PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2008 | 17 | 4 |

Tytuł artykułu

Effects of perinatal MeHg and-or 2, 2', 4, 4', 5, 5' - hexachlorobiphenyl [PCB153] exposure on adult vulnerability to amphetamine in rats

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Methylmercury (MeHg) and polychlorinated biphenyls (PCBs) are ubiquitous and persistent environmental pollutants and known neurotoxicants. It has been recognized that dietary exposure to neurotoxic substances during pregnancy and breast feeding may affect the development of the child’s nervous system and result in various neurological and neurobehavioural alterations later in life. One of the suspected consequences of such exposure may be an increased propensity to psychostimulant abuse and psychostimulant addiction. Data from animal studies indicate that behavioural sensitivity to psychostimulants is a good predictor of the propensity to psychostimulant self-administration – an animal model of drug abuse in humans. The aim of this study was to find out whether and how perinatal exposure to MeHg and/or PCB153 determines behavioural sensitivity and sensitizability to the psychostimulant amphetamine (AMPH) in adulthood. The subjects were adult rats, Wistars, born to mothers exposed, via drinking water, to MeHg (CH₃HgCl) at 0.5 mg/kg/day; or PCB153 (2,2’,4,4’,5,5’-hexachlorobiphenyl) at 5.0 mg/kg/day by gavage, or jointly MeHg (0.5 mg/kg/day, and PCB153 (5.0 mg/kg/day), from day 7 of pregnancy to day 21 post partum. The testing started at the age of 3 months. It consisted in measuring the behavioural response to a test dose of AMPH (0.5 mg/kg. i.p.) twice: 1) before a sensitization treatment in order to assess the rat’s “normal” sensitivity to the psychostimulant, and 2) three weeks after the sensitizing treatment. The sensitization treatment consisted in a repeated (once a day for five consecutive days) administration of AMPH at 2.5 mg/kg. Results: 1) Before the sensitization treatment there were no differences between the exposed and the control rats in the response to the psychostimulant. 2) Three weeks after the sensitizing treatment the response to an AMPH challenge was increased in all rats. However, in males exposed perinatally to MeHg alone, this increase was significantly more pronounced than in males of the control group. A similar effect was not present in MeHg-exposed females as well as males or females exposed to PCB153 alone or in combination with MeHg. Perinatal exposure to MeHg may result in an increased susceptibility to psychostimulant sensitization in the male progeny. Co- exposure to PCB153 may compromise this effect of MeHg-exposure.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

17

Numer

4

Opis fizyczny

p.557-567,fig.,ref.

Twórcy

autor
  • Nofer Institute of Occupational Medicine, Sw.Teresy 8, 91-348 Lodz, Poland
autor
autor
autor

