Bradykinin inhibits M current via phospholipase C and Ca2+ release from IP3-sensitive Ca2+ stores in rat sympathetic neurons
about
Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsyInactivation as a new regulatory mechanism for neuronal Kv7 channelsGAP43 stimulates inositol trisphosphate-mediated calcium release in response to hypotonicityThe conductance underlying the parallel fibre slow EPSP in rat cerebellar Purkinje neurones studied with photolytic release of L-glutamateAKAP150 signaling complex promotes suppression of the M-current by muscarinic agonistsIon channel genes and human neurological disease: recent progress, prospects, and challenges.The endocannabinoid 2-AG controls skeletal muscle cell differentiation via CB1 receptor-dependent inhibition of Kv7 channelsModulation of spontaneous and stimulation-evoked transmitter release from rat sympathetic neurons by the cognition enhancer linopirdine: insights into its mechanisms of action.Structural requirements for differential sensitivity of KCNQ K+ channels to modulation by Ca2+/calmodulin.Receptor-induced depletion of phosphatidylinositol 4,5-bisphosphate inhibits inwardly rectifying K+ channels in a receptor-specific mannerNerve growth factor sensitizes adult sympathetic neurons to the proinflammatory peptide bradykinin.Cutaneous C-polymodal fibers lacking TRPV1 are sensitized to heat following inflammation, but fail to drive heat hyperalgesia in the absence of TPV1 containing C-heat fibers.Reconstituted slow muscarinic inhibition of neuronal (Ca(v)1.2c) L-type Ca2+ channelsActivation of phospholipase C increases intramembrane electric fields in N1E-115 neuroblastoma cells.The cannabinoid agonist WIN55,212-2 increases intracellular calcium via CB1 receptor coupling to Gq/11 G proteins.Combined phosphoinositide and Ca2+ signals mediating receptor specificity toward neuronal Ca2+ channels.Sensitization of neonatal rat lumbar motoneuron by the inflammatory pain mediator bradykininAssignment of muscarinic receptor subtypes mediating G-protein modulation of Ca(2+) channels by using knockout miceOpposite Effects of the S4-S5 Linker and PIP(2) on Voltage-Gated Channel Function: KCNQ1/KCNE1 and Other Channels.Calmodulin mediates Ca2+-dependent modulation of M-type K+ channelsWhy biophysicists make models: quantifying modulation of the M currentRegulation of KCNQ2/KCNQ3 current by G protein cycling: the kinetics of receptor-mediated signaling by Gq.Coordinate regulation of gonadotropin-releasing hormone neuronal firing patterns by cytosolic calcium and store depletion.Dynamics of Phosphoinositide-Dependent Signaling in Sympathetic Neurons.Neuronal two-pore-domain potassium channels and their regulation by G protein-coupled receptors.NGF inhibits M/KCNQ currents and selectively alters neuronal excitability in subsets of sympathetic neurons depending on their M/KCNQ current background.Target-specific PIP(2) signalling: how might it work?Quantitative properties and receptor reserve of the DAG and PKC branch of G(q)-coupled receptor signalingCoupling of L-type Ca2+ channels to KV7/KCNQ channels creates a novel, activity-dependent, homeostatic intrinsic plasticity.Vascular KCNQ potassium channels as novel targets for the control of mesenteric artery constriction by vasopressin, based on studies in single cells, pressurized arteries, and in vivo measurements of mesenteric vascular resistance.Regulation of neural KCNQ channels: signalling pathways, structural motifs and functional implications.Regulation of neuronal ion channels via P2Y receptors.Potassium channels in peripheral pain pathways: expression, function and therapeutic potential.Affinity for phosphatidylinositol 4,5-bisphosphate determines muscarinic agonist sensitivity of Kv7 K+ channels.Signaling pathways from cannabinoid receptor-1 activation to inhibition of N-methyl-D-aspartic acid mediated calcium influx and neurotoxicity in dorsal root ganglion neurons.Distinct enzyme combinations in AKAP signalling complexes permit functional diversity.Coexpression and activation of TRPV1 suppress the activity of the KCNQ2/3 channel.M-type K(+) channels in peripheral nociceptive pathways.The bradykinin-cGMP-PKG pathway augments insulin sensitivity via upregulation of MAPK phosphatase-5 and inhibition of JNK.Phosphorylation regulates the sensitivity of voltage-gated Kv7.2 channels towards phosphatidylinositol-4,5-bisphosphate.
