Record Display for the EPA National Library Catalog

RECORD NUMBER: 14 OF 74

OLS Field Name OLS Field Data
Main Title Development of Adrenergic Receptor Binding Sites in Brain Regions of the Neonatal Rat: Effects of Prenatal or Postnatal Exposure to Methylmercury.
Author Bartolome, J. V. ; Kavlock, R. J. ; Cowdery, T. ; Orband-Miller, L. ; Slotkin, T. A. ;
CORP Author Duke Univ. Medical Center, Durham, NC. Dept. of Pharmacology.;Health Effects Research Lab., Research Triangle Park, NC.
Year Published 1987
Report Number EPA-R-811621; EPA/600/J-87/153;
Stock Number PB88-175880
Additional Subjects Brain ; Exposure ; Rats ; Development ; Toxicity ; Nervous system ; Reprints ; Receptors(Adrenergic) ; Mercury/methyl ; Binding sites ; Synoptic receptors
Holdings
Library Call Number Additional Info Location Last
Modified
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Status
NTIS  PB88-175880 Most EPA libraries have a fiche copy filed under the call number shown. Check with individual libraries about paper copy. 06/21/1988
Collation 15p
Abstract
In order to understand the effects of developmental exposure to methyl/mercury on the ontogeny of synaptic function, the impact of prenatal or postnatal exposure on acquisition of receptor binding sites for norepinephrine was examined. The actions of the mercurial were both regionally - and receptor subtype-selective and depended upon the maturational profile of each region. Alpha 1 and alpha 2 and Beta-receptor sites in the cerebellum, the region which develops last, were the most vulnerable to methylmercury. In contrast, the same receptor subtypes in the midbrain + brainstem, which develops earliest, were resistant to methylmercury. The cerebal cortex, which matures at a time midway between cerebellum and midbrain + brainstem, also displayed intermediate vulnerability to actions of methylmercury on receptors. Within the cerebellum, prenatal exposure to 1 mg/kg to methylmercury, interfered the most with ontogeny of alpha 1-receptor binding, less so far alpha 2-receptors and least for Beta-receptors. Lower doses of methylmercury tended to increase receptor binding for all subtypes, a fact which may contribute to promotion of neurological development seen in animals exposed to those levels.