Dopamine Receptor Expression and Function in Corticotroph Pituitary Tumors

Rosario Pivonello, Diego Ferone, Wouter W. De Herder, Johan M. Kros, Maria Laura Del Basso De Caro, Marica Arvigo, Lucio Annunziato, Gaetano Lombardi, Annamaria Colao, Leo J. Hofland, Steven W J Lamberts

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The role of dopamine agonist treatment in corticotroph pituitary tumors is controversial. The aim of this study was to evaluate D2 receptor expression in 20 corticotroph pituitary tumors and to correlate it to the in vitro effect of dopamine agonists on ACTH secretion and the in vivo effect of short-term cabergoline treatment on cortisol secretion. D2 expression was evaluated by receptor-ligand binding, immunohistochemistry, and RT-PCR. A 50% or more decrease in daily urinary cortisol levels was considered a significant clinical response. At receptor-ligand binding, specific binding of [125I]epidepride was found in 80% of cases. At immunohistochemistry, specific D2 immunostaining was found in 75% of cases. D2 expression was found in 83.3% of cases (D2long in 40%, D2short in 20%, and both in 40%) by RT-PCR. Significant in vitro inhibition of ACTH secretion was found in 100% of D2-positive cases, but not in 100% of D2-negative cases by either bromocriptine or cabergoline. A significant in vivo inhibition of cortisol secretion after 3-month cabergoline treatment was found in 60%, although a normalization of cortisol secretion was found in 40% of cases. All cabergoline-responsive cases were associated with D2 expression, whereas all noncabergoline-responsive cases but one were not associated with D2 expression. In conclusion, functional D2 receptors were expressed in approximately 80% of corticotroph pituitary tumors. The effectiveness of cabergoline in normalizing cortisol secretion in 40% of cases supports its therapeutic use in the management of Cushing's disease.

Original languageEnglish
Pages (from-to)2452-2462
Number of pages11
JournalJournal of Clinical Endocrinology and Metabolism
Issue number5
Publication statusPublished - May 2004

ASJC Scopus subject areas

  • Biochemistry
  • Endocrinology, Diabetes and Metabolism


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