Parallel stimulation of ACTH, beta-LPH + beta-endorphin and alpha-MSH release by alpha-adrenergic agents in rat anterior pituitary cells in culture

Mol Cell Endocrinol. 1981 Jun;22(3):295-303. doi: 10.1016/0303-7207(81)90038-1.

Abstract

Characteristics of the alpha-adrenergic stimulation of ACTH, beta-endorphin + beta-LPH and alpha-MSH release were studied in rat anterior pituitary cells in primary culture. Parallel changes of ACTH, beta-endorphin + beta-LPH and alpha-MSh release were found under all stimulatory and inhibitory conditions by natural and synthetic catecholamine agonists and antagonists. (-)Epinephrine and (-)norepinephrine lead to a 8--10-fold stimulation of peptide release at ED50 values of 20 and 90 nM, respectively. The stereoselectivity of the alpha-adrenergic stimulatory action on peptide release is indicated by a 100-fold higher activity of (-)- than (+)norepinephrine while (-)epinephrine is 10 times more potent than the corresponding (+) stereoisomer. The involvement of a typical alpha-adrenergic mechanism in the control of release of ACTH, beta-endorphin and related peptides in rat anterior pituitary gland is indicated by the following order of potency of a series of catecholaminergic agents (ED50 values): (-)epinephrine (20 nM) greater than (-)norepinephrine (90 nm) greater than phenylephrine (400 nM) greater than isoproterenol (6000 nM). The stimulatory effect of (-)epinephrine or phenylephrine is completely reversed by low concentrations of the alpha-adrenergic antagonist phentolamine while the beta-adrenergic antagonist propranolol has no effect up to 10 muM. Beside providing an easily accessible pure population of post-synaptic alpha-adrenergic receptors having potential applications as a model for other less accessible alpha-adrenergic brain systems, the present data suggest the possibility of the direct involvement of a catecholamine in the physiological control of ACTH secretion in the rat anterior pituitary gland.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic alpha-Agonists / pharmacology*
  • Adrenocorticotropic Hormone / metabolism*
  • Animals
  • Cells, Cultured
  • Dopamine / pharmacology
  • Endorphins / metabolism*
  • Epinephrine / pharmacology
  • Female
  • Isoproterenol / pharmacology
  • Melanocyte-Stimulating Hormones / metabolism*
  • Norepinephrine / pharmacology
  • Phenylephrine / pharmacology
  • Pituitary Gland, Anterior / metabolism*
  • Rats
  • Serotonin / pharmacology
  • beta-Endorphin
  • beta-Lipotropin / metabolism*

Substances

  • Adrenergic alpha-Agonists
  • Endorphins
  • Phenylephrine
  • Serotonin
  • beta-Endorphin
  • Adrenocorticotropic Hormone
  • Melanocyte-Stimulating Hormones
  • beta-Lipotropin
  • Isoproterenol
  • Dopamine
  • Norepinephrine
  • Epinephrine