Identification
Name Fluocinolone Acetonide
Accession Number DB00591 (APRD00977)
Type small molecule
Description A glucocorticoid derivative used topically in the treatment of various skin disorders. It is usually employed as a cream, gel, lotion, or ointment. It has also been used topically in the treatment of inflammatory eye, ear, and nose disorders. (From Martindale, The Extra Pharmacopoeia, 30th ed, p732). It is also being investigatied by pSivida and Alimera, under the brand name Medidur, as a sustained release intraocular implant for the treatment of diabetic macular edema.
Structure
Categories (*)
Molecular Weight 452.4882
Groups approved
Monoisotopic Weight 452.201045102
Pharmacology
Indication For the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. Also for the treatment of chronic non-infectious uveitis affecting the posterior segment of the eye (Retisert).
Mechanism of action Fluocinolone Acetonide is a corticosteroid that binds to the cytosolic glucocorticoid receptor. After binding the receptor the newly formed receptor-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 the increase in expression of specific target genes. The anti-inflammatory actions of corticosteroids are thought to involve lipocortins, phospholipase A2 inhibitory proteins which, through inhibition arachidonic acid, control the biosynthesis of prostaglandins and leukotrienes. Specifically glucocorticoids induce lipocortin-1 (annexin-1) synthesis, which then binds to cell membranes preventing the phospholipase A2 from coming into contact with its substrate arachidonic acid. This leads to diminished eicosanoid production. Cyclooxygenase (both COX-1 and COX-2) expression is also suppressed, potentiating the effect. In another words, the two main products in inflammation Prostaglandins and Leukotrienes are inhibited by the action of Glucocorticoids. Glucocorticoids also stimulate the lipocortin-1 escaping to the extracellular space, where it binds to the leukocyte membrane receptors and inhibits various inflammatory events: epithelial adhesion, emigration, chemotaxis, phagocytosis, respiratory burst and the release of various inflammatory mediators (lysosomal enzymes, cytokines, tissue plasminogen activator, chemokines etc.) from neutrophils, macrophages and mastocytes. Additionally the immune system is suppressed by corticosteroids due to a decrease in the function of the lymphatic system, a reduction in immunoglobulin and complement concentrations, the precipitation of lymphocytopenia, and interference with antigen-antibody binding. Like other glucocorticoid agents Fluocinolone acetonide acts as a physiological antagonist to insulin by decreasing glycogenesis (formation of glycogen). It also promotes the breakdown of lipids (lipolysis), and proteins, leading to the mobilization of extrahepatic amino acids and ketone bodies. This leads to increased circulating glucose concentrations (in the blood). There is also decreased glycogen formation in the liver.
Absorption Rapidly absorbed (15 minutes)
Protein binding Not Available
Biotransformation Primarily hepatic, corticosteroids are metabolized primarily in the liver and are then excreted by the kidneys.
Route of elimination Corticosteroids are metabolized primarily in the liver and are then excreted by the kidneys. Some of the topical corticosteroids and their metabolites are also excreted into the bile.
Toxicity Not Available
Affected organisms
  • Humans and other mammals
Interactions
Drug Interactions Not Available
Food Interactions Not Available
Glucocorticoid receptor
Name Glucocorticoid receptor
Gene Name NR3C1
Pharmacological action yes
Actions agonist
References
  • Nehme A, Lobenhofer EK, Stamer WD, Edelman JL: Glucocorticoids with different chemical structures but similar glucocorticoid receptor potency regulate subsets of common and unique genes in human trabecular meshwork cells. BMC Med Genomics. 2009 Sep 10;2:58. - Pubmed
DTHybrid score 1.2037
Cytosolic phospholipase A2
Name Cytosolic phospholipase A2
Gene Name PLA2G4A
Actions inhibitor
References
