EVALUATION OF THE ANTIOXIDANT POTENTIAL FOR DIFFERENT EXTRACTS OF AL-TAIF POMEGRANATE (PUNICA GRANATUM L) INDUCED BY ATRAZINE AND MALATHION PESTICIDES IN LIVER OF MALE ALBINO MICE

Authors

  • Reham Z. Hamza Taif University, Zagazig University
  • Asmaa M. Abd El-azez Taif University, Al-Azhar University
  • Nahed A. Hussien Cairo University

Keywords:

Malathion, Atrazine, Pomegranate peel, Hepatic functions, Oxidative stress

Abstract

Objective: The objective of the present study was to evaluate the antioxidant potential of Al-Taif Pomegranate Peel extract (PPE) and juice (PJ) induced by atrazine (Atra) and malathion (Mal) toxicity in male mice by using biochemical and histopathological assays.

Methods: Male mice were divided into ten groups and treated orally as following: Negative control; Mal group (27 mg/kg); Atra group (120 mg/kg); PPE group (0.4 g/Kg); PJ group (0.4 g/Kg);Mal + PPE group (27 mg/Kg + 0.4 g/Kg, respectively); Mal + PJ group (27mg/Kg + 0.4 g/Kg, respectively); Atra + PPE group (120mg/Kg + 0.4 g/Kg, respectively); Atra + PJ group (120mg/Kg + 0.4 g/Kg, respectively); Mal + Atra + PPE + PJ combined co-administration group.

Results: Biochemical results showed a significant decrease in the antioxidant enzyme levels represented by SOD, GPxand CAT for Mal or Atra groups, while they afforded a highly significant increase in lipid peroxidation end product, MDA level. In contrast, co-administration of PPE and/or PJ and Atra and/or Mal-treated groups restored almost most of these antioxidant defense capacities to normal levels. On the other hand, treatmentwith eitherAtra or Mal resulted in histopathological hepatic alterations. However, co-administration of PPEand/or PJ and Atra and/or Mal-treated animals improved the hepatic damage and alleviated pesticides toxic effect.

Conclusion: The present study suggested that Atra and Mal exposure lead to oxidative damage in the liver tissues of mice and concomitant treatment with different extracts of Al-Taif Pomegranate protected the liver tissues from oxidative damage.

 

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References

Allen JL, Gonzales F, Boyne JV. Larvin brand thiodicarb insecticide. A new carbamate insecticide. Mededelingen-van-de-Faculteit Landbouwwetenschappen. Rijksuniversiteit-Gent 1989;36:1167–71.

Cserháti T, Szőgyi M. Chromatographic determination of pesticides in foods and food products. Eur Chem Bull 2012;1:58–68.

Goldman LR. Atrazine, simazine and cyanazine: notice of initiation of special review. Fed Regist 1994;59:60412–43.

Purcell M, Neault JF, Malonga H, Arakawa H, Carpentier R, Tajmir-Riahi HA. Interactions of atrazine and 2,4-D with human serum albumin studied by gel and capillary electrophoresis, and FTIR spectroscopy. Biochem Biophys Acta 2001;1548(1):129–38.

Singh M, Sandhir R, Kiran R. Erythrocyte antioxidant enzymes in toxicological evaluation of commonly used organophosphate pesticides. Indian J Exp Biol 2006;44:580–3.

Firestone JA, Smith-Weller T, Franklin G, Swanson P, Longstreth WT, Checkoway H. Pesticides and risk of Parkinson disease: a population-based case control study. Arch Neurol 2005;62:91–5.

Ribas G, Ferenzilli G, Barale R, Marcos R. Herbicide-induced DNA damage in human lymphocytes evaluated by single-cell gel electrophoresis (SCGE) assay. Mutat Res 1995;344:41–54.

Grover P, Danadevi K, Mahboob M, Rozati R, Saleha Banu B, Rahman MF. Evaluation of genetic damage in workers employed in pesticide production utilizing the Comet assay. Mutagen 2003;18:201–5.

Lander BF, Knudsen LE, Gamborg MO, Järventaus H, Norppa H. Chromosome aberrations in pesticide-exposed green house workers. Scand J Work Environ Health 2000;26:436–42.

Rezg R, Mornagui B, El-Fazaa S, Gharbi N. Biochemical evaluation of hepatic damage in subchronic exposure to malathion in rats: effect on superoxide dismutase and catalase activities using native PAGE. CR Biol 2008a;331:655–62.

Lasram MM, Annabi AB, Elj N, Selmi S, Kamoun A, El-Fazaa S, Gharbi N. Metabolic disorders of acute exposure to malathion in adult Wistar rats. J Hazard Mater 2009;163:1052–5.

Mansour SA, Mossa ATH. Oxidative damage, biochemical and histopathological alterations in rats exposed to chlorpyrifos and the antioxidant role of zinc. Pestic Biochem Physiol 2010;96:14–23.

Jin Y, Wang L, Chen G, Lin X, Miao W, Fu Z. Exposure of mice to atrazine and its metabolite diaminochlorotriazine elicits oxidative stress and endocrine disruption. Environ Toxicol Pharmacol 2014;37(2):782-90.

Durak D, Uzun FG, Kalender S, Ogutcu A, Uzunhisarcikli M, Kalender Y. Malathion-induced oxidative stress in human erythrocytes and the protective effect of vitamins C and E in vitro. Environ Toxicol 2009;24(3):235-42.

Muniz JF, McCauley L, Scherer J, Lasarev M, Koshy M, Kow YW, Nazar-Stewart V, et al. Biomarkers of oxidative stress and DNA damage in agricultural workers: a pilot study. Toxicol Appl Pharmacol 2008;227(1):97–107.

