It might be a big family but the pain remains-last chance saloon for selective 5-HT receptor ligands?

被引:10
作者
Andrews, Nick [1 ]
O'Neill, Michael F. [2 ]
机构
[1] Pfizer Labs, Sandwich, Kent, England
[2] Eolasbio Biosci, London, England
关键词
POLYMERASE-CHAIN-REACTION; SUBTYPE MESSENGER-RNAS; NECROSIS-FACTOR-ALPHA; NEUROPATHIC PAIN; INDUCED INFLAMMATION; SEROTONIN RECEPTORS; MOLECULAR-CLONING; SPINAL-CORD; ACTIVATION; EXPRESSION;
D O I
10.1016/j.coph.2011.02.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The following brief overview reflects our own opinion of where the most likely advances to treating pain (unrelated to IBS and migraine) may come from with respect to ligands directly interacting with specific 5-HT receptors. It is fully appreciated, and possibly more likely, that 5-HT plays a modulatory role in the mediation of analgesic effects of certain compounds, for example tricyclic antidepressants and the newer, safer class of serotonin/noradrenaline re-uptake inhibitors, for example duloxetine and milnacipran. However, we find that recent pre-clinical findings highlight the potential of peripherally acting 5-HT1 and 5-HT2A receptor agonists and centrally penetrating 5-HT7 receptor agonists to reduce chronic pain. We encourage experimentation using human tissues and healthy volunteers to improve the confidence in rationale of targeting such receptors tor treatment of pain in humans. However for this to happen the available pharmacological toolbox will also need to be further improved and any safety concerns understood to provide the necessary impetus to go to the clinic.
引用
收藏
页码:39 / 44
页数:6
相关论文
共 37 条
[1]  
BARD JA, 1993, J BIOL CHEM, V268, P23422
[2]   A review of central 5-HT receptors and their function [J].
Barnes, NM ;
Sharp, T .
NEUROPHARMACOLOGY, 1999, 38 (08) :1083-1152
[3]   Activation of 5-HT1B/1D receptor in the periaqueductal gray inhibits nociception [J].
Bartsch, T ;
Knight, YE ;
Goadsby, PJ .
ANNALS OF NEUROLOGY, 2004, 56 (03) :371-381
[4]  
Bourgoin S, 2008, FUND CLIN PHARMACOL, V22, P127
[5]   5-HT7 receptor activation inhibits mechanical hypersensitivity secondary to capsaicin sensitization in mice [J].
Brenchat, Alex ;
Romero, Luz ;
Garcia, Monica ;
Pujol, Marta ;
Burgueno, Javier ;
Torrens, Antoni ;
Hamon, Michel ;
Manuel Baeyens, Jose ;
Buschmann, Helmut ;
Zamanillo, Daniel ;
Miguel Vela, Jose .
PAIN, 2009, 141 (03) :239-247
[6]  
*CLIN, NCT00305188 CLIN
[7]  
Colpaert FC, 2006, CURR OPIN INVEST DR, V7, P40
[8]   Systemic morphine produce antinociception mediated by spinal 5-HT7, but not 5-HT1A and 5-HT2 receptors in the spinal cord [J].
Dogrul, A. ;
Seyrek, M. .
BRITISH JOURNAL OF PHARMACOLOGY, 2006, 149 (05) :498-505
[9]   Pre- and postsynaptic localization of the 5-HT7 receptor in rat dorsal spinal cord:: Immunocytochemical evidence [J].
Doly, S ;
Fischer, J ;
Brisorgueil, MJ ;
Vergé, D ;
Conrath, M .
JOURNAL OF COMPARATIVE NEUROLOGY, 2005, 490 (03) :256-269
[10]   Role of peripheral 5-HT4, 5-HT6, and 5-HT7 receptors in development and maintenance of secondary mechanical allodynia and hyperalgesia [J].
Godinez-Chaparro, Beatriz ;
Barragan-Iglesias, Paulino ;
Castaneda-Corral, Gabriela ;
Rocha-Gonzalez, Hector I. ;
Granados-Soto, Vinicio .
PAIN, 2011, 152 (03) :687-697