Abstract
Introduction: Pancreatic β-cells synthetize and store Serotonin (5-Hydroxytriptamine, 5HT) which
is co-released with insulin. It has been proposed that extracellular 5HT binds to
specific cell surface receptors and modulate insulin secretion. On the other hand,
Selective Serotonin Reuptake Inhibitor (SSRI) fluoxetine seems to reduce Glucose-Stimulated
Insulin Secretion (GSIS). However, it is unknown whether this effect results from
changes in extracellular 5HT concentration owed to the blockade of 5HT transporter
(SERT) or from non-5HT dependent actions. The aims of this work were: 1) to quantify
extracellular 5HT levels and GSIS in β-cell lines, 2) to determine whether extracellular
5HT levels and GSIS are changed by fluoxetine or 5-Hydroxytryptophan (5HTP, the immediate
5HT biosynthetic precursor), and 3) to quantify the expression of Slc6a4 gene (encoding
SERT) in β-cell lines in relation to other genes involved in 5HT system.
Material and Methods: β-cell lines MIN6 and RINm5f were subjected to GSIS protocols, after treatment with
fluoxetine, 5HTP or 5HT. Insulin and 5HT were quantified by ELISA and HPLC, respectively.
Relative mRNA expression was quantified by RT-qPCR.
Results: MIN6 β-cells secretes 5HT in response to glucose, showing a sharp increase in 5HT
release when cells were preloaded with 5HTP. Treatment with 5HT or fluoxetine reduces
GSIS. Fluoxetine fails to further increases 5HTP-induced elevation of secreted 5HT.
MIN6 β-cells express both isoforms of Tryptophan Hydroxylase (Tph1 and Tph2), and
have high expression levels of L-Dopa decarboxylase (Ddc), both enzymes involved in
5HT biosynthetic pathway, but do not express the 5HT transporters Slc6a4 or Slc6a3
(the Dopamine-5HT transporter) genes.
Conclusion: The inhibitory effect of fluoxetine on β-cell glucose stimulated insulin secretion
is not mediated by blockage of 5HT transporter through SERT.
Key words
β-cell - insulin secretion - serotonin - fluoxetine