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Novel drug developmental strategies for treatment‐resistant depression

Major depressive disorder is a leading cause of disability worldwide. Because conventional therapies are ineffective in many patients, novel strategies are needed to overcome treatment‐resistant depression (TRD). Limiting factors of successful drug development in the last decades were the lack of (1...

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Autores principales: Borbély, Éva, Simon, Mária, Fuchs, Eberhard, Wiborg, Ove, Czéh, Boldizsár, Helyes, Zsuzsanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303797/
https://www.ncbi.nlm.nih.gov/pubmed/34822719
http://dx.doi.org/10.1111/bph.15753
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author Borbély, Éva
Simon, Mária
Fuchs, Eberhard
Wiborg, Ove
Czéh, Boldizsár
Helyes, Zsuzsanna
author_facet Borbély, Éva
Simon, Mária
Fuchs, Eberhard
Wiborg, Ove
Czéh, Boldizsár
Helyes, Zsuzsanna
author_sort Borbély, Éva
collection PubMed
description Major depressive disorder is a leading cause of disability worldwide. Because conventional therapies are ineffective in many patients, novel strategies are needed to overcome treatment‐resistant depression (TRD). Limiting factors of successful drug development in the last decades were the lack of (1) knowledge of pathophysiology, (2) translational animal models and (3) objective diagnostic biomarkers. Here, we review novel drug targets and drug candidates currently investigated in Phase I–III clinical trials. The most promising approaches are inhibition of glutamatergic neurotransmission by NMDA and mGlu(5) receptor antagonists, modulation of the opioidergic system by κ receptor antagonists, and hallucinogenic tryptamine derivates. The only registered drug for TRD is the NMDA receptor antagonist, S‐ketamine, but add‐on therapies with second‐generation antipsychotics, certain nutritive, anti‐inflammatory and neuroprotective agents seem to be effective. Currently, there is an intense research focus on large‐scale, high‐throughput omics and neuroimaging studies. These results might provide new insights into molecular mechanisms and potential novel therapeutic strategies.
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spelling pubmed-93037972022-07-28 Novel drug developmental strategies for treatment‐resistant depression Borbély, Éva Simon, Mária Fuchs, Eberhard Wiborg, Ove Czéh, Boldizsár Helyes, Zsuzsanna Br J Pharmacol Review Articles Major depressive disorder is a leading cause of disability worldwide. Because conventional therapies are ineffective in many patients, novel strategies are needed to overcome treatment‐resistant depression (TRD). Limiting factors of successful drug development in the last decades were the lack of (1) knowledge of pathophysiology, (2) translational animal models and (3) objective diagnostic biomarkers. Here, we review novel drug targets and drug candidates currently investigated in Phase I–III clinical trials. The most promising approaches are inhibition of glutamatergic neurotransmission by NMDA and mGlu(5) receptor antagonists, modulation of the opioidergic system by κ receptor antagonists, and hallucinogenic tryptamine derivates. The only registered drug for TRD is the NMDA receptor antagonist, S‐ketamine, but add‐on therapies with second‐generation antipsychotics, certain nutritive, anti‐inflammatory and neuroprotective agents seem to be effective. Currently, there is an intense research focus on large‐scale, high‐throughput omics and neuroimaging studies. These results might provide new insights into molecular mechanisms and potential novel therapeutic strategies. John Wiley and Sons Inc. 2022-01-26 2022-03 /pmc/articles/PMC9303797/ /pubmed/34822719 http://dx.doi.org/10.1111/bph.15753 Text en © 2021 The Authors. British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Review Articles
Borbély, Éva
Simon, Mária
Fuchs, Eberhard
Wiborg, Ove
Czéh, Boldizsár
Helyes, Zsuzsanna
Novel drug developmental strategies for treatment‐resistant depression
title Novel drug developmental strategies for treatment‐resistant depression
title_full Novel drug developmental strategies for treatment‐resistant depression
title_fullStr Novel drug developmental strategies for treatment‐resistant depression
title_full_unstemmed Novel drug developmental strategies for treatment‐resistant depression
title_short Novel drug developmental strategies for treatment‐resistant depression
title_sort novel drug developmental strategies for treatment‐resistant depression
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303797/
https://www.ncbi.nlm.nih.gov/pubmed/34822719
http://dx.doi.org/10.1111/bph.15753
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