OBJECTIVE: We compared the anti-allodynic effect of Neurotropin
® (an extract from the inflamed skin of rabbits inoculated with vaccinia virus, NTP) with those of anti-inflammatory drugs and anti-depressants in rats with L5 spinal nerve ligation (L5-SNL). Additionally, we investigated the combinational effect of NTP and milnacipran in L5-SNL rats.
METHODS: The left fifth lumbar nerve of rats was tightly ligated with silk sutures under pentobarbital anesthesia. Mechanical allodynia was confirmed by measuring the hindpaw withdrawal threshold in response to the application of von Frey filaments. Behavioral tests were performed at 28 days after nerve ligation. NTP, non-steroidal anti-inflammatory drug (NSAID, loxoprofen), COX-2 inhibitor (celecoxib), selective serotonin reuptake inhibitor (SSRI, paroxetine) and serotonin-noradrenaline reuptake inhibitor (SNRI, milnacipran) were administered orally. Dose-response curves were established and the 30% effective dose values were determined for NTP and milnacipran. An isobolographic analysis was performed to clarify the interaction of NTP and milnacipran.
RESULTS: NTP (400 NU/kg) showed an anti-allodynic action in L5-SNL rats. Loxoprofen (100 mg/kg) and celecoxib (100 mg/kg) had no effect in L5-SNL rats. On the other hand, milnacipran(100 mg/kg) elicited an anti-allodynic action, but paroxetine (10 mg/kg) did not inhibit allodynia in L5-SNL rats. The combination of NTP and milnacipran showed an additive effect in L5-SNL rats.
CONCLUSION: These results suggest that NTP is more effective than NSAID and SSRI, and the combination of NTP with SNRI is useful for treatment of neuropathic pain.
View full abstract