SODIUM FLUORIDE-INDUCED OXIDATIVE STRESS AND HISTOLOGICAL CHANGES IN LIVER OF SWISS ALBINO MICE AND AMELIORATION BY OCIMUM SANCTUM LINN.

Authors

  • Bhagwendra Prakash Department of Zoology, Environmental Toxicology Laboratory, Centre for Advanced Studies, University of Rajasthan, Jaipur, Rajasthan, India.
  • Suresh Kumar Sabal Department of Zoology, Environmental Toxicology Laboratory, Centre for Advanced Studies, University of Rajasthan, Jaipur, Rajasthan, India.
  • Rajbala Verma Department of Zoology, Environmental Toxicology Laboratory, Centre for Advanced Studies, University of Rajasthan, Jaipur, Rajasthan, India.
  • John Pj Department of Zoology, Environmental Toxicology Laboratory, Centre for Advanced Studies, University of Rajasthan, Jaipur, Rajasthan, India.
  • Inderpal Soni Department of Zoology, Environmental Toxicology Laboratory, Centre for Advanced Studies, University of Rajasthan, Jaipur, Rajasthan, India.

DOI:

https://doi.org/10.22159/ajpcr.2018.v11i9.26840

Keywords:

Fluoride, Mice, Drinking water, Hepatotoxicity, Amelioration, Ocimum sanctum Linn

Abstract

Objective: The present study was designed to evaluate hepatotoxicity induced by sodium fluoride (NaF) in Swiss albino mice and amelioration by Ocimum sanctum Linn.

Methods: Mice were divided into six groups, Group I received tap water, Group II received low dose of NaF (8 mg/L), Group III high dose of NaF (80 mg/L) in drinking water, Group IV tap water along with 250 mg/kg body weight/day leaf extract of O. sanctum Linn., Group V 8 mg/L NaF in drinking water and 250 mg/kg body weight leaf extract of O. sanctum Linn., and Group VI 80 mg/L NaF in drinking water along with leaf extract of O. sanctum Linn. 250 mg/kg body weight/day for 90 days. On the 91st day, the animals were autopsied and liver tissue samples were taken to assess histopathological changes and oxidative stress by estimating glutathione peroxidase, superoxide dismutase, and catalase.

Results: A highly significant decrease in the activity of antioxidant enzymes occurred with the high dose (Group III). Hepatic histopathological architecture exhibited deformities, namely, ballooning, hypertrophy, hepatocellular necrosis, infiltration of mononuclear cells, deformed central vein, sinusoidal dilation, and binucleated cells. Low-dose group (Group II) showed a significant decrease in antioxidant enzyme levels as compared to control group, and histological sections of liver showed dilated sinusoids, infiltration of mononuclear cells, ballooning, and hypertrophy of hepatocytes. Groups IV and V showed no pathological features. Group VI showed less damage to the liver as compared to Group III.

Conclusion: The results revealed that the administration of leaf extract of O. sanctum Linn. elicited protection against NaF-induced hepatotoxicity and oxidative stress. It may, therefore, be inferred that fluoride caused hepatotoxicity in Swiss albino mice at the tested dose levels can be ameliorated by O. sanctum Linn.

Downloads

Download data is not yet available.

References

WHO. Environmental health criteria 36. Fluor Fluorid 1984;1:25-36.

Li Y, Dunipace AJ, Stookey GK. Genotoxic effects of fluoride: A controversial issue. Mutant Res 1988;195:127-36.

Medical Research Council Working Group. Water Fluoridation and Health Report. London: MRC; 2002.

WHO. Guidelines for Drinking-Water Quality: Fourth Edition Incorporating the First Addendum, 2017.

Das S, Maiti R, Ghosh D. Management of fluoride-induced testicular disorders by calcium and Vitamin-E co-administration in the albino rat. Reprod Toxicol 2006;22:606-12.

Wang YN, Xiao QX, Liu JL, Dallner G, Guan ZZ. Effect of long-term fluoride exposure on lipid composition in rat liver. Toxicology 2000;146:161-9.

Djouadi A, Derouiche S. Study of fluoride-induced hematological alterations and liver oxidative stress in rats. World J Pharm Pharm Sci 2017;6:211-21.

Shashi A, Thapar SP. Histopathology of fluoride-induced hepatotoxicity in rabbits. Fluoride 2000;34:34-42.

