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The effect of allicin on blood and tissue lead content in mice

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Abstract

Previous experimental results have revealed that garlic (Alium sativum) can reduce lead toxicity and tissue lead content in lead-exposed rodents. In the present study, the effects of different doses of allicin, the main active constituent of garlic, in reducing of organ and blood lead levels were evaluated in mice exposed to 1,000 ppm of lead acetate in drinking water. Three groups of mice received allicin at doses of 12, 24, and 48 µg/kg orally (twice daily) during ongoing 14-day lead exposure. Mice were killed on experimental day 15. Allicin treatment reduced lead retention in blood and tissues. Reduction of lead concentration in blood and tissues was dose dependent. With the highest dose of allicin, the greatest rate of reduction of lead concentrations were observed in liver (73.7%), kidney (45%), brain (45%), and bone (44.4%), respectively. Liver zinc concentration was significantly reduced in all treated groups. It was concluded that allicin administered during lead exposure in mice can reduce tissue lead retention and, therefore, might have some therapeutic effect on lead poisoning.

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References

  • Adegbesan BO, Adenuga GA (2007) Effect of lead exposure on liver lipid peroxidative and antioxidant defense systems of protein-undernourished rats. Biol Trace Elem Res 116:219–225

    Article  PubMed  CAS  Google Scholar 

  • Aga M, Iwaki K, Ueda Y, Ushio S, Masaki N, Fukuda S, Kimoto T, Ikeda M, Kuromoto M (2001) Preventive effect of Corindrum sativum (Chinese parsley) on localized lead deposition in ICR mice. J Ethnopharmacol 77:203–208

    Article  PubMed  CAS  Google Scholar 

  • Amagase H, Petesch BL, Matsuura H, Kasuga S, Itakura Y (2001) Intake of garlic and its bioactive compounds. J Nutr 131:955s–962s

    PubMed  CAS  Google Scholar 

  • Aykin-Burns N, Laegeler N, Kellogg G, Ercal N (2003) Oxidative effect of lead in young and adult Fisher 344 rats. Arch Environ Contam Toxicol 44:417–420

    Article  PubMed  CAS  Google Scholar 

  • Badiei K, Pourjaafar M, Nowrooziasl A (2005) Effect of dried garlic powder (Allium sativum) on lead content of different tissues following subclinical lead poisoning in goats. Ir J Vet Res 6:12–16

    Google Scholar 

  • Campbell JR, Rosier RN, Novotny L, Puzas JE (2004) The association between environmental lead exposure and bone density in children. Environ Health Perspec 112:1200–1203

    Article  CAS  Google Scholar 

  • Casteel SW (2006) Lead. In: Peterson ME, Talcott PA (eds) Small animal toxicology, 2nd edn. Saunders-Elsevier, St. Louis, pp 795–805

    Chapter  Google Scholar 

  • Chiado LM, Jacobson SW, Jacobson JL (2004) Neurodevelopment effects of postnatal lead exposure at very low levels. Neurotoxicol Teratol 26:359–371

    Article  Google Scholar 

  • Chung LY (2006) The antioxidant properties of garlic compounds: allyl cystein, alliin, allicin and allyl disulfide. J Med Food 9:205–213

    Article  PubMed  CAS  Google Scholar 

  • Coppi A, Cabinian M, Mirelman D, Sinnis P (2006) Antimalarial activity of allicin, a biologically active compound from garlic cloves. Antimicrob Agents Chemother 50:1731–1737

    Article  PubMed  CAS  Google Scholar 

  • Degernes L, Heilman S, Trogdon M, Jordan M, Davison M, Kraege D, Correa M, Cowen P (2006) Epidemiologic investigation of lead poisoning in trumpeter and tundra swans in Washington state, USA, 2000–2002. J Wild Life Dis 42:345–358

    Google Scholar 

  • Denver MC, Tell LA, Galey FD, Trupkiewicz JG (2000) Comparison of two heavy metal chelators for treatment of lead toxicosis in cockatiels. Am J Vet Res 61:935–940

    Article  PubMed  CAS  Google Scholar 

  • Flora SJS, Bhattacharya R, Vijayaraghavan R (1995) Combined therapeutic potential of meso-2, 3-Dimercaptosuccinic acid and calcium disodium edentate on the mobilization and distribution of lead in experimental lead intoxication in rats. Fund Appl Toxicol 25:233–240

    Article  CAS  Google Scholar 

  • Germain E, Auger J, Gines C, Siess MH, Teyssier C (2002) In vivo metabolism of diallyl disulphide in the rat: identification of two new metabolites. Xenobiotica 32:1127–1138

    Article  PubMed  CAS  Google Scholar 

  • Gilbert SG, Weiss B (2006) Rational for lowering the blood lead level from l0 to 2 µg/dl. Neurotoxicol 27:693–701

    Article  CAS  Google Scholar 

  • Gulson BL, Mizon KJ, Korsch MJ, Palmer JM, Donnelly JB (2003) Mobilization of lead from bone tissue during pregnancy and lactation — a summary of long-term research. Sci Total Environ 303:79–104

