Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5138728 | Journal of Trace Elements in Medicine and Biology | 2018 | 10 Pages |
Abstract
Expressions of N-methyl-d-aspartic acid receptors (NMDARs) in the brains of rats and primary neurons exposed to high fluoride were investigated. Sprague-Dawley rats were divided randomly into a fluorosis group (50Â ppm fluoride in the drinking water for 6 months) and controls (<0.5Â ppm fluoride) and the offspring from these rats sacrificed on postnatal days 1, 7, 14, 21 and 28. The primary cultured neurons from the hippocampus of neonatal rats were treated with 5 and 50Â ppm fluoride for 48Â h. NMDAR subunits at protein or mRNA levels were quantified by Western blotting or real-time PCR. The phosphorylated calmodulin-protein kinase II (CaMKII) was determined by Western blotting, concentration of Ca2+ in neurons by laser confocal microscopy and apoptosis by flow cytometry. In the brains of adult rats and pups as well as in primary neurons exposed to high fluoride, the mRNAs encoding GluN1 and GluN2Â B subunits and the corresponding proteins were elevated, the GluN3A lowered and the GluN2A unchanged. In addition, the level of phosphor-CaMKII was reduced, and Ca2+ influx and apoptosis enhanced in the brains of rats and cultured neurons exposed to high fluoride. The results indicate that such modifications may involve brain damage induced by chronic fluorosis.
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Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Na Wei, Yang-Ting Dong, Jie Deng, Ya Wang, Xiao-Lan Qi, Wen-Feng Yu, Yan Xiao, Jian-Jiang Zhou, Zhi-Zhong Guan,