Bibliografia

  • 1. GRANDEJAN P., LANDRIGAN P. J. Developmental neurotoxicity of industrial chemicals. Lancet 368, 2167, 2006.
  • 2. WEISS B., STERN S., COX C., BALYS M. Perinatal and lifetime exposure to methylmercury in the mouse: behavioral effects. Neurotoxicology 26, 675, 2005.
  • 3. NATION J.R., SMITH K.R., BRATTON G.R. Early developmental lead exposure increases sensitivity to cocaine in a self-administration paradigm. Pharmacol. Biochem. Behav. 77, 127, 2004.
  • 4. CASTOLDI A.F., BLANDINI F., RANDINE G., SAMUELE A., MANZO L., COCCINI T. Brain monoaminergic neurotransmission parameters in weanling rats after perinatal exposure to methylmercury and 2,2’,4,4’,5,5’- hexachlorobiphenyl (PCB 153). Brain Res. 1112, 91, 2006.
  • 5. AMIN-ZAKI L., MAJEED M.A., ELHASSANI S.B., CLARKSON T.W., GREENWOOD M.R., DOHERTY R.A. Prenatal methylmercury poisoning. Clinical observations over five years. Am J Dis Child. 133, 172, 1979.
  • 6. TAKEUCHI T., ETO K., KINJO Y., TOKUNGA H. Human brain disturbance by methylmercury poisoning, focusing on the long-term effect on brain weight. Neurotoxicology 17, 187, 1996.
  • 7. KONDO K. Incidence of Minamata disease in communities along the Agano river, Niigata, Japan-patterns of the exposure and official diagnosis of patients. Nippon Eiseigaku Zasshi. 51, 599, 1996.
  • 8. SANFELIU C., SEBASTIA J., CRISTOFOL R., RODRIGUEZ – FARRE E. Neurotoxicity of organomercurial compounds. Neurotox Res. 5, 283, 2003.
  • 9. SCHETTLER T. Toxic threats to neurologic development of children. Environ Health Perspect. 6, 813, 2001.
  • 10. DAVIDSON P. W., MYJERS G. J., COX C., AXTELL C., SHAMLAYE C., SLOANE – REEVES J., CERNICHARI E., NEEDHAM L., CHOI A., WANG Y., BERLIN M., CLARKSON T.W. Effects of prenatal and postnatal methylmercury exposure from fish consumption on neurodevelopment: outcomes at 66 months of age in the Seychelles Child Development Study. JAMA. 26, 280, 1998.
  • 11. GRANDJEAN P., WEIHE P., WHITE R.F., DEBES F., ARAKI S., YOKOYAMA K., MURATA K., SORENSEN N., DAHL R., JORGENSEN P.J. Cognitive deficit in 7-year-old children with prenatal exposure to methylmercury. Neurotoxicol Teratol. 19, 418, 1997.
  • 12. WINNEKE G., WALKOWIAK J., LILIENTHAL H. PCBinduced neurodevelopmental toxicity in human infants and its potential mediation by endocrine dysfunction. Toxicology. 27, 181, 2002.
  • 13. SEEGAL R.F. Epidemiological and laboratory evidence of PCB-induced neurotoxicity. Crit Rev Toxicol. 26, 709, 1996.
  • 14. JACOBSON J.L., JACOBSON S. W. Evidence for PCBs as neurodevelopmental toxicants in humans. Neurotoxicology. 18, 415, 1997.
  • 15. DARVILL T., LONKY E., REIHAM J., STEWART P., PAGANO J. Prenatal exposure to PCBs and infant performance on the fagan test of infant intelligence. Neurotoxicology. 21, 1029, 2000.
  • 16. BUSHNELL P.J., MOSER V.C., MACPHAIL R.C., OSHIRO W.M., DERR-YELLIN E.C., PHILIPS P.M., KODAVANTI P.R. Neurobehavioral assessments of rats perinatally exposed to a commercial mixture of polychlorinated biphenyls. Toxicol Sci. 68, 109, 2002.
  • 17. BEMIS J.C., SEEGAL R.F. Polychlorinated biphenyls and methylmercury act synergistically to reduce rat brain dopamine content in vitro. Environ Health Perspect. 107, 879, 1999.
  • 18. BEMIS J.C., SEEGAL R.F. Polychlorinated biphenyls and methylmercury alter intracellular calcium concentrations in rat cerebellar granule cells. Neurotoxicology. 21, 1123, 2000.
  • 19. GRANDJEAN P, WEIHE P, BURSE V.W., NEEDHAM L.L., STORR-HANSEN E., HEINZOW B., DEBES F., MURATA K., SIMONSEN H., ELLEFSEN P., BUDTZJORGENSEN E., KEIDING N., WHITE R. F. Neurobehavioral deficits associated with PCB in 7-year-old children prenatally exposed to seafood neurotoxicants. Neurotoxicol Teratol. 23, 305, 2001.
