Cortifen: Difference between revisions
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== Cortifen == | |||
[[File:Cortifen.svg|thumb|right|Chemical structure of Cortifen]] | |||
Cortifen is used | '''Cortifen''' is a synthetic [[corticosteroid]] used primarily for its anti-inflammatory and immunosuppressive properties. It is commonly prescribed in the treatment of various inflammatory and autoimmune conditions. Cortifen is known for its efficacy in reducing inflammation and modulating the immune response, making it a valuable therapeutic agent in clinical medicine. | ||
== Pharmacology == | |||
Cortifen functions by mimicking the effects of naturally occurring [[glucocorticoids]] in the body. It binds to the [[glucocorticoid receptor]], which then translocates to the cell nucleus and influences the expression of specific genes. This action results in the suppression of pro-inflammatory cytokines and the promotion of anti-inflammatory proteins. | |||
=== Mechanism of Action === | |||
The primary mechanism of action of Cortifen involves the inhibition of [[phospholipase A2]], an enzyme responsible for the release of [[arachidonic acid]] from membrane phospholipids. This inhibition leads to a decrease in the synthesis of [[prostaglandins]] and [[leukotrienes]], which are potent mediators of inflammation. | |||
=== Pharmacokinetics === | |||
Cortifen is well absorbed when administered orally, with peak plasma concentrations occurring within 1 to 2 hours. It is extensively metabolized in the liver and excreted primarily in the urine. The half-life of Cortifen is approximately 3 to 4 hours, but its biological effects can last much longer due to its influence on gene expression. | |||
== Clinical Uses == | |||
Cortifen is indicated for a variety of conditions, including: | |||
* [[Rheumatoid arthritis]] | |||
* [[Systemic lupus erythematosus]] | |||
* [[Asthma]] | * [[Asthma]] | ||
* [[ | * [[Inflammatory bowel disease]] | ||
* [[ | * [[Allergic reactions]] | ||
It is also used in the management of [[adrenal insufficiency]] and as part of the treatment regimen for certain [[cancers]]. | |||
== Side Effects == | == Side Effects == | ||
[[File:Cortifen.svg|thumb|left|Cortifen molecule]] | |||
The use of Cortifen can lead to a range of side effects, particularly with long-term use. Common side effects include: | |||
* [[Hypertension]] | |||
* [[Hyperglycemia]] | |||
* [[Osteoporosis]] | |||
* [[Weight gain]] | * [[Weight gain]] | ||
* [[Mood changes]] | * [[Mood changes]] | ||
Patients on prolonged Cortifen therapy are also at risk for [[adrenal suppression]], which necessitates careful tapering of the drug to avoid withdrawal symptoms. | |||
== | == Contraindications == | ||
Cortifen is contraindicated in patients with systemic fungal infections and those with known hypersensitivity to the drug. Caution is advised in patients with [[peptic ulcer disease]], [[diabetes mellitus]], and [[hypertension]]. | |||
== | == Related pages == | ||
* [[ | * [[Corticosteroid]] | ||
* [[Glucocorticoid]] | |||
* [[Inflammation]] | * [[Inflammation]] | ||
* [[ | * [[Immunosuppression]] | ||
[[Category:Pharmacology]] | |||
[[Category:Anti-inflammatory agents]] | |||
Latest revision as of 04:02, 13 February 2025
Cortifen[edit]
Cortifen is a synthetic corticosteroid used primarily for its anti-inflammatory and immunosuppressive properties. It is commonly prescribed in the treatment of various inflammatory and autoimmune conditions. Cortifen is known for its efficacy in reducing inflammation and modulating the immune response, making it a valuable therapeutic agent in clinical medicine.
Pharmacology[edit]
Cortifen functions by mimicking the effects of naturally occurring glucocorticoids in the body. It binds to the glucocorticoid receptor, which then translocates to the cell nucleus and influences the expression of specific genes. This action results in the suppression of pro-inflammatory cytokines and the promotion of anti-inflammatory proteins.
Mechanism of Action[edit]
The primary mechanism of action of Cortifen involves the inhibition of phospholipase A2, an enzyme responsible for the release of arachidonic acid from membrane phospholipids. This inhibition leads to a decrease in the synthesis of prostaglandins and leukotrienes, which are potent mediators of inflammation.
Pharmacokinetics[edit]
Cortifen is well absorbed when administered orally, with peak plasma concentrations occurring within 1 to 2 hours. It is extensively metabolized in the liver and excreted primarily in the urine. The half-life of Cortifen is approximately 3 to 4 hours, but its biological effects can last much longer due to its influence on gene expression.
Clinical Uses[edit]
Cortifen is indicated for a variety of conditions, including:
- Rheumatoid arthritis
- Systemic lupus erythematosus
- Asthma
- Inflammatory bowel disease
- Allergic reactions
It is also used in the management of adrenal insufficiency and as part of the treatment regimen for certain cancers.
Side Effects[edit]
The use of Cortifen can lead to a range of side effects, particularly with long-term use. Common side effects include:
Patients on prolonged Cortifen therapy are also at risk for adrenal suppression, which necessitates careful tapering of the drug to avoid withdrawal symptoms.
Contraindications[edit]
Cortifen is contraindicated in patients with systemic fungal infections and those with known hypersensitivity to the drug. Caution is advised in patients with peptic ulcer disease, diabetes mellitus, and hypertension.
