ANTINOCICEPTIVE EFFECTS OF NEUROTROPIN IN A RAT MODEL OF PAINFUL PERIPHERAL MONONEUROPATHY

Citation
K. Toda et al., ANTINOCICEPTIVE EFFECTS OF NEUROTROPIN IN A RAT MODEL OF PAINFUL PERIPHERAL MONONEUROPATHY, Life sciences, 62(10), 1998, pp. 913-921
Citations number
28
Categorie Soggetti
Biology,"Medicine, Research & Experimental","Pharmacology & Pharmacy
Journal title
ISSN journal
00243205
Volume
62
Issue
10
Year of publication
1998
Pages
913 - 921
Database
ISI
SICI code
0024-3205(1998)62:10<913:AEONIA>2.0.ZU;2-K
Abstract
A non-protein extract isolated from the inflamed skin of rabbits inocu lated with vaccinia virus (Neurotropin, NTP), has been clinically used in Japan for the treatment of chronic painful conditions such as low back pain, osteoarthritis, postherpetic neuralgia, subacute myelo-opti coneuropathy, and so on, Recent studies have shown its efficacy on pat ients with complex regional pain syndrome (CRPS). The chronic constric tion injury (CCl) model described by Bennett and Xie has been thought to show similar painful conditions to those seen in CRPS patients. Thu s, the antinociceptive effects of NTP were tested in CCl model. In rat s with mechanical hyperalgesia 2 weeks after nerve injury, i.p, inject ion of NTP (100 Neurotropin Unit, NU/kg) produced an analgesic effect that lasted for at least 50 min. An analgesic effect lasting up to 30 min. was observed in rats with heat hyperalgesia 2 weeks after nerve i njury. Seven daily i.p, injections (50 NU/kg) of NTP commencing 1 week after surgery produced an early recovery from heat hyperalgesia. Prio r studies suggest that NTP produces analgesia by activation of a desce nding pain inhibitory system. Thus, our findings suggest the possibili ty that the dysfunction of the descending pain inhibitory system could be related to the hyperalgesia in the nerve injury model, and perhaps also in people who suffer from painful peripheral neuropathies.