Docherty R J, Farrag K J
King's College London, Wolfson Centre for Age-Related Diseases, Guy's Campus, London Bridge, London SE1 9RT, UK.
Neuropharmacology. 2006 Nov;51(6):1047-57. doi: 10.1016/j.neuropharm.2006.06.021. Epub 2006 Aug 23.
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.
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。