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  1. Article ; Online: Advancing preclinical chronic stress models to promote therapeutic discovery for human stress disorders.

    Gyles, Trevonn M / Nestler, Eric J / Parise, Eric M

    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology

    2023  Volume 49, Issue 1, Page(s) 215–226

    Abstract: There is an urgent need to develop more effective treatments for stress-related illnesses, which include depression, post-traumatic stress disorder, and anxiety. We view animal models as playing an essential role in this effort, but to date, such ... ...

    Abstract There is an urgent need to develop more effective treatments for stress-related illnesses, which include depression, post-traumatic stress disorder, and anxiety. We view animal models as playing an essential role in this effort, but to date, such approaches have generally not succeeded in developing therapeutics with new mechanisms of action. This is partly due to the complexity of the brain and its disorders, but also to inherent difficulties in modeling human disorders in rodents and to the incorrect use of animal models: namely, trying to recapitulate a human syndrome in a rodent which is likely not possible as opposed to using animals to understand underlying mechanisms and evaluating potential therapeutic paths. Recent transcriptomic research has established the ability of several different chronic stress procedures in rodents to recapitulate large portions of the molecular pathology seen in postmortem brain tissue of individuals with depression. These findings provide crucial validation for the clear relevance of rodent stress models to better understand the pathophysiology of human stress disorders and help guide therapeutic discovery. In this review, we first discuss the current limitations of preclinical chronic stress models as well as traditional behavioral phenotyping approaches. We then explore opportunities to dramatically enhance the translational use of rodent stress models through the application of new experimental technologies. The goal of this review is to promote the synthesis of these novel approaches in rodents with human cell-based approaches and ultimately with early-phase proof-of-concept studies in humans to develop more effective treatments for human stress disorders.
    MeSH term(s) Animals ; Humans ; Anxiety Disorders/therapy ; Stress Disorders, Post-Traumatic ; Anxiety ; Brain ; Rodentia ; Disease Models, Animal
    Language English
    Publishing date 2023-06-22
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 639471-1
    ISSN 1740-634X ; 0893-133X
    ISSN (online) 1740-634X
    ISSN 0893-133X
    DOI 10.1038/s41386-023-01625-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Astrocytic CREB in nucleus accumbens promotes susceptibility to chronic stress.

    Holt, Leanne M / Gyles, Trevonn M / Parise, Eric M / Minier-Toribio, Angelica / Markovic, Tamara / Rivera, Matthew / Yeh, Szu-Ying / Nestler, Eric J

    bioRxiv : the preprint server for biology

    2024  

    Abstract: Background: Increasing evidence implicates astrocytes in stress and depression in both rodent models and human Major Depressive Disorder (MDD). Despite this, little is known about the transcriptional responses to stress of astrocytes within the nucleus ... ...

    Abstract Background: Increasing evidence implicates astrocytes in stress and depression in both rodent models and human Major Depressive Disorder (MDD). Despite this, little is known about the transcriptional responses to stress of astrocytes within the nucleus accumbens (NAc), a key brain reward region, and their influence on behavioral outcomes.
    Methods: We used whole cell sorting, RNA-sequencing, and bioinformatic analyses to investigate the NAc astrocyte transcriptome in male mice in response to chronic social defeat stress (CSDS). Immunohistochemistry was used to determine stress-induced changes in astrocytic CREB within the NAc. Finally, astrocytic regulation of depression-like behavior was investigated using viral-mediated manipulation of CREB in combination with CSDS.
    Results: We found a robust transcriptional response in NAc astrocytes to CSDS in stressed mice, with changes seen in both stress-susceptible and stress-resilient animals. Bioinformatic analysis revealed CREB, a transcription factor widely studied in neurons, as one of the top-predicted upstream regulators of the NAc astrocyte transcriptome, with opposite activation states seen in resilient versus susceptible mice. This bioinformatic result was confirmed at the protein level with immunohistochemistry. Viral overexpression of CREB selectively in NAc astrocytes promoted susceptibility to chronic stress.
    Conclusions: Together, our data demonstrate that the astrocyte transcriptome responds robustly to CSDS and, for the first time, that transcriptional regulation in astrocytes contributes to depressive-like behaviors. A better understanding of transcriptional regulation in astrocytes may reveal unknown molecular mechanisms underlying neuropsychiatric disorders.
    Language English
    Publishing date 2024-01-16
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2024.01.15.575728
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Sex-Specific Regulation of Stress Susceptibility by the Astrocytic Gene

