Learning to cope with biting flies: rapid NMDA-mediated acquisition of conditioned analgesia

M Kavaliers1, D D Colwell, E Choleris

  • 1Department of Psychology, University of Western Ontario, London, Canada. kavalier@julian.uwo.ca

Insights

Biting flies trigger pain relief (analgesia) in mice through opioid pathways. Prior exposure to biting flies creates a conditioned pain relief response, mediated by N-methyl-D-aspartate (NMDA) receptors.

Area of Science:

  • Neuroscience
  • Animal Behavior
  • Immunology

Background:

  • Insect bites can elicit complex physiological responses in mammals.
  • Pain perception and modulation involve intricate neural pathways, including opioid and NMDA receptor systems.

Purpose of the Study:

  • To investigate the mechanisms of analgesia induced by biting flies in deer mice.
  • To explore the role of opioid and N-methyl-D-aspartate (NMDA) receptors in both immediate and conditioned analgesic responses to insect bites.

Main Methods:

  • Exposure of male deer mice to intact stable flies, altered stable flies (mouthparts removed), and nonbiting house flies.
  • Administration of naloxone (opioid antagonist) and NPC 12626 (NMDA antagonist) to assess receptor involvement.
  • Testing for immediate analgesia and conditioned analgesia upon subsequent exposure to altered flies.

Main Results:

  • A 30-minute exposure to intact stable flies induced opioid-mediated analgesia.
  • Previous exposure to intact flies resulted in conditioned analgesia to altered stable flies, indicating a learned response.
  • NMDA receptor blockade prevented the acquisition of conditioned analgesia, while opioid blockade did not affect it.

Conclusions:

  • The study demonstrates an opioid-mediated immediate analgesic response to intact biting flies.
  • A learned, N-methyl-D-aspartate (NMDA)-dependent conditioned analgesic response can be acquired following exposure to a natural aversive stimulus (biting flies).
  • These findings highlight the complex interplay between sensory input, learning, and pain modulation in response to insect-induced stress.