Exemplos de uso de Nicotinic acetylcholine em Inglês e suas traduções para o Português
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Cytisine is a partial nicotinic acetylcholine agonist with a half-life of 4.8 hours.
Arecoline has been compared to nicotine; however,nicotine acts primarily on the nicotinic acetylcholine receptor.
System(nicotinic acetylcholine receptors), resulting in subsequent paralysis and death of the fleas.
Like varenicline, cytisine is a partial agonist of nicotinic acetylcholine receptors nAChRs.
Nicotine acts through nicotinic acetylcholine receptors(nachrs), which are involved in a wide range of processes in central nervous system.
Of course we will do this for receptors in addition to this example, the nicotinic acetylcholine receptor.
Nicotinic acetylcholine receptors can be blocked by curare, hexamethonium and toxins present in the venoms of snakes and shellfishes, like α-bungarotoxin.
Monepantel acts on the nematode specific nicotinic acetylcholine receptor sub-unit Hco- MPTL-1.
The active substance in CHAMPIX, varenicline, can bind to some of these receptors,the α 4β 2 nicotinic acetylcholine receptors.
Since muscular response to acetylcholine is mediated through nicotinic acetylcholine receptors, atropine does not counteract the muscular symptoms.
The active substance in Champix, varenicline, can bind to some of these receptors,the α4β2 nicotinic acetylcholine receptors.
In myasthenia gravis mg, the immune system produces antibodies against nicotinic acetylcholine receptors located in the neuromuscular junction, preventing muscular activation.
Sugammadex quickly encapsulates steroidal neuromuscular blockers, increasing the amount of encapsulated steroidal neuromuscular blockers in plasma andseparating the blockers from the nicotinic acetylcholine receptors.
The thiamethoxam insecticides that belongs to this class acts as an agonist at nicotinic acetylcholine receptors in the central nervous system of insects.
Role in health and disease==Nicotinic acetylcholine receptors can be blocked by curare, hexamethonium and toxins present in the venoms of snakes and shellfishes, like α-bungarotoxin.
Pigs are one of four known mammalian species which possess mutations in the nicotinic acetylcholine receptor that protect against snake venom.
The¿7 nicotinic acetylcholine receptor(¿7nachr) is involved in the cholinergic anti-inflammatory pathway and its activation leads to protective effects in different cell types, including neurons and other cells of the central nervous system.
Its structure is derived from the neurotransmitter acetylcholine and acts on nicotinic acetylcholine receptors of the insect nerve synapse.
Dinotefuran acts on nerve receptors called nicotinic acetylcholine receptors and permethrin interferes with sodium channels on nerves that play a role in transmitting signals; when given together they reinforce each other's action.
Biological Activity Positive allosteric modulator of the a 7 neuronal nicotinic acetylcholine receptor and the purinergic P2X 4 receptor.
This directly influences attention while also affecting learning and memory by facilitating acetylcholine, glutamate, dopamine, noradrenaline, serotonin, andgamma-aminobutyric acid GABA releases from the presynaptic nicotinic acetylcholine receptors nAChRs.
One of the active substances in Trifexis,spinosad interferes with certain specific receptors(nicotinic acetylcholine receptors) in the fleas' nervous system, which results in their subsequent paralysis and death.
ACh binds to nicotinic acetylcholine receptors on the surface of the muscle cell and opens ion channels, allowing sodium ions to flow into the cell and potassium ions to flow out; this ion movement causes a depolarization, which allows for the release of calcium ions within the cell.
The active substance in Comfortis, spinosad,is an insecticide which works by interfering with certain receptors(nicotinic acetylcholine receptors) in the fleas' nervous system, which results in their subsequent paralysis and death.
Spinosad has been one of the most used insecticides to manage spodoptera frugiperda(j. e. smith) in brazil,due to its efficacy and unique mode of action nicotinic acetylcholine receptor allosteric modulator.
Glycopyrronium has little effect on cholinergic stimuli at nicotinic acetylcholine receptors, on structures innervated by postganglionic cholinergic neurons, and on smooth muscles that respond to acetylcholine but have no cholinergic innervation.
PBMC express the glucose transporter 1 GLUT1 and various neurotransmitter receptors such as dopamine D2, 5-Hydroxytryptamine HT 2A, 5HT2C,5HT1A and nicotinic acetylcholine receptors, which are similar to those found in the brain.
Varenicline binds with high affinity andselectivity at the α4β2 neuronal nicotinic acetylcholine receptors, where it acts as a partial agonist- a compound that has both agonist activity, with lower intrinsic efficacy than nicotine, and antagonist activities in the presence of nicotine.
The phenotype of skeletal muscle change for faster pattern in the muscles of the limbs andfor a slower pattern in the diaphragm muscle, in addition an increase in the expression of nicotinic acetylcholine receptors(nachr) at the neuromuscular junction nmj.
The cholinergic anti-inflammatory reflex is activated by the vagus nerve andby the¿7 subunit of the nicotinic acetylcholine receptors(¿7nachr) reduces the activation of nf-kb and consequently decreases the production of tnf¿and intensity of the immune response.