TY - JOUR
T1 - Activation of peripheral κ opioid receptors inhibits capsaicin-induced thermal nociception in rhesus monkeys
AU - Ko, Mei Chuan
AU - Butelman, Eduardo R.
AU - Woods, James H.
N1 - Copyright:
Copyright 2007 Elsevier B.V., All rights reserved.
PY - 1999/4
Y1 - 1999/4
N2 - 8-Methyl-N-vanillyl-6-nonenamide (capsaicin) was locally applied in the tail of rhesus monkeys to evoke a nociceptive response, thermal allodynia, which was manifested as reduced tail-withdrawal latencies in normally innocuous 46°C water. Coadministration of three κ opioid ligands, U50,488 (3.2-100 μg), bremazocine (0.1-3.2 μg), and dynorphin A(1-13) (3.2-100 μg), with capsaicin in the tail dose-dependently inhibited capsaicin- induced allodynia. This local antinociception was antagonized by a small dose of an opioid antagonist, quadazocine; (0.32 mg), applied in the tail; however, this dose of quadazocine injected s.c. in the back did not antagonize local U50,488. Comparing the relative potency of either agonist or antagonist after local and systemic administration confirmed that the site of action of locally applied κ opioid agonists is in the tail. In addition, local nor-binaltorphimine (0.32 mg) and oxilorphan (0.1-10 μg) antagonist studies raised the possibility of κ opioid receptor subtypes in the periphery, which indicated that U50,488 produced local antinociception by acting on κ1 receptors, but bremazocine acted probably on non-κ1 receptors. These results provide functional evidence that activation of peripheral κ opioid receptors can diminish capsaicin-induced allodynia in primates. This experimental pain model is a useful tool for evaluating peripherally antinociceptive actions of κ agonists without central side effects and suggests new approaches for opioid pain management.
AB - 8-Methyl-N-vanillyl-6-nonenamide (capsaicin) was locally applied in the tail of rhesus monkeys to evoke a nociceptive response, thermal allodynia, which was manifested as reduced tail-withdrawal latencies in normally innocuous 46°C water. Coadministration of three κ opioid ligands, U50,488 (3.2-100 μg), bremazocine (0.1-3.2 μg), and dynorphin A(1-13) (3.2-100 μg), with capsaicin in the tail dose-dependently inhibited capsaicin- induced allodynia. This local antinociception was antagonized by a small dose of an opioid antagonist, quadazocine; (0.32 mg), applied in the tail; however, this dose of quadazocine injected s.c. in the back did not antagonize local U50,488. Comparing the relative potency of either agonist or antagonist after local and systemic administration confirmed that the site of action of locally applied κ opioid agonists is in the tail. In addition, local nor-binaltorphimine (0.32 mg) and oxilorphan (0.1-10 μg) antagonist studies raised the possibility of κ opioid receptor subtypes in the periphery, which indicated that U50,488 produced local antinociception by acting on κ1 receptors, but bremazocine acted probably on non-κ1 receptors. These results provide functional evidence that activation of peripheral κ opioid receptors can diminish capsaicin-induced allodynia in primates. This experimental pain model is a useful tool for evaluating peripherally antinociceptive actions of κ agonists without central side effects and suggests new approaches for opioid pain management.
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M3 - Article
C2 - 10087027
AN - SCOPUS:0032946440
VL - 289
SP - 378
EP - 385
JO - Journal of Pharmacology and Experimental Therapeutics
JF - Journal of Pharmacology and Experimental Therapeutics
SN - 0022-3565
IS - 1
ER -