Long-lasting hyperalgesia induced by
fentanyl in rats: preventive effect of ketamine
by
Celerier E, Rivat C, Jun Y, Laulin JP, Larcher A, Reynier P, Simonnet G
Institut National de la Sante et de la Recherche Medicale (INSERM) U 259,
Bordeaux, France.
Anesthesiology 2000 Feb; 92(2):465-72

ABSTRACT

BACKGROUND: It has been reported that mu-opioid receptor activation leads to a sustained increase in glutamate synaptic effectiveness at the N-methyl-D-aspartate (NMDA) receptor level, a system associated with central hypersensitivity to pain. One hypothesis is that postoperative pain may result partly from the activation of NMDA pain facilitatory processes induced by opiate treatment per se. The authors tested here the effectiveness of the opiate analgesic fentanyl for eliciting a delayed enhancement in pain sensitivity. METHODS: The consequences of four bolus injections (every 15 min) of fentanyl (20-100 microg/kg per injection, subcutaneously) on immediate (for several hours) and long-term (for several days) sensitivity to nociceptive stimuli in the rat (paw-pressure vocalization test) were evaluated. The effects of the combination of the NMDA-receptor antagonist ketamine (10 mg/kg, subcutaneously) with fentanyl also were assessed. RESULTS: Fentanyl administration exhibited a biphasic time-dependent effect: first, an early response (for 2-5 h) associated with a marked increase in nociceptive threshold (analgesia), and second, a later response associated with sustained lowering of the nociceptive threshold (5 days for the longest effect) below the basal value (30% of decrease for the maximal effect) indicative of hyperalgesia. The higher the fentanyl dose used, the more pronounced was the fentanyl-induced hyperalgesia. Ketamine pretreatment, which had no analgesic effect on its own, enhanced the earlier response (analgesia) and prevented the development of long-lasting hyperalgesia. CONCLUSIONS: Fentanyl activates NMDA pain facilitatory processes, which oppose analgesia and lead to long-lasting enhancement in pain sensitivity.

Pain
Heroin
Sources
Overdose
Tramadol
Sufentanil
Oxycodone
Mu receptors
Endomorphins
Opiated worms
Zero tolerance?
Fentanyl for cats
Fentanyl analogs
Fentanyl: synthesis
Transdermal fentanyl
Push-button fentanyl
Gene therapy for pain
The poppy-seed defence
Fentanyl: subjective effects
Opioids, mood and cognition
Fentanyl plus ketamine for pain-relief

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