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Qaagi - Book of Why

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PubMed ABSTRACT Two - pore potassium channelscan influenceneuronal excitability

Full AccessRestricted Access A cytoplasmic intron - containing mRNA encoding a potassium channel subunitinfluencesneuronal excitability

Satellite glial cellsinfluenceneuronal excitability

Axon initial segment ( AIS ) geometrycritically influencesneuronal excitability

increased autophagy , apoptosis and proteasome activity Adropin acts in the rat paraventricular nucleusto influenceneuronal excitability

a multitude of neuroactive molecules ... in turnwill influenceneuronal excitability

authors Gary Yellen Brain metabolismcan profoundly influenceneuronal excitability

abnormal expression and function of membrane ion channels(passive) caused byneuronal excitability ,

the targeting of Nav β4 to the axon initial segmentshould ... influenceneuronal excitability

K+ channelsinfluenceneuronal excitability

Fitzgerald and Fulton 1992).One family of ion channelscan ... influenceneuronal excitability

10.7554 / eLife.32721 Brain metabolismcan ... influenceneuronal excitability

the activation of potassium channels and inhibition of voltage - gated calcium channels(passive) caused byneuronal excitability

many of the volt - age - gated sodiuan , potassium , and calcium channelsinfluencingneuronal excitability

Kv7.2 ( KCNQ2 ... gated M - channelinfluencesneuronal excitability

that both dopamine D1- and D2-receptor - expressing MSNs ( D - MSNs ) additionally harbor extrasynaptic GABAARs incorporating α4 , β , and δ subunits that mediate tonic inhibitionthereby influencingneuronal excitability

While sodium channels are knownto influenceneuronal excitability

Sally N. Lawson Ihinfluencesneuronal excitability

QxMD https://www.readbyqxmd.com/read/28100478/adropin-acts-in-the-rat-paraventricular-nucleus-to-influence-neuronal-excitability Adropin acts in the rat paraventricular nucleusto influenceneuronal excitability

a multitude of neuroactive molecules such as glutamate , ATP , nitric oxide ( NO ... in turninfluencesneuronal excitability

Inhibition of the Müller cell KIR channels by the neurotransmitter glutamate ... in turninfluencesneuronal excitability

authors G LeesBrain research2003Anandamide ... diffusible lipid moleculesinfluencesneuronal excitability

authors G. J. Lees Anandamide ... diffusible lipid moleculesinfluencesneuronal excitability

a variety of neuroactive molecules including glutamate , ATP , nitric oxide , prostaglandins , atrial natriuretic peptide ( ANP ) , and d - serine ... in turninfluencesneuronal excitability

the fraction of sodium channels that are available to open at subthreshold membrane potentials(passive) can also be influenced byNeuronal excitability

More ) Cristian G. Acosta , Simon McMullan , +5 authors Sally N. Lawson I(hinfluencesneuronal excitability

opioid posts outside the kind of brain nerve pathway activation emitted from the rod to the spinal cord(passive) caused byneuronal excitability

Their roles in dorsal root ganglion ( DRG ) neurons normally , and in … ( More ) Cristian Acosta , Simon McMullan , +5 authors Sally N. Lawson I(hinfluencesneuronal excitability

In both neocortical and amygdalar neurons , α - DTX - sensitive channels are strategically located at the soma ( Bekkers and Delaney 2001 ) or the primary apical dendrite ( Faber and Sah 2004to influenceneuronal excitability

an increase in threshold levels requiredto triggerneuronal excitability

extracellular pH.(passive) can be influenced byneuronal excitability

Regulation of extracellular levels of ions and neuro - transmitters , especially K+ and glutamatestrongly influencesneuronal excitability

the plateau potential(passive) caused byneuronal excitability

neuroactive steroidsmay influenceneuronal excitability

aspartate and glutamatecausingneuronal excitability

peptide hormonescan influenceneuronal excitability

noradrenergic projections from the midbraincan influenceneuronal excitability

acting on glia and neuronsinfluenceneuronal excitability

persistent form of inhibitioninfluencesneuronal excitability

changes in corticosterone , glutamate , or GABA rather than stress - induced dendritic growth in BLA neurons(passive) caused byneuronal excitability

