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Last Updated: 3 years ago

Possible Interaction: Bromocriptine and Adrenocorticotropic Hormone

Research Papers that Mention the Interaction

Previous studies have found that bromocriptine , cyproheptadine, and valproic acid can reduce ACTH secretion in Nelson's syndrome, but none of these agents has achieved widespread use due to their failure to normalize ACTH in most patients.
We conclude that at the doses studied, bromocriptine had the greatest acute effect in suppressing ACTH secretion in Nelson's syndrome, and that combined administration with valproic acid and cyproheptadine did not further increase this acute ACTH-suppressive effect.
The Journal of clinical endocrinology and metabolism  •  1997  |  View Paper
In some cases of Cushing’s syndrome both bromocriptine and lisuride inhibit the secretion of ACTH but it is still unknown if they act at pituitary or at higher levels.
Journal of endocrinological investigation  •  1985  |  View Paper
Significant in vitro inhibition of ACTH secretion was found in 100% of D(2)-positive cases, but not in 100% of D(2)-negative cases by either bromocriptine or cabergoline.
The Journal of clinical endocrinology and metabolism  •  2004  |  View Paper
The administration of bromocriptine was extremely effective in reducing excessive adrenocorticotrophic hormone (ACTH) and cortisol in the blood, which were previously not suppressed by 8 mg dexamethasone and persisted even after removal of the ACTH-producing adenoma in the hypophysis.
Japanese journal of medicine  •  1990  |  View Paper
Cyproheptadine and bromocriptine have been reported to be therapeutic in suppressing ACTH levels in Cushing's disease and Nelson's syndrome.
Clinical endocrinology  •  1990  |  View Paper
We postulate that bromocriptine therapy acted directly on carcinoid tumor cells to directly inhibit corticotropin production by a dopaminergic mechanism.
Archives of internal medicine  •  1987  |  View Paper
A group of cases due to corticotroph adenoma has been reported whose excessive ACTH secretion is reduced by treatment with the dopamine agonist bromocriptine , in which it is suggested that the tumour cells arise from a subset of corticotrophs of pars intermedia origin.(ABSTRACT TRUNCATED AT 400 WORDS)
Clinics in endocrinology and metabolism  •  1985  |  View Paper
Oral administration of either bromocriptine (2.5 mg) or cyproheptadine (8 mg) caused a marked drop in plasma ACTH levels.
Short-term (3-week) treatment with either bromocriptine (7.5 mg/day) or cyproheptadine (12 mg/day) resulted in a marked suppression of basal ACTH release.
Endocrinologia japonica  •  1984  |  View Paper
In this report, we describe a patient with Cushing’s disease in whom an acute inhibition of ACTH and cortisol was demonstrated following bromocriptine and in whom the long term administration of bromocriptine as the sole therapy produced a transient beneficial response.
Subsequently, an inhibitory effect on ACTH secretion was reported using bromocriptine in Cushing’s disease.
Journal of endocrinological investigation  •  1982  |  View Paper
Somatostatin, dexamethasone, bromocriptine , and cyproheptadine in a concentration of 1 microM each inhibited ACTH release by 25 +/- 2%, 35 +/- 2%, 52 +/- 2%, and 61 +/- 4%, respectively, while lysine vasopressin (0.1 microM) and dibutyryl cAMP (5 mM) stimulated ACTH release by 112 +/- 8% and 220 +/- 4%, respectively.
The Journal of clinical endocrinology and metabolism  •  1981  |  View Paper
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