyl, lipid peroxidation levels, lactate dehydrogenase and myeloperoxidase activities were increased in the group that was given Indo. Administration of vitamins-selenium and Ran reversed the levels and activities of the tested parameter in the Indo group.
Conclusion: We suggest that vitamins, selenium and Ran have powerful protective effects on Indo-induced tongue injury in rats.

References

  • Abdallah, D.M. (2010). Nicotinamide alleviates indomethacin- induced gastric ulcers: a novel antiulcer agent. European Journal of Pharmacolology, 627(1-3), 276-280. https://doi.org/10.1016/j. ejphar.2009.10.037
  • Abdel-Raheem, I.T. (2010). Gastroprotective effect of rutin against indomethacin-induced ulcers in rats. Basic & Clinical Pharmacol- ogy & Toxicology, 107(3), 742-750. https://doi.org/10.1111/j.1742- 7843.2010.00568.x
  • Aebi, H. (1984). Catalase in vitro. Methods in Enzymology, 105, 121- 126. https://doi.org/10.1016/S0076-6879(84)05016-3
  • Ali, S.S., Ahsan, H., Zia, M.K., Siddiqui, T., & Khan, F.H. (2020). Un- derstanding oxidants and antioxidants: Classical team with new players. Journal of Food Biochemistry, 44:e13145. https://doi. org/10.1111/jfbc.13145
  • Atalay, F., Odabasoglu, F., Halici, M., Cadirci, E., Aydin, O., Halici, Z., & Cakir, A. (2016). N-acetyl cysteine has both gastro-protective and anti-inflammatory effects in experimental rat models: Its gastro-protective effect is related to its in vivo and in vitro antioxidant properties. Journal of Cellular Biochemistry, 117(2), 308-319. https://doi.org/10.1002/jcb.25193
  • Assi, M. (2017). The differential role of reactive oxygen species in early and late stages of cancer. American Journal of Physiology- Regulatory, Integrative and Comparative Physiology, 313, R646- R653. https://doi.org/10.1152/ajpregu.00247.2017
  • Bacchi, S., Palumbo, P., Sponta, A., & Coppolino, M.F. (2012). Clinical pharmacology of non-steroidal anti-in- flammatory drugs: a review. Anti-Inflammatory & Anti-Al- lergy Agents in Medicinal Chemistry, 11, 52-64. https://doi. org/10.2174/187152312803476255
  • Baek, M.K., Lee, H., Kim, K.O., Kwon, H.J., Chung, M.H., Park, H.M.,…, Kim, D.Y. (2017). Age-related changes in nuclear factor ery- throid 2-related factor 2 and reactive oxygen species and mi- tochondrial structure in the tongues of fischer 344 rats. Clinical and Experimental Otorhinolaryngology, 10, 357-362. https://doi. org/10.21053/ceo.2016.01095
  • Bais, R., & Philcox, M. (1994). Approved recommendation on IFCC methods for the measurement of catalytic concentration of en- zymes. Part 8. IFCC method for lactate dehydrogenase (I-Lactate: NAD+Oxidoreductase, EC 1.1.1.27). International Federation of Clinical Chemistry (IFCC), European Journal of Clinical Chemistry and Clinical Biochemistry, 32, 639-655. https://pubmed.ncbi.nlm. nih.gov/7819436/
  • Baker, M., & Perazella, M.A. (2020). NSAIDs in CKD: Are they safe? American Journal of Kidney Diseases, 76, 546-557. https://doi. org/10.1053/j.ajkd.2020.03.023
  • Banerjee, D., Maity, B., Nag, S.K., Bandyopadhyay, S.K., & Chatto- padhyay, S. (2008). Healing potential of Picrorhiza kurroa (Scrofu- lariaceae) rhizomes against indomethacin-induced gastric ulcer- ation: a mechanistic exploration. BMC Complementary Medicine and Therapies, 8:3. https://doi.org/10.1186/1472-6882-8-3
  • Basivireddy, J., Jacob, M., & Balasubramanian, K.A. (2005). Indo- methacin induces free radical-mediated changes in renal brush border membranes. Archives of Toxicology, 79, 441-450. https:// doi.org/10.1007/s00204-005-0658-4
  • Bayrak, B.B., Arda-Pirincci, P., Bolkent, S., & Yanardag, R. (2021). Zinc prevents ethanol-induced oxidative damage in tongue tissues of rats. Biological Trace Element Research, https://doi.org/10.1007/ s12011-021-02682-6
  • Ben Amara, I., Soudani, N., Troudi, A., Bouaziz, H., Boudawara, T., & Zeghal, N. (2011). Antioxidant effect of vitamin E and selenium on hepatotoxicity induced by dimethoate in female adult rats. Ecotoxicology and Environmental Safety, 74, 811-819. https://doi. org/10.1016/j.ecoenv.2010.11.007
  • Beutler, E. (1975). Glutathione in Red Cell Metabolism, A Manual of Bio- chemical Methods, 2nd ed., Grune and Stratton, New York, p 112.
  • Bindu, S., Mazumder, S., & Bandyopadhyay, U. (2020). Non-steroi- dal anti-inflammatory drugs (NSAIDs) and organ damage: A cur- rent perspective. Biochemical Pharmacology, 180, 114147. https:// doi.org/10.1016/j.bcp.2020.114147
  • Cai, Z., Zhang, J., & Li, H. (2019). Selenium, aging and aging-related diseases. Aging Clinical and Experimental Research, 31, 1035-1047. https://doi.org/10.1007/s40520-018-1086-7
  • Chattopadhyay, I., Bandyopadhyay, U., Biswas, K., Maity, P., & Ba- nerjee, R.K. (2006). Indomethacin inactivates gastric peroxidase to induce reactive-oxygen-mediated gastric mucosal injury and curcumin protects it by preventing peroxidase inactivation and scavenging reactive oxygen. Free Radical Biology and Medicine, 40, 1397–1408. https://doi.org/10.1016/j.freeradbiomed.2005.12.01678
  • Ching, T.L., Haenen, G.R., & Bast, A. (1993). Cimetidine and other H2 receptor antagonists as powerful hydroxyl radical scaven- gers. Chemico-Biological Interactions, 86, 119–127. https://doi. org/10.1016/0009-2797(93)90116-G
  • de Araújo, E.R.D., Guerra, G.C.B., Araújo, D.F.S., de Araújo, A.A., Fernandes, J.M., de Araújo Júnior, R.F., …., Zucolotto, S.M. (2018). Gastroprotective and antioxidant activity of Kalanchoe brasiliensis and Kalanchoe pinnata leaf juices against indomethacin and eth- anol-induced gastric lesions in rats. International Journal of Mo- lecular Sciences, 19, 1265. https://doi.org/10.3390/ijms19051265
  • Dragnev, K.H., Rigas, J.R., & Dmitrovsky, E. (2000). The retinoids and cancer prevention mechanisms. The Oncologist, 5, 361-368. https://doi.org/10.1634/theoncologist.5-5-361
  • Eraslan, E., Tanyeli, A., Güler, M.C., Kurt, N., & Yetim, Z. (2020). Agomelatine prevents indomethacin-induced gastric ul- cer in rats. Pharmacological Reports, 72, 984-991. https://doi. org/10.1007/s43440-019-00049-2
  • Gill, M., Sanyal, S.N., & Sareen, M.L. (1991). Interaction of H2-re- ceptor antagonists, cimetidine and ranitidine with microsomal drug metabolizing and other systems in liver. Indian Journal of Experimental Biology, 9, 852-856. https://pubmed.ncbi.nlm.nih. gov/1794870/
  • Guillin, O.M., Vindry, C., Ohlmann, T., & Chavatte, L. (2019). Seleni- um, selenoproteins and viral infection. Nutrients, 11, 2101. https:// doi.org/10.3390/nu11092101
  • Habig, W.H., & Jakoby, W.B. (1981). Assays of differentiation of glutathione S-transferases. Methods in Enzymology, 77, 398-405. https://doi.org/10.1016/S0076-6879(81)77053-8
  • Hariharan, S., & Dharmaraj, S. (2020). Selenium and selenopro- teins: it’s role in regulation of inflammation. Inflammopharmacol- ogy, 28, 667-695. https://doi.org/10.1007/s10787-020-00690-x
  • Jomova, K., & Valko, M. (2011). Advances in metal-induced oxida- tive stress and human disease. Toxicology, 283, 65-87. https://doi. org/10.1016/j.tox.2011.03.001
  • Kajarabille, N., & Latunde-Dada, G.O. (2019). Programmed cell- death by ferroptosis: Antioxidants as mitigators. International Journal of Molecular Sciences, 20, 4968. https://doi.org/10.3390/ ijms20194968
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There are 60 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Original Article
Authors

