PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2015 | 24 | 2 |

Tytuł artykułu

The effect of perfluorooctanoic acid on the planarian Dugesia japonica

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Perfluorooctanoic acid (PFOA) has been found to distribute and accumulate widely in the environment. In this study, the acute toxicity, behavioral activity, regeneration, antioxidant enzyme activities, and cell apoptosis effects of PFOA on planarian Dugesia japonica have been investigated. The results show that the mortality is directly proportional to the PFOA concentration, and planarian locomotor velocity (pLMV) is significantly reduced with increasing both the exposure time and PFOA concentration. The recovery of the motility for planarians pre-treated with PFOA is found to be time- and dose-dependent, and all planarians recover their motility completely after 72 hr. The appearance of auricles in regenerating animals is more easily affected by PFOA exposure in comparison to the appearance of eyespot. The SOD activities and CAT activities are changed in the PFOA-exposed planarians. Increasing PFOA exposure time or concentration can cause an obvious increase of apoptosis in the brain, eye, and parenchyma region. The results suggest that PFOA is much more toxic for inducing oxidative stress, cell apoptosis, and development toxicity in planarians.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

24

Numer

2

Opis fizyczny

p.801-807,fig.,ref.

Twórcy

autor
  • School of Life Sciences, Shandong University of Technology, 12 Zhangzhou Road, Zibo, PR China
autor
  • School of Life Sciences, Shandong University of Technology, 12 Zhangzhou Road, Zibo, PR China
autor
  • School of Life Sciences, Shandong University of Technology, 12 Zhangzhou Road, Zibo, PR China
autor
  • School of Life Sciences, Shandong University of Technology, 12 Zhangzhou Road, Zibo, PR China
autor
  • School of Life Sciences, Shandong University of Technology, 12 Zhangzhou Road, Zibo, PR China

