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Dextromethorphan inhibition of voltage-gated proton currents in BV2 microglial cells
被引:10
|作者:
Song, Jin-Ho
[1
]
Yeh, Jay Z.
[2
]
机构:
[1] Chung Ang Univ, Coll Med, Dept Pharmacol, Seoul 156756, South Korea
[2] Northwestern Univ, Feinberg Sch Med, Dept Mol Pharmacol & Biol Chem, Chicago, IL 60611 USA
基金:
新加坡国家研究基金会;
关键词:
Microglial BV2 cell;
Voltage-gated proton channel;
Dextromethorphan;
Dextrorphan;
3-Hydroxymorphinan;
NADPH OXIDASE;
SUPEROXIDE-PRODUCTION;
DOPAMINERGIC-NEURONS;
IN-VITRO;
CHANNELS;
DEXTRORPHAN;
ACTIVATION;
DEPENDENCE;
PROTECT;
DAMAGE;
D O I:
10.1016/j.neulet.2012.03.065
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Dextromethorphan, an antitussive drug, has a neuroprotective property as evidenced by its inhibition of microglial production of pro-inflammatory cytokines and reactive oxygen species. The microglial activation requires NADPH oxidase activity, which is sustained by voltage-gated proton channels in microglia as they dissipate an intracellular acid buildup. In the present study, we examined the effect of dextromethorphan on proton currents in microglial BV2 cells. Dextromethorphan reversibly inhibited proton currents with an IC50 value of 51.7 mu M at an intracellular/extracellular pH gradient of 5.5/7.3. Dextromethorphan did not change the reversal potential or the voltage dependence of the gating. Dextrorphan and 3-hydroxymorphinan, major metabolites of dextromethorphan, and dextromethorphan methiodide were ineffective in inhibiting proton currents. The results indicate that dextromethorphan inhibition of proton currents would suppress NADPH oxidase activity and, eventually, microglial activation. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
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页码:94 / 98
页数:5
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