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2017 | 26 | 5 |

Tytuł artykułu

Protective potential of quercetin on Cd-induced hepatorenal damage

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Industrial and environmental pollution are sources of cadmium (Cd) exposure that cause serious health hazards. In this work we investigated the protective effect of quercetin on Cd-induced hepatorenal damage in rats. Cd toxicity was confirmed by evaluating its level in serum and tissues. Liver function enzymes, bilirubin, albumin, creatinine, uric acid, and urea were assessed in serum. However, lipid peroxidation and the activity of the antioxidant enzymes were examined in tissues. In addition, liver and kidney were studied histologically. Our results showed that the concentration of Cd was higher in tissues of Cd-treated rats while in the Cd and quercetin co-treated group, the Cd concentration was significantly reduced. Co-administration of Cd with quercetin improved the liver function as evident by the reduced levels of ALP, ALT, AST, bilirubin, and the increase in concentration of total protein and albumin. Also, kidney restored its normal function as well as lipid peroxidation, and the antioxidant enzymes partially restored their normal values. In addition, the protective effect of quercetin on the hepatorenal damage induced by Cd was confirmed histologically. In conclusion, quercetin treatment may provide protection against the damages induced by Cd exposure.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

26

Numer

5

Opis fizyczny

p.2197-2205,fig.,ref.

Twórcy

autor
  • Zoology Department, Faculty of Science, Alexandria University, Alexandria, Egypt
autor
  • Biology Department, Faculty of Applied Science, Umm-Al Qura University, King Saudi Arabia
autor
  • Chemistry Department, Faculty of Science, Tanta University, Tanta, Egypt
  • Chemistry Department,College of Science, King Faisal University, Al Ahsaa, P.B. Box 380, Hufof 31982, Saudi Arabia
autor
  • Physiology Department, Faculty of Medicine, Aswan University

