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Major Depressive Disorder and Kappa Opioid Receptor Antagonists
Major depressive disorder (MDD) is a common psychiatric disease worldwide. The clinical use of tricyclic antidepressants (TCAs), monoamine oxidase inhibitors (MAOIs) and selective serotonin reuptake inhibitors (SSRIs)/serotonin–norepinephrine reuptake inhibitor (SNRIs) for this condition have been w...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871611/ https://www.ncbi.nlm.nih.gov/pubmed/27213169 |
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author | Li, Wei Sun, Huijiao Chen, Hao Yang, Xicheng Xiao, Li Liu, Renyu Shao, Liming Qiu, Zhuibai |
author_facet | Li, Wei Sun, Huijiao Chen, Hao Yang, Xicheng Xiao, Li Liu, Renyu Shao, Liming Qiu, Zhuibai |
author_sort | Li, Wei |
collection | PubMed |
description | Major depressive disorder (MDD) is a common psychiatric disease worldwide. The clinical use of tricyclic antidepressants (TCAs), monoamine oxidase inhibitors (MAOIs) and selective serotonin reuptake inhibitors (SSRIs)/serotonin–norepinephrine reuptake inhibitor (SNRIs) for this condition have been widely accepted, but they were challenged by unacceptable side-effects, potential drug-drug interactions (DDIs) or slow onset/lack of efficacy. The endogenous opioid system is involved in stress and emotion regulatory processes and its role in MDD has been implicated. Although several KOR antagonists including JDTic and PF-04455242 were discontinued in early clinical trials, ALKS 5461 and CERC-501(LY-2456302) survived and entered into Phase-III and Phase-II trials, respectively. Considering the efficacy and safety of early off-label use of buprenorphine in the management of the treatment-resistant depression (TRD), it will be not surprising to predict the potential success of ALKS 5461 (a combination of buprenorphine and ALKS-33) in the near future. Moreover, CERC-501 will be expected to be available as monotherapy or adjuvant therapy with other first-line antidepressants in the treatment of TRD, if ongoing clinical trials continue to provide positive benefit-risk profiles. Emerging new researches might bring more drug candidates targeting the endogenous opioid system to clinical trials to address current challenges in MDD treatment in clinical practice. |
format | Online Article Text |
id | pubmed-4871611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-48716112016-05-18 Major Depressive Disorder and Kappa Opioid Receptor Antagonists Li, Wei Sun, Huijiao Chen, Hao Yang, Xicheng Xiao, Li Liu, Renyu Shao, Liming Qiu, Zhuibai Transl Perioper Pain Med Article Major depressive disorder (MDD) is a common psychiatric disease worldwide. The clinical use of tricyclic antidepressants (TCAs), monoamine oxidase inhibitors (MAOIs) and selective serotonin reuptake inhibitors (SSRIs)/serotonin–norepinephrine reuptake inhibitor (SNRIs) for this condition have been widely accepted, but they were challenged by unacceptable side-effects, potential drug-drug interactions (DDIs) or slow onset/lack of efficacy. The endogenous opioid system is involved in stress and emotion regulatory processes and its role in MDD has been implicated. Although several KOR antagonists including JDTic and PF-04455242 were discontinued in early clinical trials, ALKS 5461 and CERC-501(LY-2456302) survived and entered into Phase-III and Phase-II trials, respectively. Considering the efficacy and safety of early off-label use of buprenorphine in the management of the treatment-resistant depression (TRD), it will be not surprising to predict the potential success of ALKS 5461 (a combination of buprenorphine and ALKS-33) in the near future. Moreover, CERC-501 will be expected to be available as monotherapy or adjuvant therapy with other first-line antidepressants in the treatment of TRD, if ongoing clinical trials continue to provide positive benefit-risk profiles. Emerging new researches might bring more drug candidates targeting the endogenous opioid system to clinical trials to address current challenges in MDD treatment in clinical practice. 2016 /pmc/articles/PMC4871611/ /pubmed/27213169 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Li, Wei Sun, Huijiao Chen, Hao Yang, Xicheng Xiao, Li Liu, Renyu Shao, Liming Qiu, Zhuibai Major Depressive Disorder and Kappa Opioid Receptor Antagonists |
title | Major Depressive Disorder and Kappa Opioid Receptor Antagonists |
title_full | Major Depressive Disorder and Kappa Opioid Receptor Antagonists |
title_fullStr | Major Depressive Disorder and Kappa Opioid Receptor Antagonists |
title_full_unstemmed | Major Depressive Disorder and Kappa Opioid Receptor Antagonists |
title_short | Major Depressive Disorder and Kappa Opioid Receptor Antagonists |
title_sort | major depressive disorder and kappa opioid receptor antagonists |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871611/ https://www.ncbi.nlm.nih.gov/pubmed/27213169 |
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