Protective Role of Capsaicin against Sodium Fluoride-induced Oxidative Damage of Liver in Rats

Jump To References Section

Authors

  • Department of Physiology (UG and PG), Serampore College, Serampore, Hooghly – 712201, West Bengal ,IN
  • Department of Physiology (UG and PG), Serampore College, Serampore, Hooghly – 712201, West Bengal ,IN
  • Department of Statistics, Serampore College, Serampore, Hooghly – 712201, West Bengal ,IN
  • Department of Physiology (UG and PG), Serampore College, Serampore, Hooghly – 712201, West Bengal ,IN
  • Department of Physiology (UG and PG), Hooghly Mohsin College, Chinsurah, Hooghly – 712101, West Bengal ,IN

DOI:

https://doi.org/10.18311/ti/2021/v28i1/25920

Keywords:

Antioxidant, Capsaicin, Fluoride, Hepatotoxicity, NaF, Oxidative Stress
oxidative stress

Abstract

Capsaicin, a bioactive component of hot chili pepper, is a potent antioxidant and effective in ailments of diverse health problems. The present study evaluated the possible protective effectiveness of capsaicin (Caps) against sodium fluoride (NaF) - induced oxidative damage in liver tissue. Rats treated with NaF (10.3mg/kg b.wt/day) orally for five weeks showed marked elevation of serum level of ALT, AST and bilirubin which are the biochemical markers of liver lesions. Results also showed that NaF exposure significantly elevated LPO level and NO generation in the liver with a parallel significant decline in activities of SOD, CAT, and content of GSH. While, Caps supplementation (0.5 mg/kg b.wt/day) was significantly reversed the NaF-induced oxidative stress; amended AST, ALT levels and bilirubin content; and restored normal histology of the liver. Therefore, it can be concluded that Caps plays a protective role against hepatic toxicity produced by NaF exposure.

Downloads

Download data is not yet available.

Published

2021-03-24

How to Cite

Ray, D., Jadav, P., Panda, P., Mukherjee, S., & Ghosh, S. (2021). Protective Role of Capsaicin against Sodium Fluoride-induced Oxidative Damage of Liver in Rats. Toxicology International, 28(1), 31–38. https://doi.org/10.18311/ti/2021/v28i1/25920

Issue

Section

Original Research
Received 2020-08-20
Accepted 2020-12-07
Published 2021-03-24

 

References

Andezhath SK, Susheela AK, Ghosh G. Fluorosis management in India: The impact due to networking between health and rural drinking water supply agencies. Interdiscip Perspect Drink Water Risk Assess Manag. 2000; 260:159–65.

Fawell J, Bailey K, Chilton J, Dahi E, Fewtrell L, Magara Y (WHO). Fluoride in drinking water. London, UK: IWA Publishing Company; 2002.

Nabavi SF, Nabavi SM, Habtemariam S, Moghaddam AH, Sureda A, Jafari M, Latifi AM. Hepatoprotective effect of gallic acid isolated from Peltiphyllum peltatum against sodium fluoride-induced oxidative stress in rat's kidney. Mol Cell Biochem. 2013; 372:233–9.PMid: 23014933. https://doi.org/10.1007/s11010-012-1464-y DOI: https://doi.org/10.1007/s11010-012-1464-y

Karadeniz A, Altıntas L. Effects of Panax Ginseng on fluoride-induced haematological pattern changes in mice. Fluoride. 2008; 41:67–71.

Deng H, Kuang P, Cui H, Chen L, Luo Q, Zhao L. Sodium fluoride (NaF) induces the splenic apoptosis via Endoplasmic Reticulum (ER) stress pathway in vivo and in vitro. Aging. 2016; 8:3552–67. PMid: 28039491 PMCid: PMC5270686. https://doi.org/10.18632/aging. 101150 DOI: https://doi.org/10.18632/aging.101150

Barbier O, Arreola-Mendoza L, Del-Razo LM. Molecular mechanisms of fluoride toxicity. Chem Biol Interact. 2010; 188: 319–33. PMid: 20650267. https://doi.org/10.1016/j.cbi.2010.07.011 DOI: https://doi.org/10.1016/j.cbi.2010.07.011

Hassan HA, Yousef MI. Mitigating effects of antioxidant properties of black berry juice on sodium fluoride induced hepatotoxicity and oxidative stress in rats. Food Chem Toxicol. 2009; 47(9):2332–7. PMid: 19540898. https://doi.org/10.1016/j.fct.2009.06.023 DOI: https://doi.org/10.1016/j.fct.2009.06.023

