Comparison of mechanical allodynia and the affective component of inflammatory pain in rats

被引:46
作者
Boyce-Rustay, Janel M. [1 ]
Zhong, Chengmin [1 ]
Kohnken, Rebecca [1 ]
Baker, Scott J. [1 ]
Simler, Gricelda H. [1 ]
Wensink, Erica J. [1 ]
Decker, Michael W. [1 ]
Honore, Prisca [1 ]
机构
[1] Abbott Labs, Neurosci Res, Global Pharmaceut Res & Dev, Abbott Pk, IL 60064 USA
关键词
Inflammatory; Pain; Mechanical allodynia; Affective; Place escape; VENTRAL BED NUCLEUS; ANTERIOR CINGULATE; ESCAPE/AVOIDANCE BEHAVIOR; REUPTAKE INHIBITORS; STRIA TERMINALIS; DOUBLE-BLIND; MODELS; ACTIVATION; DULOXETINE; PLACEBO;
D O I
10.1016/j.neuropharm.2009.08.008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Most animal models of pain cannot separate the sensory and affective components of pain. One model that has been used to assess affective pain is the place escape avoidance paradigm (PEAP). The aim of the current study is two-fold. First, validate PEAP with Complete Freund's Adjuvant (CFA)-induced inflammation for the assessment of the affective component of pain using the reference analgesics celecoxib, diclofenac and duloxetine; fluoxetine and scopolamine were tested as negative controls. Secondly, determine if there is a difference in efficacy in PEAP in comparison to the effects of the same compounds on von Frey-evoked mechanical allodynia in CFA animals. All compounds were tested in mechanical allodynia, place escape/avoidance, and for potentially confounding side effects in locomotor activity. Results show that celecoxib, diclofenac, and duloxetine significantly increased the time spent on the side associated with stimulation of the injured paw, whereas fluoxetine and scopolamine had no effect. Higher doses of celecoxib, diclofenac, duloxetine, and fluoxetine were required to attenuate von Frey-evoked mechanical allodynia. In the side effect assays, only fluoxetine decreased locomotor activity at doses used in PEAR These results show that in inflammatory pain induced by CFA injection, PEAP is more sensitive to the effects of pain relieving compounds than mechanical allodynia. Fluoxetine showed efficacy in the mechanical allodynia test, but not PEAR, whereas duloxetine showed efficacy in mechanical allodynia and PEAR These studies show that methods other than reflex based measures of pain such as affective pain models could be more predictive of efficacy/potency in the clinic. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:537 / 543
页数:7
相关论文
共 38 条
[1]   A randomized, double-blind, placebo-controlled trial of duloxetine in the treatment of women with fibromyalgia with or without major depressive disorder [J].
Arnold, LM ;
Rosen, A ;
Pritchett, YL ;
D'Souza, DN ;
Goldstein, DJ ;
Iyengar, S ;
Wernicke, JF .
PAIN, 2005, 119 (1-3) :5-15
[2]  
AUVRAY M, 2008, NEUROSCI BIOBEHAV RE
[3]   Pharmacological modulation of movement-evoked pain in a rat model of osteoarthritis [J].
Chandran, Prasant ;
Pai, Madhavi ;
Blomme, Eric A. ;
Hsieh, Gin C. ;
Decker, Michael W. ;
Honore, Prisca .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2009, 613 (1-3) :39-45
[4]   QUANTITATIVE ASSESSMENT OF TACTILE ALLODYNIA IN THE RAT PAW [J].
CHAPLAN, SR ;
BACH, FW ;
POGREL, JW ;
CHUNG, JM ;
YAKSH, TL .
JOURNAL OF NEUROSCIENCE METHODS, 1994, 53 (01) :55-63
[5]   High-efficacy 5-hydroxytryptamine 1A receptor activation counteracts opioid hyperallodynia and affective conditioning [J].
Colpaert, FC ;
Deseure, K ;
Stinus, L ;
Adriaensen, H .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2006, 316 (02) :892-899
[6]   Activation of the β-adrenoceptor-protein kinase A signaling pathway within the ventral bed nucleus of the stria terminalis mediates the negative affective component of pain in rats [J].
Deyama, Satoshi ;
Katayama, Takahiro ;
Ohno, Atsushi ;
Nakagawa, Takayuki ;
Kaneko, Shuji ;
Yamaguchi, Taku ;
Yoshioka, Mitsuhiro ;
Minami, Masabumi .
JOURNAL OF NEUROSCIENCE, 2008, 28 (31) :7728-7736
[7]   Role of enhanced noradrenergic transmission within the ventral bed nucleus of the stria terminalis in visceral pain-induced aversion in rats [J].
Deyama, Satoshi ;
Katayama, Takahiro ;
Kondoh, Naoto ;
Nakagawa, Takayuki ;
Kaneko, Shuji ;
Yamaguchi, Taku ;
Yoshioka, Mitsuhiro ;
Minami, Masabumi .
BEHAVIOURAL BRAIN RESEARCH, 2009, 197 (02) :279-283
[8]   Catastrophizing and pain in arthritis, fibromyalgia, and other rheumatic diseases [J].
Edwards, RR ;
Bingham, CO ;
Bathon, J ;
Haythornthwaite, JA .
ARTHRITIS & RHEUMATISM-ARTHRITIS CARE & RESEARCH, 2006, 55 (02) :325-332
[9]   Anticipatory brainstem activity predicts neural processing of pain in humans [J].
Fairhurst, Merle ;
Wiech, Katja ;
Dunckley, Paul ;
Tracey, Irene .
PAIN, 2007, 128 (1-2) :101-110
[10]   Duloxetine vs. placebo in patients with painful diabetic neuropathy [J].
Goldstein, DJ ;
Lu, YL ;
Detke, MJ ;
Lee, TC ;
Iyengar, S .
PAIN, 2005, 116 (1-2) :109-118