Alteration of G alpha subunits mRNA levels in bromocriptine resistant prolactinomas

J Neuroendocrinol. 1996 Oct;8(10):737-46. doi: 10.1046/j.1365-2826.1996.04902.x.

Abstract

Patients with prolactinoma are commonly treated with the D2 dopamine agonist bromocriptine, which in most cases, normalizes prolactin (PRL) levels. However, resistance to bromocriptine has been observed in 5 to 18% of tested prolactinomas and is associated to a decrease in both D2 receptor density and mRNA levels. In this study, we used quantitative RT-PCR to investigate whether expression of G alpha proteins could be also modified in bromocriptine resistant prolactinomas. No difference in G alpha o mRNA levels or in the relative expression of G alpha s between bromocriptine sensitive and bromocriptine resistant prolactinomas was observed. In contrast, the relative expression of G alpha i2 was found to be decreased in bromocriptine resistant prolactinomas when compared to that of bromocriptine sensitive prolactinomas. Interestingly, the relative G alpha i2 expression was correlated to both bromocriptine inhibition of in vitro PRL secretion and D2 receptor mRNA levels. Bromocriptine resistance could thus result from a decrease in D2 dopamine receptors associated with a decrease in G alpha i2 expression.

MeSH terms

  • Adenoma / drug therapy
  • Adenoma / metabolism
  • Adult
  • Bromocriptine / pharmacology*
  • Dopamine Agonists / pharmacology*
  • Drug Resistance, Neoplasm
  • Female
  • GTP-Binding Protein alpha Subunits, Gi-Go / biosynthesis*
  • GTP-Binding Protein alpha Subunits, Gi-Go / genetics
  • Humans
  • Macromolecular Substances
  • Male
  • Pituitary Neoplasms / drug therapy
  • Pituitary Neoplasms / metabolism*
  • Polymerase Chain Reaction
  • Prolactinoma / drug therapy
  • Prolactinoma / metabolism*
  • RNA, Messenger / metabolism*
  • Receptors, Dopamine D2 / agonists
  • Receptors, Dopamine D2 / biosynthesis
  • Reproducibility of Results
  • Transcription, Genetic

Substances

  • Dopamine Agonists
  • Macromolecular Substances
  • RNA, Messenger
  • Receptors, Dopamine D2
  • Bromocriptine
  • GTP-Binding Protein alpha Subunits, Gi-Go