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2) °ÇÑ ¸ÀÀ̳ª ¾à°£ÀÇ ¾ó¾óÇÑ ´À³¦ÀÌ ´À²¸Áú ¶§±îÁö ¾ÃÀº ÈÄ, °ÇÑ ¸ÀÀ̳ª ¾ó¾óÇÑ ´À³¦ÀÌ ÁøÁ¤µÉ ¶§±îÁö ²À» Àá½Ã º¼ ¾È¿¡ µÐ´Ù.
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4) ÀÌ¿Í °°Àº ¹æ¹ýÀ¸·Î 30ºÐ°£ °è¼Ó ¾Ã´Â´Ù.
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¿ÏÀüÇÑ ±Ý¿¬À» À¯ÁöÇϱâ À§ÇØ Èí¿¬ Ãæµ¿ÀÌ ÀÖÀ» ¶§¸¶´Ù ´ÏÄÚ·¹Æ® ²À» »ç¿ëÇÑ´Ù. Åë»ó ÇÏ·ç¿¡ 2mg ² ȤÀº 4mg ²À¸·Î 8~12°³¸¦ ¾Ã°í, ÇÏ·ç ÃÑ »ç¿ë·®ÀÌ 15°³¸¦ ³ÑÁö ¾Êµµ·Ï ÇÑ´Ù.
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2) ºÒ¾ÈÁ¤ Çù½ÉÁõ ¶Ç´Â Çù½ÉÁõ ¾ÇÈ[ÇÁ¸°Áî¸ÞÅ» Çù½ÉÁõ(Prinzmetal's angina: º¯Çü¼º Çù½ÉÁõ) Æ÷ÇÔ] ȯÀÚ, ÃÖ±Ù 3°³¿ù À̳»¿¡ ½É±Ù°æ»öÀ» °æÇèÇÑ È¯ÀÚ, ±Þ¼º °æ»öÁõ Èıâ(post-infarction period) ȯÀÚ, ÁßÁõ(½ÉÇÑ Áõ»ó)ÀÇ ½ÉºÎÁ¤¸Æ ȯÀÚ µî ÀÓ»óÀûÀ¸·Î °ü·ÃÀÌ ÀÖ´Â ½ÉºÎÁ¤¸Æ ȯÀÚ, Àü½Å °íÇ÷¾Ð ¶Ç´Â ¸»ÃÊÇ÷°üÁúȯ µî ÁßÁõ(½ÉÇÑ Áõ»ó)ÀÇ ½ÉÇ÷°ü°è Áúȯ ȯÀÚ
3) ±Þ¼º ³úÁ¹ÁßÀ̳ª ÃÖ±Ù ³úÇ÷°ü ÀÌ»óÀÌ ÀÖ¾ú´ø ȯÀÚ µî ³úÇ÷°ü¼º ÁúȯÀÌ Àִ ȯÀÚ
4) ÀÓ»êºÎ
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2) Æó»ö(´ÝÇô¼ ¸·Èû)¼º µ¿¸ÆÁúȯ, ¾ÈÁ¤Çü Çù½ÉÁõ, ½ÉºÎÀü, ºñ´ë»ó¼º ½ÉºÎÀü, ½É±Ù°æ»ö, ½ÉºÎÁ¤¸Æ, Ç÷°ü°æ·Ã, Á¶ÀýµÇÁö ¾Ê´Â °íÇ÷¾Ð, µ¿¸ÆÇ÷°ü ¹ÙÀÌÆÐ½º ÀÌ½Ä ¶Ç´Â Ç÷°ü¼ºÇü¼ú ȯÀÚ µî ½ÉÇ÷°ü°è Áúȯ ȯÀÚ
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ȯÀÚ¿¡ ÀÇÇØ º¸°íµÈ ´ëºÎºÐÀÇ ÀÌ»ó¹ÝÀÀÀº ´ë°³ Ä¡·á ½ÃÀÛ Ã¹ 3-4ÁÖ¿¡ ³ªÅ¸³µ´Ù. ÀÌ ¾àÀÇ ÀÌ»ó¹ÝÀÀÀº ÁÖ·Î ¾Ã´Â ¹æ¹ýÀÌ À߸øµÇ¾ú°Å³ª ´ÏÄÚÆ¾ÀÇ ¿ë·®-ºñ·ÊÀûÀÎ ¾à¸®ÇÐÀû ¿µÇâÀ¸·Î ÀÎÇØ ¹ß»ýÇÏ¿´´Ù.
