Skip to main content
Environmental Health Perspectives logoLink to Environmental Health Perspectives
. 2002 Oct;110(Suppl 5):855–858. doi: 10.1289/ehp.02110s5855

Cognitive deficits and changes in gene expression of NMDA receptors after prenatal methylmercury exposure.

Mario Baraldi 1, Paola Zanoli 1, Fabio Tascedda 1, Joan M C Blom 1, Nicoletta Brunello 1
PMCID: PMC1241260  PMID: 12426146

Abstract

Previous studies showed learning and memory deficit in adult rats that were prenatally exposed to methylmercury chloride (MMC) in an advanced stage of pregnancy (15 days). Under these conditions, the cognitive deficits found at 60 days of age paralleled particularly changes in the N-methyl-D-aspartate (NMDA) receptor characteristics. In the present study, we report the behavioral effects of a single oral dose of MMC (8 mg/kg) administered earlier at gestational day 8. The use of different learning and memory tests (passive avoidance, object recognition, water maze) showed a general cognitive impairment in the in utero-exposed rats tested at 60 days of age compared with matched controls. Considering the importance of the glutamatergic receptor system and its endogenous ligands in learning and memory process regulation, we surmised that MMC could affect the gene expression of NMDA receptor subtypes. The use of a sensitive RNase protection assay allowed the evaluation of gene expression of two families of NMDA receptors (NR-1 and NR-2 subtypes). The result obtained in 60-day-old rats prenatally exposed to MMC, showed increased mRNA levels of the NR-2B subunit in the hippocampus but not in the frontal cortex. The data suggest that the behavioral abnormalities of MMC-exposed rats might be ascribed to a neurotoxic effect of the metal that alters the gene expression of a specific NMDA receptor subunit in the hippocampus.

Full Text

The Full Text of this article is available as a PDF (160.6 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Cagiano R., De Salvia M. A., Renna G., Tortella E., Braghiroli D., Parenti C., Zanoli 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. 1990 Jan-Feb;12(1):23–28. doi: 10.1016/0892-0362(90)90108-o. [DOI] [PubMed] [Google Scholar]
  2. Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem. 1987 Apr;162(1):156–159. doi: 10.1006/abio.1987.9999. [DOI] [PubMed] [Google Scholar]
  3. 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. 1984 May-Jun;6(3):249–254. [PubMed] [Google Scholar]
  4. Eccles C. U., Annau Z. Prenatal methyl mercury exposure: I. Alterations in neonatal activity. Neurobehav Toxicol Teratol. 1982 May-Jun;4(3):371–376. [PubMed] [Google Scholar]
  5. Eccles C. U., Annau Z. Prenatal methyl mercury exposure: II. Alterations in learning and psychotropic drug sensitivity in adult offspring. Neurobehav Toxicol Teratol. 1982 May-Jun;4(3):377–382. [PubMed] [Google Scholar]
  6. Ennaceur A., Delacour J. A new one-trial test for neurobiological studies of memory in rats. 1: Behavioral data. Behav Brain Res. 1988 Nov 1;31(1):47–59. doi: 10.1016/0166-4328(88)90157-x. [DOI] [PubMed] [Google Scholar]
  7. Hollmann M., Heinemann S. Cloned glutamate receptors. Annu Rev Neurosci. 1994;17:31–108. doi: 10.1146/annurev.ne.17.030194.000335. [DOI] [PubMed] [Google Scholar]
  8. Landrigan P. J., Graham D. G., Thomas R. D. Environmental neurotoxic illness: research for prevention. Environ Health Perspect. 1994 Jun;102 (Suppl 2):117–120. doi: 10.1289/ehp.94102117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Mohn A. R., Gainetdinov R. R., Caron M. G., Koller B. H. Mice with reduced NMDA receptor expression display behaviors related to schizophrenia. Cell. 1999 Aug 20;98(4):427–436. doi: 10.1016/s0092-8674(00)81972-8. [DOI] [PubMed] [Google Scholar]
  10. Olney J. W., Farber N. B. Glutamate receptor dysfunction and schizophrenia. Arch Gen Psychiatry. 1995 Dec;52(12):998–1007. doi: 10.1001/archpsyc.1995.03950240016004. [DOI] [PubMed] [Google Scholar]
  11. Riva M. A., Tascedda F., Lovati E., Racagni G. Regulation of NMDA receptor subunit messenger RNA levels in the rat brain following acute and chronic exposure to antipsychotic drugs. Brain Res Mol Brain Res. 1997 Oct 15;50(1-2):136–142. doi: 10.1016/s0169-328x(97)00175-7. [DOI] [PubMed] [Google Scholar]
  12. Seeburg P. H. The TINS/TiPS Lecture. The molecular biology of mammalian glutamate receptor channels. Trends Neurosci. 1993 Sep;16(9):359–365. doi: 10.1016/0166-2236(93)90093-2. [DOI] [PubMed] [Google Scholar]
  13. Tascedda F., Lovati E., Blom J. M., Muzzioli P., Brunello N., Racagni G., Riva M. A. Regulation of ionotropic glutamate receptors in the rat brain in response to the atypical antipsychotic seroquel (quetiapine fumarate). Neuropsychopharmacology. 1999 Aug;21(2):211–217. doi: 10.1016/S0893-133X(99)00034-2. [DOI] [PubMed] [Google Scholar]
  14. Vorhees C. V. Behavioral effects of prenatal methylmercury in rats: a parallel trial to the Collaborative Behavioral Teratology Study. Neurobehav Toxicol Teratol. 1985 Nov-Dec;7(6):717–725. [PubMed] [Google Scholar]
  15. Zanoli P., Cannazza G., Baraldi M. Prenatal exposure to methyl mercury in rats: focus on changes in kynurenine pathway. Brain Res Bull. 2001 May 15;55(2):235–238. doi: 10.1016/s0361-9230(01)00460-9. [DOI] [PubMed] [Google Scholar]
  16. Zanoli P., Truzzi C., Veneri C., Braghiroli D., Baraldi M. Methyl mercury during late gestation affects temporarily the development of cortical muscarinic receptors in rat offspring. Pharmacol Toxicol. 1994 Nov;75(5):261–264. doi: 10.1111/j.1600-0773.1994.tb00358.x. [DOI] [PubMed] [Google Scholar]
  17. Zanoli P., Truzzi C., Veneri C., Brandoli C., Baraldi M. Prenatal exposure to methylmercury during late gestation affects cerebral opiatergic system in rat offspring. Environ Res. 1997;74(1):48–53. doi: 10.1006/enrs.1997.3729. [DOI] [PubMed] [Google Scholar]

Articles from Environmental Health Perspectives are provided here courtesy of National Institute of Environmental Health Sciences

RESOURCES