Effects of fluoride on neural cell adhesion molecules mRNA and protein expression levels in primary rat hippocampal neurons.
- Author:
Tao XIA
1
;
Ming ZHANG
;
Wei-Hong HE
;
Ping HE
;
Ai-Guo WANG
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Cells, Cultured; Fluorides; toxicity; Gene Expression; Hippocampus; cytology; Neural Cell Adhesion Molecule L1; biosynthesis; genetics; Neurons; drug effects; metabolism; RNA, Messenger; genetics; Rats; Rats, Sprague-Dawley
- From: Chinese Journal of Preventive Medicine 2007;41(6):475-478
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the effects of fluoride on the growth and viability, and mRNA and protein expression levels of neural cell adhesion molecules (NCAM) in primary rat hippocampal neurons.
METHODSThe growth and development, the rate of cell survivor, and the mRNA and protein expression levels of NCAM were measured by MTT, RT-PCR, and Western blot respectively after the hippocampal neurons were incubated with 20, 40, and 80 microg/ml sodium fluoride for 24 hours in vitro.
RESULTSAs compared with the control group, the number of cells, the length and number of neuritis, and rate of cell survivor were significantly decreased in 80 microg/ml fluoride-treated group (P < 0.05). The mRNA expression levels of NCAM in 40 and 80 microg/ml fluoride-treated groups were significantly lower than that in the control group and decreased with the increasing fluoride concentration. Compared with the control group, the mRNA expression level of NCAM in 20 microg/ml fluoride-treated group was decreased, but the difference was not statistically significant (P > 0.05). The NCAM-180 protein expression levels in 40 and 80 microg/ml fluoride-treated groups, the NCAM-140 protein expression levels in all fluoride-treated groups, and NCAM-120 protein expression level in 80 microg/ml fluoride-treated group were significantly lower than those in the control group (P < 0.05, P < 0.05, P < 0.05, respectively).
CONCLUSIONFluoride might restrain the growth and survival of rat hippocampal neurons, and decrease mRNA and protein expression levels of NCAM. The impairment of developmental hippocampus might be one of the neurotoxicant target sites for fluoride toxicity.