to pain or seizuresleadsto pain or seizures

to enhanced brain activity before clinical manifestations of the diseaseleadingto enhanced brain activity before clinical manifestations of the disease

to the pain processmay contributeto the pain process

to the generation of seizurescontributesto the generation of seizures

to epileptic seizurescould ... contributeto epileptic seizures

to seizures ... 17leadsto seizures ... 17

to seizures ( 139leadingto seizures ( 139

to neurological disorders accompanied by inflammatory responseleadingto neurological disorders accompanied by inflammatory response

to seizure generation ( Frankenhaeuser & Hodgkin 1956leadingto seizure generation ( Frankenhaeuser & Hodgkin 1956

to increased pain perceptionleadingto increased pain perception

to seizures ( of which migraine is a part ofleadingto seizures ( of which migraine is a part of

to sedative effect of Pramipexoleleadingto sedative effect of Pramipexole

to sedative and sublingual tabletsleadingto sedative and sublingual tablets

in phase opposition with the glial membrane potential ... establishing that only the first 30 % of the neuronal depolarization is efficient for synaptic volleys within cortical neuronal networksresultedin phase opposition with the glial membrane potential ... establishing that only the first 30 % of the neuronal depolarization is efficient for synaptic volleys within cortical neuronal networks

to seizures , Brain , ( 2009 ) in pressleadingto seizures , Brain , ( 2009 ) in press

to sedative effect of Hypnotics ( Nonbenzodiazepineleadingto sedative effect of Hypnotics ( Nonbenzodiazepine

in devastating medical conditions such as chronic painresultingin devastating medical conditions such as chronic pain

to chronic pain and mechanical hypersensitivity.15leadsto chronic pain and mechanical hypersensitivity.15

an exaggerated pain response in the absence of ongoing measurable tissue damagecausingan exaggerated pain response in the absence of ongoing measurable tissue damage

to the repetitive generation of action potentials that can occur during spontaneous seizures in epilepsymay contributeto the repetitive generation of action potentials that can occur during spontaneous seizures in epilepsy

to sedative effect of MetyroSINE . Monitor therapy Magnesium Sulfateleadingto sedative effect of MetyroSINE . Monitor therapy Magnesium Sulfate

to the onset of sporadic spontaneous seizures accompanied by changes in extracellular amino acid concentration in the hippocampusleadingto the onset of sporadic spontaneous seizures accompanied by changes in extracellular amino acid concentration in the hippocampus

in rare small fiber neuropathic pain conditions including primary erythromelalgia ( iEM ) and paroxysmal extreme pain disorder ( PEPDresultingin rare small fiber neuropathic pain conditions including primary erythromelalgia ( iEM ) and paroxysmal extreme pain disorder ( PEPD

to neuroprotectionleadingto neuroprotection

to altered brain functionleadingto altered brain function

the headache and extreme sensitivity to light , sound , smells , and motioncausesthe headache and extreme sensitivity to light , sound , smells , and motion

in enhanced firing probability following an excitatory stimulus , such as kainate - induced depolarizationcould resultin enhanced firing probability following an excitatory stimulus , such as kainate - induced depolarization

in stress and tensionresultingin stress and tension

the brain from becoming hyperactivepreventsthe brain from becoming hyperactive

in an increase in seizure activity.(5resultingin an increase in seizure activity.(5

further mast cell activationcausingfurther mast cell activation

hyperalgesia and allodyniacausinghyperalgesia and allodynia

in a greater state of calmresultingin a greater state of calm

to increased periods of wakefulnessleadsto increased periods of wakefulness

to hypersensitivity in painful processesleadingto hypersensitivity in painful processes

to trigeminal inflammatory hyperalgesiathereby contributingto trigeminal inflammatory hyperalgesia

spontaneous recurrent seizure formation in adult rats with pilocarpine - induced status epilepticuscould preventspontaneous recurrent seizure formation in adult rats with pilocarpine - induced status epilepticus

to the generation and conduction of action potentialsleadingto the generation and conduction of action potentials

from altered biophysical properties in the hNav1.7-A1632 G mutant channelresultingfrom altered biophysical properties in the hNav1.7-A1632 G mutant channel

in a calming effectresultingin a calming effect

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