TIME COURSE OF THE ALTERATION IN DORSAL HORN SUBSTANCE-P LEVELS FOLLOWING FORMALIN - BLOCKADE BY NALOXONE

被引:34
作者
MCCARSON, KE [1 ]
GOLDSTEIN, BD [1 ]
机构
[1] MED COLL GEORGIA,DEPT PHARMACOL & TOXICOL,AUGUSTA,GA 30912
关键词
(Rat); Dorsal horn; Formalin test; Naloxone; Nociception; Substance P;
D O I
10.1016/0304-3959(90)91113-W
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Substance P (SP) found in the dorsal horn of the spinal cord has been proposed as a mediator of nociception. Formalin injected into the hind paw of a rat as a nociceptive stimulus has been shown to increase the amount of immunoreactive SP in the dorsal horn, perhaps by decreasing SP release from primary afferent neurons. These SP changes may be due to the actions of endogenous opiates which can block SP release from primary afferent neurons. In order to determine the time course of SP changes in the dorsal horn and their modulation by naloxone, anesthetized rats pretreated subcutaneously with naloxone or saline were injected in the right hind paw with 0.4 ml of either sahne or 5% formalin. After various time intervals, the animals were perfused and the lumbar enlargement of the spinal cord removed. Immunohistochemical staining and manual photometry were used to quantitate SP-like immunoreactivity (SPLI) in the dorsal horn. The results show that saline injection produced an increase in SPLI lasting 20 min, while formalin produced a biphasic effect with early (0-20 min) and late (20-60 min) increases in SPLI. Naloxone pretreatment 30 min prior to hind paw injection partially blocked the initial SPLI increase due to saline or formahn. However, this was not the case if naloxone was injected 2 min following hind paw injection. The formalin-induced late SPLI increase was blocked by naloxone only if it was administered prior to the formalin. This blockade of SPLI increases in the dorsal horn by naloxone implies that endogenous opioid systems play a role in the control of SP levels in the dorsal horn during nociception. © 1990.
引用
收藏
页码:95 / 100
页数:6
相关论文
共 26 条
  • [1] ORIGIN, DISTRIBUTION AND SYNAPTIC RELATIONSHIPS OF SUBSTANCE-P AXONS IN RAT SPINAL-CORD
    BARBER, RP
    VAUGHN, JE
    SLEMMON, JR
    SALVATERRA, PM
    ROBERTS, E
    LEEMAN, SE
    [J]. JOURNAL OF COMPARATIVE NEUROLOGY, 1979, 184 (02) : 331 - 351
  • [2] SUBCUTANEOUS FORMALIN-INDUCED ACTIVITY OF DORSAL HORN NEURONS IN THE RAT - DIFFERENTIAL RESPONSE TO AN INTRATHECAL OPIATE ADMINISTERED PRE-FORMALIN OR POST-FORMALIN
    DICKENSON, AH
    SULLIVAN, AF
    [J]. PAIN, 1987, 30 (03) : 349 - 360
  • [3] DOI T, 1981, N-S ARCH PHARMACOL, V317, P135, DOI 10.1007/BF00500069
  • [4] FORMALIN TEST - QUANTITATIVE STUDY OF ANALGESIC EFFECTS OF MORPHINE, MEPERIDINE, AND BRAIN-STEM STIMULATION IN RATS AND CATS
    DUBUISSON, D
    DENNIS, SG
    [J]. PAIN, 1977, 4 (02) : 161 - 174
  • [5] AFFERENT-FIBERS MEDIATE THE INCREASE OF MET-ENKEPHALIN ELICITED IN RAT SPINAL-CORD BY LOCALIZED PAIN
    FACCINI, E
    UZUMAKI, H
    GOVONI, S
    MISSALE, C
    SPANO, PF
    COVELLI, V
    TRABUCCHI, M
    [J]. PAIN, 1984, 18 (01) : 25 - 31
  • [6] IS SUBSTANCE-P A PRIMARY AFFERENT NEUROTRANSMITTER FOR NOCICEPTIVE INPUT .1. ANALYSIS OF PAIN-RELATED BEHAVIORS RESULTING FROM INTRATHECAL ADMINISTRATION OF SUBSTANCE-P AND 6 EXCITATORY COMPOUNDS
    FRENK, H
    BOSSUT, D
    URCA, G
    MAYER, DJ
    [J]. BRAIN RESEARCH, 1988, 455 (02) : 223 - 231
  • [7] RELEASE OF SUBSTANCE-P FROM THE CAT SPINAL-CORD
    GO, VLW
    YAKSH, TL
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1987, 391 : 141 - 167
  • [8] HENRY JL, 1983, BRAIN RES BULL, V10, P727, DOI 10.1016/0361-9230(83)90043-6
  • [9] EFFECTS OF SUBSTANCE-P ON FUNCTIONALLY IDENTIFIED UNITS IN CAT SPINAL-CORD
    HENRY, JL
    [J]. BRAIN RESEARCH, 1976, 114 (03) : 439 - 451
  • [10] MET-ENKEPHALIN AND MORPHINE BUT NOT DYNORPHIN INHIBIT NOXIOUS STIMULI-INDUCED RELEASE OF SUBSTANCE-P FROM RABBIT DORSAL HORN INSITU
    HIROTA, N
    KURAISHI, Y
    HINO, Y
    SATO, Y
    SATOH, M
    TAKAGI, H
    [J]. NEUROPHARMACOLOGY, 1985, 24 (06) : 567 - 570