Mercury-Induced Acute Nephrotoxicity in Rats:Treatment with Aqueous Extract of Pistacia atlantica (Desf)

doi.org/10.26538/tjnpr/v5i12.3

Authors

  • Benahmed Fatiha Laboratory of Experimental Biotoxicology, Department of Biology, Faculty of Life and Natural Sciences, University of Oran1, Ahmed Ben Bella, 1524 EL M Naouer 31000 Oran, Algeria
  • Kharoubi Omar Laboratory of Experimental Biotoxicology, Department of Biology, Faculty of Life and Natural Sciences, University of Oran1, Ahmed Ben Bella, 1524 EL M Naouer 31000 Oran, Algeria
  • Mehrab El azhari Department of Biology, Faculty of Sciences and Technology, University of Ahmed Zabana of Relizane , Algeria

Keywords:

Mercury, Liver, Kidney, Redox status, Pistacia atlantica, Rat

Abstract

Mercury is known to accumulate in living organisms, causing serious damage. An important characteristic of mercury toxicity is the generation of free radicals. The purpose of this study is to evaluate the protective effect of the aqueous extract of Pistacia atlantica against mercury-induced oxidative stress in rats. Mercury chloride (HgCl2) was administered intraperitoneally (at 2.5 mg/kg once per week), and P. atlantica was given orally by gavage at a daily dose of 150 \mg/kg body weight to rats for 32 days. These results show that HgCl2 caused a significant depletion of the glutathione level and the enzymatic activity of the antioxidant system catalase (CAT), Glutathion peroxidase (GPx,), Glutathion S transferase (GST) at the renal level. These changes were associated with increased lipid peroxidation expressed by a high level of renal Malondialdehyde (MDA) and hydroperoxides (LOOH). However, supplementation with the aqueous extract of Pistacia atlantica modified the toxic effects of mercury by reducing lipid peroxidation. These findings may indicate an antioxidant and protective effect of this plant's extract against mercury's harmful effect. 

Author Biography

Benahmed Fatiha, Laboratory of Experimental Biotoxicology, Department of Biology, Faculty of Life and Natural Sciences, University of Oran1, Ahmed Ben Bella, 1524 EL M Naouer 31000 Oran, Algeria

Department of Biology, Faculty of Sciences and Technology, University of Ahmed Zabana of Relizane , Algeria

References

da Luz Fiuza, T., Leitemperger, J., Severo, E. S., Marins, A. T., do Amaral, A. B., Pereira, M. E., & Loro, V. L. Effects of diphenyl diselenide diet on a model of mercury poisoning. Mol Biol Rep, 2018: 45(6), 2631-2639.,

Bjørklund G, Dadar M, Mutter J, Aaseth J. The toxicology of mercury: Current research and emerging trends. Environ Res. 2017; (159):545-554

Benahmed F, Rached W, Kerroum F and El Belhouari HFZ. Protective effect of Pistacia atlantica Desf leaves on Mercury-Induced toxicity in Rats. South Asian J Exp Biol. 2020; 10(3):152-161.

Gochfeld M and Burger J. Mercury interactions with selenium and sulfur and the relevance of the Se:Hg molar ratio to fish consumption advice. Environ Sci Pollut Res. 2021; (28):18407-18420.

Migdal C and Serres M. Reactive oxygen species and oxidative stress. Med Sci Paris. 2011; (27):405-412.

Yamin Y, Sabarudin S, Zubaydah WOS, Sahumena MH, Arba M, Elnawati E, Andriani R and Suryani S. Determination of Antiradical Activity, Total Phenolic and Flavonoid Contents of Kamena-mena (Clerodendrum paniculatum. L) Leaves. Trop J Nat Prod Res. 2021; 5(2):287-293.

Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979; 95(2):351-358.

Ellman GL. Tissue sulfhydryl groups. Arch Biochem Biophys. 1959; 82(1):70-77.

Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. Biol Chem. 1951; (193):265-275.

Aebi H. Catalase. In: Bergmeyer, H.U., Ed., Methods of Enzymatic Analysis. 1974; 2(2):673-684.

Rotruck JT, Pope AL, Ganther HE, Swanson AB, Hafeman DG, Hoekstra WG. Selenium: biochemical role as a component of glutathione peroxidase. Sci. 1973; (179):588-590.

Habig WH, Pabst MJ, Jakoby WB. Glutathione Stransferases: the first enzymatic step in mercapturic acid formation. Biol Chem. 1974; 249:7130-7139.

Marklund S and Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem. 1974; (47):469-474.

Ahmad S and Mahmood R. Mercury chloride toxicity in human erythrocytes: enhanced generation of ROS and RNS, hemoglobin oxidation, impaired antioxidant power, and inhibition of plasma membrane redox system. Environ Sci Pollut Res. 2019; (26):5645-5657.

Björkman L, Lygre GB, Haug K, Skjærven R. Perinatal death and exposure to dental amalgam fillings during pregnancy in the population-based MoBa cohort. PLOS ONE. 2018; 13(12):e0208803.

Mohamed NES. Protective Effect of Origanum Oil on Alterations of Some Trace Elements and Antioxidant Levels Induced by Mercuric Chloride in Male Rats. Biol Trace Elem Res. 2018; 182:49-56.

Mironczuk-Chodakowska I, Witkowska AM, Zujko ME. Endogenous non-enzymatic antioxidants in the human body. Adv Med Sci. 2018; 63:68-78.

Ekstrand J, Nielsen JB, Havarinasab S, Zalups RK, Söderkvist P and Hultman P. Mercury toxicokineticsdependency on strain and gender. Toxicol Appl Pharmacol. 2010; 243:283-291.

Mleiki A, Marigómez I, El Menif NT. Effects of dietary Pb and Cd and their combination on glutathion-S-transferase and catalase enzyme activities in digestive gland and foot of the green garden snail, Cantareus apertus (Born, 1778). Bull Environ Contam Toxicol. 2015; 94:738-743.

Agarwal AS, Goel R, Beharia J. Detoxification and antioxidant effects of curcumin in rats experimentally exposed to mercury. J Appl Toxicol. 2010; (30):457-468.

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Published

2021-12-01

How to Cite

Fatiha, B., Omar, K., & El azhari, M. (2021). Mercury-Induced Acute Nephrotoxicity in Rats:Treatment with Aqueous Extract of Pistacia atlantica (Desf): doi.org/10.26538/tjnpr/v5i12.3. Tropical Journal of Natural Product Research (TJNPR), 5(12), 2063–2067. Retrieved from https://tjnpr.org/index.php/home/article/view/216