Action potential conduction in the terminal arborisation of nociceptive C-fibre afferents

被引:32
作者
Weidner, C
Schmidt, R
Schmelz, M
Torebjörk, HE
Handwerker, HO
机构
[1] Univ Erlangen Nurnberg, Inst Physiol & Expt Pathophysiol, Dept Physiol & Expt Pathophysiol, D-91054 Erlangen, Germany
[2] Univ Uppsala, Dept Clin Neurophysiol, S-75105 Uppsala, Sweden
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2003年 / 547卷 / 03期
关键词
D O I
10.1113/jphysiol.2002.028712
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recordings of single human peroneal C-fibres and rat saphenous C-fibres confirm two different patterns of conduction at branching points. In general, an action potential (AP) arising from one terminal branch may be propagated not only centrally, but also antidromically into the other branches of the terminal arborisation. If a stimulus activates several converging branches of one unit, at each branching point only the AP arriving first from the simultaneously activated daughter branches will be propagated centrally, resetting the slower branches. However, occasionally a single electrical stimulus may evoke a double response in the parent axon. In this case, these two responses apparently originate from different terminal branches and require unidirectional conduction block to prevent the faster AP from invading and resetting the slower-conducting terminal. This conclusion is supported by the notion that when such a double response occurs, both responses immediately show additional activity-dependent slowing of the conduction velocity due to frequency increase in the parent axon (two spikes per stimulus, one from each of the two excited branches). A comparable discharge pattern in the stem axon can be induced by repetitive paired stimulation of one terminal branch. Then the slowing is induced by the doubled frequency along the whole nerve fibre including the terminal branch. Since in this case not only the stem axon, but also the terminal branches carry two spikes per pulse, activity-dependent slowing is predictably more pronounced. Unidirectional block thus provides insight into the differential amount of activity-dependent slowing (and hence postexcitatory hyperpolarisation) in the stem axon and terminal branches of cutaneous C-fibres. This comparison reveals that more than two-thirds of the slowing can be attributed to the terminal branches, since it is two- to fourfold that observed during double stimulation as compared with the unidirectional block condition. This indicates that the terminal branches are equipped with membrane proteins that are different from those of the parent axon.
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收藏
页码:931 / 940
页数:10
相关论文
共 36 条
[21]   SENSORY RECEPTORS IN MAMMALIAN SKIN IN AN INVITRO PREPARATION [J].
REEH, PW .
NEUROSCIENCE LETTERS, 1986, 66 (02) :141-146
[22]  
SCHMELZ M, 1995, EXP BRAIN RES, V104, P331
[23]   Which nerve fibers mediate the axon reflex flare in human skin? [J].
Schmelz, M ;
Michael, K ;
Weidner, C ;
Schmidt, R ;
Torebjörk, HE ;
Handwerker, HO .
NEUROREPORT, 2000, 11 (03) :645-648
[24]   Innervation territories of mechanically activated C nociceptor units in human skin [J].
Schmidt, R ;
Schmelz, M ;
Ringkamp, M ;
Handwerker, HO ;
Torebjork, HE .
JOURNAL OF NEUROPHYSIOLOGY, 1997, 78 (05) :2641-2648
[25]  
SCHMIDT R, 1995, J NEUROSCI, V15, P333
[26]   Mechano-insensitive nociceptors encode pain evoked by tonic pressure to human skin [J].
Schmidt, R ;
Schmelz, M ;
Torebjörk, HE ;
Handwerker, HO .
NEUROSCIENCE, 2000, 98 (04) :793-800
[27]   Two types of TTX-resistant and one TTX-sensitive Na+ channel in rat dorsal root ganglion neurons and their blockade by halothane [J].
Scholz, A ;
Appel, N ;
Vogel, W .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1998, 10 (08) :2547-2556
[28]   MECHANISMS OF ACTION-POTENTIAL PROPAGATION FAILURE AT SITES OF AXON BRANCHING IN THE CRAYFISH [J].
SMITH, DO .
JOURNAL OF PHYSIOLOGY-LONDON, 1980, 301 (APR) :243-259
[29]  
STONEY SD, 1990, EXP BRAIN RES, V80, P512
[30]   DOUBLE FLUORESCENCE LABELING SUPPORTS ELECTRO-PHYSIOLOGICAL EVIDENCE FOR DICHOTOMIZING PERIPHERAL SENSORY NERVE-FIBERS IN RATS [J].
TAYLOR, DCM ;
PIERAU, FK .
NEUROSCIENCE LETTERS, 1982, 33 (01) :1-6