Effects of peripheral κ opioid receptor activation on inflammatory mechanical hyperalgesia in male and female rats

被引:45
作者
Auh, Q-Schick [2 ]
Ro, Jin Y. [1 ,2 ]
机构
[1] Univ Maryland, Sch Dent, Dept Neural & Pain Sci, Program Neurosci, Baltimore, MD 21201 USA
[2] Kyung Hee Univ, Sch Dent, Dept Oral Med, Seoul, South Korea
关键词
Sex; Peripheral; Kappa opioid receptor; Inflammation; Mechanical hyperalgesia; EXPERIMENTAL HUMAN PAIN; DORSAL-ROOT GANGLIA; SEX-DIFFERENCES; ANALGESIA; AGONIST; ANTINOCICEPTION; DELTA; ASIMADOLINE; INVOLVEMENT; OXYCODONE;
D O I
10.1016/j.neulet.2012.07.018
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Activation of peripheral kappa opioid receptors (KOR) effectively relieves pain and hyperalgesia in preclinical and clinical models of pain. Although centrally located KOR activation results in sexually dimorphic effects, it is unclear whether peripheral KOR also produces sex dependent effects in persistent inflammatory pain conditions. In this study, we investigated whether local administration of a specific KOR agonist, U50, 488 relieve mechanical hyperalgesia induced by the injection of complete Freund's adjuvant (CFA) in the rat hindpaw, and whether there are sex differences. The effects of U50, 488 were assessed three days after the induction of CFA-induced inflammation, a time point at which mechanical hyperalgesia was most prominent. There were no sex differences in baseline and CFA-induced changes in mechanical thresholds between male and female rats. Local treatment of U50, 488 produced moderate, but significant, anti-hyperalgesia in both male and female rats. However, U50, 488 was significantly more effective in male rats at the highest dose of U50, 488. We confirmed that the highest dose of U50, 488 used in this study did not produce systemic effects, and that the drug effect is receptor specific. On the basis of these results, we suggest that local KOR agonists are effective in mitigating mechanical hyperalgesia under a persistent inflammatory pain condition and that sex differences in anti-hyperalgesic effects become more evident at high doses. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:111 / 115
页数:5
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