Protective effects of melatonin against fluoride-induced oxidative stress in rats at high altitude


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Authors

  • PRINCE VIVEK PhD Scholar, Defence Institute of High Altitude Research, DRDO, Leh-Ladakh, Jammu and Kashmir 194 101 India
  • VIJAY K BHARTI 2Scientist-D, Defence Institute of High Altitude Research, DRDO, Leh-Ladakh, Jammu and Kashmir 194 101 India
  • SAHIL KALIA PhD Scholar, Defence Institute of High Altitude Research, DRDO, Leh-Ladakh, Jammu and Kashmir 194 101 India
  • ARUP GIRI PhD Scholar, Defence Institute of High Altitude Research, DRDO, Leh-Ladakh, Jammu and Kashmir 194 101 India
  • KRISHNA KUMAR Technical Officer, Defence Institute of High Altitude Research, DRDO, Leh-Ladakh, Jammu and Kashmir 194 101 India
  • BHUVNESH KUMAR Scientist-G, Defence Institute of High Altitude Research, DRDO, Leh-Ladakh, Jammu and Kashmir 194 101 India

https://doi.org/10.56093/ijans.v89i1.86377

Keywords:

Antioxidant, Fluoride, Haematology, High altitude, Melatonin, Oxidative stress, Rats

Abstract

This study was conducted to evaluate the protective effects of melatonin against fluoride-induced oxidative stress-mediated haematological and biochemical changes in rat at high altitude. Adult male Wistar rats (6) were given the basal diet and drinking water ad lib. for first 7-days which was considered as the control period. Thereafter, they were exposed to NaF (@ 50 ppm) per-oral through drinking water for the next 14 days followed by melatonin treatment (@ 15 mg/kg BW, p.o.) for the next 14 days. The result showed induction of oxidative stress during NaF treatment alone, which caused significant increase in alkaline phosphatase (ALP), alanine aminotransferase (ALT), and aspartate aminotransferase (AST) activity, and % inhibition of DPPH, MDA, and water intake. Whereas, total antioxidant capacity (FRAP) and body weight gain were significantly reduced during NaF exposure. Haemogram analysis indicated significant decrease in haemoglobin, packed cell volume, erythrocytes, lymphocytes, platelets count, whereas increase in MCH, monocytes, neutrophil, and eosinophil during NaF exposure. However, melatonin administration after 14 days of fluoride treatment resulted in significant amelioration of adverse changes occurred in different blood-biochemical parameters and also increased the total antioxidant status. Notably, the body weight gain improved during melatonin administration. These findings indicated induction of oxidative stress-mediated adverse change in haematology and biochemical parameters, and amelioration effect of oral dose of melatonin in rats under high altitude stress condition. Hence it can be concluded that melatonin acts as a potent antioxidant agent, which may be orally supplemented for amelioration of fluoride-mediated oxidative stress even under prevalent high altitude stress.

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References

Ahmed H H, Essawy G S, Salem H A and Abdel Daim M A. 2005. Melatonin has a strong antioxidant activity and improves liver and kidney functions in broiler chicks. Egyptian Journal of Basic and Applied Sciences 4: 77–92.

Addya S, Chakravarti K, Das M, Ghosh N, Chakravarti D and Chatterjee G C. 1986. Effects of mercuric chloride antioxidant defense components of rat erythrocyte and plasma: influence of vitamin E supplementation. Indian Journal of Experimental Biology 24: 468–70.

Arjun L K, Shankar R G and Vakdevi V. 2017. Dental fluorosis, nutritional status, kidney damage, and thyroid function along with bone metabolic indicators in school-going children living in fluoride-affected hilly areas of Doda district, Jammu and Kashmir, India. Environmental Monitoring and Assessment 189: 579. DOI: https://doi.org/10.1007/s10661-017-6288-5

Akosu T J and Zoakah A I. 2008. Risk factors associated with dental fluorosis in Central Plateau state, Nigeria. Community DOI: https://doi.org/10.1111/j.1600-0528.2007.00387.x

Dentistry and Oral Epidemiology 36(2): 144–48

Bakonyi T and Radak Z. 2004. High altitude and free radicals. Journal of Sports Science and Medicine 3: 64–69.

Bharti V K and Srivastava R S. 2011. Effect of pineal proteins and melatonin on certain biochemical parameters of rats exposed to high-fluoride drinking water. Fluoride 44: 30–36.

Bharti V K and Srivastava R S. 2009. Protective role of buffalo pineal proteins on arsenic-induced oxidative stress in blood

and kidney of rats. Health 1: 167–72.

Bharti V K, Srivastava R S and Anand A K. 2012. Effect of melatonin and buffalo epiphyseal proteins on vital organs tissues proteins. Indian Journal of Animal Sciences 82: 176– 79.

