Morphine-induced Modulation of Nociceptive Spinal Dorsal Horn Neuronal Activities after Formalin-induced Inflammatory Pain.
- Author:
Joo Min PARK
1
;
Kang Wu LI
;
Sung Jun JUNG
;
Jun KIM
;
Sang Jeong KIM
Author Information
1. Department of Physiology & Biophysics, Seoul National University College of Medicine, Seoul 110-799, Korea. sangjkim@snu.ac.kr
- Publication Type:Original Article
- Keywords:
Nociceptive dorsal horn neurons;
Morphine;
spinal cord;
GABAA basal tone;
Subacute inflammatory state
- MeSH:
Animals;
Bicuculline;
Cats;
Formaldehyde;
GABA Agonists;
Inflammation;
Injections, Intradermal;
Morphine;
Muscimol;
Neurons;
Nociceptors;
Posterior Horn Cells*;
Spinal Cord
- From:The Korean Journal of Physiology and Pharmacology
2005;9(2):77-86
- CountryRepublic of Korea
- Language:English
-
Abstract:
In this study, we examined the morphine-induced modulation of the nociceptive spinal dorsal horn neuronal activities before and after formalin-induced inflammatory pain. Intradermal injection of formalin induced time-dependent changes in the spontaneous activity of nociceptive dorsal horn neurons. In naive cats before the injection of formalin, iontophoretically applied morphine attenuated the naturally and electrically evoked neuronal responses of dorsal horn neurons. However, neuronal responses after the formalin-induced inflammation were significantly increased by morphine. Bicuculline, GABAA antagonist, increased the naturally and electrically evoked neuronal responses of dorsal horn neurons. This increase in neuronal responses due to bicuculline after the formalin-induced inflammation was larger than that in the naive state, suggesting that basal GABAA tone increased after the formalin injection. Muscimol, GABAA agonist, reduced the neuronal responses before the treatment with formalin, but not after formalin treatment, again indicating an increase in the GABAergic basal tone after the formalin injection which saturated the neuronal responses to GABA agonist. Morphine-induced increase in the spinal nociceptive responses after formalin treatment was inhibited by co-application of muscimol. These data suggest that formalin-induced inflammation increases GABAA basal tone and the inhibition of this augmented GABAA basal tone by morphine results in a paradoxical morphine- induced increase in the spinal nociceptive neuronal responses after the formalin-induced inflammation.