Kapoor V, Prasad T, Bhatia KC. Effect of dietary fluorine on histopathological changes in calves. Fluoride 1993;26:105-10.

Mamczar E, Machoy Z, Tarnawski R, Birkner E, Mamczar A. Influence of long-term sodium fluoride administration on selected parameters of rat blood serum and liver function. Fluoride 1997;30:157-64.

Kolodziejczyk L, Put A, Grzela P. Liver morphology and histochemistry in rats resulting from ingestion of Sodium selenite and sodium fluoride. Fluoride 2000;33:6-16.

Vats V, Yadav SP, Grover JK. Ethanolic extract of Ocimum sanctum leaves partially attenuates streptozotocin-induced alterations in glycogen content and carbohydrate metabolism in rats. J Ethnopharmacol 2004;90:155-60.

Hannan JM, Marenah L, Ali L, Rokeya B, Flatt PR, Abdel-Wahab YH, et al. Ocimum sanctum leaf extracts stimulate insulin secretion from perfused pancreas, isolated islets and clonal pancreatic beta-cells. J Endocrinol 2006;189:127-36.

Gupta S, Mediratta PK, Singh S, Sharma KK, Shukla R. Antidiabetic, antihypercholesterolaemic and antioxidant effect of Ocimum sanctum (Linn) seed oil. Indian J Exp Biol 2006;44:300-4.

Magesh V, Lee JC, Ahn KS, Lee HJ, Lee HJ, Lee EO, et al. Ocimum sanctum induces apoptosis in A549 lung cancer cells and suppresses the in vivo growth of lewis lung carcinoma cells. Phytother Res 2009;23:1385-91.

Batra A, Sastry VG. Extraction of ursolic acid from Ocimum sanctum and synthesis of its derivatives: Comparative evaluation of antioxidant activities. J Pharm Sci Res 2014;5:5059-65.

Pemminati S, Swati B, Shreyasi C, Chandrasekhar R, Gopalakrishna HN, Pai MR. Anxiolytic activity of ethanolic extract of leaves of Ocimum sanctum in rats. Drug Invent Today 2010;2:115-8.

Basu A, Mitra E, Mukherjee D, Ghosh AK, Firdaus SB, Ghosh D, et al. Aqueous tulsi leaf (Ocimum sanctum L.) extract protects against piroxicam-induced gastric ulceration in rats: Involvement of antioxidant mechanisms. Int J Pharm Pharm Sci 2013;5:438-47.

Sridevi M, Bright J, Yamini K. Anti-cancer effect of Ocimum sanctum ethanolic extract in non-small cell lung carcinoma cell line. Int J Pharm Pharm Sci 2016;8:242-6.

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

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;47:469-74.21.

Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med 1967;70:158-69.

Lowry OH, Rosebrough NJ, Farr Al, Randall RJ. Protein measurement with the folin phenol reagent. J Biol Chem 1951;193:265-75.

Shanthakumari D, Srinivasalu S, Subramanian S. Effect of fluoride intoxication on lipidperoxidation and antioxidant status in experimental rats. Toxicology 2004;204:219-28.

Vani ML, Reddy KP. Effect of fluoride accumulation on some enzyme of brain and gastrocnemius muscle of mice. Fluoride 2000;33:17-26.

Patel D, Chinoy NJ. Influence of fluoride on biological free radical reactions in ovary of mice and its reversal. Fluoride 1998;31:S27.

Krechniak J, Inkielewicza I. Correlations between fluoride concentrations and free radical parameters in soft tissues of rats. Fluoride 2005;38:293-6.

Chouhan S, Flora SJ. Effects of fluoride on the tissue oxidative stress and apoptosis in rats: Biochemical assays supported by IR spectroscopy data. Toxicology 2008;254:61-7.

Ailani V, Gupta RC, Gupta SK, Gupta K. Oxidative stress in cases of chronic fluoride intoxication. Indian J Clin Biochem 2009;24:426-9.

Hassan HA, Abdel-Aziz AF. Evaluation of free radical-scavenging and anti-oxidant properties of blackberry against fluoride toxicity in rats. Food Chem Toxicol 2010;48:1999-2004.

Chattopadhyay A, Podder S, Agarwal S, Bhattacharya S. Fluoride-induced histopathology and synthesis of stress protein in liver and kidney of mice. Arch Toxicol 2011;85:327-35.