Buege J A and Aust S D. 1978. Microsomal lipid peroxidation. Methods in Enzymology 52: 302–10. DOI: https://doi.org/10.1016/S0076-6879(78)52032-6

Benzie Iris F F and Strain J J. 1996. The ferric reducing ability of plasma (FRAP) as a measure of ‘‘antioxidant power’’: The FRAP assay. Analytical Biochemistry 239: 70–76. DOI: https://doi.org/10.1006/abio.1996.0292

Blios M S. 1958. Antioxidant determinations by the use of a stable free radical. Nature 26: 1199–1200. DOI: https://doi.org/10.1038/1811199a0

Blaszczyk I, Grucka-Mamczar E, Kasperczyk S and Birkner E. 2008. Influence of fluoride on rat kidney antioxidant system: effects of methionine and vitamin E. Biological Trace Element Research 121: 51–59. DOI: https://doi.org/10.1007/s12011-007-8030-6

Bulle F, Mavier P, Zafrani E S, Preaux A M, Lescs M C and Siegrist S. 1990. Mechanism of gamma-glutamyl transpeptidase release in serum during intrahepatic and extrahepatic cholestasis in the rat: a histochemical, biochemical and molecular approach. Hepatology 11: 545–50. DOI: https://doi.org/10.1002/hep.1840110404

Chlubek D. 2003. Fluoride and oxidative stress [editorial review]. Fluoride 36: 217–28.

Chawla S L, Yadav R, Shah D and Rao M V. 2008. Protective action of melatonin against fluoride-induced hepatotoxicity in adult female mice. Fluoride 41: 44–51.

Eren E, Ozturk M and Mumcu E F. 2005. Fluorosis and its haematological effects. Toxicology and Industrial Health 21: 255–58. DOI: https://doi.org/10.1191/0748233705th236oa

Giri D K, Ghosh R C, Kashyap D K, Dewangan G and Maiti S K. 2015. Haemato-biochemical alterations in subacute oral toxicity of sodium fluoride in wistar rats. Journal of Animal Research 5: 595–98. DOI: https://doi.org/10.5958/2277-940X.2015.00100.X

Haijun Y, Jianghua C and Xizhou Z et al. 2008. Ultrasonographic analysis of the liver, spleen and kidney in young emigrants to high altitude areas. Shanghai Medical Imaging 17: 149–52.

Hou R, Mi Y, Xu Q, Wu F, Ma Y, Xue P and Yang W. 2014. Oral health survey and oral health questionnaire for high school students in Tibet, China. Head and Face Medicine 10: 17. DOI: https://doi.org/10.1186/1746-160X-10-17

Kalia S, Bharti V K, Gogoi D, Giri Arup and Kumar B. 2017. Studies on the growth performance of different broiler strains at high altitude and evaluation of probiotic effect on their survivability. Scientific Reports. #Article ID 46074. DOI: https://doi.org/10.1038/srep46074

Karadeniz A and Altintas L. 2008. Effects of panax ginseng on fluoride-induced haematological pattern changes in mice. Fluoride 41: 67–71.

Kant V, Verma P K and Pankaj N K. 2009. Haematological profile of sub acute oral toxicity of fluoride and ameliorative efficacy of aluminium sulphate in goats. Toxicology International 16: 31–35.

Karimungi M G and Joshi B N. 1996. Diurnal sensitivity in melatonin-induced hematological changes in the male albino rat. Biological Signals 5: 283–90. DOI: https://doi.org/10.1159/000109201

Kumar A, Tripathi N and Tripathi M. 2007. Fluoride-induced biochemical changes in fresh water catfish (Clarias batrachus

L.). Fluoride 40: 37–41.

Manocha S L, Warner H and Olkowski Z L. 1975. Cytochemical response of kidney, liver, and nervous system of fluoride ions in drinking water. Histochemical Journal 7: 343–55. DOI: https://doi.org/10.1007/BF01007019

Miller L E, McGinnis G R, Kliszczewicz B, Slivka D, Hailes W, Cuddy J, Dumke C, Ruby B and Quindry J C. 2013. Blood oxidative-stress markers during a high-altitude trek. International Journal of Sport Nutrition and Exercise Metabolism 23: 65–72. DOI: https://doi.org/10.1123/ijsnem.23.1.65

Narayana K D, Souza U J and Rao K P. 2002. Effect of ribavirin on epididymal spermcount in rat. Indian Journal of Physiology and Pharmacology 46: 97–101.

Pohanka M, Sobotka J, Jilkova M and Stetina R. 2010. Oxidative stress after sulfur mustard intoxication and its reduction by melatonin: efficacy of antioxidant therapy during serious intoxication. Drug and Chemical Toxicology 34: 85–91. DOI: https://doi.org/10.3109/01480545.2010.505238

Plateau State, Nigeria. Community Dentistry and Oral Epidemiology. 36: 144–148.

Patil G P and Dhande R R. 2000. Effect of HgCl and CdCl on haematobiochemical parameters of the fresh water fish, Channa punctatus. Journal of Ecotoxicology and Environmental Monitoring 10: 177–81.

