Characteristics of late Na+ current in adult rat small sensory neurons

被引:13
作者
Kiernan, MC
Baker, MD
Bostock, H
机构
[1] Prince Wales Med Res Inst, Randwick, NSW 2031, Australia
[2] Univ New S Wales, Kensington, NSW 2033, Australia
[3] Inst Neurol, Sobell Dept Neurophysiol, London WC1N 3BG, England
[4] UCL, Dept Biol, Mol Nocicept Grp, London WC1E 6BT, England
基金
英国医学研究理事会;
关键词
dorsal root ganglion; tetrodotoxin; patch-clamp; excitability; pain;
D O I
10.1016/S0306-4522(03)00194-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Na+ currents were recorded using patch-clamp techniques from small-diameter (<25 mum) dorsal root ganglion neurons, cultured from adult rats (>150 g). Late Na+ currents maintained throughout long-duration voltage-clamp steps (greater than or equal to200 ms) were of two types: a low-threshold, tetrodotoxin-sensitive (TTX-s) current that was largely blocked by 200 nM TTX, and a high-threshold, TTX-resistant (TTX-r) current. TTX-s late current was found in approximately 28% (10/36) of small-diameter neurons and was recorded only in neurons exhibiting TTX-s transient current. TTX-s transient current activation/inactivation gating overlap existed over a narrow potential range, centered between -30 and -40 mV, whereas late current operated over a wider range. The kinetics associated with de-inactivation of TTX-s late current were slow (tau approximately 37 ms at -50 mV), strongly suggesting that different subpopulations of TTX-s channel generate transient and late current. High-threshold TTX-r late current was only present in neurons generating TTX-r transient current. TTX-r late current operated over the same potential range as that for TTX-r transient current activation/inactivation gating overlap, and activation/inactivation gating overlap could be measured even after 1.5-s-duration pre-pulses. We suggest that TTX-s late sodium current results from channel openings different from those generating transient current. As in large-diameter sensory neurons, TTX-s channels generating late openings may play a key role in controlling membrane excitability. In contrast, a single population of high-threshold TTX-r channels may account for both transient and late TTX-r currents. (C) 2003 IBRO. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:653 / 660
页数:8
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