J Physiol Society Membership
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Volume 554, Number 2, 301-308, January 15, 2004 DOI: 10.1113/jphysiol.2003.048587
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
554/2/301    most recent
jphysiol.2003.048587v1
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by North, R. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by North, R. A.
Related Collections
Right arrow Review articles

SYMPOSIUM REPORT

P2X3 receptors and peripheral pain mechanisms

R. Alan North

Institute of Molecular Physiology, University of Sheffield, Western Bank, Sheffield S10 2TN, UK

ATP released from damaged or inflamed tissues can act at P2X receptors expressed on primary afferent neurones. The resulting depolarization can initiate action potentials that are interpreted centrally as pain. P2X3 subunits are found in a subset of small-diameter, primary afferent neurones, some of which are also sensitive to capsaicin. They can form homo-oligomeric channels, or they can assemble with P2X2 subunits into hetero-oligomers. Studies with antagonists selective for P2X3-containing receptors, experiments with antisense oligonucleotides to reduce P2X3 subunit levels, and behavioural testing of P2X3 knock-out mice, all suggest a role for the P2X2/3 receptor in the signalling of chronic inflammatory pain and some features of neuropathic pain. The availability of such tools and experimental approaches promises to accelerate our understanding of the other physiological roles for P2X receptors on primary afferent neurones.

(Received 4 June 2003; accepted after revision 25 June 2003; first published online 27 June 2003)
Corresponding author R. A. North: Institute of Molecular Physiology, University of Sheffield, Western Bank, Sheffield S10 2TN, UK.  Email: r.a.north{at}sheffield.ac.uk


This report was presented at The Journal of Physiology Symposium on Ion Channels: Their Structure, Function and Control, Fukuoka, Kyushu, Japan, 24 March 2003. It was commissioned by the Editorial Board and reflects the views of the author.




This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
A. R. Light, R. W. Hughen, J. Zhang, J. Rainier, Z. Liu, and J. Lee
Dorsal Root Ganglion Neurons Innervating Skeletal Muscle Respond to Physiological Combinations of Protons, ATP, and Lactate Mediated by ASIC, P2X, and TRPV1
J Neurophysiol, September 1, 2008; 100(3): 1184 - 1201.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
Y. H. Zhang, X. X. Chi, and G. D. Nicol
Brain-derived neurotrophic factor enhances the excitability of rat sensory neurons through activation of the p75 neurotrophin receptor and the sphingomyelin pathway
J. Physiol., July 1, 2008; 586(13): 3113 - 3127.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. Tashiro, K. Okamoto, S. B. Milam, and D. A. Bereiter
Differential Effects of Estradiol on Encoding Properties of TMJ Units in Laminae I and V at the Spinomedullary Junction in Female Rats
J Neurophysiol, December 1, 2007; 98(6): 3242 - 3253.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
Z. Gerevich, Z. S. Zadori, L. Koles, L. Kopp, D. Milius, K. Wirkner, K. Gyires, and P. Illes
Dual Effect of Acid pH on Purinergic P2X3 Receptors Depends on the Histidine 206 Residue
J. Biol. Chem., November 23, 2007; 282(47): 33949 - 33957.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
C. Wang, Y. Gu, G.-W. Li, and L.-Y. M. Huang
A critical role of the cAMP sensor Epac in switching protein kinase signalling in prostaglandin E2-induced potentiation of P2X3 receptor currents in inflamed rats
J. Physiol., October 1, 2007; 584(1): 191 - 203.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. D'Arco, R. Giniatullin, M. Simonetti, A. Fabbro, A. Nair, A. Nistri, and E. Fabbretti
Neutralization of Nerve Growth Factor Induces Plasticity of ATP-Sensitive P2X3 Receptors of Nociceptive Trigeminal Ganglion Neurons
J. Neurosci., August 1, 2007; 27(31): 8190 - 8201.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
E. Sokolova, A. Skorinkin, I. Moiseev, A. Agrachev, A. Nistri, and R. Giniatullin
Experimental and Modeling Studies of Desensitization of P2X3 Receptors
Mol. Pharmacol., July 1, 2006; 70(1): 373 - 382.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
R. Hausmann, J. Rettinger, Z. Gerevich, S. Meis, M. U. Kassack, P. Illes, G. Lambrecht, and G. Schmalzing
The Suramin Analog 4,4',4'',4'''-(Carbonylbis(imino-5,1,3-benzenetriylbis (carbonylimino)))tetra-kis-benzenesulfonic Acid (NF110) Potently Blocks P2X3 Receptors: Subtype Selectivity Is Determined by Location of Sulfonic Acid Groups
Mol. Pharmacol., June 1, 2006; 69(6): 2058 - 2067.
[Abstract] [Full Text] [PDF]


Home page
Pharmacol. Rev.Home page
G. Burnstock
Pathophysiology and therapeutic potential of purinergic signaling.
Pharmacol. Rev., March 1, 2006; 58(1): 58 - 86.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
S. M Brierley, R Carter, W Jones III, L. Xu, D. R Robinson, G. A Hicks, G. F Gebhart, and L. A. Blackshaw
Differential chemosensory function and receptor expression of splanchnic and pelvic colonic afferents in mice
J. Physiol., August 15, 2005; 567(1): 267 - 281.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
G.-Y. Xu and L.-Y. M. Huang
Ca2+/calmodulin-dependent protein kinase II potentiates ATP responses by promoting trafficking of P2X receptors
PNAS, August 10, 2004; 101(32): 11868 - 11873.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 The Physiological Society.