Differential slow inactivation and use-dependent inhibition of Nav1.8 channels contribute to distinct firing properties in IB4+ and IB4- DRG neurons

被引:70
作者
Choi, Jin-Sung
Dib-Hajj, Sulayman D.
Waxman, Stephen G.
机构
[1] Yale Univ, Sch Med, Dept Neurol, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Ctr Neurosci & Regenerat Res, New Haven, CT 06510 USA
[3] Vet Adm Connecticut Healthcare Syst, Rehabil Res Ctr, West Haven, CT USA
关键词
D O I
10.1152/jn.01033.2006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Nociceptive dorsal root ganglion ( DRG) neurons can be classified into nonpeptidergic IB4+ and peptidergic IB4- subtypes, which terminate in different layers in dorsal horn and transmit pain along different ascending pathways, and display different firing properties. Voltage-gated, tetrodotoxin- resistant ( TTX- R) Na-v 1.8 channels are expressed in both IB4+ and IB4- cells and produce most of the current underlying the depolarizing phase of action potential ( AP). Slow inactivation of TTX- R channels has been shown to regulate repetitive DRG neuron firing behavior. We show in this study that use-dependent reduction of Na-v 1.8 current in IB4+ neurons is significantly stronger than that in IB4- neurons, although voltage dependency of activation and steady-state inactivation are not different. The time constant for entry of Na v 1.8 into slow inactivation in IB4+ neurons is significantly faster and more Na-v 1.8 enter the slow inactivation state than in IB4+ neurons. In addition, recovery from slow inactivation of Na-v 1.8 in IB4+ neurons is slower than that in IB4- neurons. Using current- clamp recording, we demonstrate a significantly higher current threshold for generation of APs and a longer latency to onset of firing in IB4+, compared with those of IB4- neurons. In response to a ramp stimulus, IB4+ neurons produce fewer APs and display stronger adaptation, with a faster decline of AP peak than IB4- neurons. Our data suggest that differential use- dependent reduction of Na(v)1.8 current in these two DRG subpopulations, which results from their different rate of entry into and recovery from the slow inactivation state, contributes to functional differences between these two neuronal populations.
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页码:1258 / 1265
页数:8
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