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Nicotine ¿¡ ´ëÇÑ µ¶¼ºÁ¤º¸ : Á¤º¸º¸±â
Ãâó: ±¹¸³µ¶¼º°úÇпø µ¶¼º¹°ÁúÁ¤º¸DB : http://www.nitr.go.kr/nitr/contents/m134200/view.do
Mechanism of Action
Nicotine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Nicotine binds to the nicotinic acetylcholine receptor. Stimulation of nicotinic receptors leads to a variety of cholinergic and adrenergic effects; tachycardia or bradycardia mediated by either stimulation or interference with sympathetic or parasympathetic pathways, stimulation of receptors in the carotic and aortic bodies, release of epinephrine from the adrenal medulla, and stimulation of the chemoreceptor-trigger zone.
Pharmacology
Nicotine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Nicotine, the primary alkaloid in tobacco products binds stereo-selectively to nicotinic-cholinergic receptors on autonomic ganglia, the adrenal medulla, neuromuscular junctions and in the brain. Nicotine exerts two effects, a stimulant effect exerted at the locus ceruleus and a reward effect in the limbic system. Itranvenous administration of nicotine causes release of acetylcholine, norepinephrine, dopamine, serotonine, vasopressin, beta-endorphin and ACTH. Nicotine is a highly addictive substance. Nicotine also induces peripheral vasoconstriction, tachycardia and elevated blood pressure. Nicotine inhalers and patches are used to treat smoking withdrawl syndrome. Nicotine is classified as a stimulant of autonomic ganglia.
Metabolism
Nicotine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 2A6 (CYP2A6)Cytochrome P450 2E1 (CYP2E1)Cytochrome P450 2A13 (CYP2A13)Monoamine oxidase type A (MAO-A)Monoamine oxidase type B (MAO-B)Cytochrome P450 2B6 (CYP2B6)
Protein Binding
Nicotine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Less than 5%
Half-life
Nicotine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Cotinine has a half life of 15-20 hours, while nicotine has a half life of 1-3 hours
Absorption
Nicotine¿¡ ´ëÇÑ Absorption Á¤º¸ Absorption of nicotine through the buccal mucosa is relatively slow and the high and rapid rise followed by the decline in nicotine arterial plasma concentrations seen with cigarette smoking are not achieved with the inhaler. About 10% of absorbed nicotine is excreted unchanged in urine.
Biotransformation
Nicotine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Primarily hepatic, cotinine is the primary metabolite.
Toxicity
Nicotine¿¡ ´ëÇÑ Toxicity Á¤º¸ Symptoms of overdose include nausea, abdominal pain, vomiting, diarrhea, diaphoresis, flushing, dizziness, disturbed hearing and vision, confusion, weakness, palpitations, altered respiration and hypotension. LD50 = 24 mg/kg (orally in mice).
Drug Interactions
Nicotine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Drug Target
[Drug Target]
Description
Nicotine¿¡ ´ëÇÑ Description Á¤º¸ Nicotine is highly toxic alkaloid. It is the prototypical agonist at nicotinic cholinergic receptors where it dramatically stimulates neurons and ultimately blocks synaptic transmission. Nicotine is also important medically because of its presence in tobacco smoke. [PubChem]
Drug Category
Nicotine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-craving AgentsAutonomic drugsCentral Nervous System AgentsGanglionic StimulantsNicotinic Agonists
Smiles String Canonical
Nicotine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CN1CCCC1C1=CN=CC=C1
Smiles String Isomeric
Nicotine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CN1CCC[C@@H]1C1=CN=CC=C1
InChI Identifier
Nicotine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C10H14N2/c1-12-7-3-5-10(12)9-4-2-6-11-8-9/h2,4,6,8,10H,3,5,7H2,1H3
Chemical IUPAC Name
Nicotine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 3-(1-methylpyrrolidin-2-yl)pyridine
Drug-Induced Toxicity Related Proteins
NICOTINE ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein :Cytochrome P450 1A2 Drug :Nicotine Toxicity :tardive dyskinesia in schizophrenia. [¹Ù·Î°¡±â] Replated Protein :Choline O-acetyltransferase Drug :nicotine Toxicity :development of tolerance. [¹Ù·Î°¡±â] Replated Protein :Collagen Drug :nicotine Toxicity :reduced cell proliferation, disrupted cell architecture, disintegration of cells, and extracellular matrix. [¹Ù·Î°¡±â]
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