  • 20. STEWART P.W., REIHMAN J., LONKY E. I., DARVILL T. J., PAGANO J. cognitive development in preschool children prenatally exposed to PCBs and MeHg. Neurotoxicol. Teratol. 25, 11, 2003.
  • 21. ROEGGE C.S., SCHANTZ S. Motor function following developmental exposure to PCBs and/or MeHg. Neurotoxicol. Teratol. 28, 260, 2006.
  • 22. SAFE S. Polychlorinated biphenyls (PCBs): environmental impact, biochemical and toxic responses, and implications for risk assessment. Crit Rev Toxicol. 24, 87, 1994.
  • 23. LONGNECKER M.P., WOLFF M. S., GLADEN B.C., BROCK J. W., GRANDJEAN P., JACOBSON J.L., KORRICK S.A., ROGAN W.J., WEISGLAS-KUPERUS N., HERTZ-PICCIOTO I., AYOTTE P., STEWART P., WINNEKE G., CHARLES M.J., JACOBSON S. W., DEWAILLY E., BOERSMA E.R., ALTSHUL L.M., HEINZOW B., PAGANO J.J., JENSEN A.A. Comparison of polychlorinated biphenyl levels across studies of human neurodevelopment. Environ. Health Perspect. 111, 65, 2003.
  • 24. FAUSTMAN E.M., SILBERNAGEL S.M., FENSKE R.A., BURBACHER T.M., PONCE R.A. Mechanisms underlying Children's susceptibility to environmental toxicants. Environ Health Perspect. 108, 13, 2000.
  • 25. CAGIANO R., DE SALVIA M.A., RENNA G., TORTELLA E., BRAGHIROLI D., PARENTI C., ZANOLLI P., BARALDI M., ANNAU Z., CUOMO V. Evidence that exposure to methyl mercury during gestation induces behavioral and neurochemical changes in offspring of rats. Neurotoxicol Teratol. 12, 23, 1990.
  • 26. ROSSI A.D., AHLBOM E., OGREN S.O., NICOTERA P., CECCATELLI S. Prenatal exposure to methylmercury alters locomotor activity of male but not female rats. Exp Brain Res. 117, 428, 1997.
  • 27. RASMUSSEN E.B., NEWLAND M.C. Developmental exposure to methylmercury alters behavioral sensitivity to D-amphetamine and pentobarbital in adult rats. Neurotoxicol Teratol. 23, 45, 2001.
  • 28. DARE E., FETISSOV S., HOKFELT T., HALL H., OGREN S.O., CECCATELLI S. Effects of prenatal exposure to methylmercury on dopamine-mediated locomotor activity and dopamine D2 receptor binding. Naunyn Schmiedebergs Arch Pharmacol. 367, 500, 2003.
  • 29. WAGNER G.C., REUHL K.R., MING X., HALLADAY A. Behavioral and neurochemical sensitization to amphetamine following early postnatal administration of methylmercury (MeHg). Neurotoxicology. 28, 59, 2007.
  • 30. CERNICHIARI E., BREWER R., MYERS G.J., MARSH D.O., LAPHAM L.W., COX C., SHAMLAYE C.F., BERLIN M., DAVIDSON P.W., CLARKSON T.W. Monitoring methylmercury during pregnancy: maternal hair predicts fetal brain exposure. Neurotoxicology. 16, 705, 1995.
  • 31. HOLENE E., NAFSTAD I., SKAARE J.U., SAGVOLDEN T. Behavioural hyperactivity in rats following postnatal exposure to sub-toxic doses of polychlorinated biphenyl congeners 153 and 126. Behav Brain Res. 94, 213, 1998.
  • 32. WEISS B., STERN S., CERNICHIARI E., GELEIN R. Methylmercury Contamination of Laboratory Animal Diets. Environ Health Perspect. 113, 1120, 2005.
  • 33. POLI D., CAGLIERI A., GOLDONI M., VETTORI M.V., COCCINI T., CASTOLDI S., CECCATELLI S., MUTTI A. PCB153 and methylmercury (MeHg) assessment of target tissues doses in rats after single and combined exposures: Mothers versus pups comparisons. Toxicology Letters 164, S177, 2006.
  • 34. LUTZ P., WIADERNA D., GRALEWICZ S., KUR B. Exposure to chlorphenvinphos, an organophosphate insecticide, prevents from behavioral sensitization to amphetamine. Int J Occup Med Environ Health. 19, 132, 2006.
