Effects of early postnatal exposure to dieldrin on synaptic development of striatum in mice.
- Author:
Ye GAO
1
;
Qu-nan WANG
;
Shan WU
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Animals, Newborn; Corpus Striatum; drug effects; growth & development; Dieldrin; toxicity; Female; Glial Fibrillary Acidic Protein; metabolism; Male; Mice; Mice, Inbred ICR; Nerve Tissue Proteins; metabolism; Post-Synaptic Density; drug effects
- From: Chinese Journal of Industrial Hygiene and Occupational Diseases 2012;30(2):97-102
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the effects of early postnatal exposure to dieldrin on striatum synaptic development in lactation, adolescence and adulthood of mice.
METHODSThe pups were divided into 5 groups randomly. Three groups were exposed to dieldrin (0.01% DMSO solution) at doses of 0.2, 2.0 and 20.0 microg/kg and two control groups were exposed to DMSO or saline by intraperitoneal injection of every other day from postnatal days (PND) 3 to PND13. The striatum were isolated from brain in lactation (PND14), adolescence (PND36) and adulthood (PND98). Western blot assay was used to detect the expression levels of striatal synaptic proteins.
RESULTSThe postnatal exposure to dieldrin could reduce the level of growth associated protein (GAP43) of striatum in lactation in a dose-dependent manner. In adolescence, the level of glial fibrillary acidic protein (GFAP) in striatum increased and the levels of tyrosine hydroxylase (TH), GAP43 and post-synaptic density protein 95 (PSD95) decreased with exposure doses. The level of Synapsin I decreased in adolescence male mice. The changes of expression levels of GFAP, TH and PSD95 proteins lasted to adulthood.
CONCLUSIONEarly postnatal exposure to dieldrin could affect the expression level of GAP43 protein in striatum. The expression levels of TH and PSD95 proteins in striatum decreased in adolescence and adulthood. These results indicated that the early postnatal exposure to dieldrin may persistently interfere in the striatal synaptic development.