Muscarinic suppression of the M-current in the rat sympathetic ganglion is mediated by receptors of the M1-subtype.
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Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptorsKCNQ potassium channels in sensory system and neural circuitsMuscarinic M-current inhibition via G alpha q/11 and alpha-adrenoceptor inhibition of Ca2+ current via G alpha o in rat sympathetic neuronesM-type potassium channels modulate Schaffer collateral-CA1 glutamatergic synaptic transmission.Intracellular retention of recombinant GABAB receptors.Receptor-induced depletion of phosphatidylinositol 4,5-bisphosphate inhibits inwardly rectifying K+ channels in a receptor-specific mannerInhibition of post-synaptic Kv7/KCNQ/M channels facilitates long-term potentiation in the hippocampusPotassium channels in gastrointestinal smooth muscle.Disruption of the m1 receptor gene ablates muscarinic receptor-dependent M current regulation and seizure activity in mice.M-type K+ currents in rat cultured thoracolumbar sympathetic neurones and their role in uracil nucleotide-evoked noradrenaline release.Excitatory muscarinic modulation strengthens virtual nicotinic synapses on sympathetic neurons and thereby enhances synaptic gainElectrostatic interaction of internal Mg2+ with membrane PIP2 Seen with KCNQ K+ channels.Characterization of muscarinic receptor subtypes inhibiting Ca2+ current and M current in rat sympathetic neuronsModulation of Kv7 channels and excitability in the brain.Activation of a PTX-insensitive G protein is involved in histamine-induced recombinant M-channel modulation.Neuronal expression of the rat M1 muscarinic acetylcholine receptor gene is regulated by elements in the first exon.Structure of the m1 muscarinic acetylcholine receptor gene and its promoter.Facilitation of long-term potentiation by muscarinic M(1) receptors is mediated by inhibition of SK channels.Nicotine inhibits potassium currents in Aplysia bag cell neurons.An M2-like muscarinic receptor enhances a delayed rectifier K+ current in rat sympathetic neurones.Ion channel regulation by phosphoinositides analyzed with VSPs-PI(4,5)P2 affinity, phosphoinositide selectivity, and PI(4,5)P2 pool accessibility.Selective activation of heterologously expressed G protein-gated K+ channels by M2 muscarinic receptors in rat sympathetic neurones.Muscarinic acetylcholine response in pyramidal neurones of rat cerebral cortex.Modulation of N-type calcium currents by presynaptic imidazoline receptor activation in rat superior cervical ganglion neurons.Excitation of rat sympathetic neurons via M1 muscarinic receptors independently of Kv7 channels.Enhancing m currents: a way out for neuropathic pain?Selective inhibition of M-type potassium channels in rat sympathetic neurons by uridine nucleotide preferring receptors.An M-like outward current regulates the excitability of spinal motoneurones in the adult turtle.Activation of M1 muscarinic receptors triggers transmitter release from rat sympathetic neurons through an inhibition of M-type K+ channels.Desensitization of alpha7 nicotinic receptors potentiated the inhibitory effect on M-current induced by stimulation of muscarinic receptors in rat superior cervical ganglion neurons.L- and N-current but not M-current inhibition by M1 muscarinic receptors requires DAG lipase activity.Muscarinic modulation of TREK currents in mouse sympathetic superior cervical ganglion neurons.SR 46559A: a novel and potent muscarinic compound with no cholinergic syndrome.Disparate cholinergic currents in rat principal trigeminal sensory nucleus neurons mediated by M1 and M2 receptors: a possible mechanism for selective gating of afferent sensory neurotransmission.PIP(2)-dependent inhibition of M-type (Kv7.2/7.3) potassium channels: direct on-line assessment of PIP(2) depletion by Gq-coupled receptors in single living neurons.Muscarinic M1 receptors activate phosphoinositide turnover and Ca2+ mobilisation in rat sympathetic neurones, but this signalling pathway does not mediate M-current inhibition.Genotypic m3-Muscarinic Receptors Preferentially Inhibit M-currents in DNA-transfected NG108-15 Neuroblastoma x Glioma Hybrid Cells.Some Actions of 9-Amino-1,2,3,4-Tetrahydroacridine (THA) on Cholinergic Transmission and Membrane Currents in Rat Sympathetic Ganglia.
P2860
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P2860
Muscarinic suppression of the M-current in the rat sympathetic ganglion is mediated by receptors of the M1-subtype.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
@zh-cn
name
Muscarinic suppression of the ...... y receptors of the M1-subtype.
@en
Muscarinic suppression of the ...... y receptors of the M1-subtype.
@nl
type
label
Muscarinic suppression of the ...... y receptors of the M1-subtype.
@en
Muscarinic suppression of the ...... y receptors of the M1-subtype.
@nl
prefLabel
Muscarinic suppression of the ...... y receptors of the M1-subtype.
@en
Muscarinic suppression of the ...... y receptors of the M1-subtype.
@nl
P2093
P2860
P1476
Muscarinic suppression of the ...... y receptors of the M1-subtype.
@en
P2093
P2860
P304
P356
10.1111/J.1476-5381.1989.TB12630.X
P407
P577
1989-10-01T00:00:00Z