Activation of G-protein-coupled receptor 30 increases T-type calcium currents in trigeminal ganglion neurons via the cholera toxin-sensitive protein kinase A pathway

被引:7
|
作者
Yue, Jingxia [1 ]
Zhang, Yi [1 ]
Li, Xuemin [1 ]
Gong, Shan [1 ]
Tao, Jin [1 ]
Jiang, Xinghong [1 ]
机构
[1] Soochow Univ, Coll Med, Dept Physiol & Neurobiol, Suzhou 215123, Peoples R China
来源
PHARMAZIE | 2014年 / 69卷 / 11期
基金
中国国家自然科学基金;
关键词
CHANNEL ACTIVITY; SENSORY NEURONS; CA2+ CHANNELS; RAT; MODULATION; GPR30; PAIN; NOCICEPTION; MOUSE; CELLS;
D O I
10.1691/ph.2014.4650
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
G protein-coupled receptor 30 (GPR30) is a seven transmembrane domain G protein coupled receptor. In our study, GPR30 expression was found in trigeminal ganglia (TG) in mice, detected by RT-PCR and western blotting. We examined the effects of GPR30 activation on T-type calcium channels using GPR30-specific compound 1 (G-1), a GPR30-selective agonist, in TG neurons and demonstrated that G-1 induced an increase in T-type calcium channel currents (T-currents) in TGs. Intracellular infusion of GDP-beta-S and pre-treatment of the neurons with cholera toxin (CTX) blocked the effects of G-1, suggesting that the G(s)-protein was involved. Intracellular application of the protein kinase A (PKA) inhibitor PKI 6-22 or pretreatment of the neurons with H89 abolished G-1-induced enhancement of T-currents in TG neurons. However, incubation with PKC inhibitor elicited no such effects. In conclusion, our study shows that activation of GPR30 by G-1 increases T-currents via the CTX-sensitive and PKA-dependent pathway.
引用
收藏
页码:804 / 808
页数:5
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