Evaluation of possible protective role of Chrysin against arsenic-induced nephrotoxicity in rats

References

• Ahad, A., et al., 2014. Chrysin, an anti-inflammatory molecule, abrogates renal dysfunction in type 2 diabetic rats. Toxicology and applied pharmacology, 279 (1), 1–7.
   PubMed Web of Science ®Google Scholar
• Ahmad, L., et al., 2021. The effect of different repeated doses of cypermethrin on the behavioral and histological alterations in the brain of rabbits (Oryctolagus cuniculi). International journal of veterinary science, 10, 347–354.
   Google Scholar
• Ahmed, H.H., et al., 2021. Efficacy of melatonin against oxidative stress, DNA damage and histopathological changes induced by nicotine in liver and kidneys of male rats. International journal of veterinary science, 10, 31–36.
   Google Scholar
• Ali, B.H., et al., 2015. Ameliorative effect of chrysin on adenine-induced chronic kidney disease in rats. PLoS One, 10 (4), e0125285.
   PubMed Web of Science ®Google Scholar
• Anwar-Mohamed, A., et al., 2012. Differential modulation of aryl hydrocarbon receptor regulated enzymes by arsenite in the kidney, lung, and heart of C57BL/6 mice. Archives of toxicology, 86 (6), 897–910.
   PubMed Web of Science ®Google Scholar
• Aydin, B., et al., 2011. The antioxidant and antigenotoxic effects of pycnogenol(®) on rats treated with cisplatin. Biological trace element research, 142 (3), 638–650.
   PubMed Web of Science ®Google Scholar
• Azqueta, A., et al., 2013. Measurement of DNA base and nucleotide excision repair activities in mammalian cells and tissues using the comet assay-a methodological overview. DNA repair, 12 (11), 1007–1010.
   PubMed Web of Science ®Google Scholar
• Baş, H., Pandır, D., and Kalender, S., 2016. Furan-induced hepatotoxic and hematologic changes in diabetic rats: the protective role of lycopene. Arhiv za Higijenu Rada i Toksikologiju, 67 (3), 194–202.
   PubMed Web of Science ®Google Scholar
• Bhuyan, B., 2011. Assessment of arsenic and iron contamination of groundwater in four development blocks of Lakhimpur District, Assam, India. Der Chemica Sinica, 2 (4), 316–323.
   Google Scholar
• Cárdenas-González, M., et al., 2016. Environmental exposure to arsenic and chromium in children is associated with kidney injury molecule-1. Environmental research, 150, 653–662.
   PubMed Web of Science ®Google Scholar
• Chance, B., and Maehly, A.C., 1995. Assay of catalase and peroxidase. Methods in enzymology, 2, 764–775.
   Web of Science ®Google Scholar
• Ciftci, O., et al., 2012. Beneficial effects of chrysin on the reproductive system of adult male rats. Andrologia, 44 (3), 181–186.
   PubMed Web of Science ®Google Scholar
• Dangleben, N.L., Skibola, C.F., and Smith, M.T., 2013. Arsenic immunotoxicity: a review. Environmental health, 12 (1), 15–73.
   PubMedGoogle Scholar
• Das, A.K., et al., 2010. Protective effect of Corchorus olitorius leaves on sodium arsenic induced toxicity in experimental rats. Food and chemical toxicology, 48 (1), 326–335.
   PubMed Web of Science ®Google Scholar
• Dasheng, L.I., et al., 2001. Arsenic induces DNA damage via reactive oxygen species in human cells. Environmental health and preventive medicine, 6 (1), 27–32.
   PubMedGoogle Scholar
• Dhawan, A., Bajpayee, M., and Parmar, D., 2009. Comet assay: a reliable tool for the assessment of DNA damage in different models. Cell biology and toxicology, 25 (1), 5–32.
   PubMed Web of Science ®Google Scholar
• Ellman, G.L., 1959. Tissue sulfhydryl groups. Archives of biochemistry and biophysics, 82 (1), 70–77.
   PubMed Web of Science ®Google Scholar
• Guillamet, E., 2004. In vitro DNA damage by arsenic compounds in a human lymphoblastoid cell line (TK6) assessed by the alkaline Comet assay. Mutagenesis, 19 (2), 129–135.
   PubMed Web of Science ®Google Scholar
• Gul, S.T., et al., 2020. Toxico-pathological effects of thiamethoxam on hemato-biochemical and productive performance of commercial laying hens. Pakistan veterinary journal, 40 (4), 449–454.
