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 6 条
  • [1] The effects of novel, selective 5-hydroxytryptamine (5-HT)(4) receptor ligands in rat spatial navigation
    Fontana, DJ
    Daniels, SE
    Wong, EHF
    Clark, RD
    Eglen, RM
    NEUROPHARMACOLOGY, 1997, 36 (4-5) : 689 - 696
  • [2] The antipsychotic potential of subtype-selective 5-HT receptor ligands based on interactions with mesolimbic dopamine systems
    Tricklebank, MD
    BEHAVIOURAL BRAIN RESEARCH, 1996, 73 (1-2) : 15 - 17
  • [3] Effects of selective h5-HT1B (SB-216641) and h5-HT1D (BRL-15572) receptor ligands on guinea-pig and human 5-HT auto- and heteroreceptors
    E. Schlicker
    K. Fink
    G. J. Molderings
    G. W. Price
    M. Duckworth
    L. Gaster
    D. N. Middlemiss
    J. Zentner
    J. Likungu
    M. Göthert
    Naunyn-Schmiedeberg's Archives of Pharmacology, 1997, 356 : 321 - 327
  • [4] Effects of selective h5-HT1B (SB-216641) and h5-HT1D (BRL-15572) receptor ligands on guinea-pig and human 5-HT auto- and heteroreceptors
    Schlicker, E
    Fink, K
    Molderings, GJ
    Price, GW
    Duckworth, M
    Gaster, L
    Middlemiss, DN
    Zentner, J
    Likungu, J
    Gothert, M
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1997, 356 (03) : 321 - 327
  • [5] FURTHER ASSESSMENT OF THE ANTAGONIST PROPERTIES OF THE NOVEL AND SELECTIVE 5-HT(1A) RECEPTOR LIGANDS (+)-WAY-100-135 AND SDZ-216-525
    LANFUMEY, L
    HAJDAHMANE, S
    HAMON, M
    EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 249 (01) : 25 - 35
  • [6] THE 5-HT(1A) RECEPTOR SELECTIVE LIGANDS, (R)-8-OH-DPAT AND (S)-UH-301, DIFFERENTIALLY AFFECT THE ACTIVITY OF MIDBRAIN DOPAMINE NEURONS
    ARBORELIUS, L
    CHERGUI, K
    MURASE, S
    NOMIKOS, GG
    HOOK, BB
    CHOUVET, G
    HACKSELL, U
    SVENSSON, TH
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1993, 347 (04) : 353 - 362