OPIOID RECEPTOR ANTAGONIST NALMEFENE STEREOSPECIFICALLY INHIBITS GLUTAMATE RELEASE DURING GLOBAL CEREBRAL-ISCHEMIA

被引:16
作者
GRAHAM, SH
SHIMIZU, H
NEWMAN, A
WEINSTEIN, P
FADEN, AI
机构
[1] GEORGETOWN UNIV,SCH MED,DEPT NEUROL,WASHINGTON,DC 20007
[2] GEORGETOWN UNIV,SCH MED,DEPT PHARMACOL,WASHINGTON,DC 20007
[3] UNIV CALIF SAN FRANCISCO,DEPT NEUROL,SAN FRANCISCO,CA 94121
[4] UNIV CALIF SAN FRANCISCO,DEPT NEUROSURG,SAN FRANCISCO,CA 94121
[5] WALTER REED ARMY INST RES,DEPT APPL BIOCHEM,WASHINGTON,DC 20307
关键词
OPIOID ANTAGONIST; MICRODIALYSIS; STROKE; EXCITATORY AMINO ACID;
D O I
10.1016/0006-8993(93)91175-R
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The opioid receptor antagonist nalmefene improves cellular bioenergetics and attenuates the reduction in tissue glutamate levels after global cerebral ischemia/reperfusion. The latter finding suggests that nalmefene might inhibit glutamate release during ischemia. To test this hypothesis, we used microdialysis techniques to examine the effect of nalmefene pretreatment on extracellular excitatory amino acid levels during global cerebral ischemia in rats. Saline, (-)-nalmefene (20, 100 or 500 mu g/kg) or the inactive nalmefene enantiomer (+)-nalmefene (100 mu g/kg) were given 15 min prior to induction of ischemia using a multi-vessel occlusion model. Pretreatment with (-)-nalmefene decreased peak dialysate glutamate in a dose-dependent fashion as compared to saline-treated controls, whereas (+)-nalmefene had no effect. These results suggest that opioid receptors may modulate glutamate release during ischemia and that inhibition of excitatory amino acid release may contribute to the protective actions of opioid receptor antagonists in cerebral ischemia.
引用
收藏
页码:346 / 350
页数:5
相关论文
共 38 条
  • [1] N-METHYL-D-ASPARTATE (NMDA) AND OPIOID RECEPTORS MEDIATE DYNORPHIN-INDUCED SPINAL-CORD INJURY - BEHAVIORAL AND HISTOLOGICAL STUDIES
    BAKSHI, R
    NI, RX
    FADEN, AI
    [J]. BRAIN RESEARCH, 1992, 580 (1-2) : 255 - 264
  • [2] DYNORPHIN-A-(1-17) INDUCES ALTERATIONS IN FREE FATTY-ACIDS, EXCITATORY AMINO-ACIDS, AND MOTOR FUNCTION THROUGH AN OPIATE-RECEPTOR-MEDIATED MECHANISM
    BAKSHI, R
    NEWMAN, AH
    FADEN, AI
    [J]. JOURNAL OF NEUROSCIENCE, 1990, 10 (12) : 3793 - 3800
  • [3] ELEVATION OF THE EXTRACELLULAR CONCENTRATIONS OF GLUTAMATE AND ASPARTATE IN RAT HIPPOCAMPUS DURING TRANSIENT CEREBRAL-ISCHEMIA MONITORED BY INTRACEREBRAL MICRODIALYSIS
    BENVENISTE, H
    DREJER, J
    SCHOUSBOE, A
    DIEMER, NH
    [J]. JOURNAL OF NEUROCHEMISTRY, 1984, 43 (05) : 1369 - 1374
  • [4] NEUROPROTECTIVE ACTIONS OF GR89696, A HIGHLY POTENT AND SELECTIVE KAPPA-OPIOID RECEPTOR AGONIST
    BIRCH, PJ
    ROGERS, H
    HAYES, AG
    HAYWARD, NJ
    TYERS, MB
    SCOPES, DIC
    NAYLOR, A
    JUDD, DB
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 1991, 103 (03) : 1819 - 1823
  • [5] OPIOIDS AND NON-OPIOID ENANTIOMERS SELECTIVELY ATTENUATE N-METHYL-D-ASPARTATE NEUROTOXICITY ON CORTICAL-NEURONS
    CHOI, DW
    VISESKUL, V
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 155 (1-2) : 27 - 35
  • [6] CHOI DW, 1987, J NEUROSCI, V7, P369
  • [7] CLARK JA, 1989, J PHARMACOL EXP THER, V251, P461
  • [8] EVALUATION OF U-50,488H ANALOGS FOR NEUROPROTECTIVE ACTIVITY IN THE GERBIL
    CONTRERAS, PC
    RAGAN, DM
    BREMER, ME
    LANTHORN, TH
    GRAY, NM
    IYENGAR, S
    JACOBSON, AE
    RICE, KC
    DECOSTA, BR
    [J]. BRAIN RESEARCH, 1991, 546 (01) : 79 - 82
  • [9] CORDON J J, 1990, Society for Neuroscience Abstracts, V16, P934
  • [10] CELLULAR-ORIGIN OF ISCHEMIA-INDUCED GLUTAMATE RELEASE FROM BRAIN-TISSUE INVIVO AND INVITRO
    DREJER, J
    BENVENISTE, H
    DIEMER, NH
    SCHOUSBOE, A
    [J]. JOURNAL OF NEUROCHEMISTRY, 1985, 45 (01) : 145 - 151