    Article  PubMed  CAS  Google Scholar 

  • Hanafy MS, Shalaby SM, El-Fouly MA (1994) Effect of garlic on lead content in chicken tissues. DTW Dtsch Tieraztl Wonchenschr 10:157–158

    Google Scholar 

  • Jones MM, Basinger MA, Gale GR, Atkins LM, Smith AB, Stone A (1994) Effect of chelate treatment on kidney, bone and brain lead level of lead-intoxicated mice. Toxicol 89:91–100

    Article  CAS  Google Scholar 

  • Jones MM, Singh PK, Kostial K, Blanus M, Piasek M, Restek SN (1997) Comparative in vivo lead mobilization of meso- and rac-2, 3-dimercaptosuccinic acid in albino Wistar rats. Pharmacol Toxicol 80:182–186

    Article  PubMed  CAS  Google Scholar 

  • Kalia K, Flora SJS (2005) Strategies for safe and effective therapeutic measures for chronic arsenic and lead poisoning. J Occup Health 47:1–21

    Article  PubMed  CAS  Google Scholar 

  • Kessler M, Durand PY, Huu TC, Royer-Morot MJ, Chanliau J, Netter P, Duc M (1999) Mobilization of lead from bone in end-stage renal failure patients with secondary hyperparathyroidism. Nephrol Dial Transplant 14:2731–2733

    Article  PubMed  CAS  Google Scholar 

  • Kim JS, Hamilton DL, Blakley BR, Roussraux CG (1992) The effect of thiamin on lead metabolism: organ distribution of lead 203. Can J Vet Res 56:256–259

    PubMed  CAS  Google Scholar 

  • Knight TE, Kent M (2001) Succimer for treatment of lead toxicosis in two cats. J Am Vet Med Assoc 218:1946–1948

    Article  PubMed  CAS  Google Scholar 

  • Kostial K, Blanusa M, Piasek M, Restek-Samarzija N, Jones MM, Singh PK (1999) Combined chelation therapy in reducing tissue lead concentrations in suckling rats. J Appl Toxicol 19:143–147

    Article  PubMed  CAS  Google Scholar 

  • Massadeh AM, Al-Safi SA, Momani IF, Alomary AA, Jaradat QM, Alkofahi AS (2007) Garlic (Allium sativum L.) as a potential antidote for cadmium and lead intoxication: cadmium and lead distribution and analysis in different mice organs. Biol Trace Elem Res 120:227–234

    Article  PubMed  CAS  Google Scholar 

  • Meldrum JB, Ko KW (2003) Effects of calcium disodium EDTA and meso-2, 3-dimercaptosuccinic acid of tissue concentrations of lead for use in treatment of calves with experimentally induced lead toxicosis. Am J Vet Res 6:672–676

    Article  Google Scholar 

  • Miron T, Rabinkov A, Wilchek M, Weiner L (2000) The mode of action of allicin: its ready permeability through phospholipids membranes may contribute to its biological activity. Biochem Biophys Acta 1463:20–30

    Article  PubMed  CAS  Google Scholar 

  • Miron T, Bercovici T, Rabinkov A, Wilchek M, Mrelman D (2004) Allicin: preparation and applications. Anal Biochem 331:364–369

    Article  PubMed  CAS  Google Scholar 

  • Mudipali A (2007) Lead hepatotoxicity and potential health effect. Ind J Med Res 126:518–527

    Google Scholar 

  • Okada Y, Tanaka K, Sato E, Okajima H (2006) Kinetic and mechanistic studies of allicin as an antioxidant. Org Biol Chem 4:4113–4117

    Article  CAS  Google Scholar 

  • Osweiler GD (1999) Toxicology, 1st edn. Williams and Wilkins, Philadelphia, pp 195–196

    Google Scholar 

  • Pande M, Mehta A, Pant BP, Flora SJS (2001) Combined administration of a chelating agent and an antioxidant in the prevention and treatment of acute lead intoxication in rats. Environ Toxicol Pharmacol 9:173–184

    Article  PubMed  CAS  Google Scholar 

  • Pappas JB, Ahlquist JT, Allen EM, Banner W (1995) Oral dimercaptosuccinic acid and ongoing exposure to lead: effects on heme synthesis and lead distribution in rat model. Toxicol Appl Pharmacol 133:121–129

    Article  PubMed  CAS  Google Scholar 

  • Patrick L (2006a) Lead toxicity, a review of the literature. Part I: exposure, evaluation and treatment. Alt Med Rev 11:2–22

    Google Scholar 

  • Patrick L (2006b) Lead toxicity, part II: the role of free radical damage and the use of antioxidants in the pathology and treatment of lead toxicity. Alt Med Rev 11:114–126

    Google Scholar 

  • Pounds JG, Long GJ, Rosen JF (1991) Cellular and molecular toxicity of lead in bone. Environ Health Perspect 91:17–32

