Background: The research on conductive analgesia induced by perineural opio
ids generated a large body of conflicting data. In this study we reassessed
the antinociceptive response to perineural administration of morphine, fen
tanyl or meperidine in a rat model.
Methods: Analgesia was assessed using the hind paw withdrawal latency (HPWL
) response to radiant heat. The opioid dose producing 20% of maximal possib
le effect (20%MPE) for systemic analgesia was calculated for each drug. The
n sciatic blockade was performed with the dose corresponding to 20%NME. The
injected hind paw was used to measure direct perineural effect and the con
tralateral hind paw was used as an indicator of systemic effect.
Results: The response latency produced by morphine or fentanyl was not sign
ificantly different for ipsilateral (perineural effect) or contralateral (s
ystemic effect) paw (27 +/- 11 vs 28 +/- 16 and 31 +/- 16 vs 23 +/- 16 s, r
espectively). However, the meperidine group showed significantly higher %MP
E for the ipsilateral paw (79 +/- 32 s) than for the contralateral paw (27
+/- 99 s).
Conclusions: The results indicate that perineural fentanyl or morphine do n
ot produce analgesia. Perineural block produced by meperidine was attribute
d to local anesthetic-like effect, rather than to drug interaction with opi
oid receptor.