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Ameliorative Effect of Resveratrol Against Fluoride-Induced Alteration of Thyroid Function in Male Wistar Rats

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Abstract

Resveratrol (3,4,5-trihydroxystilbene), a polyphenol and well-known natural antioxidant has been evaluated for its protective effect against fluoride-induced metabolic dysfunctions in rat thyroid gland. Fluoride, the most abundant anions present in groundwater throughout the world, creates a major problem in safe drinking water and causes metabolic, structural, and functional injuries in different organ systems. Sub-acute exposure to sodium fluoride at a dose of 20 mg/kg b.w./day orally to rat for 30 days induces thyroidal dysfunction including suppressed synthetic machinery of the thyroid gland to produce nucleic acids and thyroid hormones, mainly T3 and T4. Other functional changes are alteration of certain metabolic enzyme activities like Na+-K+-ATPase, thyroid peroxidase, and 5,5′-deiodinase. Structural abnormality of thyroid follicles by fluoride intoxication clearly indicates its thyrotoxic manifestation. Resveratrol supplementation in fluoride-exposed animals appreciably prevented metabolic toxicity caused by fluoride and restored both functional status and ultra-structural organization of the thyroid gland towards normalcy. This study first establishes the therapeutic efficacy of resveratrol as a natural antioxidant in thyroprotection against toxic insult caused by fluoride.

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References

  1. Sharma BS, Agrawal J, Gupta AK (2011) Emerging challenge: fluoride contamination in groundwater in agra district, Uttar Pradesh. Asian J Exp Biol Sci 2:131–134

    CAS  Google Scholar 

  2. Toyoda A, Taira T (2000) A new method for treating fluorine wastewater to reduce sludge and running costs. IEEE Trans Semicond Manuf 13:305–309

    Article  Google Scholar 

  3. Sorg TJ (1978) Treatment technology to meet the interim primary drinking water regulations for inorganics. J Am Water Works Assoc 106–112

  4. Hussain J, Sharma KC, Hussain I (2004) Fluoride in drinking water in Rajasthan and its ill effects on human health. J Tissue Res 4:263–273

    Google Scholar 

  5. Das K, Chainy GB (2004) Thyroid hormone influences antioxidant defense system in adult rat brain. Neurochem Res 29:1755–1766

    Article  CAS  PubMed  Google Scholar 

  6. Zeng Q, Cui YS, Zhang L et al (2012) Studies of fluoride on the thyroid cell apoptosis and mechanism. Zhonghua Yu Fang Yi Xue Za Zhi 46:233–236

  7. Hosur MB, Puranik RS, Vanaki S, Puranik SR (2012) Study of thyroid hormones free triiodothyronine (FT3), free thyroxine (FT4) and thyroid stimulating hormone (TSH) in subjects with dental fluorosis. Eur J Dent 6:184–190

    PubMed Central  PubMed  Google Scholar 

  8. Yu YN (1985) Effects of chronic fluorosis in the thyroid gland. Chinese Med J 65:747–759

    CAS  Google Scholar 

  9. Hassan HA, Yousef MI (2009) Mitigating effects of antioxidant properties of black berry juice on sodium fluoride induced hepatotoxicity and oxidative stress in rats. Food Chem Toxicol 47:2332–2337

    Article  CAS  PubMed  Google Scholar 

  10. Altuntas I, Delibas N, Sutcu R (2002) The effects of organophosphate insecticide methidathion on lipid peroxidation and anti-oxidant enzymes in rat erythrocytes: role of vitamins E and C. Hum Exp Toxicol 21:681–685

    Article  CAS  PubMed  Google Scholar 

  11. Zhao XY, Li GY, Liu Y et al (2008) Resveratrol protects against arsenic trioxide-induced cardiotoxicity in vitro and in vivo. Br J Pharmacol 154:105–133

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  12. Xu Y, Nie L, Yin YG et al (2012) Resveratrol protects against hyperglycemiainduced oxidative damage to mitochondria by activating SIRT1 in rat mesangial cells. Toxicol Appl Pharmacol 259:395–401

    Article  CAS  PubMed  Google Scholar 

  13. Sarkar C, Pal S, Das N, Dinda B (2014) Ameliorative effects of oleanolic acid on fluoride induced metabolic and oxidative dysfunctions in rat brain: experimental and biochemical studies. Food Chem Toxicol 66:224–236

    Article  CAS  PubMed  Google Scholar 

  14. Chirumari K, Reddy PK (2007) Dose-dependent effects of fluoride on neurochemical milieu in the hippocampus and neocortex of rat brain. Fluoride 40:101–110

    CAS  Google Scholar 

  15. Kaczur V, Vereb G, Molnar I et al (1997) Effect of anti-thyroid peroxidase (TPO) antibodies on TPO activity measured by chemiluminescence assay. Clin Chem 43:1392–1396

    CAS  PubMed  Google Scholar 

  16. Chandra AK, De N, Choudhury SR (2011) Effect of different doses of un-fractionated green and black tea extracts on thyroid physiology. Hum Exp Toxicol 30:884–896

    Article  CAS  PubMed  Google Scholar 

  17. Baginski ES, Foa PP, Zak B (1967) Determination of phosphate: study of labile organic phosphate interference. Clin Chim Acta 15:155–158

    Article  CAS  Google Scholar 

  18. Stroev EA, Makarova VG (1989) Determination of bilirubin and its fractions in blood serum. In: Laboratory Manual in Biochemistry, Mir publisher; Moscow, pp 66

