Effects of analgesics on the plantar incision-induced drop of the noxious heat threshold measured with an increasing-temperature water bath in the rat

被引:16
作者
Fueredi, Reka [1 ]
Boeskei, Kata [2 ,3 ]
Szolcsanyi, Janos [1 ]
Petho, Gabor [1 ]
机构
[1] Univ Pecs, Dept Pharmacol & Pharmacotherapy, H-7624 Pecs, Hungary
[2] Univ Pecs, Analgest Res Lab, H-7624 Pecs, Hungary
[3] Gedeon Richter Plc, H-7624 Pecs, Hungary
关键词
Thermonociception; Noxious heat threshold; Increasing-temperature water bath; Surgical incision; Analgesics; THERMAL HYPERALGESIA; TRPV1; RECEPTOR; IN-VITRO; MODEL; PAIN; MECHANISMS; ANTAGONIST; CAPSAICIN; MORPHINE; INJURY;
D O I
10.1016/j.ejphar.2008.12.035
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The behavioural noxious heat threshold i.e. the lowest temperature evoking nocifensive behaviour was previously shown to decrease in short-lasting, but not in sustained, inflammatory thermal hyperalgesias. The aim of this study was to examine whether the surgical incision-induced lasting heat hyperalgesia involves a drop of the heat threshold and to assess the effects of conventional opioid and non-opioid analgesics in this model. One of the hind paws of rats was immersed into a water bath whose temperature was near-linearly increased from 30 degrees C until the animal withdrew its paw from the water. The corresponding bath temperature was considered as the behavioural noxious heat threshold. Hyperalgesia to heat was induced by a standardized plantar surgical incision performed under pentobarbital anaesthesia which led to a 5-7 degrees C decrease of the noxious heat threshold for seven days. Morphine, diclofenac, and paracetamol administered intraperitoneally 18 h after incision dose-dependently inhibited the drop of heat threshold with minimum effective doses of 0.3, 1, and 100 mg/kg, respectively, as assessed 20, 30 and 40 min after treatment. Thermal hyperalgesia was also decreased by intraplantar treatment with morphine (10 mu g) or diclofenac (100 mu g). In conclusion, the incision-induced sustained thermal hyperalgesia in rats involves a drop of the heat threshold suggesting that mechanisms of postsurgical pain are distinct from those of pure inflammatory pain. The thermal anti hyperalgesic actions of systemically and/or locally applied morphine, diclofenac and paracetamol could be detected with high temporal resolution and sensitivity in this model. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:63 / 67
页数:5
相关论文
共 26 条
[1]   Effect of resiniferatoxin on the noxious heat threshold temperature in the rat:: a novel heat allodynia model sensitive to analgesics [J].
Almási, R ;
Pethö, G ;
Bölcskei, K ;
Szolcsányi, J .
BRITISH JOURNAL OF PHARMACOLOGY, 2003, 139 (01) :49-58
[2]   Actions of 3-methyl-N-oleoyldopamine, 4-methyl-N-oleoyldopamine and N-oleoylethanolamide on the rat TRPV1 receptor in vitro and in vivo [J].
Almasi, Robert ;
Szoeke, Eva ;
Boelcskei, Kata ;
Varga, Angelika ;
Riedl, Zsuzsanna ;
Sandor, Zoltan ;
Szolcsanyi, Janos ;
Petho, Gabor .
LIFE SCIENCES, 2008, 82 (11-12) :644-651
[3]   Spontaneous discharge and increased heat sensitivity of rat C-fiber nociceptors are present in vitro after plantar incision [J].
Banik, RK ;
Brennan, TJ .
PAIN, 2004, 112 (1-2) :204-213
[4]   Oral administration of Ginkgo biloba extract, EGb-761 inhibits thermal hyperalgesia in rodent models of inflammatory and post-surgical pain [J].
Biddlestone, L. ;
Corbett, A. D. ;
Dolan, S. .
BRITISH JOURNAL OF PHARMACOLOGY, 2007, 151 (02) :285-291
[5]   Heat injury-induced drop of the noxious heat threshold measured with an increasing-temperature water bath:: A novel rat thermal hyperalgesia model [J].
Bolcskei, Kata ;
Horvath, Dora ;
Szolcsanyi, Janos ;
Petho, Gabor .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2007, 564 (1-3) :80-87
[6]   Characterization of a rat model of incisional pain [J].
Brennan, TJ ;
Vandermeulen, EP ;
Gebhart, GF .
PAIN, 1996, 64 (03) :493-501
[7]  
Field MJ, 1997, J PHARMACOL EXP THER, V282, P1242
[8]   A NEW AND SENSITIVE METHOD FOR MEASURING THERMAL NOCICEPTION IN CUTANEOUS HYPERALGESIA [J].
HARGREAVES, K ;
DUBNER, R ;
BROWN, F ;
FLORES, C ;
JORIS, J .
PAIN, 1988, 32 (01) :77-88
[9]   ENHANCEMENT OF DYNORPHIN GENE-EXPRESSION IN SPINAL-CORD FOLLOWING EXPERIMENTAL INFLAMMATION - STIMULUS SPECIFICITY, BEHAVIORAL PARAMETERS AND OPIOID RECEPTOR-BINDING [J].
IADAROLA, MJ ;
BRADY, LS ;
DRAISCI, G ;
DUBNER, R .
PAIN, 1988, 35 (03) :313-326
[10]   The TRPV1 receptor and nociception [J].
Immke, David C. ;
Gavva, Narender R. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2006, 17 (05) :582-591