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Comparative Excretion and Tissue Distribution of Selenium in Mice and Rats Following Treatment with Diphenyl Diselenide

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Abstract

The purpose of this study was to provide data about in vivo tissue distribution and excretion of diphenyl diselenide ((PhSe)2) in rats and mice through determination of selenium levels in different biological samples. (PhSe)2 (500 mg/kg, dissolved in canola oil) was administered to animals once a day per oral. After this, mice and rats were housed in metabolic cages (one animal per cage) and urine and feces were collected at specific times after treatment. Three to five animals per group (for each time-point) were anesthetized and blood samples were collected at 0 and 30 min, 24 h, at day 5, 15, and 30 after (PhSe)2 administration. The plasma and red blood cells were separated. Brain, liver, lungs, kidneys, and adipose tissue were also collected. The determination of selenium levels was performed by inductively coupled plasma atomic emission spectrometry. The main results indicate that: (1) urine is an important route of excretion of selenium originated from (PhSe)2 in mice and rats; (2) a large amount of (PhSe)2 or some of its metabolites are stored in fat; (3) the content of selenium found in plasma was low; and (4) liver and kidneys are the tissues with high amounts of selenium.

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References

  1. Nogueira CW, Zeni G, Rocha JBT (2004) Organoselenium and organotellurium compounds: toxicology and pharmacology. Chem Rev 104:6255–6286

    Article  PubMed  CAS  Google Scholar 

  2. Rosa RM, Roesler R, Braga AL, Saffi J, Henriques JA (2007) Pharmacology and toxicology of diphenyl diselenide in several biological models. Braz Med Biol Res 40:1287–1304

    Article  CAS  Google Scholar 

  3. Nogueira CW, Rocha JBT (2010) Diphenyl diselenide a janus-faced molecule. J Braz Chem Soc 21:2055–2071

    Article  CAS  Google Scholar 

  4. Meotti FC, Stangherlin EC, Zeni G, Rocha JBT, Nogueira CW (2004) Protective role of aryl and alkyl diselenides on lipid peroxidation. Environ Res 94:276–282

    Article  PubMed  CAS  Google Scholar 

  5. Luchese C, Brandao R, de Oliveira R, Nogueira CW, Santos FW (2007) Efficacy of diphenyl diselenide against cerebral and pulmonary damage induced by cadmium in mice. Toxicol Lett 173(3):181–190

    Article  PubMed  CAS  Google Scholar 

  6. Prigol M, Luchese C, Nogueira CW (2009) Antioxidant effect of diphenyl diselenide on oxidative stress caused by acute physical exercise in skeletal muscle and lungs of mice. Cell Biochem Funct 27:216–222

    Article  PubMed  CAS  Google Scholar 

  7. Borges LP, Nogueira CW, Panatieri RB et al (2006) Acute liver damage induced by 2-nitropropane in rats: effect of diphenyl diselenide on antioxidant defenses. Chem Biol Interact 160:99–107

    Article  PubMed  CAS  Google Scholar 

  8. Savegnago L, Trevisan M, Alves D et al (2006) Antisecretory and antiulcer effects of diphenyl diselenide. Environ Toxicol Pharmacol 21:86–92

    Article  PubMed  CAS  Google Scholar 

  9. Ghisleni G, Porciúncula LO, Cimarosti H et al (2003) Diphenyl diselenide protects rat hippocampal slices submitted to oxygen–glucose deprivation and diminishes inducible nitric oxide synthase immunocontent. Brain Res 986:196–199

    Article  PubMed  CAS  Google Scholar 

  10. Savegnago L, Jesse CR, Pinto LG, Rocha JBT, Nogueira CW (2007) Diphenyl diselenide attenuates acute thermal hyperalgesia and persistent inflammatory and neuropathic pain behavior in mice. Brain Res 1175:54–59

    Article  PubMed  CAS  Google Scholar 

  11. Ghisleni G, Kazauckas V, Both FL, Pagnussat N, Mioranzza S, Rocha JBT, Souza DO (2008) Diphenyl diselenide exerts anxiolytic-like effect in Wistar rats: putative roles of GABAA and 5HT receptors. Prog Neuro-Psychopharmacol 32:1508–1515

    Article  CAS  Google Scholar 

  12. Maciel EN, Bolzan RC, Braga AL, Rocha JBT (2000) Diphenyl diselenide and diphenyl ditelluride differentially affect δ-aminolevulinate dehydratase from liver, kidney and brain of mice. J Biochem Mol Toxicol 14:310–319

    Article  PubMed  CAS  Google Scholar 

  13. Meotti FC, Borges VC, Zeni G, Rocha JBT, Nogueira CW (2003) Potential renal and hepatic toxicity of diphenil diselenide, diphenil ditelluride and Ebselen for rats and mice. Toxicol Lett 143:9–16

    Article  PubMed  CAS  Google Scholar 

  14. Borges VC, Rocha JBT, Nogueira CW (2005) Effect of diphenyl diselenide, diphenyl ditelluride and ebselen on cerebral Na+, K+-ATPase activity in rats. Toxicology 215:191–197

