Axotomy- and autotomy-induced changes in Ca2+ and K+ channel currents of rat dorsal root ganglion neurons

被引:168
作者
Abdulla, FA
Smith, PA
机构
[1] Univ Alberta, Dept Pharmacol, Edmonton, AB T6G 2H7, Canada
[2] Univ Alberta, Div Neurosci, Edmonton, AB T6G 2H7, Canada
[3] Tennessee State Univ, Dept Phys Therapy, Nashville, TN 37209 USA
关键词
D O I
10.1152/jn.2001.85.2.644
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Sciatic nerve section (axotomy) increases the excitability of rat dorsal root ganglion (DRG) neurons. The changes in Ca2+ currents, K+ currents, Ca2+ sensitive K+ current, and hyperpolarization-activated cation current (I-H) that may be associated with this effect were examined by whole cell recording. Axotomy affected the same conductances in all types of DRG neuron. In general, the largest changes were seen in "small" cells and the smallest changes were seen in "large" cells. High-voltage-activated Ca2+-channel current (HVA-I-Ba) was reduced by axotomy. Although currents recorded in axotomized neurons exhibited increased inactivation, this did not account for all of the reduction in HVA-I-Ba. Activation kinetics were unchanged, and experiments with nifedipine and/or omega -conotoxin GVIA showed that there was no change in the percentage contribution of L-type, N-type, or "other" HVA-I-Ba to the total current after axotomy. T-type (low-voltage-activated) I-Ba was not affected by axotomy. Ca2+-sensitive K+ conductance (g(K,Ca)) appeared to be reduced, but when voltage protocols were adjusted to elicit similar amounts of Ca2+ influx into control and axotomized cells, I-K,I-Ca(s) were unchanged. After axotomy, Cd2+-insensitive, steady-state K+ channel current, which primarily comprised delayed rectifier K+ current (I-K), was reduced by about 60% in small, medium, and large cells. These data suggest that axotomy-induced increases in excitability are associated with decreases in I-K and/or decreases in g(K,Ca) that are secondary to decreased Ca2+-influx. Because I-H was reduced by axotomy, changes in this current do not contribute to increased excitability. The amplitude and inactivation of I-Ba in all cell types was changed more profoundly in animals that exhibited self-mutilatory behavior (autotomy). The onset of this behavior corresponded with significant reduction in I-Ba of large neurons. This finding supports the hypothesis that autotomy, that may be related to human neuropathic pain, is associated with changes in the properties of large myelinated sensory neurons.
引用
收藏
页码:644 / 658
页数:15
相关论文
共 63 条
[1]  
Abdulla FA, 1997, J NEUROSCI, V17, P1633
[2]   Nerve injury increases an excitatory action of neuropeptide Y and Y2-agonists on dorsal root ganglion neurons [J].
Abdulla, FA ;
Smith, PA .
NEUROSCIENCE, 1999, 89 (01) :43-60
[3]   Axotomy- and autotomy-induced changes in the excitability of rat dorsal root ganglion neurons [J].
Abdulla, FA ;
Smith, PA .
JOURNAL OF NEUROPHYSIOLOGY, 2001, 85 (02) :630-643
[4]  
Abdulla Fuad A., 1995, Society for Neuroscience Abstracts, V21, P566
[5]   M-CURRENTS AND OTHER POTASSIUM CURRENTS IN BULLFROG SYMPATHETIC NEURONS [J].
ADAMS, PR ;
BROWN, DA ;
CONSTANTI, A .
JOURNAL OF PHYSIOLOGY-LONDON, 1982, 330 (SEP) :537-572
[6]   CHARACTERIZATION OF POTASSIUM CURRENTS IN ADULT-RAT SENSORY NEURONS AND MODULATION BY OPIOIDS AND CYCLIC-AMP [J].
AKINS, PT ;
MCCLESKEY, EW .
NEUROSCIENCE, 1993, 56 (03) :759-769
[7]   In vitro characterization of a peripheral afferent pathway of the rat after chronic sciatic nerve section [J].
Babbedge, RC ;
Soper, AJ ;
Gentry, CT ;
Hood, VC ;
Campbell, EA ;
Urban, L .
JOURNAL OF NEUROPHYSIOLOGY, 1996, 76 (05) :3169-3177
[8]   Voltage-gated calcium currents in axotomized adult rat cutaneous afferent neurons [J].
Baccei, ML ;
Kocsis, JD .
JOURNAL OF NEUROPHYSIOLOGY, 2000, 83 (04) :2227-2238
[9]   RESPONSE OF CUTANEOUS SENSORY UNITS WITH UNMYELINATED FIBERS TO NOXIOUS STIMULI [J].
BESSOU, P ;
PERL, ER ;
SCHMITTR.LA .
JOURNAL OF NEUROPHYSIOLOGY, 1969, 32 (06) :1025-&
[10]   3 TYPES OF SODIUM-CHANNELS IN ADULT-RAT DORSAL-ROOT GANGLION NEURONS [J].
CAFFREY, JM ;
ENG, DL ;
BLACK, JA ;
WAXMAN, SG ;
KOCSIS, JD .
BRAIN RESEARCH, 1992, 592 (1-2) :283-297