Demeclocycline: Difference between revisions
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'''Demeclocycline''' (marketed as '''Declomycin''', '''Declostatin''' and '''Ledermycin''') is a member of the [[tetracycline antibiotics]] group used in various types of [[bacteria]]l [[infection]]s. One of its other registered uses is the treatment of [[hyponatremia]] (low blood [[sodium]] concentration) due to the [[syndrome of inappropriate antidiuretic hormone]] (SIADH) where fluid restriction alone has been ineffective. It is derived from the ''Streptomyces aureofaciens'' fungal strain. | '''Demeclocycline''' (marketed as '''Declomycin''', '''Declostatin''' and '''Ledermycin''') is a member of the [[tetracycline antibiotics]] group used in various types of [[bacteria]]l [[infection]]s. One of its other registered uses is the treatment of [[hyponatremia]] (low blood [[sodium]] concentration) due to the [[syndrome of inappropriate antidiuretic hormone]] (SIADH) where fluid restriction alone has been ineffective. It is derived from the ''Streptomyces aureofaciens'' fungal strain. | ||
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Revision as of 00:34, 9 August 2012
File:Demeclocycline structure.svg | |
Clinical data | |
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Pregnancy category |
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Routes of administration | Oral 150 mg/300 mg |
ATC code | |
Pharmacokinetic data | |
Protein binding | 41-50% |
Metabolism | Hepatic |
Elimination half-life | 10-17 hours |
Identifiers | |
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CAS Number | |
PubChem CID | |
DrugBank | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C21H21ClN2O8 |
Molar mass | 464.853 g/mol |
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Demeclocycline (marketed as Declomycin, Declostatin and Ledermycin) is a member of the tetracycline antibiotics group used in various types of bacterial infections. One of its other registered uses is the treatment of hyponatremia (low blood sodium concentration) due to the syndrome of inappropriate antidiuretic hormone (SIADH) where fluid restriction alone has been ineffective. It is derived from the Streptomyces aureofaciens fungal strain.
Mode of action
Its use as an antibiotic is particularly in Lyme disease, acne and bronchitis. Resistance is gradually becoming more common. As with related tetracycline antibiotics, demeclocycline acts by binding to the 30S- and 50S-RNA, which impairs protein synthesis by bacteria. It is therefore bacteriostatic (it impairs bacterial growth but does not kill bacteria directly). Demeclocycline is rarely used for infections.
The use in SIADH actually relies on a side-effect of tetracycline antibiotics; many may cause diabetes insipidus (dehydration due to the inability to concentrate urine). It is not completely understood why demeclocycline impairs the action of antidiuretic hormone, but it is thought that it blocks the binding of the hormone to its receptor.[1]
Side-effects and interactions
These are similar to other tetracyclines. Hypersensitivity may occur. Skin reactions with sunlight have been reported.
Contraindications
As other tetracyclines, demeclocycline is contraindicated in children and pregnant or nursing women. All members of this class interfere with bone development and may discolour teeth. Tetracyclines bind with cations such as calcium and magnesium and becomes insoluble and inabsorbable for the GI tract. Tetracyclines should not be given with milk or antacids.
References
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- Tetracycline antibiotics