「norepinephrine」の共起表現(1語右で並び替え)

「norepinephrine」の共起表現一覧(1語右で並び替え)

norepinephrine

1語右で並び替え

該当件数:101件

acting as an inhibitor while dopamine and norepinephrine act as a stimulator of sexual desire.
oduced in the synthesis of dopa, dopamine, norepinephrine and epinephrine.
in, bufotenine, bufothionine, epinephrine, norepinephrine, and serotonin.
es, reduces levels of dopamine and cardiac norepinephrine, and inactivates tyrosine hydroxylase.
A deficiency of norepinephrine and epinephrine that causes orthostatic hy
take inhibitor of serotonin, dopamine, and norepinephrine, and also has some weak releasing activity
Two catecholamines, norepinephrine and dopamine, act as neuromodulators in th
n to inhibit the reuptake of serotonin and norepinephrine, and to possibly induce their release.
ne likely acts via inducing the release of norepinephrine and dopamine as with its analogues pemolin
transmitters (chemical nerve in the brain) norepinephrine and dopamine by blocking the action of the
levels, although thus possibly decreasing norepinephrine and epinephrine.
ransmitters that is membrane-bound, making norepinephrine and epinephrine the only transmitters synt
It increases serotonin, norepinephrine, and dopamine levels in the brain and is b
ansmitter systems and to block reuptake of norepinephrine and serotonin from the synapse, therefore
eased extracellular concentrations of both norepinephrine and dopamine and therefore an increase in
2C receptor which normally acts to inhibit norepinephrine and dopamine release, thereby promoting ou
inhibitor of the reuptake of serotonin and norepinephrine and instead acts predominantly as a 5-HT2
s not induce the release of epinephrine or norepinephrine and instead acts as a selective β-adrenerg
ated to be a releasing agent of serotonin, norepinephrine and dopamine (with serotonin being the pri
hich are shared and sometimes contested by norepinephrine and GABA.
ity for the serotonin transporter over the norepinephrine and dopamine transporters, as transporter-
rmation of creatine, carnitine, DNA, tRNA, norepinephrine, and other compounds, it is transformed in
he production of neurotransmitters such as norepinephrine and serotonin, as well as supplementing wi
y have stronger effects on the reuptake of norepinephrine and/or serotonin than quinupramine itself.
e) are thought to stimulate the release of norepinephrine and/or dopamine from storage sites in nerv
as saturation of these receptors inhibits norepinephrine and/or dopamine release.
s most, including serotonin, dopamine, and norepinephrine, are absorbed from the synaptic cleft rath
neurotransmitters serotonin, dopamine and norepinephrine by interacting with the serotonin transpor
, adrenaline (epinephrine), noradrenaline ( norepinephrine), cortisol, and growth hormone.
Normetanephrine is a metabolite of norepinephrine created by action of catechol-O-methyl tra
Some people refer to this as norepinephrine deficiency.
Norepinephrine degradation.
tors triggers the release or inhibition of norepinephrine depending on species, presumably from the
The synthesis of norepinephrine depends on the presence of tyrosine, an am
It has been found to be effective when norepinephrine does not help.
esponding amines, for example epinephrine, norepinephrine, dopamine or serotonin.
ers, primarily glutamate, and also such as norepinephrine, dopamine, epinephrine, and serotonin, all
ous neurotransmitters including serotonin, norepinephrine, dopamine, GABA, and glutamate.
ally released epinephrine (adrenaline) and norepinephrine during periods of stress.
se of stored monoamines, such as dopamine, norepinephrine, epinephrine.
Norepinephrine) has a positive ionotropic effect on heart
In vertebrates, octopamine replaces norepinephrine in sympathetic neurons with chronic use of
It stimulates the release of norepinephrine in mammals, working as a stimulant.
h a variety of animals suggest the role of norepinephrine in olfactory learning, in which norepineph
stimulates the generation of serotonin and norepinephrine in the brain.
s and increases the levels of dopamine and norepinephrine in the brain through reuptake inhibition o
d is approximately 10x and 20x stronger on norepinephrine in comparison, respectively.
This effect is mediated by norepinephrine increasing the calcium uptake and therefor
glionic nerve cells, although they release norepinephrine into the blood.
