Ahmad-Molaei L, Ordikhani-Seyedlar M, Ziaei M, Khademi R, Rouzmeh P, Haghparast A. Analgesic effect of morphine microinjected into the nucleus raphe magnus after electrolytic lesion of nucleus cuneiformis in tail-flick and formalin tests in rat . Physiol Pharmacol 2011; 15 (3) :371-384
URL:
http://ppj.phypha.ir/article-1-735-en.html
Abstract: (12510 Views)
Introduction: The antinociceptive effect of morphine is, in part, mediated through the activation of a descending
pathway. One of the major components of this pathway is the nucleus raphe magnus (NRM). Our previous study
demonstrated the involvement of NRM in the analgesic effect of morphine microinjected into the nucleus cuneiformis
(NCF) in a descending manner. The aim of the current study was to investigate another aspect of the interaction
between these two nuclei in both acute and chronic inflammatory pain models.
Methods: In order to calculate 50% effective dose (ED50) of morphine, animals received bilateral morphine
injections (1, 2.5, 5 and 10 μg/0.5 μl saline) into the NRM. The obtained ED50 of morphine was applied into the NRM
with/without bilateral electrolytic lesion (500 μA, 30 sec) of the NCF. Tail-flick and formalin tests were applied as
behavioral analgesic tests in this study.
Results: Results interestingly showed that the intra-NRM morphine injection (ED50 1 μg/0.5 μl saline) resulted in
an increase in tail flick latencies (morphine-induced antinociception) at 30-min intervals, while bilateral electrolytic
lesions in the NCF could notably decreased the morphine-induced antinociception during 30-90 min after the injection
of morphine. Data also showed that bilateral morphine microinjected into the NRM, dose-dependently increases the
antinociceptive responses during both early and late phases of formalin test. The antinociceptive effect of morphine
microinjected into the NRM was significantly attenuated at the late phase but not early phase following the bilateral
destruction of NCF in formalin test.
Conclusion: It could be concluded that there is a reciprocal interaction between NRM and NCF during morphine -
induced antinociception in both acute and chronic inflammatory pain models in rat.