Bibliografia

  • 1. Kedam T.R., Sheik R.B., Bai M.M., HaseenaBhanu S.K. A histological study on acrylamide and Cd chloride altered chick embryonic liver. IOSR J Pharm. 2 (1), 1, 2012.
  • 2. Stohs S.J., Bagachi D., Hassoun E., Baguchi M. Oxidative mechanisms in the toxicity of Chromium and Cd ions. J Environ Path Toxicol Oncol. 19, 201, 2000.
  • 3. Velickov A., Jancic N., Dinidic N., Rancic I., Bojanic N., Krstic M. Histological and histochemical characteristics of rat myocardium in Cd toxicosis. Acta Medica Medianae. 52 (2), 15, 2013.
  • 4. Michael C., Jorge P. Endocrine disruption by Cd, a common environmental toxicant with paradoxical effects on reproduction. Exp Biol Med. 229 (5), 383, 2004.
  • 5. Kara H., Karatas F., Canatan H., Servi K. Effects of exogenous metallothionein on acute Cd toxicity in rats. Biol Trace Elem. Res. 104 (3), 223, 2005.
  • 6. Brzoska M.M. Moniuszko-Jakoniuk J., Pilat-Marcinkiewicz B., Sawicki B. Liver and kidney function and histology in rats exposed to Cd and ethanol. Alcohol Alcolism. 38 (1), 2, 2003.
  • 7. Kang M.Y., Cho S.H., Lin Y.H., Seo J.C., Hong Y.C. Effects of environmental Cd exposure on liver function in adults. Occup Environ Med. 70, 268, 2016.
  • 8. Solaiman D., Jonah M.M., Miyazaki W.H.O.G., Bhatlacharyya M.H. Increased metallothionin in mouse liver, kidneys and duodenum during lactation. Toxicol Sci. 60, 184, 2001.
  • 9. Ojo O.A., Ajiboye B.O., Oyinloye B.E., Ojo A.B., Olarewaju O.I. Protective effect of Irvingia gabonensis stem bark against Cd-induced toxicity in albino rats. Advances in Pharmaceutics. Hindiwi Publishing Co-operation; Article ID 894610, 8, 2014.
  • 10. Maheswari C. Venkatnarayanan R. Protective effect of orithosiphon stamineus leaves against lead acetate and Cd chloride included renal dysfunction in rats. Int Res J Pharm. 4 (14), 232, 2013.
  • 11. Albasha M., Azab A. Effect of Cd on liver and amelioration by aqueous extracts of fenugreek seeds, rosemary, and cinnamon in guinea pigs: Histological and biochemical study. Cell Biol. 2 (2), 7, 2014.
  • 12. El-Refaiy A.I., Eissa F.I. Histopathological and cytotoxicity as biomarkers in treated rats with Cd and some therapeutic agents. Saudi J Biol Sci. 20, 265, 2013.
  • 13. Renugadevi J., Prabu S.M. Cd induced hepatotoxicity in rats and the protective effect of maringenin. Exp Toxicol Pathol. 62 (2), 171, 2010.
  • 14. Galati G., Sabzevari O., Wilson J.X., O'Bren P.J. Prooxidant activity and cellular effects of phenoxyl radicals of dietary flavonoids and other polyphenolics. Toxicology. 177, 91, 2002.
  • 15. Pedrielli P., Skibsted L.H. Antioxidant synergy and regeneration effects of quercetin, (-) epicatechin, and (+) catechin on α tocopherol in homogeneous solutions of peroxidating methyl linoleate. J Agricult Food Chem. 50, 7138, 2003.
  • 16. Lu Y.X., Zhang Q., Li J., Sun Y.X., Wang L.K., Cheng W.M., Hu X.Y. Antidiabetic effects of total flavonoids from Litsea coreana leave on fat-fed, streptozotocin induced type 2 diabetic rats. Am J Chin Med. 38, 713, 2010.
  • 17. Jin G., Kan J., Zhu Y., Lei N. Spectrophotometric determination of Cd (II) using the chromogenic reagent 4-(o-diazoaminophenylarsonic acid) azobenzene. Indian J Chem. 39A, 1227, 2000.
  • 18. Lowry O.H., Rosebrough N.J., Farr A.L., Randa R.J. Protein measurement with the Folin phenol reagent. J Biol Chem. 193 (1), 265, 1951.
  • 19. Buege J.A., Aust S.D. Microsomal lipid peroxidation. Methods Enzymol. 52 (C), 1302, 1978.
  • 20. McCord J.M., Fridovich I. Superoxide dismutase. An enzymatic function for erythrocupein (hemocuprein). J Biol Chem. 244 (22), 64049, 1969.
  • 21. Aebi H. Catalase estimation in methods of enzymatic analysis, H.V. Bermeye, Verlag Chemis, Ed. 673, 1974.
  • 22. Rotruck J.T., Pope A.L., Ganther H.E., Swanson A.S., Hafema D.G., Hoekstra W.G. Selenium: biochemical role as a component of glutathione peroxidase. Science. 179 (4073), 588, 1973.
  • 23. Bancroft D., Gamble M. The theory and practice of histological technique. 5th edition. Churchil Living Stone. 75, 2002.
  • 24. Ibiam A.V., Ugwuja E.I., Ejeogo C., Ugwu O. Cd-induced toxicity and the hepatoprotective potentials of aqueous extract of Jessiaea nervosa leaf. Advanced Pharmaceutical Bulletin. 3 (2), 309, 2013.
  • 25. Jaramillo-Jurez F., Rodrguez-Vzquez M.L., Rincn-Snchez A.R., Consolacin Martnez C.M., Ortiz G.G., Lianas J. Acute renal failure induced by carbon tetrachloride in rats with hepatic cirrhosis. Ann Hepatol. 7 (4), 331, 2003.
  • 26. El-Kady A.A., Sharaf H.A., Abou-Donia M.A., Abbes S., Naguib K., Ouestatli R., Abdel-Wahhab M.A. Adsorption of cd²⁺ ions on an Egyptian montmorillonite and toxicological effects in rats. Appl Clay Sci. 44 (1-2), 59, 2009.