Cam M, Hisil Y, Durmaz G. Classification of eight pomegranate juices based on antioxidant capacity measured by four methods. Food Chem 2009;112:721-6.

Aviram M, Dornfeld L. Pomegranate juice consumption inhibits serum angiotensin converting enzyme activity and reduces systolic blood pressure. Atheroscler 2001;158:195-8.

Malik A, Afaq F, Sarfaraz S, Adhami VM, Syed DN, Mukhtar H. Pomegranate fruit juice for chemoprevention and chemotherapy of prostate cancer. Proc Natl Acad Sci USA 2005;102:14813-8.

Al-Zoreky NS. Antimicrobial activity of pomegranate (Punica granatum L) fruit peels. Int J Food Microbiol 2009;134:244-8.

Uzun FG, Kalender S, Durak D, Demir F, Kalender Y. Malathion-induced testicular toxicity in male rats and the protective effect of vitamins C and E. Food Chem Toxicol 2009;47(8):1903-8.

Kniewald J, Jakominic M, Tomljenovic A, Simic B, Romac P, Vranesic D, et al. Disorders of male rat reproductive tract under the influence of atrazine. J Appl Toxicol 2000;20:61–8.

Bhaskar A, Kumar A. Antihyperglycemic, antioxidant and hypolipidemic effect of Punica granatum L flower extract in streptozotocin induced diabetic rats. Asian Pac J Trop Biomed 2012;3 Suppl:1764-9.

Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 1979;95:351–8.

Marklund S, Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem 1974;47:469–74.

Aebi H. Catalase in vitro. Methods Enzymol 1984;105:121–6.

Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med 1967;70:158.

Carleton HM. Carleton’s Histological Technique. (4th Ed), Pub. London, New York, Toronto, Oxford university press; 1967.

Qin YY, Zhang ZH, Li L, Xiong W, Shi JY, Zhao TR, Fan J. Antioxidant effect of pomegranate rind powder extract, pomegranate juice, and pomegranate seed powder extract as antioxidants in raw ground pork meat. Food Sci Biotechnol 2013;22(4):1063-9.

Nwani CD, Lakra WS, Nagpure NS, Kumar R, Kushwaha B, Srivastava SK. Toxicity of the herbicide atrazine: effects on lipid peroxidation and activities of antioxidant enzymes in the freshwater fish Channapunctatus (Bloch). Int J Environ Res Public Health 2010;7(8):3298-312.

Akunna GG, Saalu CL, Ogunmodede OS, Ogunlade B, Bello AJ. Aqueous extract of date fruit (phoenix dactylifera) protects testis against atrazine-induced toxicity in rat. World J Life Sci Medical Res 2012;2(2):100.

EI-Gharieb MA, EI-Masry TA, Emara AM, Hashem MA. Potential hepatoprotective effects of vitamin E and Nigella sativa oil on hepatotxicity induced by chronic exposure tomalathion in human and male albino rats. Egypt Soc Pharmacol Exp Ther 2008;29(2):347-68.

Kalender S, Uzun FG, Durak D, Demir F, Kalender Y. Malathion-induced hepatotoxicity in rats: the effects of vitamins C and E. Food Chem Toxicol 2010;48(2):633-8.

Gokcimen A, Gulle K, Demirin H, Bayram D, Kocak A, Altuntas I. Effects of diazinon at different doses on rat liver and pancreas tissues. Pestic Biochem Phys 2007;87:103–8.

Campos-Pereira FD, Oliveira CA, Pigoso AA, Silva-Zacarin EC, Barbieri R, Spatti EF, et al. Early cytotoxic and genotoxic effects of atrazine on Wistar rat liver: a morphological, immunohistochemical, biochemical, and molecular study. Ecotoxicol Environ Saf 2012;78:170-7.

Liu XM, Shao JZ, Xiang LX, Chen XY. Cytotoxic effects and apoptosis induction of atrazine in a grass carp (Ctenopharyngodonidellus) cell line. Environ Toxicol 2006;21(1):80-9.

Yin XM, Ding WX, Gao W. Autophagy in the liver. Hepatol 2008;47(5):1773-85.

Jain V, Murugananthan G, Deepak M, Viswanatha GL, Manohar D. Isolation and standardization of various phytochemical constituents from methanolic extracts of fruit rinds of punicagranatum. Chin J Nat Med 2011;9(6):0414−20.

Bors W, Heller W, Michel C, Saran M. Flavonoids as antioxidants: determination of radical-scavenging efficiencies. Methods Enzymol 1990;186:343-55.

Blokhina O, Virolainen E, Fagerstedt KV. Antioxidants, oxidative damage and oxygen deprivation stress: a review. Ann Bot 2003;91:179-94.

Verstraeten SV, Keen CL, Schmitz HH, Fraga CG, Oteiza PI. Flavan-3-ols and procyanidins protect liposomes against lipid oxidation and disruption of the bilayer structure. Free Radic Biol Med 2003;34(1):84-92.

Khan AG, Kuek C, Chaudhry TM, Khoo CS, Hayes WJ. Role of plants, mycorrhizae and phytochelators in heavy metal contaminated land remediation. Chemosphere 2000;41(1-2):197-207.

Published

01-01-2015

How to Cite

Hamza, R. Z., A. M. Abd El-azez, and N. A. Hussien. “EVALUATION OF THE ANTIOXIDANT POTENTIAL FOR DIFFERENT EXTRACTS OF AL-TAIF POMEGRANATE (PUNICA GRANATUM L) INDUCED BY ATRAZINE AND MALATHION PESTICIDES IN LIVER OF MALE ALBINO MICE”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 7, no. 1, Jan. 2015, pp. 89-94, https://journals.innovareacademics.in/index.php/ijpps/article/view/3525.

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