Lu Y, Luo Q, Cui H, Deng H, Kuang P, Liu H, Fang J, Zuo Z, Deng J, Li Y, Wang X, Zhao L. Sodium fluoride causes oxidative stress and apoptosis in the mouse liver. Aging. 2017; 9(6):1623–39. PMid: 28657544 PMCid: PMC5509460. https://doi.org/10.18632/aging.101257 DOI: https://doi.org/10.18632/aging.101257

Zhou BH, Zhao J, Liu J, Zhang JL, Li J, Wang HW. Fluoride induced oxidative stress is involved in the morphological damage and dysfunction of liver in female mice. Chemosphere. 2015; 139:504–11. PMid: 26295688. https://doi.org/10.1016/j.chemosphere.2015.08.030 DOI: https://doi.org/10.1016/j.chemosphere.2015.08.030

Xiong X, Liu J, He W, Xia T, He P, Chen X, Yang K, Wang A. Dose-effect relationship between drinking water fluoride levels and damage to liver and kidney functions in children. Environ Res. 2007; 103:112–6. PMid: 16834990. https://doi.org/10.1016/j.envres.2006.05.008 DOI: https://doi.org/10.1016/j.envres.2006.05.008

Kogure K, Goto S, Nishimura M. Mechanism of potent antiperoxidative effect of capsaicin. Biochim Biophys Acta. 2002; 1573: 84–92. https://doi.org/10.1016/S0304- 4165(02)00335-5 DOI: https://doi.org/10.1016/S0304-4165(02)00335-5

Anandakumar P, Kamaraj S. Capsaicin modulates pulmonary antioxidant defense system during Benzo (a) pyrene-induced Lung Cancer in Swiss Albino Mice. Phytother Res. 2008; 22:529–33. PMid: 18338764. https://doi.org/10.1002/ptr.2393 DOI: https://doi.org/10.1002/ptr.2393

Luqman S, Rizvi SI. Protection of lipid peroxidation and carbonyl formation in proteins by capsaicin in human erythrocytes subjected to oxidative stress. Phytother Res. 2006; 20:303–6. PMid: 16557614. https://doi.org/10.1002/ptr.1861 DOI: https://doi.org/10.1002/ptr.1861

Kempaiah RK, Srinivasan K. Influence of dietary curcumin, capsaicin and garlic on the antioxidant status of red blood cells and the liver in high-fat-fed rats. Annals Nutr Metab. 2004; 48(5):314–20. PMid: 15467281. https://doi.org/10.1159/000081198 DOI: https://doi.org/10.1159/000081198

Huang M, Cheng G, Tan H, Qin R, Zou Y, Wang Y, Zhang Y. Capsaicin protects cortical neurons against ischemia/reperfusion injury via downregulating NMDA receptors. Exp Neurol. 2017; 295:66–76. PMid: 28479337 PMCid: PMC5991616. https://doi.org/10.10 16/j.expneurol.2017.05.001 DOI: https://doi.org/10.1016/j.expneurol.2017.05.001

Reitman S, Frankel S. A colorimetric method for the determination of serum glutamic oxaloacetic acid and glutamic pyruvic transaminases. Am J Clin Pathol.1957; 28:56–63. PMid: 13458125. https://doi.org/10.1093/ajcp/ 28.1.56 DOI: https://doi.org/10.1093/ajcp/28.1.56

Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. The J of Biol Chemistry. 1951; 193(1):265–75. https://doi.org/10.1016/S0021-9258(19)52451-6 DOI: https://doi.org/10.1016/S0021-9258(19)52451-6

Giuseppina MR, Rosario M, Oreste G, Maria P, Raffaele DC. Prolactin induction of nitric oxide synthase in rat C6 Glioma cells. J Neurochem. 1999; 73:2272–7. PMid: 10582584. https://doi.org/10.1046/j.1471-4159.1999.073 2272.x DOI: https://doi.org/10.1046/j.1471-4159.1999.0732272.x

Wills ED. Evaluation of lipid peroxidation in lipids and biological membranes. Snell K, Mullock B. (Eds.) Biochemical Toxicology: A practical approach. Oxford (England): IRL Press; 1987; 138–40.

