Reduction of spike frequency adaptation and blockade of M-current in rat CA1 pyramidal neurones by linopirdine (DuP 996), a neurotransmitter release enhancer.
about
M1-muscarinic receptors promote fear memory consolidation via phospholipase C and the M-currentNeural KCNQ (Kv7) channelsNew molecular targets for antiepileptic drugs: alpha(2)delta, SV2A, and K(v)7/KCNQ/M potassium channelsCharacterization of KCNQ5/Q3 potassium channels expressed in mammalian cellsFormation and Dynamics of Waves in a Cortical Model of Cholinergic ModulationFrom pan-reactive KV7 channel opener to subtype selective opener/inhibitor by addition of a methyl groupK(V)7/KCNQ channels are functionally expressed in oligodendrocyte progenitor cellsAKAP150 signaling complex promotes suppression of the M-current by muscarinic agonistsM-type potassium channels modulate the intrinsic excitability of infralimbic neurons and regulate fear expression and extinctionProtein Phosphatase 2a and glycogen synthase kinase 3 signaling modulate prepulse inhibition of the acoustic startle response by altering cortical M-Type potassium channel activityRescue of homeostatic regulation of striatal excitability and locomotor activity in a mouse model of Huntington's disease.Ion channel genes and human neurological disease: recent progress, prospects, and challenges.Gain control in CA1 pyramidal cells using changes in somatic conductance.Modulation of spontaneous and stimulation-evoked transmitter release from rat sympathetic neurons by the cognition enhancer linopirdine: insights into its mechanisms of action.KCNQ4 channels expressed in mammalian cells: functional characteristics and pharmacology.Controlling potassium channel activities: Interplay between the membrane and intracellular factors.Distinct muscarinic acetylcholine receptor subtypes mediate pre- and postsynaptic effects in rat neocortex.Retigabine/Ezogabine, a KCNQ/K(V)7 channel opener: pharmacological and clinical data.M-type potassium conductance controls the emergence of neural phase codes: a combined experimental and neuron modelling study.M1 and M4 receptors modulate hippocampal pyramidal neurons.Tamoxifen inhibition of kv7.2/kv7.3 channelsContributions of Kv7-mediated potassium current to sub- and suprathreshold responses of rat layer II/III neocortical pyramidal neurons.Kv7.2 regulates the function of peripheral sensory neurons.KCNQ currents and their contribution to resting membrane potential and the excitability of interstitial cells of Cajal from the guinea pig bladderp75 and TrkA signaling regulates sympathetic neuronal firing patterns via differential modulation of voltage-gated currents.The mechanisms of repetitive spike generation in an axonless retinal interneuron.Spike phase locking in CA1 pyramidal neurons depends on background conductance and firing rate.The motor cortex: a network tuned to 7-14 HzEthanol inhibition of m-current and ethanol-induced direct excitation of ventral tegmental area dopamine neurons.Functional expression of KCNQ (Kv7) channels in guinea pig bladder smooth muscle and their contribution to spontaneous activity.K+ channel modulators for the treatment of neurological disorders and autoimmune diseasesDopamine terminals from the ventral tegmental area gate intrinsic inhibition in the prefrontal cortex.Modulation of Kv7 channels and excitability in the brain.Antiepileptic Drug Discovery and Development: What Have We Learned and Where Are We Going?Memory recall and spike-frequency adaptationModulation of ERG channels by XE991.Age- and Sex-Dependent Impact of Repeated Social Stress on Intrinsic and Synaptic Excitability of the Rat Prefrontal Cortex.CA1 pyramidal cells have diverse biophysical properties, affected by development, experience, and agingMechanisms underlying modulation of neuronal KCNQ2/KCNQ3 potassium channels by extracellular protonsActivation of P2Y1 nucleotide receptors induces inhibition of the M-type K+ current in rat hippocampal pyramidal neurons.
P2860
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P2860
Reduction of spike frequency adaptation and blockade of M-current in rat CA1 pyramidal neurones by linopirdine (DuP 996), a neurotransmitter release enhancer.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Reduction of spike frequency a ...... otransmitter release enhancer.
@en
type
label
Reduction of spike frequency a ...... otransmitter release enhancer.
@en
prefLabel
Reduction of spike frequency a ...... otransmitter release enhancer.
@en
P2093
P2860
P1476
Reduction of spike frequency a ...... otransmitter release enhancer.
@en
P2093
P2860
P304
P356
10.1111/J.1476-5381.1995.TB15019.X
P407
P577
1995-08-01T00:00:00Z