The NSAID dexketoprofen trometamol is as potent as μ-opioids in the depression of wind-up and spinal cord nociceptive reflexes in normal rats

This publication has 22 references indexed in Scilit:

• Prostanoids synthesized by cyclo‐oxygenase isoforms in rat spinal cord and their contribution to the development of neuronal hyperexcitability
  British Journal of Pharmacology, 1997
• Preclinical and Clinical Development of Dexketoprofen
  Drugs, 1996
• Stimulus intensity and the comparative efficacy of ω- and κ-opioid agonists on nociceptive spinal reflexes in the rat
  Brain Research, 1994
• Non-steroidal anti-inflammatory drugs and spinal nociceptive processing
  PAIN®, 1994
• The Spinal Actions of Nonsteroidal Anti-Inflammatory Drugs and the Dissociation between their Anti-Inflammatory and Analgesic Effects
  Drugs, 1994
• Stereoselective cyclooxygenase inhibition in cellular models by the enantiomers of ketoprofen
  Chirality, 1993
• Pure Enantiomers of 2‐Arylpropionic Acids: Tools in Pain Research and Improved Drugs in Rheumatology
  The Journal of Clinical Pharmacology, 1992
• Evidence for involvement ofN-methylaspartate receptors in ‘wind-up’ of class 2 neurones in the dorsal horn of the rat
  Brain Research, 1987
• Evidence for a role of the NMDA receptor in the frequency dependent potentiation of deep rat dorsal horn nociceptive neurones following c fibre stimulation.
  Neuropharmacology, 1987
• Physiological properties of unmyelinated fiber projection to the spinal cord
  Experimental Neurology, 1966