NMDA receptor antagonists in pain therapy.

被引:7
作者
Weber, C [1 ]
机构
[1] Heidelberg Univ, Klinikum Stadt Mannheim, Fak Klin Med Mannheim, Inst Anasthesiol & Operat Intens Med, D-68167 Mannheim, Germany
来源
ANASTHESIOLOGIE INTENSIVMEDIZIN NOTFALLMEDIZIN SCHMERZTHERAPIE | 1998年 / 33卷 / 08期
关键词
NMDA receptor antagonists; central sensitization; ketamine; opioid tolerance; neuropathic pain;
D O I
10.1055/s-2007-994794
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
The treatment of patients suffering from chronic neuropathic pain remains a clinical challenge, particularly in cases where opioid therapy fails to provide sufficient pain relief. Spinal sensitization might be one cause for induction and maintenance of such states of pain, frequently accompanied by symptoms like allodynia, hyperalgesia and temporal summation of second pain. Experimental data concerning the role of NMDA-mediated processes in central sensitization and the effects of NMDA receptor antagonists in different models of neuropathic pain are reviewed. In clinical trials ketamine and other NMDA receptor blokking agents caused a significant reduction of hypersensitive states of pain, but nearly all authors described psychomimetic and other side effects. Aminoadamantanes like memantine and amantadine also have NMDA blocking properties and are widely used in the treatment of Parkinson's disease. Further clinical studies may reveal whether these substances will play a role as adjuncts in future pain treatment. Improving the efficacy of opioids by blocking NMDA receptor-mediated activity constitutes another clinically relevant concept for pain management. Numerous experiments have shown synergistic effects of NMDA antagonists and opioids in analgesia, while the development of opioid tolerance was prevented.
引用
收藏
页码:475 / 483
页数:11
相关论文
共 110 条
[21]   ANTAGONISM AT THE GLYCINE SITE ON THE NMDA RECEPTOR REDUCES SPINAL NOCICEPTION IN THE RAT [J].
DICKENSON, AH ;
AYDAR, E .
NEUROSCIENCE LETTERS, 1991, 121 (1-2) :263-266
[22]   EVIDENCE FOR A ROLE OF THE NMDA RECEPTOR IN THE FREQUENCY-DEPENDENT POTENTIATION OF DEEP RAT DORSAL HORN NOCICEPTIVE NEURONS FOLLOWING C-FIBER STIMULATION [J].
DICKENSON, AH ;
SULLIVAN, AF .
NEUROPHARMACOLOGY, 1987, 26 (08) :1235-1238
[23]   ELECTROPHYSIOLOGICAL STUDIES ON THE EFFECTS OF INTRATHECAL MORPHINE ON NOCICEPTIVE NEURONS IN THE RAT DORSAL HORN [J].
DICKENSON, AH ;
SULLIVAN, AF .
PAIN, 1986, 24 (02) :211-222
[24]   HYPERALGESIA AND EXPANDED RECEPTIVE-FIELDS [J].
DUBNER, R .
PAIN, 1992, 48 (01) :3-4
[25]   CONTINUOUS SUBCUTANEOUS ADMINISTRATION OF THE N-METHYL-D-ASPARTIC ACID (NMDA) RECEPTOR ANTAGONIST KETAMINE IN THE TREATMENT OF POSTHERPETIC NEURALGIA [J].
EIDE, PK ;
STUBHAUG, A ;
OYE, I ;
BREIVIK, H .
PAIN, 1995, 61 (02) :221-228
[26]   RELIEF OF POSTHERPETIC NEURALGIA WITH THE N-METHYL-D-ASPARTIC ACID RECEPTOR ANTAGONIST KETAMINE - A DOUBLE-BLIND, CROSS-OVER COMPARISON WITH MORPHINE AND PLACEBO [J].
EIDE, PK ;
JORUM, E ;
STUBHAUG, A ;
BREMNES, J ;
BREIVIK, H .
PAIN, 1994, 58 (03) :347-354
[27]   THE EFFECTS OF THE CLINICALLY TESTED NMDA RECEPTOR ANTAGONIST MEMANTINE ON CARRAGEENAN-INDUCED THERMAL HYPERALGESIA IN RATS [J].
EISENBERG, E ;
LACROSS, S ;
STRASSMAN, AM .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1994, 255 (1-3) :123-129
[28]   THE NMDA ANTAGONIST MEMANTINE BLOCKS PAIN BEHAVIOR IN A RAT MODEL OF FORMALIN-INDUCED FACIAL-PAIN [J].
EISENBERG, E ;
VOS, BP ;
STRASSMAN, AM .
PAIN, 1993, 54 (03) :301-307
[29]   DEXTROMETHORPHAN ATTENUATES AND REVERSES ANALGESIC TOLERANCE TO MORPHINE [J].
ELIOTT, K ;
HYNANSKY, A ;
INTURRISI, CE .
PAIN, 1994, 59 (03) :361-368
[30]   N-METHYL-D-ASPARTATE (NMDA) RECEPTORS, MU-OPIOID AND KAPPA-OPIOID TOLERANCE, AND PERSPECTIVES ON NEW ANALGESIC DRUG DEVELOPMENT [J].
ELLIOTT, K ;
KEST, B ;
MAN, A ;
KAO, B ;
INTURRISI, CE .
NEUROPSYCHOPHARMACOLOGY, 1995, 13 (04) :347-356