Intracellular Ca2+ buffers disrupt muscarinic suppression of Ca2+ current and M current in rat sympathetic neurons.
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Elevation of intracellular calcium by muscarinic receptor activation induces a block of voltage-activated rat ether-à-go-go channels in a stably transfected cell lineActivation of m1 muscarinic acetylcholine receptor induces surface transport of KCNQ channels through a CRMP-2-mediated pathway.Orientation of palmitoylated CaVbeta2a relative to CaV2.2 is critical for slow pathway modulation of N-type Ca2+ current by tachykinin receptor activation.Structural requirements for differential sensitivity of KCNQ K+ channels to modulation by Ca2+/calmodulin.Conduction properties of the M-channel in rat sympathetic neurons.Time course of receptor-channel coupling in frog sympathetic neurons.Nerve growth factor sensitizes adult sympathetic neurons to the proinflammatory peptide bradykinin.Reconstituted slow muscarinic inhibition of neuronal (Ca(v)1.2c) L-type Ca2+ channelsCombined phosphoinositide and Ca2+ signals mediating receptor specificity toward neuronal Ca2+ channels.Arachidonic acid mediates muscarinic inhibition and enhancement of N-type Ca2+ current in sympathetic neurons.Hysteresis of gating underlines sensitization of TRPV3 channels.Assignment of muscarinic receptor subtypes mediating G-protein modulation of Ca(2+) channels by using knockout micePotent block of potassium currents in rat isolated sympathetic neurones by the uncharged form of amitriptyline and related tricyclic compoundsCharacterization of acute homologous desensitization of mu-opioid receptor-induced currents in locus coeruleus neurones.Effects on K+ currents in rat cerebellar granule neurones of a membrane-permeable analogue of the calcium chelator BAPTA.Optimization of neuronal cultures from rat superior cervical ganglia for dual patch recording.Block of potassium currents in rat isolated sympathetic neurones by tricyclic antidepressants and structurally related compounds.Regulators of G protein signaling attenuate the G protein-mediated inhibition of N-type Ca channelsCalmodulin mediates Ca2+-dependent modulation of M-type K+ channelsWhy biophysicists make models: quantifying modulation of the M currentDynamics of Phosphoinositide-Dependent Signaling in Sympathetic Neurons.Bradykinin inhibits M current via phospholipase C and Ca2+ release from IP3-sensitive Ca2+ stores in rat sympathetic neuronsNeuronal two-pore-domain potassium channels and their regulation by G protein-coupled receptors.Somatostatin modulates voltage-gated K(+) and Ca(2+) currents in rod and cone photoreceptors of the salamander retina.Regulation of neural KCNQ channels: signalling pathways, structural motifs and functional implications.Functional effects of KCNQ K(+) channels in airway smooth muscleCharacterization of muscarinic receptor subtypes inhibiting Ca2+ current and M current in rat sympathetic neuronsAffinity for phosphatidylinositol 4,5-bisphosphate determines muscarinic agonist sensitivity of Kv7 K+ channels.Regulation of voltage-gated Ca2+ channels by lipids.Scanning mutagenesis of the I-II loop of the Cav2.2 calcium channel identifies residues Arginine 376 and Valine 416 as molecular determinants of voltage dependent G protein inhibition.Speed of Ca2+ channel modulation by neurotransmitters in rat sympathetic neurons.Phosphatidylinositol 4,5-bisphosphate hydrolysis mediates histamine-induced KCNQ/M current inhibition.Ionic permeation and conduction properties of neuronal KCNQ2/KCNQ3 potassium channels.Muscarinic modulation of erg potassium current.The actions of Pasteurella multocida toxin on neuronal cells.Mechanisms underlying modulation of neuronal KCNQ2/KCNQ3 potassium channels by extracellular protonsThe antidepressant imipramine inhibits M current by activating a phosphatidylinositol 4,5-bisphosphate (PIP2)-dependent pathway in rat sympathetic neurones.Pharmacological discrimination between muscarinic receptor signal transduction cascades with bethanechol chlorideMuscarinic (M1) receptor-mediated inhibition of K(+)-evoked [3H]-noradrenaline release from human neuroblastoma (SH-SY5Y) cells via inhibition of L- and N-type Ca2+ channels.Ca2+ and phosphatidylinositol 4,5-bisphosphate stabilize a Gbeta gamma-sensitive state of Ca V2 Ca 2+ channels.
P2860
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P2860
Intracellular Ca2+ buffers disrupt muscarinic suppression of Ca2+ current and M current in rat sympathetic neurons.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on January 1991
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Intracellular Ca2+ buffers dis ...... nt in rat sympathetic neurons.
@en
Intracellular Ca2+ buffers dis ...... nt in rat sympathetic neurons.
@nl
type
label
Intracellular Ca2+ buffers dis ...... nt in rat sympathetic neurons.
@en
Intracellular Ca2+ buffers dis ...... nt in rat sympathetic neurons.
@nl
prefLabel
Intracellular Ca2+ buffers dis ...... nt in rat sympathetic neurons.
@en
Intracellular Ca2+ buffers dis ...... nt in rat sympathetic neurons.
@nl
P2860
P356
P1476
Intracellular Ca2+ buffers dis ...... ent in rat sympathetic neurons
@en
P2093
P2860
P304
P356
10.1073/PNAS.88.2.652
P407
P577
1991-01-01T00:00:00Z