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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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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. |
format | Online Article Text |
id | pubmed-9303797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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