Central antinociceptive effects of meloxicam on rat spinal cord in vitro

被引:26
作者
Lopez-Garcia, JA [1 ]
Laird, JMA [1 ]
机构
[1] Univ Alcala de Henares, Sch Med, Dept Physiol, E-28871 Madrid, Spain
关键词
analgesia; cyclooxygenase; indomethacin; inflammation; meloxicam; NSAIDs; pain; spinal transmission;
D O I
10.1097/00001756-199803090-00016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
NON-STEROIDAL anti-inflammatory drugs inhibit constitutive (COX-1) and induced cyclooxygenase (COX-2), blocking prostaglandin production. We have compared the effects on nociceptive reflexes of meloxicam, which is COX-2 selective, with indomethacin, which is non-selective, using an in vitro spinal cord preparation. Cords were taken from naive rats, and from rats with carrageenan-induced hyperalgesia of one hindpaw. Reflex thresholds were lower in carrageenan preparations. Superfusion with meloxicam (10-100 mu M) dose-dependently inhibited baseline reflexes and wind-up in normal and carrageenan preparations, whereas indomethacin (100-300 mu M) had no effect. Thus meloxicam inhibits spinal reflexes, whereas indomethacin does not, despite its high affinity for both COX isoforms. We conclude that meloxicam has spinal antinociceptive actions which cannot be explained by the current concept of COX inhibition.
引用
收藏
页码:647 / 651
页数:5
相关论文
共 23 条
[1]   BEHAVIORAL AND ELECTROPHYSIOLOGICAL EVIDENCE FOR AN ANALGESIC EFFECT OF A NON-STEROIDAL ANTI-INFLAMMATORY AGENT, SODIUM DICLOFENAC [J].
ATTAL, N ;
KAYSER, V ;
ESCHALIER, A ;
BENOIST, JM ;
GUILBAUD, G .
PAIN, 1988, 35 (03) :341-348
[2]   Up-regulation of cyclooxygenase-2 mRNA in the rat spinal cord following peripheral inflammation [J].
Beiche, F ;
Scheuerer, S ;
Brune, K ;
Geisslinger, G ;
GoppeltStruebe, M .
FEBS LETTERS, 1996, 390 (02) :165-169
[3]   DEPRESSION BY MORPHINE AND THE NON-OPIOID ANALGESIC AGENTS, METAMIZOL (DIPYRONE), LYSINE ACETYLSALICYLATE, AND PARACETAMOL, OF ACTIVITY IN RAT THALAMUS NEURONS EVOKED BY ELECTRICAL-STIMULATION OF NOCICEPTIVE AFFERENTS [J].
CARLSSON, KH ;
MONZEL, W ;
JURNA, I .
PAIN, 1988, 32 (03) :313-326
[4]   THE SPINAL AND PERIPHERAL ROLES OF BRADYKININ AND PROSTAGLANDINS IN NOCICEPTIVE PROCESSING IN THE RAT [J].
CHAPMAN, V ;
DICKENSON, AH .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 219 (03) :427-433
[6]   Meloxican: Influence on arachidonic acid metabolism .2. In vivo findings [J].
Engelhardt, G ;
Bogel, R ;
Schnitzler, C ;
Utzmann, R .
BIOCHEMICAL PHARMACOLOGY, 1996, 51 (01) :29-38
[7]   ANTIINFLAMMATORY, ANALGESIC, ANTIPYRETIC AND RELATED PROPERTIES OF MELOXICAM, A NEW NONSTEROIDAL ANTIINFLAMMATORY AGENT WITH FAVORABLE GASTROINTESTINAL TOLERANCE [J].
ENGELHARDT, G ;
HOMMA, D ;
SCHLEGEL, K ;
UTZMANN, R ;
SCHNITZLER, C .
INFLAMMATION RESEARCH, 1995, 44 (10) :423-433
[8]   A classification of NSAIDs according to the relative inhibition of cyclooxygenase isoenzymes [J].
Frolich, JC .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1997, 18 (01) :30-34
[9]   ASPIRIN CLEARLY DEPRESSES RESPONSES OF VENTROBASAL THALAMUS NEURONS TO JOINT STIMULI IN ARTHRITIC RATS [J].
GUILBAUD, G ;
BENOIST, JM ;
GAUTRON, M ;
KAYSER, V .
PAIN, 1982, 13 (02) :153-163
[10]   Reversal by naloxone of the spinal antinociceptive actions of a systemically-administered NSAID [J].
Herrero, JF ;
Headley, PM .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 118 (04) :968-972