Inflammatory mediators potentiate ATP-gated channels through the P2X(3) subunit.
about
Molecular and functional properties of P2X receptors--recent progress and persisting challengesProtein kinase C regulation of P2X3 receptors is unlikely to involve direct receptor phosphorylationModeling and analysis of the molecular basis of pain in sensory neurons.Sensitization of cutaneous neuronal purinergic receptors contributes to endothelin-1-induced mechanical hypersensitivityEndogenous purinergic control of bladder activity via presynaptic P2X3 and P2X2/3 receptors in the spinal cord.Regulation of ATP-gated P2X channels: from redox signaling to interactions with other proteinsContributions of P2X3 homomeric and heteromeric channels to acute and chronic pain.Air-stimulated ATP release from keratinocytes occurs through connexin hemichannels.The penultimate arginine of the carboxyl terminus determines slow desensitization in a P2X receptor from the cattle tick Boophilus microplusChelerythrine and other benzophenanthridine alkaloids block the human P2X7 receptor.Drug Insight: biological effects of botulinum toxin A in the lower urinary tract.Activation and regulation of purinergic P2X receptor channelsP2X3 receptors and peripheral pain mechanisms.Crossing the pain barrier: P2 receptors as targets for novel analgesics.Emerging peripheral receptor targets for deep-tissue craniofacial pain therapies.Metabotropic P2Y receptors inhibit P2X3 receptor-channels via G protein-dependent facilitation of their desensitization.Adenosine 5'-triphosphate and its relationship with other mediators that activate pelvic nerve afferent neurons in the rat colorectum.P2X receptors: targets for novel analgesics?Allosteric modulation of ATP-gated P2X receptor channelsModulation of P2X3 and P2X2/3 Receptors by Monoclonal AntibodiesP2 receptors and chronic painFunctional up-regulation of P2X 3 receptors in the chronically compressed dorsal root ganglion.Transient receptor potential channels in pain and inflammation: therapeutic opportunities.Targeting cell surface trafficking of pain-facilitating receptors to treat chronic pain conditions.Brain natriuretic peptide constitutively downregulates P2X3 receptors by controlling their phosphorylation state and membrane localizationBradykinin Contributes to Sympathetic and Pressor Responses Evoked by Activation of Skeletal Muscle Afferents P2X in Heart Failure.Protein kinase A regulation of P2X(4) receptors: requirement for a specific motif in the C-terminus.Lipid raft association and cholesterol sensitivity of P2X1-4 receptors for ATP: chimeras and point mutants identify intracellular amino-terminal residues involved in lipid regulation of P2X1 receptors.Lack of evidence for direct phosphorylation of recombinantly expressed P2X(2) and P2X (3) receptors by protein kinase C.Molecular mechanism for opioid dichotomy: bidirectional effect of μ-opioid receptors on P2X₃ receptor currents in rat sensory neurones.G-protein-coupled receptor regulation of P2X1 receptors does not involve direct channel phosphorylationAgonist-dependence of recovery from desensitization of P2X(3) receptors provides a novel and sensitive approach for their rapid up or downregulation.Contribution of the intracellular C terminal domain to regulation of human P2X1 receptors for ATP by phorbol ester and Gq coupled mGlu(1α) receptors.Regions of the amino terminus of the P2X receptor required for modification by phorbol ester and mGluR1alpha receptors.Stable, synthetic analogs of diadenosine tetraphosphate inhibit rat and human P2X3 receptors and inflammatory painDehydroepiandrosterone potentiates native ionotropic ATP receptors containing the P2X2 subunit in rat sensory neurones.Spontaneous firing and evoked responses of spinal nociceptive neurons are attenuated by blockade of P2X3 and P2X2/3 receptors in inflamed rats.Purinergic component of mechanosensory transduction is increased in a rat model of colitis.CB1 Receptors Mediated Inhibition of ATP-Induced [Ca(2+)]i Increase in Cultured Rat Spinal Dorsal Horn Neurons.Cyclin-dependent kinase 5 modulates the P2X2a receptor channel gating through phosphorylation of C-terminal threonine 372.
P2860
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P2860
Inflammatory mediators potentiate ATP-gated channels through the P2X(3) subunit.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh
2001年學術文章
@zh-hant
name
Inflammatory mediators potentiate ATP-gated channels through the P2X
@nl
Inflammatory mediators potentiate ATP-gated channels through the P2X(3) subunit.
@en
type
label
Inflammatory mediators potentiate ATP-gated channels through the P2X
@nl
Inflammatory mediators potentiate ATP-gated channels through the P2X(3) subunit.
@en
prefLabel
Inflammatory mediators potentiate ATP-gated channels through the P2X
@nl
Inflammatory mediators potentiate ATP-gated channels through the P2X(3) subunit.
@en
P2093
P2860
P356
P1476
Inflammatory mediators potentiate ATP-gated channels through the P2X(3) subunit.
@en
P2093
Geisler HS
Glowatzki E
Osteroth R
Ruppersberg JP
P2860
P304
21077-21082
P356
10.1074/JBC.M101465200
P407
P577
2001-03-22T00:00:00Z