    Article  PubMed  CAS  Google Scholar 

  • Prasad K, Laxdal VA, Yu M, Raney BL (1995) Antioxidant activity of allicin, an active principle in garlic. Mol Cell Biochem 148:183–189

    Article  PubMed  CAS  Google Scholar 

  • Rabinowitz MB (1991) Toxicokinetics of bone lead. Environ Health Perspect 91:33–37

    Article  PubMed  CAS  Google Scholar 

  • Radostits OM, Gay CC, Hinchcliff KW, Constable PD (2007) Veterinary medicine, 10th edn. Elsevier, London, pp 1799–1808

    Google Scholar 

  • Rahman S, Sultana S (2006) Chemopreventive activity of glycyrrhizin on lead acetate mediated hepatic oxidative stress and its hyperproliferative activity in Wistar rats. Chemico-Biol Inter 160:61–69

    Article  CAS  Google Scholar 

  • Riess ML, Halm JK (2007) Lead poisoning in an adult: lead mobilization by pregnancy. J Gener Int Med 22:1212–1215

    Article  Google Scholar 

  • Rosen RT, Hiserodt RD, Fukuda EK, Ruiz RJ, Zhou Zh, Lech J, Rosen SL, Hartman TG (2001) Determination of allicin, s-allylcystein and volatile metabolites of garlic in breath, plasma or simulated gastric fluids. J Nutr 131:968s–971s

    PubMed  CAS  Google Scholar 

  • Senapati SK, Dey S, Dwivedi SK, Swarup D (2001) Effect of garlic (Allium sativum) extract on tissue lead level in rats. J Ethnopharmacol 76:229–232

    Article  PubMed  CAS  Google Scholar 

  • Silbergeld EK (1991) Lead in bone: implications for toxicology during pregnancy and lactation. Environ Health Perspect 91:63–70

    Article  PubMed  CAS  Google Scholar 

  • Smith D, Bayer L, Strupp BJ (1998) Efficacy of succimer chelation for reducing brain lead levels in a rodent model. Environ Res 78:168–176

    Article  PubMed  CAS  Google Scholar 

  • Soltaninejad K, Kebriaeezadeh A, Minaiee B, Ostad SN, Hosseini R, Azizi E, Abdollahi M (2003) Biochemical and ultrastructural evidences for toxicity of lead through free radicals in rat brain. Hum Exp Toxicol 22:417–423

    PubMed  CAS  Google Scholar 

  • Tellez-Rojo MM, Hernandez-Avila M, Gonzales-Cossio T, Romieu I, Aro A, Palazuelos E, Schwartz J, Hu H (2002) Impact of breast feeding on the mobilization of lead from bone. Am J Epidemiol 155:420–428

    Article  PubMed  Google Scholar 

  • Tendon SK, Singh S (2000) Vitamins in treatment of lead intoxication. J Trace Elem Exp Med 13:305–315

    Article  Google Scholar 

  • Varnai VM, Piasek M, Blanusa M, Juresa D, Saric M, Kostial K (2003) Ascorbic acid supplementation does not improve efficacy of meso-dimercaptosuccinic acid treatment in lead-exposed suckling rats. Pharmacol Toxicol 93:180–185

    Article  PubMed  CAS  Google Scholar 

  • Varnai VM, Piasek M, Blanusa M, Saric MM, Juresa D, Kostial K (2004) Succimer treatment and calcium supplementation reduce tissue lead in suckling rats. J Appl Toxicol 24:123–128

    Article  CAS  Google Scholar 

  • Wang CH, Liang NC, Zhang CL, Bi YY, Shi XL, Shi Q (2007) Effect of ascorbic acid and thiamine supplementation at different concentrations on lead toxicity in liver. Anal Occup Hyg 51:563–569

    Article  CAS  Google Scholar 

  • Xu Z, Jones MM (1988) Comparative mobilization of lead by chelation agents. Toxicol 43:277–288

    Google Scholar 

  • Xu Y, Li G, Han C, Sun L, Zhao R, Cui S (2005) Protective effects of Hippophae rhamnoides L. juice on lead-induced neurotoxicity in mice. Biol Pharmacol Bull 208:490–494

    Article  Google Scholar 

  • Yassin M (2005) Prophylactic efficacy of crushed garlic lobes, block seed or olive oils on cholinesterase activity in central nervous system parts and serum of lead intoxicated rabbits. Turk J Biol 29:173–180

    Google Scholar 

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Acknowledgments

The authors wish to express their appreciation to the research council of the Ferdowsi University of Mashhad for financial support. We also wish to thank Mr. Mohsen Namei Ghasemi, Medical Toxicology Research Center Laboratory, for his assistance in toxicological analysis of the samples.

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Correspondence to Mohammad Reza Aslani.

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Aslani, M.R., Najarnezhad, V., Mohri, M. et al. The effect of allicin on blood and tissue lead content in mice. Comp Clin Pathol 20, 121–125 (2011). https://doi.org/10.1007/s00580-010-0964-y

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  • DOI: https://doi.org/10.1007/s00580-010-0964-y

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