Pain Genes

被引:124
作者
Foulkes, Tom [1 ]
Wood, John N. [2 ]
机构
[1] Natl Inst Med Res, Dept Stem Cell Biol & Dev Genet, London NW7 1AA, England
[2] UCL, Mol Nocicept Grp, London, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1371/journal.pgen.1000086
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Pain, which afflicts up to 20% of the population at any time, provides both a massive therapeutic challenge and a route to understanding mechanisms in the nervous system. Specialised sensory neurons (nociceptors) signal the existence of tissue damage to the central nervous system (CNS), where pain is represented in a complex matrix involving many CNS structures. Genetic approaches to investigating pain pathways using model organisms have identified the molecular nature of the transducers, regulatory mechanisms involved in changing neuronal activity, as well as the critical role of immune system cells in driving pain pathways. In man, mapping of human pain mutants as well as twin studies and association studies of altered pain behaviour have identified important regulators of the pain system. In turn, new drug targets for chronic pain treatment have been validated in transgenic mouse studies. Thus, genetic studies of pain pathways have complemented the traditional neuroscience approaches of electrophysiology and pharmacology to give us fresh insights into the molecular basis of pain perception.
引用
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页数:9
相关论文
共 89 条
[1]   The nature and identification of quantitative trait loci: a community's view [J].
Abiola, O ;
Angel, JM ;
Avner, P ;
Bachmanov, AA ;
Belknap, JK ;
Bennett, B ;
Blankenhorn, EP ;
Blizard, DA ;
Bolivar, V ;
Brockmann, GA ;
Buck, KJ ;
Bureau, JF ;
Casley, WL ;
Chesler, EJ ;
Cheverud, JM ;
Churchill, GA ;
Cook, M ;
Crabbe, JC ;
Crusio, WE ;
Darvasi, A ;
de Haan, G ;
Demant, P ;
Doerge, RW ;
Elliott, RW ;
Farber, CR ;
Flaherty, L ;
Flint, J ;
Gershenfeld, H ;
Gu, JPGJ ;
Gu, WK ;
Himmelbauer, H ;
Hitzemann, R ;
Hsu, HC ;
Hunter, K ;
Iraqi, FA ;
Jansen, RC ;
Johnson, TE ;
Jones, BC ;
Kempermann, G ;
Lammert, F ;
Lu, L ;
Manly, KF ;
Matthews, DB ;
Medrano, JF ;
Mehrabian, M ;
Mittleman, G ;
Mock, BA ;
Mogil, JS ;
Montagutelli, X ;
Morahan, G .
NATURE REVIEWS GENETICS, 2003, 4 (11) :911-916
[2]   The tetrodotoxin-resistant sodium channel SNS has a specialized function in pain pathways [J].
Akopian, AN ;
Souslova, V ;
England, S ;
Okuse, K ;
Ogata, N ;
Ure, J ;
Smith, A ;
Kerr, BJ ;
McMahon, SB ;
Boyce, S ;
Hill, R ;
Stanfa, LC ;
Dickenson, AH ;
Wood, JN .
NATURE NEUROSCIENCE, 1999, 2 (06) :541-548
[3]   Trans-splicing of a voltage-gated sodium channel is regulated by nerve growth factor [J].
Akopian, AN ;
Okuse, K ;
Souslova, V ;
England, S ;
Ogata, N ;
Wood, JN .
FEBS LETTERS, 1999, 445 (01) :177-182
[4]   Human brain mechanisms of pain perception and regulation in health and disease [J].
Apkarian, AV ;
Bushnell, MC ;
Treede, RD ;
Zubieta, JK .
EUROPEAN JOURNAL OF PAIN, 2005, 9 (04) :463-484
[5]   TRPA1 mediates the inflammatory actions of environmental irritants and proalgesic agents [J].
Bautista, DM ;
Jordt, SE ;
Nikai, T ;
Tsuruda, PR ;
Read, AJ ;
Poblete, J ;
Yamoah, EN ;
Basbaum, AI ;
Julius, D .
CELL, 2006, 124 (06) :1269-1282
[6]   SPTLC1 is mutated in hereditary sensory neuropathy, type 1 [J].
Bejaoui, K ;
Wu, CY ;
Sheffler, MD ;
Haan, G ;
Ashby, P ;
Wu, LC ;
de Jong, P ;
Brown, RH .
NATURE GENETICS, 2001, 27 (03) :261-262
[7]   Quantitative trait loci influencing morphine antinociception in four mapping populations [J].
Bergeson, SE ;
Helms, ML ;
O'Toole, LA ;
Jarvis, MW ;
Hain, HS ;
Mogil, JS ;
Belknap, JK .
MAMMALIAN GENOME, 2001, 12 (07) :546-553
[8]   Parallel "pain" pathways arise from subpopulation of primary afferent nociceptor [J].
Braz, JM ;
Nassar, MA ;
Wood, JN ;
Basbaum, AI .
NEURON, 2005, 47 (06) :787-793
[9]   Association of ABCB1/MDR1 and OPRM1 gene polymorphisms with morphine pain relief [J].
Campa, D. ;
Gioia, A. ;
Tomei, A. ;
Poli, P. ;
Barale, R. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2008, 83 (04) :559-566
[10]   Impaired nociception and pain sensation in mice lacking the capsaicin receptor [J].
Caterina, MJ ;
Leffler, A ;
Malmberg, AB ;
Martin, WJ ;
Trafton, J ;
Petersen-Zeitz, KR ;
Koltzenburg, M ;
Basbaum, AI ;
Julius, D .
SCIENCE, 2000, 288 (5464) :306-313