Korean J Anesthesiol.  1998 Apr;34(4):708-715. 10.4097/kjae.1998.34.4.708.

The Effect of Intrathecal NMDA and non-NMDA Receptor Antagonist on the Hyperalgesia Observed after Thermal Injury in the Rat

Affiliations
  • 1Department of Anesthesiology, Hanyang University College of Medicine, Seoul, Korea.

Abstract

BACKGROUND: Previous reports have described NMDA antagonist reduced the nerve injury induced or inflammatory thermal hyperalgesia. This study evaluated the effects of spinally administered excitatory amino acid antagonists on the thermal hyperalgesia state induced by mild burn.
METHODS
The measured response was the latency to paw withdrawal of each hindpaw after application of a focused heat lamp on the plantar surface of the paw through a glass plate upon which the animal stood. In this work, MK801, non-competitive NMDA receptor antagonist, AP5, competitive NMDA receptor antagonist, CNQX, non-NMDA receptor antagonist were injected through chronically implanted lumbar intrathecal catheters in rats with mild burn injury on the right hindpaw.
RESULTS
In the normal left hindpaw, MK801, AP5 and CNQX had little effect upon paw withdrawal latency (PWL) at intrathecal doses which do not produce readily detectable motor weakness. In the right hyperalgesic hindpaw, AP5 significantly reduced PWL at a dose-dependent fashion, MK801 reduced PWL to some extent, and CNQX did not reduced PWL.
CONCLUSIONS
These results suggested that spinal NMDA receptors play an important role in the hyperalgesia induced by mild burn injury.

Keyword

Analgesics, intrathecal: MK801; AP5; CNQX; Pain: hyperalgesia; Receptors, glutamate: NMDA

MeSH Terms

6-Cyano-7-nitroquinoxaline-2,3-dione
Animals
Burns
Catheters
Dizocilpine Maleate
Excitatory Amino Acid Antagonists
Glass
Hot Temperature
Hyperalgesia*
N-Methylaspartate*
Rats*
Receptors, N-Methyl-D-Aspartate
6-Cyano-7-nitroquinoxaline-2,3-dione
Dizocilpine Maleate
Excitatory Amino Acid Antagonists
N-Methylaspartate
Receptors, N-Methyl-D-Aspartate
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