Comparison of somatostatin and morphine action on the responses of wide dynamic range cells in the dorsal horn to peripheral noxious mechanical and heat stimulation in cats.
- Author:
Sung Jun JUNG
1
;
Young In CHOI
;
Jun KIM
Author Information
1. Department of Physiology, and Biophysics, Seoul National University College of Medicine, Seoul 110-799, Korea.
- Publication Type:Original Article
- Keywords:
WDR cells;
Somatostatin;
Morphine;
Mechanical and thermal noxious stimuli
- MeSH:
Animals;
Cats*;
Electrodes;
Horns*;
Hot Temperature*;
Morphine*;
Naloxone;
Neurons;
Nociceptors;
Somatostatin*;
Spinal Cord
- From:The Korean Journal of Physiology and Pharmacology
1998;2(2):155-163
- CountryRepublic of Korea
- Language:English
-
Abstract:
The purpose of present study was to compare the effects of somatostatin (SOM) and morphine (Mor) on the responses of wide dynamic range (WDR) cells to peripheral noxious stimulation. Single neuronal activity was recorded with a carbon-filament electrode at the lumbosacral enlargement of cat spinal cord. After identifying WDR cells, their responses to peripheral noxious mechanical or thermal stimuli were characterized and the effects of SOM and Mor, applied either iontophoretically or intrathecally, were studied. In most cells SOM and Mor suppressed noxious stimulus-evoked WDR neuronal activity, though a few WDR neurons showed no change or were excited by SOM and Mor. Systemically applied naloxone, a non-specific opioid antagonist, always reversed the Mor induced suppression of neuronal activity evoked by noxious mechanical stimuli, but did not always reverse the suppression of neuronal activity elicited by SOM. The suppressive effect of Mor on thermal stimulus-evoked neuronal activity was partially reversed by naloxone, while that of SOM were not reversed at all. The above results suggest that both Mor and SOM exert an inhibitory effect on thermal and mechanical stimulus-evoked WDR neuronal activity in cat spinal dorsal horn, but the mechanisms are dependent upon the functional populations of dorsal horn nociceptive neurons.