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1) ÁßÃ߽Űæ°è : µÎÅë, Çö±âÁõ(¾îÁö·¯¿ò), ¼ö¸é Àå¾Ö, ºÒ¾È, °¨Á¤ÀÇ ºÒ¾ÈÁ¤, ÃÊÁ¶, ºñÁ¤»óÀûÀÎ ²Þ, È¥¸ù(Á¤½ÅÀÌ È帴ÇÏ°í °¡¹°°¡¹°ÇÔ), µ¿¿ä(¾ÈÀýºÎÀý), ÁýÁßÀå¾Ö, ÇÇ·Î, ÆíµÎÅë, ¿¬Ãà(¼öÃà°ú ÀÌ¿Ï), ÇÏÁö(´Ù¸®)°æ·Ã
2) ½ÉÇ÷°ü°è : Ç÷¾ÐÀÇ º¯È, °íÇ÷¾Ð, ½É°èÇ×Áø(µÎ±Ù°Å¸²), °¡¿ªÀû ½É¹æ¼¼µ¿, ½É¹æºÎÁ¤¸Æ
3) À§Àå°ü°è : ±¸¿ª, ±¸Åä, »óº¹ºÎ ÅëÁõ, º¹ºÎ µ¿Åë(¹èºÎºÐ ÅëÁõ), ¼ÒȺҷ®, °íâ(ºÏ¹è), À§±Ë¾ç µîÀÇ À§Àå°ü Àå¾Ö, ¿¬ÇÏ °ï¶õ(»ïÅ´°ï¶õ), ±¸°¥(¸ñ¸¶¸§), ¹èº¯ ÀÌ»ó, º¯ºñ, ¼³»ç, ½Ä¿åÁõ°¡
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5) ÇǺΠ: ¾Ë·¯Áö, ÇÇÁø(ÇǺιßÁø), Ç츣Æä½ºÁø, °¡·Á¿òÁõ, µÎµå·¯±â, ¿©µå¸§, È«¹Ý(ºÓÀº¹ÝÁ¡)
6) °¨°¢±â°è : ¹Ì°¢µµÂø(¸ÀÀ» Á¦´ë·Î ¸ø´À³¦), ½Ã¾ßÀÌ»ó
7) Àû¿ëºÎÀ§ : ±¸°(ÀÔ¾È) ¹× ÀÎÈÄ(¸ñ±¸¸Û)ÀÇ ÀÚ±Ø(ÅëÁõ), ÅΰüÀý ¹× ±ÙÀ°ÀÇ ÅëÁõ, Ä¡Àº¿°(ÀÕ¸ö¿°)
8) ±âŸ : ¿ù°æ°ï¶õÁõ, ±ÙÀ°Åë, °üÀýÅë, Ä¡Åë, ¹èÅë(µî ÅëÁõ), ÈäÅë(°¡½¿ÅëÁõ), µ¿Åë(ÅëÁõ), ÀÌÅë(±ÍÅëÁõ), ¾È¸é(¾ó±¼)È«Á¶, ±¹¼ÒºÎÁ¾(ºÎ±â), üÁßÁõ°¡, °©»ó¼± ±â´ÉÀå¾Ö, Àӯļ± µ¿Åë(ÅëÁõ), ¹æ±¤¿°, ¹ßÇÑ(¶¡ÀÌ ³²)Áõ°¡, µþ±¹Áú, Ç÷°üºÎÁ¾(ºÎ±â)°ú °°Àº ¾Ë·¹¸£±â ¹ÝÀÀ
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| DUR (ÀǾàǰ»ç¿ëÆò°¡) |
º´¿ë±Ý±â :
°í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
[»óÈ£ÀÛ¿ë/º´¿ë±Ý±â°Ë»ö]
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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.
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| 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.
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| 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)
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| Protein Binding |
Nicotine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Less than 5%
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| 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
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| 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.
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| Biotransformation |
Nicotine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Primarily hepatic, cotinine is the primary metabolite.
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| 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).
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| Drug Interactions |
Nicotine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Drug Target |
[Drug Target]
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| 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]
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| Drug Category |
Nicotine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-craving AgentsAutonomic drugsCentral Nervous System AgentsGanglionic StimulantsNicotinic Agonists
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| Smiles String Canonical |
Nicotine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CN1CCCC1C1=CN=CC=C1
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| Smiles String Isomeric |
Nicotine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CN1CCC[C@@H]1C1=CN=CC=C1
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| 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
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| Chemical IUPAC Name |
Nicotine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 3-(1-methylpyrrolidin-2-yl)pyridine
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| 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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µå·°ÀÎÆ÷ ÀǾàÇмúÁ¤º¸´Â ½ÄǰÀǾàǰ¾ÈÀüóÀÇ Á¦Ç°Çã°¡»çÇ×, Çмú¹®Çå, Á¦¾àȸ»ç Á¦°øÁ¤º¸ µîÀ» ±Ù°Å·Î ÀÛ¼ºµÈ Âü°í Á¤º¸ÀÔ´Ï´Ù.
Á¤º¸ÀÇ Á¤È®¼ºÀ» À§ÇØ ³ë·ÂÇϰí ÀÖÀ¸³ª ÆíÁý»óÀÇ ¿À·ù, Çã°¡»çÇ× º¯°æ, Ãß°¡ÀûÀÎ Çмú¿¬±¸ ¶Ç´Â Àӻ󿬱¸ ¹ßÇ¥ µîÀ¸·Î ÀÎÇØ ¹ß»ýÇÏ´Â ¹®Á¦¿¡ ´ëÇØ µå·°ÀÎÆ÷´Â
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¹Ýµå½Ã Á¦Á¶¡¤¼öÀÔ»ç, ÆÇ¸Å»ç, ÀÇ»ç, ¾à»ç¿¡°Ô ÃÖÁ¾ÀûÀ¸·Î È®ÀÎÇϽñ⠹ٶø´Ï´Ù.
ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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