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二丁酰环磷腺苷对大鼠背根神经节神经元中河豚毒素敏感和耐药的电压门控钠电流的影响及其对利多卡因敏感性的影响。

The effect of dibutyryl cAMP on tetrodotoxin-sensitive and -resistant voltage-gated sodium currents in rat dorsal root ganglion neurons and the consequences for their sensitivity to lidocaine.

作者信息

Docherty R J, Farrag K J

机构信息

King's College London, Wolfson Centre for Age-Related Diseases, Guy's Campus, London Bridge, London SE1 9RT, UK.

出版信息

Neuropharmacology. 2006 Nov;51(6):1047-57. doi: 10.1016/j.neuropharm.2006.06.021. Epub 2006 Aug 23.

Abstract

Tetrodotoxin-sensitive (TTXS) sodium currents in dorsal root ganglia (DRG) neurons were enhanced by DcAMP applied acutely or by pre-treatment. Pre-treatment increased peak TTXS by 28%. This compared to the increase of tetrodotoxin-resistant sodium currents (TTXR) of 123%. In both cases the increase was associated with a hyperpolarizing shift in activation potentials. Slow inactivation was slower for both TTXR and TTXS in DcAMP treated neurons but rates of recovery from inactivation were not altered. Lidocaine blocked TTX-R with an IC(50) of 0.51+/-0.15mM (n=9) which was reduced to 0.14+/-0.05mM (n=8, P<0.05) in DcAMP treated cells. The sensitivity of TTX-S currents to lidocaine was not altered by DcAMP (control EC(50)=0.89+/-0.16mM, n=9; DcAMP EC(50)=0.73+/-0.19mM, n=6). It is concluded that TTXS currents in DRG are, like TTX-R currents, enhanced by cAMP but whilst the pharmacology of TTXR channels with respect to lidocaine is altered, that to TTXS channels is not.

摘要

急性应用或预处理环磷腺苷(DcAMP)可增强背根神经节(DRG)神经元中的河豚毒素敏感性(TTXS)钠电流。预处理使TTXS电流峰值增加28%。相比之下,河豚毒素抗性钠电流(TTXR)增加了123%。在这两种情况下,电流增加都与激活电位的超极化偏移有关。在DcAMP处理的神经元中,TTXR和TTXS的缓慢失活都变慢,但失活后的恢复速率没有改变。利多卡因阻断TTX-R的半数抑制浓度(IC50)为0.51±0.15mM(n = 9),在DcAMP处理的细胞中降至0.14±0.05mM(n = 8,P<0.05)。DcAMP未改变TTX-S电流对利多卡因的敏感性(对照半数有效浓度(EC50)=0.89±0.16mM,n = 9;DcAMP EC50 = 0.73±0.19mM,n = 6)。结论是,DRG中的TTXS电流与TTX-R电流一样,可被环磷酸腺苷(cAMP)增强,但虽然TTXR通道对利多卡因的药理学特性发生了改变,但TTXS通道的药理学特性未改变。

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