Примери коришћења Acetylcholine receptors на Енглеском и њихови преводи на Српски
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Nicotine acts on central nicotinic acetylcholine receptors.
Muscarinic acetylcholine receptors possess a regulatory effect on dopaminergic neurotransmission.
Research has also demonstrated that blocking acetylcholine receptors disrupts learning and memory.
It has also been shown to act as a positive allosteric modulator of α7 nicotinic acetylcholine receptors.
Other research has also shown that blocking acetylcholine receptors disrupts both learning and memory.
Although all acetylcholine receptors, by definition, respond to acetylcholine, they respond to other molecules as well.
Moreover, other studies revealed that stopping acetylcholine receptors interrupts learning and memory.
Although all acetylcholine receptors, by definition, respond to acetylcholine, they respond to other molecules as well.
PNU-282,987 is a drug that acts as a potent andselective agonist for the α7 subtype of neural nicotinic acetylcholine receptors.
They mean acetylcholine andjust the central acetylcholine receptors act on the nicotine I talked about earlier.
Rivanicline(TC-2403, RJR-2403,(E)-metanicotine) is a drug which acts as a partial agonist at neural nicotinic acetylcholine receptors.
Muscarinic acetylcholine receptors are also present and distributed throughout the local nervous system, in post-synaptic and pre-synaptic positions.
For example, atropine from deadly nightshade( Atropa belladonna)that functions as a competitive antagonist of the muscarinic acetylcholine receptors.
They may also antagonise muscarinic acetylcholine receptors, causing symptoms such as dry mouth, urinary retention and confusion in the elderly.
WAY-317538(SEN-12333) is a drug that acts as a potent andselective full agonist for the α7 subtype of neural nicotinic acetylcholine receptors.
In addition, galantamine is a ligand for nicotinic acetylcholine receptors, which may increase the presynaptic release of Ach and activate postsynaptic receptors. .
This disease of the neuromuscular junction, where the normal neuromuscular transmission pulse is broken oris not allowed antibodies to acetylcholine receptors.
Galantamine also binds allosterically with nicotinic acetylcholine receptors and may possibly potentiate the action of agonists(such as acetylcholine) at these receptors. .
Anticholinergics are classified according to the receptors that are affected:Antimuscarinic agents operate on the muscarinic acetylcholine receptors.
Nicotine, for example,by acting on nicotinic acetylcholine receptors will eventually increase dopamine in the corpus striatum(older smokers will stop shaking hands) and nucleus accumbens(a habit can occur).
It works by interfering with the transmission of nerve impulses in insects by binding irreversibly to specific insect nicotinic acetylcholine receptors.
The drug acts on what are known as nicotinic acetylcholine receptors(NCR's) and affects two main areas of the body- one called the adrenal medulla, and the other affects the central nervous system(CNS).
Atropine and related anticholinergic drugs act as antidotes to nerve agent poisoning because they block acetylcholine receptors, but they are poisonous in their own right.
Like other transmembrane receptors, acetylcholine receptors are classified according to their"pharmacology", or according to their relative affinities and sensitivities to different molecules.
Neurotoxicity can also result from the inhibition of receptors; for example, atropine from deadly nightshade(Atropa belladonna)that functions as a competitive antagonist of the muscarinic acetylcholine receptors.
Myasthenia currently considered as an autoimmune disease associated with antibodies to acetylcholine receptors, which reduce the number of effective receptors and thereby violate neuromuscular transmission pulse.
CDP Choline is hydrolyzed into Choline and cytidine in the intestines,after crossing the Blood-Brain Barrier it is reformed back into CDP Choline where is used and absorbed through the Acetylcholine receptors which are implicated in thought and memory formation.
Each of the five types of conotoxins attacks a different target:α-conotoxin inhibits nicotinic acetylcholine receptors at nerves and muscles. δ-conotoxin inhibits fast inactivation of voltage-dependent sodium channels. κ-conotoxin inhibits potassium channels. μ-conotoxin inhibits voltage-dependent sodium channels in muscles. ω-conotoxin inhibits N-type voltage-dependent calcium channels.
It is a partial agonist selective for alpha-4, beta-2 nicotinic acetylcholine receptor subtypes.
It is an alpha-4 beta-2(α4β2) nicotinic acetylcholine receptor partial agonist.