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    | Mechanism of Action | 
    
       Prednisolone¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Glucocorticoids such as Prednisolone can inhibit leukocyte infiltration at the site of inflammation, interfere with mediators of inflammatory response, and suppress humoral immune responses. The antiinflammatory actions of glucocorticoids are thought to involve phospholipase A2 inhibitory proteins, lipocortins, which control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes. Prednisolone reduces inflammatory reaction by limiting the capillary dilatation and permeability of the vascular structures. These compounds restrict the accumulation of polymorphonuclear leukocytes and macrophages and reduce the release of vasoactive kinins. Recent research suggests that corticosteroids may inhibit the release of arachidonic acid from phospholipids, thereby reducing the formation of prostaglandins. Prednisolone is a glucocorticoid receptor agonist. On binding, the corticoreceptor-ligand complex translocates itself into the cell nucleus, where it binds to many glucocorticoid response elements (GRE) in the promoter region of the target genes. The DNA bound receptor then interacts with basic transcription factors, causing an increase or decrease in expression of specific target genes, including suppression of IL2 (interleukin 2) expression. 
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    | Pharmacology | 
     
       Prednisolone¿¡ ´ëÇÑ Pharmacology Á¤º¸ Prednisolone is a synthetic glucocorticoid used as antiinflammatory or immunosuppressive agent. Prednisolone is indicated in the treatment of various conditions, including congenital adrenal hyperplasia, psoriatic arthritis, systemic lupus erythematosus, bullous dermatitis herpetiformis, seasonal or perennial allergic rhinitis, allergic corneal marginal ulcers, symptomatic sarcoidosis, idiopathic thrombocytopenic purpura in adults, leukemias and lymphomas in adults, and ulcerative colitis. Glucocorticoids are adrenocortical steroids and cause profound and varied metabolic effects. In addition, they modify the body's immune responses to diverse stimuli. 
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    | Metabolism | 
    
       Prednisolone¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4) 
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    | Protein Binding | 
    
       Prednisolone¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Very high (>90%) 
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    | Half-life | 
    
       Prednisolone¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 2-3 hours 
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    | Absorption | 
    
       Prednisolone¿¡ ´ëÇÑ Absorption Á¤º¸ Readily absorbed by gastrointestinal tract, peak plasma concentration is reached 1-2 hours after administration. 
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    | Pharmacokinetics | 
    
       PrednisoloneÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á 
- ´Ü¹é°áÇÕ : 65¡91% (¿ë·® ÀÇÁ¸Àû)
 - ´ë»ç : ÀÏÂ÷ÀûÀ¸·Î °£¿¡¼ ´ë»çµÇ³ª ´ëºÎºÐÀÇ Á¶Á÷¿¡¼µµ ´ë»ç°¡ ÀϾ¸ç ºñȰ¼ºÇü ´ë»çü°¡ »ý¼ºµÈ´Ù.
 - ¹Ý°¨±â : 3.6½Ã°£
 
	-  »ý¸®Àû ¹Ý°¨±â : 18-36½Ã°£
 
	 -  ¸»±â ½ÅÁúȯ ȯÀÚ¿¡¼ÀÇ ¹Ý°¨±â : 3¡5½Ã°£
  
 - ¼Ò½Ç : ´ëºÎºÐ glucuronides, sulfates Æ÷ÇÕü³ª ºñÆ÷ÇÕ ´ë»çü·Î ½Å¹è¼³ µÈ´Ù. 
  
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    | Biotransformation | 
    
       Prednisolone¿¡ ´ëÇÑ Biotransformation Á¤º¸ Excreted in the urine as either free or glucoconjugate. 
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    | Toxicity | 
    
       Prednisolone¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50=500 mg/kg (oral, rat), short-term side effects include high blood glucose levels and fluid retention. Long term side effects include Cushing's syndrome, weight gain, osteoporosis, glaucoma, type II diabetes and adrenal suppression. 
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    | Drug Interactions | 
    
