Pertussis toxin reduces the day-night rhythm of nociception and mu and kappa opioid peptide-mediated antinociception in the snail, Cepaea nemoralis.
There is accumulating evidence that pertussis toxin-sensitive G proteins are associated with the transduction of opioid-mediated antinociception in mammals. The present study examined the effects of hemocel injections of pertussis toxin (0.10 microgram) on the day-night rhythm of nociception and mu and kappa opioid-mediated antinociception in a mollusc, the land snail, Cepaea nemoralis. Five days after treatment, pertussis toxin significantly reduced the naloxone-sensitive, opioid-mediated nocturnal peak in the day-night rhythm of nociception [as measured by the latency of response to a thermal (40 degrees C) stimulus] in Cepaea, without affecting the daytime response latency. Pertussis toxin also significantly decreased the antinociceptive effects of the mu agonist, DAMGO, and blocked those of the kappa opioid agonist, U-69,593. These results suggest that G protein substrates of pertussis toxin are associated with the transduction of opioid-mediated nociception and antinociception in the snail, Cepaea.[1]References
- Pertussis toxin reduces the day-night rhythm of nociception and mu and kappa opioid peptide-mediated antinociception in the snail, Cepaea nemoralis. Yu, N., Kavaliers, M. Peptides (1991) [Pubmed]
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