Bibliografia

  • 1. GIESY J.P., KANNAN K. Global distribution of perfluorooctane sulfonate in wildlife. Environ. Sci. Technol. 35, (7), 1339, 2001.
  • 2. BUTENHOFF J.L., GAYLOR D.W., MOORE J.A., OLSEN G.W., RODRICKS J., MANDEL J.H., ZOBEL L.R. Characterization of risk for general population exposure to perfluorooctanoate. Regul Toxicol Pharmacol. 39, (3), 363, 2004.
  • 3. DIETZ R., BOSSI R., RIGE´T F.F., SONNE C., BORN E.W. Increasing perfluoroalkyl contaminants in east Greenland polar bears (Ursus maritimus): A new toxic threat to the Arctic bears. Environ Sci Technol. 42, (7), 2701, 2008.
  • 4. JIN Y.H., LIU W., SATO I., NAKAYAMA S.F., SASAKI K., SAITO N., TSUDA S. PFOS and PFOA in environmental and tap water in China. Chemosphere. 77, (5), 605, 2009.
  • 5. LOOS R., LOCORO G., HUBER T., WOLLGAST J., CHRISTOPH,E.H., DE JAGER A., MANFRED GAWLIK B., HANKE G., UMLAUF G., ZALDIVAR J.M. Analysis of perfluorooctanoate (PFOA) and other perfluorinated compounds (PFCs) in the River Po watershed in N-Italy. Chemosphere. 71, (2), 306, 2008.
  • 6. CALAFAT A.M., KUKLENYIK Z., REIDY J.A., CAUDILL S.P., TULLY J.S., NEEDHAM, L.L. Serum conc entrations of 11 polyfluoroalkyl compounds in the u.s. population: data from the national health and nutrition examination survey (NHANES). Environ. Sci. Technol. 41, (7), 2237, 2007.
  • 7. GURUGE K., YEUNG L.W.Y., YAMANAKA N., MIYAZAKI S., LAM P.K.S., GIESY J.P., JONES P.D., YAMASHITA N. Gene expression profiles in rat liver treated with perfluorooctanoic acid (PFOA). Toxicol. Sci. 89, (1), 93, 2006.
  • 8. KENNEDY G.L.Jr., BUTENHOFF J.L., OLSEN G.W., O'CONNOR J.C., SEACAT A.M., PERKINS R.G., BIEGEL L.B., MURPHY S.R., FARRAR D.G. The toxicology of perfluorooctanoate. Crit Rev Toxicol. 34, (4), 351, 2004.
  • 9. ANKLEY G.T., KUEHL D.W., KAHL M.D., JENSEN K.M., LINNUM A., LEINO R.L., VILLENEUVET D.A. Reproductive and developmental toxicity and bioconcentration of perfluorooctanesulfonate in a partial life-cycle test with the fathead minnow (Pimephales promelas). Environ. Toxicol. Chem. 24, (9), 2316, 2005.
  • 10. LIU C., YU K., SHI X., WANG J., LAM P.K., WU R.S., ZHOU B. Induction of oxidative stress and apoptosis by PFOS and PFOA in primary cultured hepatocytes of freshwater tilapia (Oreochromis niloticus). Aquat Toxicol. 82, (2), 135, 2007.
  • 11. LUEBKER D.J, HANSEN K.J., BASS N.M., BUTENHOFF J.L. Interactions of fluorochemicals with rat liver fatty acid-binding protein. Toxicology. 176, (3), 175, 2002.
  • 12. BIEGEL L.B., HURTT M.E., FRAME S.R., O'CONNOR J.C., COOK J.C. Mechanisms of extrahepatic tumor induction by peroxisome proliferators in male CD rats. Toxicol. Sci. 60, (1), 44, 2001.
  • 13. COOK J.C., MURRAY S.M., FRAME S.R., HURTT M.E. Induction of Leydig cell adenomas by ammonium perfluorooctanoate: A possible endocrine-related mechanism. Toxicol Appl Pharmacol. 113, (2), 209, 1992.
  • 14. SEACAT A.M., THOMFORD P.J., HANSEN K.J., CLEMEN L.A., ELDRIDGE S.R., ELCOMBE C.R., BUTENHOFF J.L. Sub-chronic dietary toxicity of potassium perfluorooctanesulfonate in rats. Toxicology. 183, (1-3), 117, 2003.
  • 15. WALTERS M.W., BJORK J.A., WALLACE K.B. Perfluorooctanoic acid stimulated mitochondrial biogenesis and gene transcription in rats. Toxicology. 264, (1-2), 10, 2009.
  • 16. WANG F., SHIH K. Adsorption of perfluorooctanesulfonate (PFOS) and perfluorooctanoate (PFOA) on alumina: influence of solution pH and cations. Water Res. 45, (9), 2925, 2011.
  • 17. NANO G.M., BINELLO A., BIANCO M.A., UGAZIO G., BURDINO S. In vitro tests to evaluate potential biological activity in natural substances. Fitoterapia. 73, (2), 140, 2002.
  • 18. SÁNCHEZ ALVARADO A. Regeneration and the need for simpler model organisms. Philos Trans R Soc Lond B Biol Sci. 359, (1445), 759, 2004.
  • 19. KOVAČEVIĆ G., GREGOROVIĆ G., KALAFATIĆ M., JAKLINOVIĆ I. The Effect of Aluminium on the Planarian Polycelis felina (Daly.) Water Air Soil Pollut. 196, 333, 2009.