   Web of Science ®Google Scholar
• Hall, A.H., 2002. Chronic arsenic poisoning. Toxicology letters, 128 (1–3), 69–72.
   PubMed Web of Science ®Google Scholar
• Hayashi, I., et al., 2007. High-throughput spectrophotometric assay of reactive oxygen species in serum. Mutation research/genetic toxicology and environmental mutagenesis, 631 (1), 55–61.
   PubMed Web of Science ®Google Scholar
• He, J., et al., 2012. In vitro and in vivo antioxidant activity of the ethanolic extract from Meconopsis quintuplinervia. Journal of ethnopharmacology, 141 (1), 104–110.
   PubMed Web of Science ®Google Scholar
• Hei, T.K., Liu, S.X., and Waldren, C., 1998. Mutagenicity of arsenic in mammalian cells: role of reactive oxygen species. Proceedings of the national academy of sciences of the United States of America, 95 (14), 8103–8107.
   PubMed Web of Science ®Google Scholar
• Hughes, F.M., 2006. Biomarkers of exposure: a case study with inorganic arsenic. Environmental health perspectives, 114 (11), 1790–1796.
   PubMed Web of Science ®Google Scholar
• Iqbal, M., et al., 1996. Glutathione metabolizing enzymes and oxidative stress in ferric nitrilotriacetate (Fe-NTA) mediated hepatic injury. Redox report, 2 (6), 385–391.
   PubMed Web of Science ®Google Scholar
• Izuta, H., et al., 2008. Protective effects of Chinese propolis and its component, chrysin, against neuronal cell death via inhibition of mitochondrial apoptosis pathway in SH-SY5Y cells. Journal of agricultural and food chemistry, 56 (19), 8944–8953.
   PubMed Web of Science ®Google Scholar
• Jiang, Y., et al., 2014. Chrysin suppressed inflammatory responses and the inducible nitric oxide synthase pathway after spinal cord injury in rats. International journal of molecular sciences, 15 (7), 12270–12279.
   PubMed Web of Science ®Google Scholar
• Jin, Y., et al., 2017. Urinary kidney injury molecule-1 as an early diagnostic biomarker of obstructive acute kidney injury and development of a rapid detection method. Molecular medicine reports, 15 (3), 1229–1235.
   PubMed Web of Science ®Google Scholar
• Kakkar, P., Das, B., and Viswanathan, P.N., 1984. A modified spectrophotometric assay of superoxide dismutase. Indian journal of biochemistry & biophysics, 21 (2), 130–132.
   PubMed Web of Science ®Google Scholar
• Kandemir, F.M., et al., 2018. Therapeutic efficacy of zingerone against vancomycin-induced oxidative stress, inflammation, apoptosis and aquaporin 1 permeability in rat kidney. Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie, 105, 981–991.
   PubMed Web of Science ®Google Scholar
• Kasala, E.R., et al., 2015. Chemopreventive and therapeutic potential of chrysin in cancer: mechanistic perspectives. Toxicology letters, 233 (2), 214–225.
   PubMed Web of Science ®Google Scholar
• Khan, R.A., et al., 2010. Prevention of CCl4-induced nephrotoxicity with Sonchus asper in rat. Food and chemical toxicology, 48 (8–9), 2469–2476.
   PubMed Web of Science ®Google Scholar
• Khoo, B.Y., Chua, S.L., and Balaram, P., 2010. Apoptotic effects of chrysin in human cancer cell lines. International journal of molecular sciences, 11 (5), 2188–2199.
   PubMed Web of Science ®Google Scholar
• Kim, S. J., 2014. Herbal chrysanthemi flos, oxidative damage and protection against diabetic complications. In: Diabetes: oxidative stress and dietary antioxidants. Cambridge: Academic Press, 201–211.
   Google Scholar
• Kligerman, A.D., Malik, S.I., and Campbell, J.A., 2010. Cytogenetic insights into DNA damage and repair of lesions induced by a monomethylated trivalent arsenical. Mutation research, genetic toxicology and environmental mutagenesis, 695 (1–2), 2–8.
   Web of Science ®Google Scholar
• Korany, R.M.S., et al., 2019. Pathological and immunohistochemical studies on the ameliorating effect of Spirulina platensis against arsenic induced reproductive toxicity in female albino rats. International journal of veterinary science, 8, 113–119.
