References
- Abdelmegui, N.E., Chmaisse, H.N., and Zeinab, N.S.A., 2010a. Protective effect of silymarin on cisplatin-induced nephrotoxicity in rats. Pakistan Journal of Nutrition, 9 (7), 624–636.
- Abdelmegui, N.E., Chmaisse, H.N., and Zeinab, N.S.A., 2010b. Silymarin ameliorates cisplatin-induced hepatotoxicity in rats: histopathological and ultrastructural studies. Pakistan Journal of Biological Sciences, 13 (10), 463–479.
- Abdullah, M.A., Abd, A.A., and Baker, S.A., 2018. A biochemical study of the effect of quercetin on cisplatin induced rat tissues toxicity. American Journal of Biochemistry, 8 (5), 87–92.
- Aebi, H., 1984. Catalase in vitro. Methods in Enzymology. 105, 121–126.
- Ali, R.I., and Ibrahim, M.A., 2018. Malathion induced testicular toxicity and oxidative damage in male mice: the protective effect of curcumin. Egyptian Journal of Forensic Sciences, 8 (1), 1–13.
- Arhoghro, E.M., Kpomah, D.E., and Uwakwe, A.A., 2012. Ocimum gratissimum aqueous extract enhances recovery in cisplatin-induced nephrotoxicity in albino wistar rats. Indian J Drugs & Diseases, 1 (5), 129–142.
- Attyah, A.M., and Ismail, S.H., 2012. Protective effect of ginger extract against cisplatin-induced hepatotoxicity and cardiotoxicity in rats. Iraqi Journal of Pharmaceutical Sciences, 21 (1), 27–33.
- Azarbarz, N., et al., 2020. Assessment of the effect of sodium hydrogen sulfide (hydrogen sulfide donor) on cisplatin-induced testicular toxicity in rats. Environmental Science and Pollution Research International, 27 (8), 8119–8128.
- Bentli, R., et al., 2013. Molsidomine prevents cisplatin-induced hepatotoxicity. Archives of Medical Research, 44 (7), 521–528.
- Bhalchandra, W., and Alqadhi, Y.A., 2019. Royal jelly and honey ameliorates cisplatin induced alterations in biomarker levels of oxidative stress in kidney of rat. Indian Journal of Public Health, 10 (2), 1053.
- Bilgic, Y., et al., 2018. Protective effect of dexpanthenol against cisplatin‑induced hepatotoxicity. Experimental and Therapeutic Medicine, 16 (5), 4049–4057.
- Bradford, M.M., 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72, 248–254.
- Cao, B.-B., et al., 2018. Effect of cisplatin on the clock genes expression in the liver, heart and kidney. Biochemical and Biophysical Research Communications, 501 (2), 593–597.
- Corsello, T., Komaravelli, N., and Casola, A., 2018. Role of hydrogen sulfide in NRF2-and sirtuin-dependent maintenance of cellular redox balance. Antioxidants, 7 (10), 129.
- Du, S., et al., 2018. Protective mechanism of hydrogen sulfide against chemotherapy-induced cardiotoxicity. Frontiers in Pharmacology, 9, 32. DOI
- Dugbartey, G.J., et al., 2016. Hydrogen sulfide: a novel nephroprotectant against cisplatin-induced renal toxicity. Nitric Oxide: Biology and Chemistry, 57, 15–20.
- El-Sawalhi, M.M., and Ahmed, L.A., 2014. Exploring the protective role of apocynin, a specific NADPH oxidase inhibitor, in cisplatin-induced cardiotoxicity in rats. Chemico-Biological Interactions, 207, 58–66.
- Fard, A., et al., 2013. Effects of hydrogen sulfide on oxidative stress, tnf-α level and kidney histological changes in cisplatin nephro-toxicity in rat. Journal of Physiology and Pharmacology Advances, 3 (3), 57–65.
- Gao, C., et al., 2018. Neuroprotective effects of hydrogen sulfide on sodium azide-induced oxidative stress in PC12 cells. International Journal of Molecular Medicine, 41 (1), 242–250.
- Gaona-Gaona, L., et al., 2011. Protective effect of sulforaphane pretreatment against cisplatin-induced liver and mitochondrial oxidant damage in rats. Toxicology, 286 (1–3), 20–27.
- Guo, R., et al., 2013. Exogenous hydrogen sulfide protects against doxorubicin-induced inflammation and cytotoxicity by inhibiting p38MAPK/NFκB pathway in H9c2 cardiac cells. Cellular Physiology and Biochemistry, 32 (6), 1668–1680.