Park K. 2011. Passmore, p 577. Textbook of Preventive and Social Medicine. 21 Edn. Banarasisdas Bhanot Publishers, Jabalpur, India.

Reiter R J, Tan D X and Maldonado M D. 2005. Melatonin as an antioxidant: physiology versus pharmacology. Journal of Pineal Research 39: 215–26. DOI: https://doi.org/10.1111/j.1600-079X.2005.00261.x

Reiter R J, Tan D X and Sainz R M. 2002. Melatonin: reducing the toxicity and increasing the efficacy of drugs. Journal of Pharmacy and Pharmacology 54: 1299–21. DOI: https://doi.org/10.1211/002235702760345374

Susheela A K. 2001. Fluorosis Indian scienario: A treatise on fluorosis. Fluorosis Research and Rural Development Foundation, New Delhi, India.

Saravanan S, Kalyani C, Vijayarani M, Jayakodi P, Felix A, Nagarajan S, Arunmozhi P and Krishnan V. 2008. Prevalence of dental fluorosis among primary school children in rural areas of Chidambaram Taluk, Cuddalore District, Tamil Nadu, India. Indian Journal of Community Medicine 33: 146–50. DOI: https://doi.org/10.4103/0970-0218.42047

Sidhu I P S, Bhatti J S and Bhatti G K. 2014. Modulatory action of melatonin against chlorpyrifos induced hepatotoxicity in Wistar rats. Asian Journal of Multidisciplinary Studies 2(9): 123–31.

Tian Y M, Zhang G Y and Dai Y R. 2003. Melatonin rejuvenates degenerated thymus and redresses peripheral immune functions in aged mice. Immunology Letters 88: 101–104. DOI: https://doi.org/10.1016/S0165-2478(03)00068-3

Tsunoda M, Aizawa Y, Nakana K, Liu Y, Horuchi T, Hai K and Tsunoda H. 2005. Changes in fluoride levels in the liver, kidney and brain and in neurotransmitters of mice after sub acute administration of fluoride. Fluoride 38: 284–92.

Thangapandiyan S and Miltonprabu S. 2013. An in vivo and in vitro studies on the antioxidant property of epigallocatechin gallate on sodium fluoride induced toxicity in rats. International Journal of Phytopharmacology 4: 245–54.

Vijayalaxmi Russel J, Reiter Dun-Xiantan, Terence S, Herman and Charles R. 2004. Melatonin as a radioprotective agent: A review. International Journal of Radiation Oncology Biology Physics 59: 639–53. DOI: https://doi.org/10.1016/j.ijrobp.2004.02.006

Vural H, Sabuncu T, Oktay Arslan S and Aksoy N. 2001. Melatonin inhibits lipid peroxidation and stimulates the antioxidant status of diabetic rats. Journal of Pineal Research 31: 193–98. DOI: https://doi.org/10.1034/j.1600-079X.2001.310301.x

Vasant R A and Narasimhacharya A V. 2012. Ameliorative effect of tamarind leaf on fluoride-induced metabolic alterations. Environmental Health and Preventive Medicine 17: 484–93. DOI: https://doi.org/10.1007/s12199-012-0277-7

Wessam M and Abdel-Wahab. 2013. Protective effect of thymoquinone on sodium fluoride-induced hepatotoxicity and oxidative stress in rats. Journal of Basic and Applied Zoology 66: 263–70. DOI: https://doi.org/10.1016/j.jobaz.2013.04.002

West J B. 2004. The physiologic basis of high-altitude diseases. Annals of Internal Medicine 141: 789–800. DOI: https://doi.org/10.7326/0003-4819-141-10-200411160-00010

Whitford G M. 1997. Determinants and mechanisms of enamel fluorosis. Ciba Foundation Symposium 205: 226–41. DOI: https://doi.org/10.1002/9780470515303.ch16

Zaghloul D M and Gad S B. 2014. Melatonin restores renal functions and histology in aged rats. Research Opinions in Animal and Veterinary Sciences 4: 249–57.

Zhipeng Fan, Yanhui Gao, Wei Wang, Hongqiang Gong, Min Guo, Shengcheng Zhao, Xuehui Liu, Bing Yu and Dianjun Sun. 2016. Prevalence of brick tea-type fluorosis in the Tibet autonomous region. Journal of Epidemiology 26: 57–63. DOI: https://doi.org/10.2188/jea.JE20150037

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2019-01-22

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2019-01-22

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How to Cite

VIVEK, P., BHARTI, V. K., KALIA, S., GIRI, A., KUMAR, K., & KUMAR, B. (2019). Protective effects of melatonin against fluoride-induced oxidative stress in rats at high altitude. The Indian Journal of Animal Sciences, 89(1), 34–39. https://doi.org/10.56093/ijans.v89i1.86377
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