   Google Scholar
• Latif, M., 2020. Study of oxidative stress and histo-biochemical biomarkers of diethyl phthalate induced toxicity in a cultureable fish. Pakistan veterinary journal, 40 (02), 202–208.
   Google Scholar
• Lei, L., et al., 2018. Value of urinary KIM-1 and NGAL combined with serum Cys C for predicting acute kidney injury secondary to decompensated cirrhosis. Scientific reports, 8 (1), 1–9.
   PubMedGoogle Scholar
• Luo, Q.H., et al., 2016. Evaluation of KIM-1 and NGAL as early indicators for assessment of gentamycin-induced nephrotoxicity in vivo and in vitro. Kidney & blood pressure research, 41 (6), 911–918.
   PubMed Web of Science ®Google Scholar
• Malak, N.M.L., et al., 2020. Using histological and chemical methods for detection of unauthorized tissues addition in emulsion type meat product. International journal of veterinary science, 9, 438–442.
   Google Scholar
• Malhotra, R., and Siew, E.D., 2017. Biomarkers for the early detection and prognosis of acute kidney injury. Clinical journal of the American society of nephrology, 12 (1), 149–173.
   PubMed Web of Science ®Google Scholar
• Mandal, B.K., and Suzuki, K.T., 2002. Arsenic round the world: a review. Talanta, 58 (1), 201–235.
   PubMed Web of Science ®Google Scholar
• Manzolli, E.S., et al., 2015. Protective effects of the flavonoid chrysin against methylmercury-induced genotoxicity and alterations of antioxidant status, in vivo. Oxidative medicine and cellular longevity, 2015, 1–7.
   Web of Science ®Google Scholar
• Mehrzadi, S., et al., 2018. Ellagic acid: a promising protective remedy against testicular toxicity induced by arsenic. Biomedicine & pharmacotherapy = biomedecine & pharmacotherapie, 103, 1464–1472.
   PubMed Web of Science ®Google Scholar
• Melekoglu, R., et al., 2018. The protective effects of glycyrrhetinic acid and chrysin against ischemia-reperfusion injury in rat ovaries. BioMed research international, 2018, 5421308.
   PubMed Web of Science ®Google Scholar
• Messarah, M., et al., 2012. Hepatoprotective role and antioxidant capacity of selenium on arsenic-induced liver injury in rats. Experimental and toxicologic pathology, 64 (3), 167–174.
   PubMedGoogle Scholar
• Mujahid, Q., et al., 2021. Allethrin induced toxicopathological alterations in adult male albino rats. Agrobiological records, 5, 8–14.
   Google Scholar
• Naseer, A., et al., 2020. Vitamin E and selenium attenuate hepatotoxicity, nephrotoxicity and oxidative stress induced by rifampicin in rabbits. Pakistan veterinary journal, 40 (3), 277–282.
   Web of Science ®Google Scholar
• Ramesh, G., et al., 2007. Endotoxin and cisplatin synergistically induce renal dysfunction and cytokine production in mice. American journal of physiology. Renal physiology, 293 (1), F325–332.
   PubMed Web of Science ®Google Scholar
• Rani, V.U., Sudhakar, M., and Ramesh, A., 2017. Protective effect of Pueraria tuberosa Linn. in arsenic induced nephrotoxicity in rats. Asian journal of pharmaceutical research, 7 (1), 15–20.
   Google Scholar
• Ratnaike, R.N., 2003. Acute and chronic arsenic toxicity. Postgraduate medical journal, 79 (933), 391–396.
   PubMed Web of Science ®Google Scholar
• Rehman, M.U., et al., 2014. Alleviation of hepatic injury by chrysin in cisplatin administered rats: probable role of oxidative and inflammatory markers. Pharmacological reports, 66 (6), 1050–1059.
   PubMed Web of Science ®Google Scholar
• Ross, J.A., and Kasum, C.M., 2002. Dietary flavonoids: bioavailability, metabolic effects and safety. Annual review of nutrition, 22 (1), 19–34.
   PubMed Web of Science ®Google Scholar
• Rotruck, J.T., et al., 1973. Selenium: biochemical role as a component of glutathione peroxidase. Science, 179 (4073), 588–590.
   PubMed Web of Science ®Google Scholar
• SAFHI, M.M., 2018. Nephroprotective effect of Zingerone against CCl4-induced renal toxicity in Swiss albino mice: molecular mechanism. Oxidative medicine and cellular longevity, 2018, 2474831.