    Parise, Eric M / Gyles, Trevonn M / Godino, Arthur / Sial, Omar K / Browne, Caleb J / Parise, Lyonna F / Torres-Berrío, Angélica / Salery, Marine / Durand-de Cuttoli, Romain / Rivera, Matthew T / Cardona-Acosta, Astrid M / Holt, Leanne / Markovic, Tamara / van der Zee, Yentl Y / Lorsch, Zachary S / Cathomas, Flurin / Garon, Juliet B / Teague, Collin / Issler, Orna /
    Hamilton, Peter J / Bolaños-Guzmán, Carlos A / Russo, Scott J / Nestler, Eric J

    bioRxiv : the preprint server for biology

    2024  

    Abstract: Major depressive disorder (MDD) is linked to impaired structural and synaptic plasticity in limbic brain regions. Astrocytes, which regulate synapses and are influenced by chronic stress, likely contribute to these changes. We analyzed astrocyte gene ... ...

    Abstract Major depressive disorder (MDD) is linked to impaired structural and synaptic plasticity in limbic brain regions. Astrocytes, which regulate synapses and are influenced by chronic stress, likely contribute to these changes. We analyzed astrocyte gene profiles in the nucleus accumbens (NAc) of humans with MDD and mice exposed to chronic stress.
    Language English
    Publishing date 2024-04-15
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2024.04.12.588724
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: The Resilient Phenotype Induced by Prophylactic Ketamine Exposure During Adolescence Is Mediated by the Ventral Tegmental Area-Nucleus Accumbens Pathway.

    Parise, Eric M / Parise, Lyonna F / Sial, Omar K / Cardona-Acosta, Astrid M / Gyles, Trevonn M / Juarez, Barbara / Chaudhury, Dipesh / Han, Ming-Hu / Nestler, Eric J / Bolaños-Guzmán, Carlos A

    Biological psychiatry

    2021  Volume 90, Issue 7, Page(s) 482–493

    Abstract: Background: Major depressive disorder is prevalent in children and adolescents and is associated with a high degree of morbidity throughout life, with potentially devastating personal consequences and public health impact. The efficacy of ketamine (KET) ...

    Abstract Background: Major depressive disorder is prevalent in children and adolescents and is associated with a high degree of morbidity throughout life, with potentially devastating personal consequences and public health impact. The efficacy of ketamine (KET) as an antidepressant has been demonstrated in adolescent rodents; however, the neurobiological mechanisms underlying these effects are unknown. Recent evidence showed that KET reverses stress-induced (i.e., depressive-like) deficits within major mesocorticolimbic regions, such as the prefrontal cortex, nucleus accumbens (NAc), and hippocampus, in adult rodents. However, little is known about KET's effect in the ventral tegmental area (VTA), which provides the majority of dopaminergic input to these brain regions.
    Methods: We characterized behavioral, biochemical, and electrophysiological effects produced by KET treatment in C57BL/6J male mice during adolescence (n = 7-10 per condition) within the VTA and its major projection regions, namely, the NAc and prefrontal cortex. Subsequently, molecular targets within the VTA-NAc projection were identified for viral gene transfer manipulations to recapitulate the effects of stress or KET treatment.
    Results: Repeated KET treatment produced a robust proresilient response to chronic social defeat stress. This effect was largely driven by Akt signaling activity within the VTA and NAc, and it could be blocked or recapitulated through direct Akt-viral-mediated manipulation. Additionally, we found that the KET-induced resilient phenotype is dependent on VTA-NAc, but not VTA-prefrontal cortex, pathway activity.
    Conclusions: These findings indicate that KET exposure during adolescence produces a proresilient phenotype mediated by changes in Akt intracellular signaling and altered neuronal activity within the VTA-NAc pathway.
    MeSH term(s) Animals ; Depressive Disorder, Major ; Ketamine ; Male ; Mice ; Mice, Inbred C57BL ; Nucleus Accumbens ; Phenotype ; Ventral Tegmental Area
    Chemical Substances Ketamine (690G0D6V8H)
    Language English
    Publishing date 2021-05-08
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 209434-4
    ISSN 1873-2402 ; 0006-3223
    ISSN (online) 1873-2402
    ISSN 0006-3223
    DOI 10.1016/j.biopsych.2021.05.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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