  • Norris JF, Ilderton E, Yardley HJ, Summerly R, Forster S: Utilization of epidermal phospholipase A2 inhibition to monitor topical steroid action. Br J Dermatol. 1984 Jul;111 Suppl 27:195-203. - Pubmed
DTHybrid score 0.4247
Id Partner name Gene Name Score
4512 Cytochrome P450 3A4 CYP3A4 0.1658
1193 Proteinase-activated receptor 1 F2R 0.0777
4118 Cytochrome P450 3A5 CYP3A5 0.0466
1588 Multidrug resistance protein 1 ABCB1 0.0449
234 Plasminogen PLG 0.0448
737 Mineralocorticoid receptor NR3C2 0.0429
614 Progesterone receptor PGR 0.0428
469 Annexin A1 ANXA1 0.0385
588 Chromodomain-helicase-DNA-binding protein 1 CHD1 0.033
6020 Aldehyde oxidase AOX1 0.0319
290 Prostaglandin G/H synthase 2 PTGS2 0.0315
1729 Solute carrier family 22 member 6 SLC22A6 0.0315
756 Sex hormone-binding globulin SHBG 0.0302
6116 Gastric triacylglycerol lipase LIPF 0.0301
1757 Myeloperoxidase MPO 0.0301
1295 Fatty acid synthase FASN 0.028
754 Pancreatic triacylglycerol lipase PNLIP 0.0268
269 Adrenodoxin, mitochondrial FDX1 0.0258
3823 Cytokine receptor common gamma chain IL2RG 0.0254
4132 Chloride channel protein ClC-Ka CLCNKA 0.0225
724 Interleukin-2 receptor alpha chain IL2RA 0.0221
717 Interleukin-2 receptor subunit beta IL2RB 0.0221
813 Neuronal acetylcholine receptor subunit alpha-2 CHRNA2 0.0219
6107 Cytochrome P450 3A7 CYP3A7 0.0209
1770 Phospholipase C PLCL1 0.0206
2841 Phospholipase C plc 0.0206
1759 85 kDa calcium-independent phospholipase A2 PLA2G6 0.0206
6500 Phospholipase A2 PLA2G1B 0.0201
4165 P2Y purinoceptor 2 P2RY2 0.0198
6139 Solute carrier organic anion transporter family member 1A2 SLCO1A2 0.0194
805 Cytochrome P450 11B1, mitochondrial CYP11B1 0.019
430 Follicle-stimulating hormone receptor FSHR 0.0179
617 Muscarinic acetylcholine receptor M2 CHRM2 0.0179
862 Multidrug resistance-associated protein 1 ABCC1 0.0178
4604 Liver carboxylesterase 1 CES1 0.0177
817 DNA topoisomerase 2-alpha TOP2A 0.0173
103 Muscarinic acetylcholine receptor M1 CHRM1 0.0171
6178 UDP-glucuronosyltransferase 2B7 UGT2B7 0.0165
2654 Complement control protein C3L 0.0161
146 Androgen receptor AR 0.0161
5766 NAD-dependent deacetylase sirtuin-5 SIRT5 0.0154
5455 Arylsulfatase A ARSA 0.0146
814 Ryanodine receptor 1 RYR1 0.0146
4203 Histamine N-methyltransferase HNMT 0.0143
3923 Cholinesterase BCHE 0.0142
381 Prolactin receptor PRLR 0.0142
489 Monocarboxylate transporter 2 SLC16A7 0.0137
4119 Cytochrome P450 2D6 CYP2D6 0.013
5718 Cytochrome P450 2A6 CYP2A6 0.0123
4924 Cytochrome P450 2C8 CYP2C8 0.0122
2981 Phospholipase A2, membrane associated PLA2G2A 0.0119
738 Monocarboxylate transporter 1 SLC16A1 0.0112
3947 Xanthine dehydrogenase/oxidase XDH 0.011
6018 UDP-glucuronosyltransferase 1-9 UGT1A9 0.0106
2751 Holliday junction ATP-dependent DNA helicase ruvB ruvB 0.0105
4755 Holliday junction ATP-dependent DNA helicase ruvB ruvB 0.0105
4615 Chain A, Red Copper Protein Nitrosocyanin NE0143 0.0093
6144 Solute carrier family 22 member 2 SLC22A2 0.009
6013 Cytochrome P450 2E1 CYP2E1 0.0085
6024 Cytochrome P450 1A1 CYP1A1 0.0084
3811 Cytochrome P450 19A1 CYP19A1 0.0083
20 Prostaglandin G/H synthase 1 PTGS1 0.0083
54 Prothrombin F2 0.0081
1758 GTPase HRas HRAS 0.0068
4200 Cytochrome P450 1A2 CYP1A2 0.0061
136 Estrogen receptor ESR1 0.0052
364 Corticosteroid 11-beta-dehydrogenase isozyme 1 HSD11B1 0.0048
2300 Lysozyme E 0.0047
3633 Lysozyme R 0.0047
5597 Lysozyme 17 0.0047
6023 Cytochrome P450 11B2, mitochondrial CYP11B2 0.0035
6016 Cytochrome P450 2C19 CYP2C19 0.0034
587 Serum albumin ALB 0.003
1732 ATP-binding cassette sub-family G member 2 ABCG2 0.0028
84 Nuclear receptor 0B1 NR0B1 0.0023
380 Cytochrome P450 17A1 CYP17A1 0.0017
6031 Cytochrome P450 3A43 CYP3A43 0.0014
468 Cytochrome P450 4A11 CYP4A11 0.0014
6017 Cholesterol side-chain cleavage enzyme, mitochondrial CYP11A1 0.0013
1898 Cytochrome P450 1B1 CYP1B1 0.0011
776 Bile salt export pump ABCB11 0.0011
7 Nitric oxide synthase, inducible NOS2 0.0011
1735 Canalicular multispecific organic anion transporter 1 ABCC2 0.0009
6030 Cytochrome P450 2B6 CYP2B6 0.0008
4757 Cytochrome P450 2C9 CYP2C9 0.0007