Abstract
Major depressive disorder (MDD) is a leading cause of morbidity, and the fourth leading cause of disease burden worldwide. While MDD is a treatable condition for many individuals, others suffer from treatment-resistant depression (TRD). Here, we suggest the immunomodulatory compound AS101 as novel therapeutic alternative. We previously showed in animal models that AS101 reduces anxiety-like behavior and elevates levels of the brain-derived neurotrophic factor (BDNF), a protein that has a key role in the pathophysiology of depression. To explore the potential antidepressant properties of AS101, we used the extensively characterized chronic mild stress (CMS) model, and the depressive rat line (DRL Finally, in Exp. 3 to attain insight into the mechanism we knocked down BDNF in the hippocampus, and demonstrated that the beneficial effect of AS101 was abrogated. Together with the previously established safety profile of AS101 in humans, these results may represent the first step towards the development of a novel treatment option for MDD and TRD.
Original language | English |
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Pages (from-to) | 437-446 |
Number of pages | 10 |
Journal | NeuroMolecular Medicine |
Volume | 22 |
Issue number | 3 |
DOIs | |
State | Published - 1 Sep 2020 |
Bibliographical note
Publisher Copyright:© 2020, Springer Science+Business Media, LLC, part of Springer Nature.
Funding
This work was partly supported by: The Comet-Walerstein Cancer Research Program; The Finckler Cancer Research Endowment and the Frida Stollman Cancer Memorial Fund.
Funders | Funder number |
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Finckler Cancer Research Endowment | |
Frida Stollman Cancer Memorial Fund | |
Damon Runyon Cancer Research Foundation |
Keywords
- AS101
- BDNF
- Chronic mild stress
- Depression
- Major depressive disorder