    Article  PubMed  CAS  Google Scholar 

  15. Prigol M, Wilhelm EA, Schneider CC, Rocha JBT, Nogueira CW, Zeni G (2007) Involvement of oxidative stress in seizures induced by diphenyl diselenide in rat pups. Brain Res 1147:226–232

    Article  PubMed  CAS  Google Scholar 

  16. Prigol M, Wilhelm EA, Stangherlin EC, Barancelli DA, Nogueira CW, Zeni G (2008) Diphenyl diselenide-induced seizures in rat pups: possible interaction with glutamatergic system. Neurochem Res 33:996–1004

    Article  PubMed  CAS  Google Scholar 

  17. Prigol M, Schumacher RF, Nogueira CW, Zeni G (2009) Convulsant effect of diphenyl diselenide in rats and mice and its relationship to plasma levels. Toxicol Lett 189(1):35–39

    Article  PubMed  CAS  Google Scholar 

  18. Adams WJ Jr, Kocsis JJ, Snyder R (1989) Acute toxicity and urinary excretion of diphenyl diselenide. Toxicol Lett 48:301–310

    Article  PubMed  CAS  Google Scholar 

  19. Paulmier C (1986) Selenoorganic functional groups. In: Paulmier C (ed) Selenium reagents and intermediates in organic synthesis, 1st edn. Pergamon, Oxford, England, pp 25–51

    Google Scholar 

  20. Maciel EN, Flores EMM, Rocha JBT, Folmer V (2003) Comparative deposition of diphenyl diselenide in liver, kidney and brain of mice. Bull Environ Contam Tox 70:470–476

    Article  CAS  Google Scholar 

  21. Sohn OS, Desai DH, Das A, Rodriguez JG, Amin SG, El-Bayoumy K (2005) Comparative excretion and tissue distribution of selenium in mice and rats following treatment with the chemopreventive agent 1,4-phenylenebis(methylene)selenocyanate. Chem Biol Interact 151:193–202

    Article  PubMed  CAS  Google Scholar 

  22. Glover JW (1979) Concentrations of arsenic, selenium and 10 heavy-metals in school shark, Galeorhinus-australis (macleay), and gummy shark, Mustelus antarcticus Gunther, from southeastern Australian waters. Aust J Mar Freshwat Res 30:505–510

    Article  CAS  Google Scholar 

  23. Nagahori H, Matsunaga H, Tomigahara Y, Isobe N, Kaneko H (2010) Metabolism of 2,6-Dichloro-4-(3,3-dichloroallyloxy)phenyl3-[5-(trifluoromethyl)-2-pyridyloxy] propyl Ether (Pyridalyl) in rats after repeated oral administration and a simple physiologically based pharmacokinetic modeling in brown and white adipose tissues. Drug Metab Dispos 38:824–832

    Article  PubMed  CAS  Google Scholar 

  24. Palin KJ, Wilson CG, Davis SS, Phillips AJ (1982) The effect of oils on the lymphatic absorption of DDT. J Pharm Pharmacol 34:707–710

    Article  PubMed  CAS  Google Scholar 

  25. Roth WL, Freeman RA, Wilson AG (1993) A physiologically based model for gastrointestinal absorption and excretion of chemicals carried by lipids. Risk Anal 13(5):531–543

    Article  PubMed  CAS  Google Scholar 

  26. Manjunath K, Venkateswarlu V (2005) Pharmacokinetics, tissue distribution and bioavailability of clozapine solid lipid nanoparticles after intravenous and intraduodenal administration. J Control Release 107(2):215–228

    Article  PubMed  CAS  Google Scholar 

  27. Shiobara Y, Suzuki KT (1998) Binding of selenium (administered as selenite) to albumin after efflux from red blood cells. J Chromatogr B: Biomed Sci Appl 710:49–56

    Article  CAS  Google Scholar 

  28. Suzuki KT, Shiobara Y, Itoh M, Ohmichi M (1998) Selective uptake of selenite by red blood cells. Analyst 123:63–67

    Article  PubMed  CAS  Google Scholar 

  29. Barbosa NB, Rocha JB, Zeni G, Emanuelli T, Beque MC, Braga AL (1998) Effect of organic forms of selenium on delta-aminolevulinate dehydratase from liver, kidney and brain of adult rats. Toxicol Appl Pharmacol 149:243–253

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

The financial support by FAPERGS, CAPES, and CNPq is gratefully acknowledged. The authors would like to thank Fabiano Kauer (Shimadzu) for the technical support in the ICPE analysis.

Conflict of interest

None of the authors has a financial or scientific conflict of interest related to the work reported in this paper.

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Correspondence to Marina Prigol.

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Prigol, M., Brüning, C.A., Martini, F. et al. Comparative Excretion and Tissue Distribution of Selenium in Mice and Rats Following Treatment with Diphenyl Diselenide. Biol Trace Elem Res 150, 272–277 (2012). https://doi.org/10.1007/s12011-012-9464-z

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  • DOI: https://doi.org/10.1007/s12011-012-9464-z

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