Ectopic Agouti protein overexpression increases stimulated corticosterone production without effect on adenylate cyclase activity in mouse adrenal cells

Eur J Endocrinol. 2004 Nov;151(5):613-8. doi: 10.1530/eje.0.1510613.

Abstract

Objective: The antagonism of Agouti protein (AP) and Agouti-related protein on melanocortin receptors suggests an inhibitory role in the regulation of steroidogenesis. However, we have previously demonstrated that ectopic AP overexpression increased restraint-induced corticosterone release and adrenal reactivity to ACTH in mice. A high steroidogenic response to ACTH may be a consequence of a stimulatory AP action on the adenylate cyclase (AC) and/or intracellular steroidogenic enzymes. The aim of the present study was to estimate the effect of ectopic AP overexpression on the activity of AC and steroidogenic intracellular enzymes.

Methods: ACTH and forskolin were used for AC stimulation, and dibutyryl cAMP and progesterone were used for stimulation of intracellular steroidogenic enzymes in isolated adrenal cells in male C57Bl/6J mice of two Agouti genotypes: A(y)/a (ectopic AP overexpression) and a/a (absence of AP in all tissues).

Results: ACTH and forskolin increased cAMP accumulation to the same extent in both A(y)/a and a/a mouse adrenal cells (P<0.001; ANOVA), but resulted in higher corticosterone production in A(y)/a mice (P<0.001 for ACTH and P<0.01 for forskolin; ANOVA). Dibutyryl cAMP- and progesterone-induced corticosterone production was higher in A(y)/a mice than in a/a mice (P<0.001 for dibutyryl cAMP and P<0.01 for progesterone; ANOVA).

Conclusions: Ectopic AP overexpression increased stimulated corticosterone production and intracellular steroidogenic enzyme reactivity to cAMP without an effect on AC activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenylyl Cyclases / metabolism*
  • Adrenal Glands / cytology
  • Adrenal Glands / drug effects
  • Adrenal Glands / enzymology
  • Adrenal Glands / metabolism*
  • Adrenocorticotropic Hormone / pharmacology
  • Agouti Signaling Protein
  • Agouti-Related Protein
  • Animals
  • Bucladesine / pharmacology
  • Colforsin / pharmacology
  • Corticosterone / biosynthesis*
  • Cyclic AMP / metabolism
  • Genes, Dominant
  • Genotype
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL / genetics
  • Mutation
  • Progesterone / pharmacology
  • Tissue Distribution

Substances

  • Agouti Signaling Protein
  • Agouti-Related Protein
  • Agrp protein, mouse
  • Intercellular Signaling Peptides and Proteins
  • a protein, mouse
  • Colforsin
  • Progesterone
  • Bucladesine
  • Adrenocorticotropic Hormone
  • Cyclic AMP
  • Adenylyl Cyclases
  • Corticosterone