  • 20. ZHOU Y.X., ZHANG Z.S. Methods of aquatic toxicology analysis. Agriculture Publisher of China, Beijing. pp. 114-122, 1989.
  • 21. RAFFA R.B., HOLLAND L.J., SCHULINGKAMP R.J. Quantitative assessment of dopamine D2 antagonist activity using invertebrate (Planaria) locomotion as a functional endpoint. J Pharmacol Toxicol Methods. 45, (3), 223, 2001.
  • 22. BRADFORD M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of proteindye binding. Anal Biochem. 72, 248, 1976.
  • 23. MARKLUND S., MARKLUND G. Involvement of superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur. J. Biochem. 47, (3), 469, 1974.
  • 24. AEBI H. Catalase in vitro, Method Enzymol. 105, 121, 1984.
  • 25. HUANG H., HUANG C., WANG L., YE X., BAI C., SIMONICH M.T., TANGUAY R.L., DONG Q. Toxicity, uptake kinetics and behavior assessment in zebrafish embryos following exposure to perfluorooctanesulphonicacid (PFOS). Aquat Toxicol. 98, (2), 139, 2010.
  • 26. LI M.H. Effects of nonionic and ionic surfactants on survival, oxidative stress, and cholinesterase activity of planarian. Chemosphere. 70, (10), 1796, 2008.
  • 27. LI M.H. Toxicity of perfluorooctane sulfonate and perfluorooctanoic acid to plants and aquatic invertebrates. Environ. Toxicol. 24, (1), 95, 2009.
  • 28. ZHENG X.M., LIU H.L., SHI W., WEI S., GIESY J.P., YU H.X. Effects of perfluorinated compounds on development of zebrafish embryos. Environ Sci Pollut Res Int.19, (7), 2498, 2011.
  • 29. ALONSO A., CAMARGO J.A. The freshwater planarian Polycelis felina as a sensitive species to assess the long-term toxicity of ammonia. Chemosphere. 84, (5), 533, 2011.
  • 30. NEWMARK P. A., SANCHEZ ALVARADO A. Not your father’s planarian: A classic model enters the era of functional genomics. Nat Rev Genet. 3, (3), 210, 2002.
  • 31. YUAN Z.Q., ZHENG M.Y., ZHANG J.Y., ZHAO S.Z., GUO L., ZHAO B.S. Effects of Anionic Surfactants Sodium Dodecyl Sulphate on Regeneration and Antioxidant Enzymes Response of Planarian Dugesia japonica. Fresen Environ Bull. 22, (1), 157, 2013.
  • 32. FATIMA M., MANDIKI S.N.M., DOUXFILS J., SILVESTRE F., COPPE P., KESTEMONT P. Combined effects of herbicideson biomarkers reflecting immune-endocrine interactions in gold fish immune and antioxidant effects. Aquat Toxicol. 81, (2), 159, 2007.
  • 33. JIN Y., PAN X., CAO L., MA B., FU Z. Embryonic exposure to cis-bifenthrin enantioselectively induces the transcription of genes related to oxidative stress, apoptosis and immunotoxicity in zebrafish (Danio rerio). Fish Shellfish Immunol. 34, (2), 717, 2013.
  • 34. SHI X., DU Y., LAM P.K., WU R.S., ZHOU B. Developmental toxicity and alteration of gene expression in zebrafish embryos exposed to PFOS. Toxicol. Appl. Pharmacol. 230, (1), 23, 2008.
  • 35. XIONG W., SUN Y., ZOU M., MUHAMMAD R.U. Molecular cloning, characterization of CAT, and eco-toxicological effects of dietary zinc oxide on antioxidant enzymes in Eisenia fetida. Environ Sci. Pollut. Res. Int. 20, (3), 1746, 2013.
  • 36. AUSTIN M.E., KASTURI B.S., BARBER M., KANNAN K., MOHANKUMAR P.S., MOHANKUMAR S.M. Neuroendocrine effects of perfluorooctane sulfonate in rats. Environ Health Perspec. 111, (12), 1485, 2003.
  • 37. MOODY C.A., MARTIN J.W., KWAN W.C., MUIR D.C.G., MABURY S.A. Monitoring perfluorinated surfactants in biota and surface water samples following an accidental release of fire-fighting foam into Etobicoke Creek. Environ Sci Technol. 36, 545, 2002.
  • 38. LEMA S.C., SCHULTZ I.R., SCHOLZ N.L., INCARDONA J.P., SWANSON P. Neural defects and cardiac arrhythmia in fish larvae following embryonic exposure to 2,2',4,4'-tetrabromodiphenyl ether (PBDE 47). Aquat. Toxicol. 82, 296, 2007.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-64185371-8995-459e-90ef-932f1a99bff6
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.