Distinct ASIC currents are expressed in rat putative nociceptors and are modulated by nerve injury

被引:83
作者
Poirot, Olivier
Berta, Temugin
Decosterd, Isabelle
Kellenberger, Stephan
机构
[1] Univ Lausanne, Dept Pharmacol & Toxicol, CH-1005 Lausanne, Switzerland
[2] Lausanne Univ Hosp, CHUV, Anaesthesiol Pain Res Grp, Dept Anaesthesiol, CH-1011 Lausanne, Switzerland
[3] Univ Lausanne, Dept Cell Biol & Morphol, Fac Biol & Med, CH-1005 Lausanne, Switzerland
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2006年 / 576卷 / 01期
关键词
D O I
10.1113/jphysiol.2006.113035
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The H+-gated acid-sensing ion channels (ASICs) are expressed in dorsal root ganglion (DRG) neurones. Studies with ASIC knockout mice indicated either a pro-nociceptive or a modulatory role of ASICs in pain sensation. We have investigated in freshly isolated rat DRG neurones whether neurones with different ASIC current properties exist, which may explain distinct cellular roles, and we have investigated ASIC regulation in an experimental model of neuropathic pain. Small-diameter DRG neurones expressed three different ASIC current types which were all preferentially expressed in putative nociceptors. Type 1 currents were mediated by ASIC1a homomultimers and characterized by steep pH dependence of current activation in the pH range 6.8-6.0. Type 3 currents were activated in a similar pH range as type 1, while type 2 currents were activated at pH < 6. When activated by acidification to pH 6.8 or 6.5, the probability of inducing action potentials correlated with the ASIC current density. Nerve injury induced differential regulation of ASIC subunit expression and selective changes in ASIC function in DRG neurones, suggesting a complex reorganization of ASICs during the development of neuropathic pain. In summary, we describe a basis for distinct cellular functions of different ASIC types in small-diameter DRG neurones.
引用
收藏
页码:215 / 234
页数:20
相关论文
共 81 条
[1]   A new member of the acid-sensing ion channel family [J].
Akopian, AN ;
Chen, CC ;
Ding, YN ;
Cesare, P ;
Wood, JN .
NEUROREPORT, 2000, 11 (10) :2217-2222
[2]   Multiple interacting sites of ectopic spike electrogenesis in primary sensory neurons [J].
Amir, R ;
Kocsis, JD ;
Devor, M .
JOURNAL OF NEUROSCIENCE, 2005, 25 (10) :2576-2585
[3]  
Amir R, 1996, J NEUROSCI, V16, P4733
[4]   ASIC-like, proton-activated currents in rat hippocampal neurons [J].
Baron, A ;
Waldmann, R ;
Lazdunski, M .
JOURNAL OF PHYSIOLOGY-LONDON, 2002, 539 (02) :485-494
[5]   Zn2+ and H+ are coactivators of acid-sensing ion channels [J].
Baron, A ;
Schaefer, L ;
Lingueglia, E ;
Champigny, G ;
Lazdunski, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (38) :35361-35367
[6]  
Basbuam A.L., 2000, The perception of pain. Principles of Neural Science, P472
[7]   Responses of adult human dorsal root ganglion neurons in culture to capsaicin and low pH [J].
Baumann, TK ;
Burchiel, KJ ;
Ingram, SL ;
Martenson, ME .
PAIN, 1996, 65 (01) :31-38
[8]   Background potassium channel block and TRPV1 activation contribute to proton depolarization of sensory neurons from humans with neuropathic pain [J].
Baumann, TK ;
Chaudhary, P ;
Martenson, ME .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2004, 19 (05) :1343-1351
[9]   trkA, CGRP and IB4 expression in retrogradely labelled cutaneous and visceral primary sensory neurones in the rat [J].
Bennett, DL ;
Dmietrieva, N ;
Priestley, JV ;
Clary, D ;
McMahon, SB .
NEUROSCIENCE LETTERS, 1996, 206 (01) :33-36
[10]  
Benson CJ, 1999, CIRC RES, V84, P921