   PubMed Web of Science ®Google Scholar
• Sahreen, S., et al., 2015. Protective effects of Carissa opaca fruits against CCl4-induced oxidative kidney lipid peroxidation and trauma in rat. Food & nutrition research, 59 (1), 28438.
   PubMed Web of Science ®Google Scholar
• Shahid, F., et al., 2014. Studies on the effect of sodium arsenate on the enzymes of carbohydrate metabolism, brush border membrane, and oxidative stress in the rat kidney. Environmental toxicology and pharmacology, 37 (2), 592–599.
   PubMed Web of Science ®Google Scholar
• Sharma, S., 2016. Nephrotoxic effects of arsenic in Albino mice. American journal of BioScience, 4 (3), 1–4.
   Google Scholar
• Singer, E., et al., 2013. Neutrophil gelatinase‐associated lipocalin: pathophysiology and clinical applications. Acta physiologica, 207 (4), 663–672.
   PubMed Web of Science ®Google Scholar
• Sinha, M., Manna, P., and Sil, P.C., 2008. Arjunolic acid attenuates arsenic-induced nephrotoxicity. Pathophysiology, 15 (3), 147–156.
   PubMedGoogle Scholar
• Subbaramaiah, K., and Dannenberg, A.J., 2003. Cyclooxygenase 2: a molecular target for cancer prevention and treatment. Trends in pharmacological sciences, 24 (2), 96–102.
   PubMed Web of Science ®Google Scholar
• Tahir, R., et al., 2021. Pesticide induced hematological, biochemical and genotoxic changes in fish: a review. Agrobiological records, 3, 41–57.
   Google Scholar
• Thangapandiyan, S., et al., 2019. Sulforaphane potentially attenuates arsenic-induced nephrotoxicity via the PI3K/Akt/Nrf2 pathway in albino Wistar rats. Environmental science and pollution research international, 26 (12), 12247–12263.
   PubMed Web of Science ®Google Scholar
• Townsend, D.M., and Tew, K.D., 2003. The role of glutathione-S-transferase in anti-cancer drug resistance. Oncogene, 22 (47), 7369–7375.
   PubMed Web of Science ®Google Scholar
• Usoh, I.F., et al., 2005. Antioxidant actions of dried flower extracts of Hibiscus sabdariffa L. on sodium arsenite-induced oxidative stress in rats. Pakistan journal of nutrition, 4 (3), 135–141.
   Google Scholar
• Vaidya, V.S., Ferguson, M.A., and Bonventre, J.V., 2008. Biomarkers of acute kidney injury. Annual review of pharmacology and toxicology, 48, 463–493.
   PubMed Web of Science ®Google Scholar
• Villar, I.C., et al., 2002. Effect of chronic chysin treatment in spontaneously hypertensive rats. Planta medica, 68 (9), 847–847.
   PubMed Web of Science ®Google Scholar
• Waalkes, M.P., et al., 2004. Mechanisms underlying arsenic carcinogenesis: hypersensitivity of mice exposed to inorganic arsenic during gestation. Toxicology, 198 (1–3), 31–38.
   PubMed Web of Science ®Google Scholar
• Wang, W., et al., 2014. Association of inorganic arsenic exposure with type 2 diabetes mellitus: a meta-analysis. Journal of epidemiology and community health, 68 (2), 176–184.
   PubMed Web of Science ®Google Scholar
• Wu, M.M., et al., 2001. Association of blood arsenic levels with increased reactive oxidants and decreased antioxidant capacity in a human population of northeastern Taiwan. Environmental health perspectives, 109 (10), 1011–1017.
   PubMed Web of Science ®Google Scholar
• Yamamura, S., et al., 2003. Drinking water guidelines and standards. Arsenic, water, and health, 2003, 18.
   Google Scholar
• Younis, T., Khan, M.R., and Sajid, M., 2016. Protective effects of Fraxinus xanthoxyloides (wall.) leaves against CCl4 induced hepatic toxicity in rat. BMC complementary and alternative medicine, 16 (1), 2–13.
   PubMedGoogle Scholar
• Zhang, W., et al., 2014. Protective effect of resveratrol on arsenic trioxide-induced nephrotoxicity in rats. Nutrition research and practice, 8 (2), 220–226.
   PubMed Web of Science ®Google Scholar