  19. Singh NP, McCoy MT, Tice RR, Schneider EL (1988) A simple technique for quantitation of low levels of DNA damage in individual cells. Exp Cell Res 175:184–191

    Article  CAS  PubMed  Google Scholar 

  20. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the folin phenol reagent. J Biol Chem 193:265–275

    CAS  PubMed  Google Scholar 

  21. Das D (1981) Statistics in biology and psychology. Academic, Calcutta, p 197

    Google Scholar 

  22. Sakamoto Y, Mikuriya H, Tayma K et al (2001) Goitrogenic effects of green tea extract catechins by dietary administration in rats. Ach Toxicol 75:591–596

    CAS  Google Scholar 

  23. Ge YM, Ning HM, Wang SL, Wang JD (2005) DNA damage in thyroid gland cells of rats exposed to long-term intake of high fluoride and low iodine. Fluoride 38:318–323

    CAS  Google Scholar 

  24. Bouaziz H, Soussia L, Guermazi F, Zeghal N (2005) Fluoride-induced thyroid proliferative changes and their reversal in female mice and their pups. Fluoride 38:185–92

    CAS  Google Scholar 

  25. Wang AG, Xia T, Chu QL et al (2004) Effects of fluoride on lipid peroxidation, DNA damage and apoptosis in human embryo hepatocytes. Biomed Environ Sci 17:217–222

    PubMed  Google Scholar 

  26. Yaming G, Hongmei N, Shaolin W, Jundong W (2005) DNA damage in thyroid gland cells of rats exposed to long-term intake of high fluoride and low iodine. Fluoride 38:318–323

    Google Scholar 

  27. Verma RJ, Guna Sherlin DM (2002) Sodium fluoride-induced hypoproteinemia and hypoglycemia in parental and F (1)-generation rats and amelioration by vitamins. Food Chem Toxicol 40:1781–1788

    Article  CAS  PubMed  Google Scholar 

  28. Leonard S, Xia C, Jiang B et al (2003) Resveratrol scavenges reactive oxygen species and affects radical-induced cellular responses. Biochem Biophys Res Commun 309:1017–1026

    Article  CAS  PubMed  Google Scholar 

  29. Zhan X, Li J, Wang M, Xu Z (2006) Effects of fluoride on growth and thyroid function in young pigs. Fluoride 39:95–100

    CAS  Google Scholar 

  30. Singla S, Shashi A (2013) Thyroid peroxidase activity as toxicity target for fluoride in patients with thyroid dysfunction. Curr Res Microbiol Biotechnol 1:53–57

    Google Scholar 

  31. Boas M, Feldt RU, Main KM (2012) Thyroid effects of endocrine disrupting chemicals. Mol Cell Endocrinol 355:240–248

    Article  CAS  PubMed  Google Scholar 

  32. Le Grow AB, Fielding DC, Pressley TA (1999) Stimulation of Na+-K+-ATPase by hypothyroidism in the thyroid gland. J Endocrinol 160:453–60

    Article  Google Scholar 

  33. Murphy AJ, Hoover JC (1992) Inhibition of the Na+-K+-ATPase by fluoride. Parallels with its inhibition of the sarcoplasmic reticulum Ca+2-ATPase. J Biol Chem 267:16995–7000

    CAS  PubMed  Google Scholar 

  34. Bocanera LV, Krawiec L, Nocetti G, Juvenal GJ, Silberschmidt D, Pisarev MA (2001) The protein kinase C pathway inhibits iodide uptake by calf thyroid cells via sodium potassium-adenosine triphosphatase. Thyroid 11:813–817

    Article  CAS  PubMed  Google Scholar 

  35. Chinoy NJ, Walimbe AS, Vyas HA, Mangla P (1994) Transient and reversible fluoride toxicity in some soft tissues of female mice. Fluoride 27:205–214

    CAS  Google Scholar 

  36. Duntas LH (2011) Resveratrol and its impact on aging and thyroid function. J Endocrinol Invest 34:788–792

    CAS  PubMed  Google Scholar 

  37. Sebai H, Hovsepian S, Ristorcelli E, Aouani E, Lombardo D, Fayet G (2010) Resveratrol increases iodide trapping in the rat thyroid cell line FRTL-5. Thyroid 20:195–203

    Article  CAS  PubMed  Google Scholar 

  38. Iwasaki K, Ray PD, Huang BW, Sakamoto K, Kobayashi T, Tsuji Y (2013) Role of AMP-activated protein kinase in ferritin H gene expression by resveratrol in human T cells. Biochemistry 52:5075–5083

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  39. Zhang M, Wang A, Xia T, He P (2008) Effects of fluoride on DNA damage, S phase cell-cycle arrest and the expression of NF-kB in primary cultured rat hippocampal neurons. Toxicol Lett 179:1–5

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

We express our sincere gratitude to DBT, New Delhi, Government of India for providing us financial support for carrying out the research work. We also express our sincere thanks to the Co-ordinator, State Biotech Hub, Tripura University for providing infrastructural facility needed for the present work. We also express our thanks to Dr. Surochita Basu, Assistant Professor, Department of Botany for her continuous support in preparation of this manuscript.

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Correspondence to Sudipta Pal.

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Sarkar, C., Pal, S. Ameliorative Effect of Resveratrol Against Fluoride-Induced Alteration of Thyroid Function in Male Wistar Rats. Biol Trace Elem Res 162, 278–287 (2014). https://doi.org/10.1007/s12011-014-0108-3

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  • DOI: https://doi.org/10.1007/s12011-014-0108-3

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