Coenzyme Q10 Inhibits the Release of Glutamate in Rat Cerebrocortical Nerve Terminals by Suppression of Voltage-Dependent Calcium Influx and Mitogen-Activated Protein Kinase Signaling Pathway

被引:14
|
作者
Chang, Yi [1 ,2 ]
Huang, Shu-Kuei [3 ]
Wang, Su-Jane [1 ]
机构
[1] Fu Jen Catholic Univ, Sch Med, New Taipei City 24205, Taiwan
[2] Shin Kong Wu Ho Su Mem Hosp, Dept Anesthesiol, Taipei 111, Taiwan
[3] Far Eastern Mem Hosp, Dept Anesthesiol, New Taipei City 22060, Taiwan
关键词
CoQ10; glutamate release; cerebrocortical nerve terminals; ERK; voltage-dependent Ca2+ channels; TRANSGENIC MOUSE MODEL; NEURONAL CELL-DEATH; OXIDATIVE STRESS; PRESYNAPTIC MODULATION; ANTIOXIDANT PROPERTIES; CA2+ ENTRY; SYNAPSIN-I; PHOSPHORYLATION; CHANNELS; BRAIN;
D O I
10.1021/jf302875k
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
This study investigates the effects and possible mechanism of coenzyme Q10 (CoQ10) on endogenous glutamate release in the cerebral cortex nerve terminals of rats. CoQ10 inhibited the release of glutamate evoked by the K+ channel blocker 4-aminopyridine (4-AP). CoQ10 reduced the depolarization-induced increase in cytosolic [Ca2+](c) but did not alter the 4-AP-mediated depolarization. The effect of CoQ10 on evoked glutamate release was abolished by blocking the Ca(v)2.2 (N-type) and Ca(v)2.1 (P/Q-type) Ca2+ channels and mitogen-activated protein kinase kinase (MEK). In addition, CoQ10 decreased the 4-AP-induced phosphorylation of extracellular signal-regulated kinase 1 and 2 (ERK1/2) and synaptic vesicle-associated protein synapsin I, a major presynaptic substrate for ERK Moreover, the inhibition of glutamate release by CoQ10 was strongly attenuated in mice without synapsin I. These results suggest that CoQ10 inhibits glutamate release from cortical synaptosomes in rats through the suppression of the presynaptic voltage-dependent Ca2+ entry and ERK/synapsin I signaling pathway.
引用
收藏
页码:11909 / 11918
页数:10
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