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(ÀÓ»ó ½ÃÇè¿¡¼ ³·Àº À§Ç輺ÀÌ º¸°íµÊ. -Briggs G, et al. Drugs in Pregnancy and Lactation 7th edit. )
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Atropine¿¡ ´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 |
Atropine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Generally, atropine lowers the "rest and digest" activity of all muscles and glands regulated by the parasympathetic nervous system. This occurs because atropine is a competitive inhibitor of the muscarinic acetylcholine receptors (acetylcholine is the neurotransmitter used by the parasympathetic nervous system).
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| Pharmacology |
Atropine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Atropine, a naturally occurring belladonna alkaloid, is a racemic mixture of equal parts of d- and l-hyoscyamine, whose activity is due almost entirely to the levo isomer of the drug. Atropine is commonly classified as an anticholinergic or antiparasympathetic (parasympatholytic) drug. More precisely, however, it is termed an antimuscarinic agent since it antagonizes the muscarine-like actions of acetylcholine and other choline esters. Adequate doses of atropine abolish various types of reflex vagal cardiac slowing or asystole. The drug also prevents or abolishes bradycardia or asystole produced by injection of choline esters, anticholinesterase agents or other parasympathomimetic drugs, and cardiac arrest produced by stimulation of the vagus. Atropine may also lessen the degree of partial heart block when vagal activity is an etiologic factor. Atropine in clinical doses counteracts the peripheral dilatation and abrupt decrease in blood pressure produced by choline esters. However, when given by itself, atropine does not exert a striking or uniform effect on blood vessels or blood pressure.
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| Metabolism |
Atropine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cholinesterase
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| Protein Binding |
Atropine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ The protein binding of atropine is 14 to 22% in plasma.
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| Half-life |
Atropine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 3.0 ¡¾ 0.9 hours in adults. The half-life of atropine is slightly shorter (approximately 20 minutes) in females than males.
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| Absorption |
Atropine¿¡ ´ëÇÑ Absorption Á¤º¸ Atropine is rapidly and well absorbed after intramuscular administration. Atropine disappears rapidly from the blood and is distributed throughout the various body tissues and fluids.
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| Pharmacokinetics |
Atropine SulfateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : ¸ðµç Á¦ÇüÀÌ Àß Èí¼öµÊ.
- ºÐÆ÷ : ü³»¿¡ ³Ð°Ô ºÐÆ÷, ÅÂ¹Ý Åë°ú, ¸ðÀ¯¿¡ ¹Ì·® ºÐÆ÷, Ç÷¾×³ú°ü¹® Åë°ú
- ´ë»ç : °£´ë»ç
- ¹Ý°¨±â : 2-3½Ã°£
- ¼Ò½Ç : ´ë»çü ¹× ¹Ìº¯Èü·Î¼ ´¢¸¦ ÅëÇØ ¹è¼³µÊ (30-50%)
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| Biotransformation |
Atropine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Much of the drug is destroyed by enzymatic hydrolysis, particularly in the liver. From 13 to 50% is excreted unchanged in the urine.
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| Toxicity |
Atropine¿¡ ´ëÇÑ Toxicity Á¤º¸ Oral, mouse: LD50 = 75 mg/kg. Symptoms of overdose includes widespread paralysis of parasympathetically innervated organs. Dry mucous membranes, widely dilated and nonresponsive pupils, tachycardia, fever and cutaneous flush are especially prominent, as are mental and neurological symptoms. In instances of severe intoxication, respiratory depression, coma, circulatory collapse and death may occur.
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| Drug Interactions |
Atropine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Atropine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Avoid alcohol.Take with food.
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| Drug Target |
[Drug Target]
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| Description |
Atropine¿¡ ´ëÇÑ Description Á¤º¸ An alkaloid, originally from Atropa belladonna, but found in other plants, mainly solanaceae. [PubChem]
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| Drug Category |
Atropine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Adjuvants, AnesthesiaAnti-Arrhythmia AgentsBronchodilator AgentsMuscarinic AntagonistsMydriaticsParasympatholytics
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| Smiles String Canonical |
Atropine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CN1C2CCC1CC(C2)OC(=O)C(CO)C1=CC=CC=C1
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| Smiles String Isomeric |
Atropine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CN1[C@H]2CC[C@@H]1C[C@H](C2)OC(=O)[C@@H](CO)C1=CC=CC=C1
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| InChI Identifier |
Atropine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3/t13-,14+,15?,16?
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| Chemical IUPAC Name |
Atropine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ [(1R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 3-hydroxy-2-phenylpropanoate
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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