Corticorelin
(Redirected from Corticorelin ovine triflutate)
What is Corticorelin?[edit | edit source]
- Corticorelin (Acthrel; Xerecept) a synthetic peptide that is used for the determination of pituitary corticotrophic responsiveness.
- Corticorelin ovine has an amino acid sequence identical to ovine corticotropin-releasing hormone (oCRH). Corticorelin ovine is an analogue of the naturally occurring human CRH (hCRH) peptide.
- Both peptides are potent stimulators of adrenocorticotropic hormone (ACTH) release from the anterior pituitary. ACTH stimulates cortisol production from the adrenal cortex.
What are the uses of this medicine?[edit | edit source]
- Corticorelin (Acthrel; Xerecept) is used for differentiating pituitary and ectopic production of ACTH in patients with ACTH-dependent Cushing's syndrome.
Differential Diagnosis: There are two forms of Cushing's syndrome:
- ACTH-dependent in which hypercortisolism is due either to pituitary hypersecretion of ACTH.
- ACTH- independent in which hypercortisolism is due to autonomous cortisol secretion by an adrenal tumor.
The corticorelin test is used to aid in establishing the source of excessive ACTH secretion.
How does this medicine work?[edit | edit source]
Acthrel® (corticorelin ovine triflutate for injection) is a sterile, nonpyrogenic, lyophilized white cake powder, containing corticorelin ovine triflutate, a trifluoroacetate salt of a synthetic peptide that is used for the determination of pituitary corticotrophic responsiveness. Corticorelin ovine has an amino acid sequence identical to ovine corticotropin-releasing hormone (oCRH). Corticorelin ovine is an analogue of the naturally occurring human CRH (hCRH) peptide. Both peptides are potent stimulators of adrenocorticotropic hormone (ACTH) release from the anterior pituitary. ACTH stimulates cortisol production from the adrenal cortex.
The corticorelin stimulation test helps to differentiate between the etiologies of ACTH-dependent hypercortisolism as follows:
- High basal plasma ACTH plus high basal plasma cortisol (20 - 40 mcg/dL). Acthrel® injection (1 mcg/kg) results in:
- Increased plasma ACTH levels
- Increased plasma cortisol levels
- Diagnosis: Cushing's disease (ACTH of pituitary origin)
High basal plasma ACTH (may be very high) plus high basal plasma cortisol (20 - 40 mcg/dL). Acthrel® injection (1 mcg/kg) results in:
- Little or no response of plasma ACTH levels
- Little or no response of plasma cortisol levels
- Diagnosis: Ectopic ACTH syndrome
Who Should Not Use this medicine ?[edit | edit source]
This medicine cannot be used in patients:
- with a history of a hypersensitivity reaction to ovine corticorelin or any of its excipients.
What drug interactions can this medicine cause?[edit | edit source]
- Tell your doctor and pharmacist what other prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking or plan to take.
Be sure to mention any of the following:
Is this medicine FDA approved?[edit | edit source]
- Corticorelin ovine triflutate is designated as an orphan drug by the US FDA on 11/24/1989, used in For use in differentiating pituitary and ectopic production of ACTH in patients with ACTH-dependent Cushings syndrome, manufactured / distributed by Ferring Laboratories, Inc.
How should this medicine be used?[edit | edit source]
Recommended dosage:
- A single intravenous dose of Acthrel® at 1 mcg/kg is recommended for the testing of pituitary corticotrophin function.
Administration:
- The preparation is intended for intravenous administration.
What are the dosage forms and brand names of this medicine?[edit | edit source]
This medicine is available in fallowing doasage form:
- As Acthrel® for injection is available in vials containing 100 mcg corticorelin ovine
This medicine is available in fallowing brand namesː
- Acthrel
What side effects can this medication cause?[edit | edit source]
The most common side effects of this medicine include:
- dyspnea
- wheezing
- urticaria
- angioedema
- flushing
- tachycardia
- hypotension
- dyspnea
- "chest compression" or tightness
What special precautions should I follow?[edit | edit source]
- The severity of adverse effects to a corticorelin injection appear to be dose-dependent. Dosages above 1 mcg/kg are not recommended. While few adverse effects have been observed at the 1 mcg/kg or 100 mcg dose, higher doses have been associated with transient tachycardia, decreased blood pressure, loss of consciousness, and asystole.
- Hypersensitivity reactions have been reported in patients receiving Acthrel. Discontinue Acthrel, monitor and treat if indicated.
- It is not known whether corticorelin is secreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Acthrel is administered to a nursing woman.
What to do in case of emergency/overdose?[edit | edit source]
Symptoms of overdosage may include:
- severe facial flushing
- cardiovascular changes
- dyspnea
Management of overdosage:
- In the event of toxic overdose, adverse effects should be treated symptomatically.
Can this medicine be used in pregnancy?[edit | edit source]
- It is also not known whether corticorelin can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity.
- Acthrel should be given to a pregnant woman only if clearly needed.
Can this medicine be used in children?[edit | edit source]
- Only a few tests have been performed on children.
- Dosages were 1 mcg/kg body weight.
What are the active and inactive ingredients in this medicine?[edit | edit source]
Active ingredients:
- CORTICORELIN OVINE TRIFLUTATE
Inactive ingredient:
- ASCORBIC ACID
- LACTOSE, UNSPECIFIED FORM
- CYSTEINE HYDROCHLORIDE
Who manufactures and distributes this medicine?[edit | edit source]
Manufactured for:
- Ferring Pharmaceuticals Inc.
- Parsippany, NJ
What should I know about storage and disposal of this medication?[edit | edit source]
- Acthrel is stable in the lyophilized form when stored refrigerated at 2°C to 8°C (36°F to 46°F) and protected from light.
- The reconstituted solution is stable up to 8 hours under refrigerated conditions.
- Discard unused reconstituted solution.
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