  • 35. WINER B.J. Statistical principles in experimental design. New York, Mac Graw Hill Book Company, 1992.
  • 36. JOYCE E.M., KOOB G.F. Amphetamine-, scopolamineand caffeine-induced locomotor activity following 6-hydroxydopamine lesions of the mesolimbic dopamine system. Psychopharmacology. 73, 311, 1981.
  • 37. SANBERG P.R., HENAULT M.A., HAGENMEYERHOUSER S.H., AGENMEYER-HOUSER S.H., RUSSELL K.H. The topography of amphetamine and scopolamineinduced hyperactivity: toward an activity print. Behav Neurosci. 101, 131, 1987.
  • 38. RIEGEL A.C., ALI S.F., FRENCH E.D. Toluene-induced locomotor activity is blocked by 6-hydroxydopamine lesions of the nucleus accumbens and the mGluR2/3 agonist LY379268. Neuropsychopharmacology. 28, 1440, 2003.
  • 39. VANDERSCHUREN L.J., KALIVAS P.W. Alterations in dopaminergic and glutamatergic transmission in the induction and expression of behavioral sensitization: a critical review of preclinical studies. Psychopharmacology 151, 99, 2000.
  • 40. DLUZEN D.E. Neuroprotective effects of estrogen upon the nigrostriatal dopaminergic system. J Neurocytol. 29, 387, 2000.
  • 41. GÖTZ M.E., KOUTSILIERI E., RIEDERER P., CECCATELLI S., DARÉ E. Methylmercury induces neurite degeneration in primary culture of mouse dopaminergic mesencephalic cells. J Neural Transm. 109, 597, 2002.
  • 42. BARTOLOME J., WHITMORE W.L., SEIDLER F.J., SLOTKIN T.A. Exposure to methylmercury in utero: effects on biochemical development of catecholamine neurotransmitter systems. Life Sci. 35, 657, 1984.
  • 43. BEYROUTY P., STAMLER Ch.,J., LIU J.N., LOUA K.M., KUBOW S., CHAN H.M. Effects of prenatal methylmercury exposure on brain monoamine oxidase activity and neurobehaviour of rats. Neurotoxicol. Teratol. 28, 251, 2006.
  • 44. CUOMO V., AMBROSI L., ANNAU Z., CAGIANO R., BRUNELLO N., RACAGNI G. Behavioural and neurochemical changes in offspring of rats exposed to methyl mercury during gestation. Neurobehav Toxicol Teratol. 6, 249, 1984.
  • 45. SEEGAL R.F., BROSCH K.O., OKONIEWSKI R.J. Effects of in utero and lactational exposure of the laboratory rat to 2,4,2',4'- and 3,4,3',4'-tetrachlorobiphenyl on dopamine function. Toxicol Appl Pharmacol. 146, 95, 1997.
  • 46. CHOKSI N.Y., KODAVANTI P.S., TILSON H.A., BOOTH R.G. Effects of polychlorinated biphenyls (PCBs) on brain tyrosine hydroxylase activity and dopamine synthesis in rats. Fundam. Appl. Toxicol. 39, 76, 1997.
  • 47. SEEGAL R.F. The neurotoxicological consequences of developmental exposure to PCBs. Toxicol Sci. 57, 1, 2000.
  • 48. SEEGAL R.F., OKONIEWSKI R.J., BROSCH K.O., BEMIS J.C. Polychlorinated biphenyls alter extraneuronal but not tissue dopamine concentrations in adult rat striatum: an in vivo microdialysis study. Environ Health Perspect. 110, 1113, 2002.
  • 49. BEMIS J.C., SEEGAL R.F. PCB-induced inhibition of the vesicular monoamine transporter predicts reductions in synaptosomal dopamine content. Toxicol Sci. 80, 288, 2004.
  • 50. COCCINI T., RODA E., CASTOLDI A. F., GOLDONI M., POLI D., BERNOCCHI G., MANZO L. Perinatal co-exposure to methylmercury and PCB153 or PCB126 in rats alters the cerebral cholinergic muscarinic receptors at weaning and puberty. Toxicology. [Epub ahead of print] 2007.
  • 51. VETTORI M.V., GOLDONI M., CAGLIERI A., POLI D., FOLESANI G., CECCATELLI S., MUTTI A. Antagonistic effects of methyl-mercury and PCB153 on PC12 cells after a combined and simultaneous exposure. Food Chem. Toxicol. 44, 1505, 2006.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-ac14dac9-f9ba-4037-9012-91eb66f86518
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.