Bitte benutzen Sie diese Kennung, um auf die Ressource zu verweisen: http://doi.org/10.25358/openscience-8402
Autoren: El Hamdaoui, Yamina
Zheng, Fang
Fritz, Nikolas
Ye, Lian
Tran, Mai Anh
Schwickert, Kevin
Schirmeister, Tanja
Braeuning, Albert
Lichtenstein, Dajana
Hellmich, Ute A.
Weikert, Dorothee
Heinrich, Markus
Treccani, Giulia
Schäfer, Michael K. E.
Nowak, Gabriel
Nürnberg, Bernd
Alzheimer, Christian
Müller, Christian P.
Friedland, Kristina
Titel: Analysis of hyperforin (St. John’s wort) action at TRPC6 channel leads to the development of a new class of antidepressant drugs
Online-Publikationsdatum: 18-Jan-2023
Erscheinungsdatum: 2022
Sprache des Dokuments: Englisch
Zusammenfassung/Abstract: St. John’s wort is an herb, long used in folk medicine for the treatment of mild depression. Its antidepressant constituent, hyperforin, has properties such as chemical instability and induction of drug-drug interactions that preclude its use for individual pharmacotherapies. Here we identify the transient receptor potential canonical 6 channel (TRPC6) as a druggable target to control anxious and depressive behavior and as a requirement for hyperforin antidepressant action. We demonstrate that TRPC6 deficiency in mice not only results in anxious and depressive behavior, but also reduces excitability of hippocampal CA1 pyramidal neurons and dentate gyrus granule cells. Using electrophysiology and targeted mutagenesis, we show that hyperforin activates the channel via a specific binding motif at TRPC6. We performed an analysis of hyperforin action to develop a new antidepressant drug that uses the same TRPC6 target mechanism for its antidepressant action. We synthesized the hyperforin analog Hyp13, which shows similar binding to TRPC6 and recapitulates TRPC6-dependent anxiolytic and antidepressant effects in mice. Hyp13 does not activate pregnan-X-receptor (PXR) and thereby loses the potential to induce drug-drug interactions. This may provide a new approach to develop better treatments for depression, since depression remains one of the most treatment-resistant mental disorders, warranting the development of effective drugs based on naturally occurring compounds.
DDC-Sachgruppe: 610 Medizin
610 Medical sciences
Veröffentlichende Institution: Johannes Gutenberg-Universität Mainz
Organisationseinheit: FB 09 Chemie, Pharmazie u. Geowissensch.
FB 04 Medizin
Veröffentlichungsort: Mainz
ROR: https://ror.org/023b0x485
DOI: http://doi.org/10.25358/openscience-8402
Version: Published version
Publikationstyp: Zeitschriftenaufsatz
Nutzungsrechte: CC BY
Informationen zu den Nutzungsrechten: https://creativecommons.org/licenses/by/4.0/
Zeitschrift: Molecular psychiatry
27
Seitenzahl oder Artikelnummer: 5070
5085
Verlag: Springer
Erscheinungsdatum: 2022
ISSN: 1476-5578
DOI der Originalveröffentlichung: 10.1038/s41380-022-01804-3
Enthalten in den Sammlungen:DFG-491381577-H

Dateien zu dieser Ressource:
  Datei Beschreibung GrößeFormat
Miniaturbild
analysis_of_hyperforin_st_joh-20230118131954936.pdf3.88 MBAdobe PDFÖffnen/Anzeigen