Weydert CJ, Cullen JJ. Measurement of superoxide dismutase, catalase and glutathione peroxidase in cultured cells and tissue. Nat Protoc 2010;5:51-66.

Bartsch H, Nair J. Ultrasensitive and specific detection method for exocyclic DNA adducts: Markers for lipid peroxidation and oxidative stress. Toxicology 2000;153:105-14.

Sharma A, Chinoy NJ. Role of free radicals in fluoride-induced toxicity in liver and kidney of mice and its reversal. Fluoride 1998;31:26-30.

Shuhua X, Ziyou L, Ling Y, Fei W, Sun G. A role of fluoride on free radical generation and oxidative stress in BV-2 microglia cells. Mediators Inflamm 2012;2012:102954.

Guo X, Sun G, Sun Y. Oxidative stress from fluoride induced hepatotoxicity in rats. Fluoride 2003;36:25-9.

Zhan XA, Min W, Rong XZ, Fen LW, Li JX. Effects of fluoride on hepatic antioxidant system and transcription of Cu/Zn SOD gene in young pigs. J Trace Elem Med Biol 2006;20:83-7.

J M, Sinha S, Ghosh M, Mukherjee A. Evaluation of multi-endpoint assay to detect genotoxicity and oxidative stress in mice exposed to sodium fluoride. Mutat Res 2013;751:59-65.

Flora SJ, Mittal M, Pachauri V, Dwivedi N. A possible mechanism for combined arsenic and fluoride induced cellular and DNA damage in mice. Metallomics 2012;4:78-90.

Bouaziz H, Ketata S, Jammoussi K, Boudawara T, Ayedi F, Ellouze F, et al. Effects of sodium fluoride on hepatic toxicity in adult mice and their suckling pups. Pestic Biochem Physiol 2006;86:124-30.

Shashi A, Singh JP, Thapar SP. Toxic effects of fluoride on rabbit kidney. Fluoride 2002;35:38-50.

Chinoy NJ, Joseph R, Sequeira E, Narayana MV. Effects of sodium fluoride on the muscle and liver of albino rats. Indian J Environ Biol 1991;1:129-34.

Bogdanffy MS, Makovec GT, Frame SR. Inhalation oncogenicity bioassay in rats and mice with vinyl fluoride. Fundam Appl Toxicol 1995;26:223-38.

Lahon K, Das S. Hepatoprotective activity of Ocimum sanctum alcoholic leaf extract against paracetamol-induced liver damage in Albino rats. Pharmacog Res 2011;3:13-8.

Chattopadhyay RR, Sarkar SK, Ganguly S, Medda C, Basu TK. Hepatoprotective activity of Ocimum sanctum leaf extracts against paracetamol-induced hepatic damage in rats. Indian J Pharmacol 1992;24:163-5.

Liu J. Pharmacology of oleanolic acid and ursolic acid. J Ethnopharmacol 1995;49:57-68.

Sen P. Therapeutic potentials of Tulsi: From experience to facts. Drugs News Views 1993;1:15-21.

Kath RK, Gupta RK. Antioxidant activity of hydroalcoholic leaf extract of Ocimum sanctum in animal models of peptic ulcer. Indian J Physiol Pharmacol 2006;50:391-6.

Siddique Y, Ara G, Beg T, Afzal M. Anti-genotoxic effect of Ocimum sanctum L. extract against cyproterone acetate induced genotoxic damage in cultured mammalian cells. Acta Biol Hung 2007;58:397-409.

Manikandan P, Murugan RS, Abbas H, Abraham SK, Nagini S. Ocimum sanctum Linn. (holy basil) ethanolic leaf extract protects against 7,12-dimethylbenz[a] anthracene-induced genotoxicity, oxidative stress, and imbalance in xenobiotic-metabolizing enzymes. J Med Food 2007;10:495-502.

Published

07-09-2018

How to Cite

Prakash, B., S. K. Sabal, R. Verma, J. Pj, and I. Soni. “SODIUM FLUORIDE-INDUCED OXIDATIVE STRESS AND HISTOLOGICAL CHANGES IN LIVER OF SWISS ALBINO MICE AND AMELIORATION BY OCIMUM SANCTUM LINN”. Asian Journal of Pharmaceutical and Clinical Research, vol. 11, no. 9, Sept. 2018, pp. 195-9, doi:10.22159/ajpcr.2018.v11i9.26840.

Issue

Section

Original Article(s)