  • 27. Finco D.R. Kidney function. In: Kaneko J.J., Harvey, Bruce M.L., editors. Clinical biochemistry of domestic animal. 5th ed. San Diego, CA: Academic Press; 462, 1997.
  • 28. El-Morsy A.M., Sakr S.A., Bayomy M.F. Ameliorative effect of aqueous leaves extract of Rosmarius officinalis on Cd induced kidney injury in albino Rats. J Biosci Appl Res. 1 (1), 10, 2015.
  • 29. El-Boshy M.E., Risha E.F., Abdelhamid F.M., Mubarak M.S., Hadda T.B. Protective effects of selenium against Cd induced hematological disturbances, immunsuppressive, oxidative stress and hepatorenal damage in rats. J. Trace Elem. Med. Biol. 29, 104, 2015.
  • 30. Sudo J., Hayashi T., Kimuto S., Kakuno K., Terui J., Takashima K., Soyama M. Mechanism of nephrotoxicity included by repeated administration of Cd chloride in rats. J Toxicol Environ Health. 48 (4), 333, 1996.
  • 31. Gibellini L., Pinti M., Nasi M., Montagna J.P., De Biasi S., Roat E., Bertoncell L., Cooper E.L., Cossarizza A. “Quercetin and Cancer Chemoprevention. Evid Based Complement Alternat Med. Article ID 591356, 15, 2011. doi:10.1093/ecam/neq053
  • 32. Heijnen C.C.M., Haenen G.R.M.N.M., Van Acker F.A.A., VanDer Vijgh W.J.F., Bast A. Flavonoids as peroxynitrite scavengers: the role of the hydroxyl groups. Toxicology in vitro. 15, 3, 2001.
  • 33. Zeashan H., Amresh G., Singh S., Rao C.V. Hepatoprotective activity of Amaranthus spinosus in experimental animals. Food Chem Toxicol. 46 (11), 3417, 2008.
  • 34. El-Sharaky A.S., Newairy A.A., Badreldeen M.M., Eweda S.M., Sheweira S.A. Protective role of selenium against renal toxicity induced by Cd in rats. Toxicology 235, 185, 2007.
  • 35. Thijissen S., Cuypers A., Maringwa J., Smeets K., Hormans N. Low Cd exposure triggers a biphasic oxidative stress response in mice kidneys. Toxicology. 236, 29, 2007.
  • 36. Stohs S.J., Bagchi D. Oxidative mechanisms in the toxicity of metal ions. Free Radic Biol Med. 18 (2), 321, 1995.
  • 37. Ogjanovic B.I., Pavlovic S.Z., Maletic S.D., Zikic R.V., Stajn A.S., Radokicic R.M., Soicic Z.S., Petrovic V.M. Protective influence of vitamin E on antioxidant defense system in the blood of rats treated with Cd. Physiol Rev. 52, 563, 2003.
  • 38. Obaiah J., Rani V.A. Amelioration effect of zinc and Iron supplementation on selected oxidative stress enzymes in liver and kidney of Cd-treated male albino rat. Toxicol Int. 22 (1), 1, 2015.
  • 39. Nagaraj M., Sumitha S., Varalakshmi P. Effect of luped, apentacyclic tritepene, on lipid peroxidation and antioxidant status in rate kidney after chronic Cd exposure. J Appl Toxicol. 20, 413, 2000.
  • 40. Filek M., Keskinen R., Harrikainen H., Azarejko I., Janiak A., Miszalski Z., Golda A. The protective role of selenium in rape seedlings subjected to Cd stress. J plant Physiol. 26; 165 (8), 1833, 2008.
  • 41. Stohs S.J., Bagchi D., Hassoun E., Bagchi M. Oxidative mechanism sin the toxicity of chromium and Cd ions. J Environ Pathol Toxicol Oncol 19, 201, 2000.
  • 42. Sunaina A., Ansari B. Biochemical markets of oxidative stress in Zebra fish Danio ratio exposed to Cd chloride. Ann Biol Res. 6 (8), 6, 2015.
  • 43. Lin W., Qianj L.S., Long H.E., Gang L.I., Yong W.Z. Protective effects of quercetin on Cd-induced cytotoxicity in primary cultures of rat proximal tubular cells. Biomed Environ Sci. 26 (4), 258, 2013.
  • 44. Kim M.R., Lee J.Y., Lee H.H., Aryal D.K., Kim Y.G., Kim S.K., Woo E.R., Kang K.W. Antioxidative effects of quercetin glycosides isolated from the flower buds of Tussilago farfare L. Food Chem Toxicol. 44, 1299, 2006.
  • 45. Tarasub N., Junseecha T., Tarasub C., AyutthayaW. Protective effects of curcumin, vitamin C, or their combination on Cd-induced hepatotoxicity. J Basic Clin Pharm. 3 (2), 273, 2012.
  • 46. Sakr S.A., Bayomy M.F., EL-Morsy A.M. Rosemary extract ameliorates Cd-induced histological changes and oxidative damage in the liver of albino rat. J Basic Appl Zool. 71, 1, 2015.
  • 47. Leo M.A., Arai M., Saro M., Lieber C.S. Hepatotoxicity of vitamin A and ethanol in the rat. Gastroenterology. 82, 194, 1982.
  • 48. Rikans L.E., Yamano T. Mechanisms of Cd-mediated acute hepatotoxicity. J Biochem Mol Toxicol. 14 (2), 110, 2000.
  • 49. Liu J., Kershaw W., Liu Y., Klaassen C.D. Cd-induced hepatic endothelial cell injury in inbred strains of mice. Toxicology. 75 (1), 51, 1992.
  • 50. Zargar S., Siddiqi N.J., Al Daihan S.K., Wanti T.A. Protective effects of quercetin on Cd fluoride induced oxidative stress at different intervals of time in mouse liver. Acta Biochem Pol. 62 (2), 207, 2015.
  • 51. Aktoz T., Kanter M., Hulya U.Y., Aktas C., Erboga M., Atakan H.I. Protective Effect of Quercetin Against Renal Toxicity Induced by Cd in Rats. Balkan Med J. 29, 56, 2012.

Typ dokumentu

Bibliografia

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Identyfikator YADDA

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