Acetaminophen reinforces descending inhibitory pain pathways

被引:99
作者
Pickering, G. [1 ,2 ,3 ]
Esteve, V. [1 ]
Loriot, M-A [4 ,5 ]
Eschalier, A. [2 ,3 ,6 ]
Dubray, C. [1 ,2 ,3 ]
机构
[1] Univ Hosp, CHU Clermont Ferrand, Clin Pharmacol Ctr, Clermont Ferrand, France
[2] Univ Hosp, Dept Pharmacol, Fac Med, INSERM,U766, Clermont Ferrand, France
[3] Univ Clermont 1, Clermont Ferrand, France
[4] Univ Paris 05, INSERM, UMRS 490, Paris, France
[5] Hop Europeen Georges Pompidou, Dept Biochem, Paris, France
[6] Univ Hosp, CHU Clermont Ferrand, Lab Pharmacol & Toxicol, Clermont Ferrand, France
关键词
D O I
10.1038/sj.clpt.6100403
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The mechanism of the analgesic action of acetaminophen involves the serotonergic system. This study explores how acetaminophen interferes with serotonergic descending pain pathways. Eighteen rapid metabolizers of tropisetron were included in this double-blind cross-over study. After ethical approval, the healthy volunteers took 1 g oral acetaminophen (A) or placebo (p) combined with either the 5-HT3 antagonist tropisetron (T) (5 mg) or saline, intravenously, at weekly intervals. Mechanical pain thresholds, determined before and after a cold pressor test (CPT), were repeated seven times during the three post-dosing hours, and area under the concentration-time curves (AUCs) of the three treatments were compared. After CPT, AUC (%*min) of Ap (1,561+/-429) was larger than before CPT (393+/-382, P<0.05); these effects were totally inhibited by tropisetron. Acetaminophen reinforces descending inhibitory pain pathways; it suggests a supraspinal target for acetaminophen's antinociceptive action. This study also confirmed that there is a central serotonergic mechanism of action for acetaminophen that is not stimulus-dependent.
引用
收藏
页码:47 / 51
页数:5
相关论文
共 35 条
[1]   Paracetamol exerts a spinal, tropisetron-reversible, antinociceptive effect in an inflammatory pain model in rats [J].
Alloui, A ;
Chassaing, C ;
Schmidt, J ;
Ardid, D ;
Dubray, C ;
Cloarec, A ;
Eschalier, A .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2002, 443 (1-3) :71-77
[2]   Tropisetron inhibits the antinociceptive effect of intrathecally administered paracetamol and serotonin [J].
Alloui, A ;
Pelissier, T ;
Dubray, C ;
Lavarenne, J ;
Eschalier, A .
FUNDAMENTAL & CLINICAL PHARMACOLOGY, 1996, 10 (04) :406-407
[3]   Molecular mechanisms of actions of interleukin-6 on the brain, with special reference to serotonin and the hypothalamo-pituitary-adrenocortical axis [J].
Barkhudaryan, N ;
Dunn, AJ .
NEUROCHEMICAL RESEARCH, 1999, 24 (09) :1169-1180
[4]   Spinal 5-HT1A receptors differentially influence nociceptive processing according to the nature of the noxious stimulus in rats:: effect of WAY-100635 on the antinociceptive activities of paracetamol, venlafaxine and 5-HT [J].
Bonnefont, J ;
Chapuy, E ;
Clottes, E ;
Alloui, A ;
Eschalier, A .
PAIN, 2005, 114 (03) :482-490
[5]   Acetaminophen recruits spinal p42/p44 MAPKs and GH/IGF-1 receptors to produce analgesia via the serotonergic system [J].
Bonnefont, Jerome ;
Daulhac, Laurence ;
Etienne, Monique ;
Chapuy, Eric ;
Mallet, Christophe ;
Ouchchane, Lemlih ;
Deval, Christiane ;
Courade, Jean-Philippe ;
Ferrara, Marc ;
Eschalier, Alain ;
Clottes, Eric .
MOLECULAR PHARMACOLOGY, 2007, 71 (02) :407-415
[6]   Raphe magnus neurons help protect reactions to visceral pain from interruption by cutaneous pain [J].
Brink, Thaddeus S. ;
Hellman, Kevin M. ;
Lambert, Aaron M. ;
Mason, Peggy .
JOURNAL OF NEUROPHYSIOLOGY, 2006, 96 (06) :3423-3432
[7]   CENTRAL ANALGESIC EFFECT OF PARACETAMOL MANIFESTED BY DEPRESSION OF NOCICEPTIVE ACTIVITY IN THALAMIC NEURONS OF THE RAT [J].
CARLSSON, KH ;
JURNA, I .
NEUROSCIENCE LETTERS, 1987, 77 (03) :339-343
[8]   5-HT receptor subtypes involved in the spinal antinociceptive effect of acetaminophen in rats [J].
Courade, JP ;
Chassaing, C ;
Bardin, L ;
Alloui, A ;
Eschalier, A .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2001, 432 (01) :1-7
[9]   INTERPRETATION OF A SIMPLE PCR ANALYSIS OF THE CYP2D6(A) AND CYP2DG(B) NULL ALLELES ASSOCIATED WITH THE DEBRISOQUINE SPARTEINE GENETIC-POLYMORPHISM [J].
DOUGLAS, AM ;
ATCHISON, BA ;
SOMOGYI, AA ;
DRUMMER, OH .
PHARMACOGENETICS, 1994, 4 (03) :154-158
[10]   Age-related differences in endogenous pain modulation: a comparison of diffuse noxious inhibitory controls in healthy older and younger adults [J].
Edwards, RR ;
Fillingim, RB ;
Ness, TJ .
PAIN, 2003, 101 (1-2) :155-165