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Vol. 56, Issue 3, 552-561, September 1999
European Institute for Peptide Research (Institut
Fédératif de Recherches Multidisciplinaires sur les
Peptides 23), Laboratory of Cellular and Molecular
Neuroendocrinology, Institut National de la Santé et de la
Recherche Médicale, Unité Associée Centre
National de la Recherche Scientifique, University of Rouen,
Mont-Saint-Aignan, France
Serotonin (5-hydroxytryptamine; 5-HT) is a potent stimulator of
aldosterone secretion in the rat adrenal gland but the type of receptor
involved in the mechanism of action of 5-HT remains unknown. The aim of
the present study was to determine the pharmacological profile and to
clone the receptor responsible for the corticotropic effect of 5-HT in
rat glomerulosa cells. A series of 10 serotonergic receptor agonists
and 12 receptor antagonists was used to characterize the receptor
mediating the effect of 5-HT on aldosterone secretion from perifused
rat adrenocortical slices. Correlation analysis between the potencies
of the different compounds in our model and those previously reported
for various recombinant 5-HT receptors showed that the rat adrenal 5-HT
receptor exhibits the same pharmacological profile as the
5-HT7 receptor transiently expressed in COS-7 cells (r = 0.82 for agonists, p < .05; r = 0.83 for antagonists,
p < .01). Polymerase chain reaction with specific
primers revealed the expression of 5-HT7 receptor mRNA in
the rat adrenal gland. Cloning of the polymerase chain reaction
product confirmed that the amplified DNA corresponded to the
5-HT7 receptor cDNA sequence. Western blot analysis showed
the presence of a protein with an apparent molecular mass of 66 kDa in
the adrenal cortex but not in the medulla. Taken together, these data
demonstrate that the rat adrenal glomerulosa expresses functional
5-HT7 receptors. Rat glomerulosa cells will thus provide a
robust and sensitive bioassay for future studies on native
5-HT7 receptors.
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