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Changed expressions of N-methyl-D-aspartate receptors in the brains of rats and primary neurons exposed to high level of fluoride
被引:14
|作者:
Wei, Na
[1
]
Dong, Yang-Ting
[1
]
Deng, Jie
[1
,3
]
Wang, Ya
[1
]
Qi, Xiao-Lan
[2
,3
]
Yu, Wen-Feng
[2
,3
]
Xiao, Yan
[2
,3
]
Zhou, Jian-Jiang
[2
,3
]
Guan, Zhi-Zhong
[1
,2
,3
]
机构:
[1] Guizhou Med Univ, Affiliated Hosp, Dept Pathol, Guiyang 550004, Guizhou, Peoples R China
[2] Guizhou Med Univ, Minist Educ, Key Lab Endem & Ethn Dis, Guiyang, Guizhou, Peoples R China
[3] Guizhou Med Univ, Key Lab Med Mol Biol, Guiyang, Guizhou, Peoples R China
关键词:
Chronic fluorosis;
NMDARs;
Rat brains;
Ca MKII alpha;
CO2+ influx;
Apoptosis;
SUBUNIT GLUN3A NR3A;
CHRONIC FLUOROSIS;
NMDA RECEPTORS;
MEDIATED EXCITOTOXICITY;
SYNAPTIC PLASTICITY;
ALZHEIMERS-DISEASE;
ADULT-MOUSE;
DISORDERS;
MEMORY;
ROLES;
D O I:
10.1016/j.jtemb.2017.09.020
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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 (50 ppm fluoride in the drinking water for 6 months) and controls (< 0.5 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 50 ppm fluoride for 48 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 InRNAs encoding GluN1 and GluN2 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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页码:31 / 40
页数:10
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