Long-term depression of C-fibre-evoked spinal field potentials by stimulation of primary afferent Aδ-fibres in the adult rat

被引:113
作者
Liu, XG [1 ]
Morton, CR [1 ]
Azkue, JJ [1 ]
Zimmermann, M [1 ]
Sandkühler, J [1 ]
机构
[1] Heidelberg Univ, Inst Physiol 2, D-69120 Heidelberg, Germany
关键词
A delta-fibre; analgesia; electrical nerve stimulation; hyperalgesia; long-term potentiation; NMDA receptors; synaptic plasticity;
D O I
10.1046/j.1460-9568.1998.00310.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Long-term potentiation (LTP) of spinal C-fibre-evoked field potentials can be induced by brief electrical stimulation of afferent C-fibres, by natural noxious stimulation of skin or by acute nerve injury. Here, we report that in urethane anaesthetized, adult rats prolonged high frequency burst stimulation of the sciatic nerve at A delta-fibre strength produced long-term depression (LTD) of C-fibre-evoked field potentials, and also depressed the increased amplitudes of C-fibre-evoked field potentials recorded after LTP had been established (depotentiation). Electrical stimulation of A beta-fibres failed to induce LTD or depotentiation. In spinalized rats, prolonged A delta-fibre conditioning stimulation induced LTP rather than LTD of C-fibre-evoked field potentials. Thus, tonic descending inhibition may determine the direction of plastic changes in C-fibre-mediated synaptic transmission. Spinal application of the N-methyl-D-aspartic acid receptor antagonist D-APV blocked induction of LTD in intact rats and LTP in spinalized rats. The presently described LTD and the depotentiation of established LTP of C-fibre-evoked field potentials in spinal dorsal horn may underlie some forms of prolonged analgesia induced by peripheral nerve stimulation procedures.
引用
收藏
页码:3069 / 3075
页数:7
相关论文
共 53 条
[1]   LONG-TERM POTENTIATION OF NICOTINIC TRANSMISSION BY A HETEROSYNAPTIC MECHANISM IN THE STELLATE GANGLION OF THE CAT [J].
BACHOO, M ;
POLOSA, C .
JOURNAL OF NEUROPHYSIOLOGY, 1991, 65 (03) :639-647
[2]   ENDOGENOUS PAIN CONTROL MECHANISMS - REVIEW AND HYPOTHESIS [J].
BASBAUM, AI ;
FIELDS, HL .
ANNALS OF NEUROLOGY, 1978, 4 (05) :451-462
[3]  
Bear Mark F., 1994, Current Opinion in Neurobiology, V4, P389, DOI 10.1016/0959-4388(94)90101-5
[4]   CONTROLLED SUPERFUSION OF THE RAT SPINAL-CORD FOR STUDYING NONSYNAPTIC TRANSMISSION - AN AUTORADIOGRAPHIC ANALYSIS [J].
BECK, H ;
SCHROCK, H ;
SANDKUHLER, J .
JOURNAL OF NEUROSCIENCE METHODS, 1995, 58 (1-2) :193-202
[5]   LONG-LASTING POTENTIATION OF SYNAPTIC TRANSMISSION IN DENTATE AREA OF ANESTHETIZED RABBIT FOLLOWING STIMULATION OF PERFORANT PATH [J].
BLISS, TVP ;
LOMO, T .
JOURNAL OF PHYSIOLOGY-LONDON, 1973, 232 (02) :331-356
[6]   A SYNAPTIC MODEL OF MEMORY - LONG-TERM POTENTIATION IN THE HIPPOCAMPUS [J].
BLISS, TVP ;
COLLINGRIDGE, GL .
NATURE, 1993, 361 (6407) :31-39
[7]   NOCICEPTOR-DRIVEN DORSAL HORN NEURONS IN LUMBAR SPINAL-CORD OF CAT [J].
CERVERO, F ;
IGGO, A ;
OGAWA, H .
PAIN, 1976, 2 (01) :5-24
[8]   PROLONGED INHIBITION OF PRIMATE SPINOTHALAMIC TRACT CELLS BY PERIPHERAL-NERVE STIMULATION [J].
CHUNG, JM ;
FANG, ZR ;
HORI, Y ;
LEE, KH ;
WILLIS, WD .
PAIN, 1984, 19 (03) :259-275
[9]   FACTORS INFLUENCING PERIPHERAL-NERVE STIMULATION PRODUCED INHIBITION OF PRIMATE SPINOTHALAMIC TRACT CELLS [J].
CHUNG, JM ;
LEE, KH ;
HORI, Y ;
ENDO, K ;
WILLIS, WD .
PAIN, 1984, 19 (03) :277-293
[10]   CONTRIBUTION OF CENTRAL NEUROPLASTICITY TO PATHOLOGICAL PAIN - REVIEW OF CLINICAL AND EXPERIMENTAL-EVIDENCE [J].
CODERRE, TJ ;
KATZ, J ;
VACCARINO, AL ;
MELZACK, R .
PAIN, 1993, 52 (03) :259-285