L-NAME BLOCKS RESPONSES TO NMDA, SUBSTANCE-P AND NOXIOUS CUTANEOUS STIMULI IN CAT DORSAL HORN

被引:38
作者
RADHAKRISHNAN, V
HENRY, JL
机构
[1] MCGILL UNIV,DEPT PHYSIOL,3655 DRUMMOND ST,MONTREAL H3G 1Y6,QUEBEC,CANADA
[2] MCGILL UNIV,DEPT PSYCHIAT,MONTREAL H3G 1Y6,QUEBEC,CANADA
基金
加拿大健康研究院;
关键词
SUBSTANCE-P; NITRIC OXIDE; PAIN; DORSAL HORN; L-NAME; NOCICEPTION; N-METHYL-D-ASPARTATE; QUISQUALATE; EXCITATORY AMINO ACID; SPINAL CORD;
D O I
10.1097/00001756-199303000-00025
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
THE nitric oxide synthase inhibitor, N(G)-nitro-L-arginine methyl ester (L-NAME), administered i.v. (50 mg kg-1) or by iontophoresis, was tested on the responses of spinal dorsal horn neurones in cats anaesthetized with alpha-chloralose and spinally transected at the L1 level. Extracellular, single-unit recordings were obtained from functionally identified dorsal horn cells. All units included in this study were wide dynamic range neurones. L-NAME significantly reduced the responses of (i) twelve neurones to noxious thermal stimulation of the receptive field, (ii) nine neurones to noxious pinch, (iii) nine neurones to iontophoretic application of N-methyl-D-aspartate (NMDA) and (iv) ten neurones to iontophoretic application of substance P. The inhibition usually lasted for 50-70 min following i.v. administration and for 5-8 min after iontophoretic application Of L-NAME. The responses of four neurones to iontophoretic application of quisqualate were not affected by L-NAME. The results suggest the possible involvement of nitric oxide in the mediation of the spinal effects of NMDA and substance P, and in the transmission of thermal and mechanical nociceptive imputs.
引用
收藏
页码:323 / 326
页数:4
相关论文
共 25 条
[1]   LOCALIZATION OF NITRIC-OXIDE SYNTHASE INDICATING A NEURAL ROLE FOR NITRIC-OXIDE [J].
BREDT, DS ;
HWANG, PM ;
SNYDER, SH .
NATURE, 1990, 347 (6295) :768-770
[2]   SUBSTANCE P-MEDIATED SLOW EXCITATORY POSTSYNAPTIC POTENTIAL ELICITED IN DORSAL HORN NEURONS INVIVO BY NOXIOUS-STIMULATION [J].
DE KONINCK, Y ;
HENRY, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (24) :11344-11348
[3]   PERIPHERAL ANALGESIA AND ACTIVATION OF THE NITRIC OXIDE-CYCLIC GMP PATHWAY [J].
DUARTE, IDG ;
LORENZETTI, BB ;
FERREIRA, SH .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 186 (2-3) :289-293
[4]   THE OBLIGATORY ROLE OF ENDOTHELIAL-CELLS IN THE RELAXATION OF ARTERIAL SMOOTH-MUSCLE BY ACETYLCHOLINE [J].
FURCHGOTT, RF ;
ZAWADZKI, JV .
NATURE, 1980, 288 (5789) :373-376
[5]   ENDOTHELIUM-DERIVED RELAXING FACTOR RELEASE ON ACTIVATION OF NMDA RECEPTORS SUGGESTS ROLE AS INTERCELLULAR MESSENGER IN THE BRAIN [J].
GARTHWAITE, J ;
CHARLES, SL ;
CHESSWILLIAMS, R .
NATURE, 1988, 336 (6197) :385-388
[6]   ELECTROPHYSIOLOGICAL EVIDENCE FOR A ROLE OF NITRIC-OXIDE IN PROLONGED CHEMICAL NOCICEPTION IN THE RAT [J].
HALEY, JE ;
DICKENSON, AH ;
SCHACHTER, M .
NEUROPHARMACOLOGY, 1992, 31 (03) :251-258
[7]   EVIDENCE FOR SPINAL N-METHYL-D-ASPARTATE RECEPTOR INVOLVEMENT IN PROLONGED CHEMICAL NOCICEPTION IN THE RAT [J].
HALEY, JE ;
SULLIVAN, AF ;
DICKENSON, AH .
BRAIN RESEARCH, 1990, 518 (1-2) :218-226
[8]   ENDOTHELIUM-DERIVED RELAXING FACTOR PRODUCED AND RELEASED FROM ARTERY AND VEIN IS NITRIC-OXIDE [J].
IGNARRO, LJ ;
BUGA, GM ;
WOOD, KS ;
BYRNS, RE ;
CHAUDHURI, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (24) :9265-9269
[9]  
KAWAGOE R, 1986, BIOMED RES-TOKYO, V7, P253
[10]   FORMATION OF NITRIC-OXIDE FROM L-ARGININE IN THE CENTRAL NERVOUS-SYSTEM - A TRANSDUCTION MECHANISM FOR STIMULATION OF THE SOLUBLE GUANYLATE-CYCLASE [J].
KNOWLES, RG ;
PALACIOS, M ;
PALMER, RMJ ;
MONCADA, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (13) :5159-5162