İsmet Burcu Turkyilmaz 0000-0003-2789-5943

Refiye Yanardağ 0000-0003-4185-4363

Publication Date April 28, 2023
Submission Date August 25, 2021
Published in Issue Year 2023 Volume: 53 Issue: 1

Cite

APA Turkyilmaz, İ. B., & Yanardağ, R. (2023). Antioxidants prevent indomethacin-induced oxidative damage in tongue tissues of rats. İstanbul Journal of Pharmacy, 53(1), 73-79.
AMA Turkyilmaz İB, Yanardağ R. Antioxidants prevent indomethacin-induced oxidative damage in tongue tissues of rats. iujp. April 2023;53(1):73-79.
Chicago Turkyilmaz, İsmet Burcu, and Refiye Yanardağ. “Antioxidants Prevent Indomethacin-Induced Oxidative Damage in Tongue Tissues of Rats”. İstanbul Journal of Pharmacy 53, no. 1 (April 2023): 73-79.
EndNote Turkyilmaz İB, Yanardağ R (April 1, 2023) Antioxidants prevent indomethacin-induced oxidative damage in tongue tissues of rats. İstanbul Journal of Pharmacy 53 1 73–79.
IEEE İ. B. Turkyilmaz and R. Yanardağ, “Antioxidants prevent indomethacin-induced oxidative damage in tongue tissues of rats”, iujp, vol. 53, no. 1, pp. 73–79, 2023.
ISNAD Turkyilmaz, İsmet Burcu - Yanardağ, Refiye. “Antioxidants Prevent Indomethacin-Induced Oxidative Damage in Tongue Tissues of Rats”. İstanbul Journal of Pharmacy 53/1 (April 2023), 73-79.
JAMA Turkyilmaz İB, Yanardağ R. Antioxidants prevent indomethacin-induced oxidative damage in tongue tissues of rats. iujp. 2023;53:73–79.
MLA Turkyilmaz, İsmet Burcu and Refiye Yanardağ. “Antioxidants Prevent Indomethacin-Induced Oxidative Damage in Tongue Tissues of Rats”. İstanbul Journal of Pharmacy, vol. 53, no. 1, 2023, pp. 73-79.
Vancouver Turkyilmaz İB, Yanardağ R. Antioxidants prevent indomethacin-induced oxidative damage in tongue tissues of rats. iujp. 2023;53(1):73-9.