Abstract

Materials and methods Eighteen healthy female subjects participated in this PET study. The selective 5-HT1A receptor antagonist [carbonyl-11C]WAY-100635 was used as radioligand. The hypothalamus as an essential part of the HPA axis and eight control regions of interest and the cerebellum as reference region were defined a priori and delineated on coregistered MR images. DHEAS and cortisol plasma levels were ascertained by morning blood collections on the PET day. The 5-HT1A receptor binding potentials of the target brain regions were correlated with DHEAS, cortisol plasma levels and the ratio of DHEAS / cortisol.

Highlights

  • Serotonin modulates the activity of the hypothalamicpituitary-adrenal (HPA) axis, to a big part through the serotonin-1A receptor (5-HT1A) [1]

  • The 5-HT1A receptor binding potentials of the target brain regions were correlated with dehydroepiandrosterone sulfate (DHEAS), cortisol plasma levels and the ratio of DHEAS / cortisol

  • We found highly significant correlations between the hypothalamic 5-HT1A receptor binding and DHEAS (p=.003) and the ratio of DHEAS / cortisol (p

Read more

Summary

Introduction

Serotonin modulates the activity of the hypothalamicpituitary-adrenal (HPA) axis, to a big part through the serotonin-1A receptor (5-HT1A) [1]. DHEAS and cortisol correlate with Hypothalamic Serotonin-1A Ulrike Moser*1, Wolfgang Wadsak2, Patrycja Stein1, Christoph Spindelegger1, Markus Mitterhauser2,3, Alexander Holik1, Christian Bieglmayer4, Kurt Kletter2, Siegfried Kasper1 and Rupert Lanzenberger1

Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.