       Prednisolone¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Ambenonium	The corticosteroid decreases the effect of anticholinesterasesEdrophonium	The corticosteroid decreases the effect of anticholinesterasesNeostigmine	The corticosteroid decreases the effect of anticholinesterasesPyridostigmine	The corticosteroid decreases the effect of anticholinesterasesWarfarin	The corticosteroid alters the anticoagulant effectAcenocoumarol	The corticosteroid alters the anticoagulant effectDicumarol	The corticosteroid alters the anticoagulant effectAnisindione	The corticosteroid alters the anticoagulant effectMidodrine	Increased arterial pressureAspirin	The corticosteroid decreases the effect of salicylatesBismuth Subsalicylate	The corticosteroid decreases the effect of salicylatesSalicylate-magnesium	The corticosteroid decreases the effect of salicylatesSalicylate-sodium	The corticosteroid decreases the effect of salicylatesSalsalate	The corticosteroid decreases the effect of salicylatesTrisalicylate-choline	The corticosteroid decreases the effect of salicylatesTalbutal	The barbiturate decreases the effect of the corticosteroidSecobarbital	The barbiturate decreases the effect of the corticosteroidQuinidine barbiturate	The barbiturate decreases the effect of the corticosteroidPrimidone	The barbiturate decreases the effect of the corticosteroidPhenobarbital	The barbiturate decreases the effect of the corticosteroidPentobarbital	The barbiturate decreases the effect of the corticosteroidMethylphenobarbital	The barbiturate decreases the effect of the corticosteroidMethohexital	The barbiturate decreases the effect of the corticosteroidHexobarbital	The barbiturate decreases the effect of the corticosteroidHeptabarbital	The barbiturate decreases the effect of the corticosteroidDihydroquinidine barbiturate	The barbiturate decreases the effect of the corticosteroidButethal	The barbiturate decreases the effect of the corticosteroidButalbital	The barbiturate decreases the effect of the corticosteroidButabarbital	The barbiturate decreases the effect of the corticosteroidAprobarbital	The barbiturate decreases the effect of the corticosteroidAmobarbital	The barbiturate decreases the effect of the corticosteroidChlorotrianisene	The estrogenic agent increases the effect of the corticosteroidClomifene	The estrogenic agent increases the effect of the corticosteroidDiethylstilbestrol	The estrogenic agent increases the effect of the corticosteroidEstradiol	The estrogenic agent increases the effect of the corticosteroidEstriol	The estrogenic agent increases the effect of the corticosteroidConjugated Estrogens	The estrogenic agent increases the effect of the corticosteroidEstrone	The estrogenic agent increases the effect of the corticosteroidEstropipate	The estrogenic agent increases the effect of the corticosteroidEthinyl Estradiol	The estrogenic agent increases the effect of the corticosteroidMestranol	The estrogenic agent increases the effect of the corticosteroidQuinestrol	The estrogenic agent increases the effect of the corticosteroidEthotoin	The enzyme inducer decreases the effect of the corticosteroidFosphenytoin	The enzyme inducer decreases the effect of the corticosteroidMephenytoin	The enzyme inducer decreases the effect of the corticosteroidPhenytoin	The enzyme inducer decreases the effect of the corticosteroidRifampin	The enzyme inducer decreases the effect of the corticosteroidItraconazole	The imidazole increases the effect and toxicity of the corticosteroidKetoconazole	The imidazole increases the effect and toxicity of the corticosteroid 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Food Interaction | 
    
       Prednisolone¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take with food to reduce gastric irritation.Avoid alcohol. Avoid caffeine. 
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    | Drug Target | 
    
      
      [Drug Target]
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    | Description | 
    
       Prednisolone¿¡ ´ëÇÑ Description Á¤º¸ A glucocorticoid with the general properties of the corticosteroids. It is the drug of choice for all conditions in which routine systemic corticosteroid therapy is indicated, except adrenal deficiency states. [PubChem] 
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    | Drug Category | 
    
       Prednisolone¿¡ ´ëÇÑ Drug_Category Á¤º¸ Adrenergic AgentsAnti-inflammatory AgentsAntineoplastic AgentsAntineoplastic Agents, HormonalGlucocorticoids 
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    | Smiles String Canonical | 
    
       Prednisolone¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC12CC(O)C3C(CCC4=CC(=O)C=CC34C)C1CCC2(O)C(=O)CO 
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    | Smiles String Isomeric | 
    
       Prednisolone¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)C=C[C@]34C)[C@@H]1CC[C@]2(O)C(=O)CO 
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    | InChI Identifier | 
    
       Prednisolone¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C21H28O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h5,7,9,14-16,18,22,24,26H,3-4,6,8,10-11H2,1-2H3/t14-,15-,16-,18+,19-,20-,21-/m0/s1 
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    | Chemical IUPAC Name | 
    
       Prednisolone¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one 
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    | Drug-Induced Toxicity Related Proteins | 
    
      PREDNISOLONE ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:DNA topoisomerase 1 Drug:prednisolone Toxicity:appearance of apoptotic cells.  [¹Ù·Î°¡±â] 
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