Beauchamp C, Fridovich I. Assays of superoxide dismutase. Analytical Biochem. 1971; 44:276–87. https://doi.org/10.1016/0003-2697(71)90370-8 DOI: https://doi.org/10.1016/0003-2697(71)90370-8

Beers RF, Sizer IW. A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J of Biol Chem.1952: 195:133–40. https://doi.org/10.1016/S0021-9258(19)50881-X DOI: https://doi.org/10.1016/S0021-9258(19)50881-X

Ellman GL. Tissue sulfhydryl groups. Arch Biochem Biophys. 1959; 82(1):70–7. https://doi.org/10.1016/0003- 9861(59)90090-6 DOI: https://doi.org/10.1016/0003-9861(59)90090-6

Liu G, Chai C, Cui L. Fluoride causing abnormally elevated serum nitric oxide levels in chicks. Environ. Toxicol Pharmacol. 2003; 1:199–204. https://doi.org /10.1016/S1382-6689(03)00002-4 DOI: https://doi.org/10.1016/S1382-6689(03)00002-4

Parihar S, Choudhary A, Gaur S. Toxicity of fluoride in liver of Albino rat and Mitigation after adopting artificial (Vitamin C and D) and natural (Aloe vera) food supplementations. Int J Adv Res Tech. 2013; 2(2):1–11.

Sharma A, Chinoy NJ. Role of free radicals in fluorideinduced toxicity in liver and kidney of mice and its reversal. Fluoride.1998; 31:S26.

Shivarajashankara YM, Shivashankara AR, Bhat G, Rao SH. Brain lipid peroxidation and antioxidant systems of young rats in chronic fluoride intoxication. Fluoride. 2002; 35(3):197–203.

Ilbey YO, Ozbek E, Cekmen M, Simsek A, Cekmen M, Otunctemur A, Somay A Chemoprotective effect of a nuclear factor-kB inhibitor, pyrrolidine dithiocarba mate, against cisplatin-induced testicular damage in rats. J Androl. 2009; 30:505–14. PMid: 19234314. https://doi.org/10.2164/jandrol.108.006270 DOI: https://doi.org/10.2164/jandrol.108.006270

Yildirim NC, Kandemir FM, Ceribasi S, Ozkaraca M, Benzer F. Pomegranate seed extract attenuates chemo therapy induced liver damage in an experimental model of rabbits. Cell Mol Biol. 2013; 59(Suppl):1842–7.

Chinoy NJ, Memon MR. Beneficial effects of some vitamins and calcium on fluoride and aluminium toxicity on gastrocnemius muscle and liver of male mice. Fluoride. 2001; 34:21–33.

Peesa JP. Nephroprotective potential of herbal medicines: a review. Asian J Pharm Tech. 2013; 3:115–8.

Nakashima H, Kinoshita M, Nakashima M, Habu Y, Shono S, Uchida T, Shinomiya N, Seki S. Superoxide produced by Kupffer cells is an essential effector in concanavalin A-induced hepatitis in mice. Hepatology. 2008; 48:1979–88. PMid: 18942689. https://doi.org/10.1002/hep.22561 DOI: https://doi.org/10.1002/hep.22561

Pemberton PW, Aboutwerat A, Smith A, Burrows PC, McMahon RF, Warnes TW. Oxidant stress in type I autoimmune hepatitis: The link between necroinflam mation and fibrogenesis? Biochim Biophys Acta. 2004; 1689:182–9. PMid: 15276644. https://doi.org/10.1016/j. bbadis.2004.01.005 DOI: https://doi.org/10.1016/j.bbadis.2004.01.005

Shimeda Y, Hirotani Y, Akimoto Y. Protective effects of capsaicin against cisplastin-induced nephrotoxicity. Biol Pharm Bull. 2005; 28:1635–8. PMid: 16141530, https://doi.org/10.1248/bpb.28.1635 DOI: https://doi.org/10.1248/bpb.28.1635

Kour K, Koul ML, Koul RL. Histological changes in liver following sodium fluoride ingestion. Fluoride.1981; 14(3):119–23.

Shashi A, Thapar SP. Histopathology of fluoride-induced hepatotoxicity in rabbits. Fluoride. 2001; 34(1):34–42.

Blaszczyk I, Birkner E, Kasperczyk S. Influence of methionine on toxicity of fluoride in the liver of rats. Biol Trace Elem Res. 2011; 139:325–31. PMid: 20306234. https://doi.org/10.1007/s12011-010-8664-7 DOI: https://doi.org/10.1007/s12011-010-8664-7

Yadav SS, Kumar R, Tripathi M. Effects of fluoride exposure on some enzymatic and histopathological changes in the liver of Heteropneustes fossilis (Bloch). Int J Fauna Biol Studies. 2014; 1(5):80–4.

Manjunatha H, Srinivasan K. Protective effect of dietary curcumin and capsaicin on induced oxidation of low-density lipoprotein, iron-induced hepatotoxicity and carrageenan-induced inflammation in experimental rats. FEBS J. 2006; 273:4528–35. PMid: 16956363. https://doi.org/10.1111/j.1742-4658.2006.05458.x DOI: https://doi.org/10.1111/j.1742-4658.2006.05458.x

Most read articles by the same author(s)