- Ibrahim, M.A., et al., 2019. Cardioprotective effect of green tea extract and vitamin E on Cisplatin-induced cardiotoxicity in mice: toxicological, histological and immunohistochemical studies. Biomedecine & Pharmacotherapie [Biomedicine & Pharmacotherapy], 113, 108731.
- Ijaz, M.U., et al., 2020. Remedial effects of casticin as an antioxidant on cisplatin induced oxidative damage in rat liver. Journal of King Saud University-Science, 32 (1), 1100–1105.
- Kalbolandi, S.M., et al., 2019. Luteolin confers renoprotection against ischemia–reperfusion injury via involving Nrf2 pathway and regulating miR320. Molecular Biology Reports, 46 (4), 4039–4047.
- Karimi, A., et al., 2017. Sodium hydrogen sulfide (NaHS) ameliorates alterations caused by cisplatin in filtration slit diaphragm and podocyte cytoskeletal in rat kidney. Journal of Nephropathology, 6 (3), 150–156.
- Khan, R., et al., 2012. Chrysin protects against cisplatin-induced colon. toxicity via amelioration of oxidative stress and apoptosis: probable role of p38MAPK and p53. Toxicology and Applied Pharmacology, 258 (3), 315–329.
- Kimura,H., Production and physiological effects of hydrogen sulfide. Antioxidants & Redox Signaling, 20 (5), 783–793.
- Nasr, A.Y., and Saleh, H.A.M., 2014. Aged garlic extract protects against oxidative stress and renal changes in cisplatin-treated adult male rats. Cancer Cell International, 14 (1), 92.
- Ohkawa, H., Ohishi, N., and Yagi, K., 1979. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry, 95 (2), 351–358.
- Pan, Z., et al., 2019. Hydrogen sulfide protects against high glucose‑induced lipid metabolic disturbances in 3T3‑L1 adipocytes via the AMPK signaling pathway. Molecular Medicine Reports, 20 (5), 4119–4124.
- Pecorelli, A., et al., 2013. NRF2 activation is involved in ozonated human serum upregulation of HO-1 in endothelial cells. Toxicology and Applied Pharmacology, 267 (1), 30–40.
- Rafiee, Z., et al., 2021. p-Coumaric acid alleviates adriamycin-induced hepatotoxicity in rats. Asian Pacific Journal of Tropical Biomedicine, 11 (3), 115.
- Ramesh, G., and Reeves, W.B., 2002. TNF-α mediates chemokine and cytokine expression and renal injury in cisplatin nephrotoxicity. Journal of Clinical Investigation, 110 (6), 835–842.
- Rjiba-Touati, K., et al., 2012. Recombinant human erythropoietin prevents cisplatin-induced genotoxicity in rat liver and heart tissues via an antioxidant process. Drug and Chemical Toxicology, 35 (2), 134–140.
- Ruan, Z., et al., 2020. Exogenous hydrogen sulfide protects fatty liver against ischemia–reperfusion injury by regulating endoplasmic reticulum stress‐induced autophagy in macrophage through mediating the class A scavenger receptor pathway in rats. Cell Biology International, 44 (1), 306–316.
- Shimizu, Y., et al., 2018. Hydrogen sulfide regulates cardiac mitochondrial biogenesis via the activation of AMPK. Journal of Molecular and Cellular Cardiology, 116, 29–40.
- Su, Y.-W., et al., 2009. Hydrogen sulfide regulates cardiac function and structure in adriamycin-induced cardiomyopathy. Circulation Journal, 73 (4), 741–749.
- Tan, G., et al., 2011. Hydrogen sulfide attenuates carbon tetrachloride-induced hepatotoxicity, liver cirrhosis and portal hypertension in rats. PLOS One, 6 (10), e25943.
- Yadav, Y.C., et al., 2010. Nephropharmacological activity of ethanolic extract Lepidium sativum L. Seeds in albino rats using cisplatin induced acute renal failure. International Journal of Pharmaceutical Science Review Research, 4 (3), 64–68. www.globalresearchonline.net.
- Yao, X., et al., 2007. Cisplatin nephrotoxicity: a review. The American Journal of the Medical Sciences, 334 (2), 115–124.
- Yousef, M.I., Saad, A.A., and El-Shennawy, L.K., 2009. Protective effect of grape seed proanthocyanidin extract against oxidative stress induced by cisplatin in rats. Food and Chemical Toxicology, 47 (6), 1176–1183.
- Yüce, A., et al., 2007. Ellagic acid prevents cisplatin‐induced oxidative stress in liver and heart tissue of rats. Basic & Clinical Pharmacology & Toxicology, 101 (5), 345–349.
- Zhou, J., et al., 2018. GYY4137 promotes mice feeding behavior via arcuate nucleus sulfur-sulfhydrylation and AMPK activation. Frontiers in Pharmacology, 9, 966.