P2860
Q24675995-AB603C59-07DF-4ED1-B008-D2D019541C2AQ24676507-F88FB3A6-A7B9-41F1-8959-DF10846173F8Q24679816-C6D25CFA-1C38-425F-97C7-FFC6993807E8Q28366928-F14C5AE1-3915-4B5E-A429-4BF3A47B7DFDQ28574598-AE1ECA08-9EE0-427C-99EA-C42C68475C77Q33603836-F8959627-F7C0-44C5-A4C4-16D366D8E89AQ33790150-7616CBB1-71CA-4624-8CE4-674E38BADAF5Q33859793-50E53DDD-FDE2-43EF-BAE0-E397D5C90C92Q33911083-7EC414FE-DA13-4BE7-BE67-D057D3FCB5C4Q33934360-7F156EA7-6088-4EA3-B8A7-28E125F8043DQ34123803-08745952-AB79-4AAD-9E96-E6C4423E3DB7Q34173925-CF444D4F-5261-4A45-B04A-E17B22BD2F3AQ34179399-F2293B33-F430-4ECF-A490-73F03C47AD52Q34181600-90FB8111-832A-41FE-A0DE-83EC821482B5Q34245210-2A64722F-65B4-449A-8535-67AF5418CE44Q34452803-CDC18AA6-E8DE-492E-AE7A-995E33CCDE77Q35541398-EBA0F67B-01BC-430A-84C9-20FAAB905039Q35636678-4560716E-83B5-4EE1-89CD-05DDB90FED7CQ36076020-8534055A-E81D-4F7C-B05F-8DFA47B63E74Q36447189-1729EA59-0A02-47E4-97CA-BC249C84B7A8Q36447368-8FBE5CDA-2FC3-44CF-B659-6E216FC27C06Q36447378-B0354F2E-338D-4277-8B1A-DC6F9F3B0E5BQ36458903-629EDEC4-1BD9-407E-95E5-B9FBFFFD424BQ36507791-018C9EBD-0368-4DF7-8EBE-150210AB423BQ36635997-BD543479-AE92-4694-A610-86A6AFBCDF28Q36667893-4B004B3A-2F68-4E6D-B7E2-DEA31919B48FQ36782546-57F855AF-CAEB-492E-8294-4BCF86BA0C91Q36804642-6E3337BC-740D-4043-A349-3085855550A0Q36957011-7ECFEBA0-9197-4796-AD48-018EB616ECF5Q37001792-67008810-BD9D-4EF4-A3B8-3AAEC85B809DQ37073174-9EFA5355-F295-4A6E-B3FE-983ECD815D85Q37135473-41D88274-064A-4D8D-8D96-88657B07E26CQ37362041-223326C6-A4FF-463E-B22C-67F03BD4683DQ37402286-C8ED4DB8-9F3C-402B-B1E3-1C4531DA97B9Q37444391-20B249FA-5662-4D64-A02E-C54C22BD89D1Q37582031-FBE13F32-3748-46EE-996E-C8C0ED2B2646Q38371584-C9DB5BCC-683A-4CB2-B1E2-C12D6EEFCAD9Q38628600-BC08DFFC-89F7-4F58-A6FF-DFCAF4B23273Q38692385-AAA7D5DE-AA4C-4F68-9077-D101B20D07AAQ39398244-F9C8FE4C-8C54-41E8-9B5B-5D86BDD1841B
P2860
Bradykinin inhibits M current via phospholipase C and Ca2+ release from IP3-sensitive Ca2+ stores in rat sympathetic neurons
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Bradykinin inhibits M current ...... res in rat sympathetic neurons
@ast
Bradykinin inhibits M current ...... res in rat sympathetic neurons
@en
type
label
Bradykinin inhibits M current ...... res in rat sympathetic neurons
@ast
Bradykinin inhibits M current ...... res in rat sympathetic neurons
@en
prefLabel
Bradykinin inhibits M current ...... res in rat sympathetic neurons
@ast
Bradykinin inhibits M current ...... res in rat sympathetic neurons
@en
P2093
P2860
P356
P1476
Bradykinin inhibits M current ...... res in rat sympathetic neurons
@en
P2093
P2860
P304
P356
10.1073/PNAS.95.12.7151
P407
P577
1998-06-01T00:00:00Z