renalase is expressed in heart muscle and norepinephrine is thought to aggravate heart attacks (myo
Norepinephrine is also released from postganglionic neuro
The catecholamine norepinephrine is a neuromodulator of the peripheral symp
Institute on Alcohol Abuse and Alcoholism, norepinephrine is secreted under stress, arousal, or thri
rane by the same mechanism that transports norepinephrine itself (NET, uptake 1), and uptake is esse
ually cause the degeneration of dopamine & norepinephrine levels in the brain, contributing to Parki
c catecholamine (dopamine, epinephrine and norepinephrine) levels.
research in the basic biology of dopamine, norepinephrine, opioid peptides in the brain, connections
rage in sympathetic neurons occurs via the norepinephrine pump; guanadrel slowly displaces norepinep
o effects on dopamine release and probably norepinephrine release as well, and as a 5-HT2A receptor
As an example, norepinephrine released from sympathetic neurons may inte
ne can essentially be considered selective norepinephrine releasing agents (NRAs).
Instead, it may act as a serotonin and/or norepinephrine releasing agent.
c effects, and instead acts as a selective norepinephrine releasing agent.
g the reuptake of serotonin, dopamine, and norepinephrine, respectively.
g the reuptake of serotonin, dopamine, and norepinephrine, respectively.
ne acts as a serotonin releasing agent and norepinephrine reuptake inhibitor.
Dibenzepin acts as a norepinephrine reuptake inhibitor, potent antihistamine,
It acts primarily as a norepinephrine reuptake inhibitor similarly to desipramin
It is known to act as a norepinephrine reuptake inhibitor, antihistamine, and ant
id agonist, serotonin releasing agent, and norepinephrine reuptake inhibitor.
It acts as a potent and highly selective norepinephrine reuptake inhibitor.
ns via the dopamine and noradrenaline (aka norepinephrine) reuptake transporters.
has desipramine-like effects, acting as a norepinephrine reuptake inhibitor without affecting the r
Dextroprotiline acts as a potent norepinephrine reuptake inhibitor and H1 receptor antagon
espite being a TCA, it acts as a selective norepinephrine reuptake inhibitor and has negligible affi
Talsupram (5-003) is a selective norepinephrine reuptake inhibitor (NRI) which was investi
Setiptiline acts as a norepinephrine reuptake inhibitor, α2-adrenergic receptor
eceptor antagonist, and weak serotonin and norepinephrine reuptake inhibitor.
pramine, it likely acts as a serotonin and norepinephrine reuptake inhibitor and serotonin, adrenena
o amitriptyline, acting as a serotonin and norepinephrine reuptake inhibitor, serotonin receptor ant
Main article: Norepinephrine reuptake inhibitor
e potently inhibits neuronal serotonin and norepinephrine reuptake, and it has been demonstrated tha
were shown to slow enzymatic breakdown of norepinephrine, serotonin and dopamine via inhibition of
thalamus, and has modest to no effects on norepinephrine, serotonin, dopamine, or glutamate levels
ture explains some of the clinical uses of norepinephrine, since a modification of the system affect
th serotonin (5-HT) and neurons containing norepinephrine that are targeted by the currently used an
For norepinephrine to be acted upon by PNMT in the cytosol, i
ce the release of serotonin, dopamine, and norepinephrine to varying extents.
to the presynaptic terminal transported by Norepinephrine transporter (NET).
It has been used to label the norepinephrine transporter in positron emission tomograph
ction of the serotonin transporter (SERT), norepinephrine transporter (NET), and dopamine transporte
as well: serotonin transporter (890 nM) > norepinephrine transporter (20,000) > dopamine transporte
"The involvement of the norepinephrine transporter (NET) in the pathophysiology a
AT), serotonin transporter (SERT), and the norepinephrine transporter (NET) in the outer cell membra
δ-opioid receptor, or for the serotonin or norepinephrine transporter.
t binding to the serotonin transporter and norepinephrine transporter.
sporter with increased selectivity for the norepinephrine transporters.
neurotransmitters/neuroregulators, such as norepinephrine, vasopressin, hypocretin (orexin), neurope
ed by AMPT may be mediated by decreases in norepinephrine, while changes in selective attention and
t the reuptake of serotonin, dopamine, and norepinephrine with IC50 values of 322 nM, 1,997 nM, and
Ca2+, ATP and catecholamines (epinephrine, norepinephrine) within the hormone storage vesicle core.