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Sex-specific prefrontal-hypothalamic control of behavior and stress responding

Depression and cardiovascular disease are both augmented by daily life stress. Yet, the biological mechanisms that translate psychological stress into affective and physiological outcomes are unknown. Previously, we demonstrated that stimulation of the ventromedial prefrontal cortex (vmPFC) has sexu...

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Autores principales: Schaeuble, Derek, Wallace, Tyler, Pace, Sebastian A., Hentges, Shane T., Myers, Brent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10369879/
https://www.ncbi.nlm.nih.gov/pubmed/37502938
http://dx.doi.org/10.1101/2023.07.09.548297
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author Schaeuble, Derek
Wallace, Tyler
Pace, Sebastian A.
Hentges, Shane T.
Myers, Brent
author_facet Schaeuble, Derek
Wallace, Tyler
Pace, Sebastian A.
Hentges, Shane T.
Myers, Brent
author_sort Schaeuble, Derek
collection PubMed
description Depression and cardiovascular disease are both augmented by daily life stress. Yet, the biological mechanisms that translate psychological stress into affective and physiological outcomes are unknown. Previously, we demonstrated that stimulation of the ventromedial prefrontal cortex (vmPFC) has sexually divergent outcomes on behavior and physiology. Importantly, the vmPFC does not innervate the brain regions that initiate autonomic or neuroendocrine stress responses; thus, we hypothesized that intermediate synapses integrate cortical information to regulate stress responding. The posterior hypothalamus (PH) directly innervates stress-effector regions and receives substantial innervation from the vmPFC. In the current studies, circuit-specific approaches examined whether vmPFC synapses in the PH coordinate stress responding. Here we tested the effects of optogenetic vmPFC-PH circuit stimulation in male and female rats on social and motivational behaviors as well as physiological stress responses. Additionally, an intersectional genetic approach was used to knock down synaptobrevin in PH-projecting vmPFC neurons. Our collective results indicate that male vmPFC-PH circuitry promotes positive motivational valence and is both sufficient and necessary to reduce sympathetic-mediated stress responses. In females, the vmPFC-PH circuit does not affect social or preference behaviors but is sufficient and necessary to elevate neuroendocrine stress responses. Altogether, these data suggest cortical regulation of stress reactivity and behavior is mediated, in part, by projections to the hypothalamus that function in a sex-specific manner.
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spelling pubmed-103698792023-07-27 Sex-specific prefrontal-hypothalamic control of behavior and stress responding Schaeuble, Derek Wallace, Tyler Pace, Sebastian A. Hentges, Shane T. Myers, Brent bioRxiv Article Depression and cardiovascular disease are both augmented by daily life stress. Yet, the biological mechanisms that translate psychological stress into affective and physiological outcomes are unknown. Previously, we demonstrated that stimulation of the ventromedial prefrontal cortex (vmPFC) has sexually divergent outcomes on behavior and physiology. Importantly, the vmPFC does not innervate the brain regions that initiate autonomic or neuroendocrine stress responses; thus, we hypothesized that intermediate synapses integrate cortical information to regulate stress responding. The posterior hypothalamus (PH) directly innervates stress-effector regions and receives substantial innervation from the vmPFC. In the current studies, circuit-specific approaches examined whether vmPFC synapses in the PH coordinate stress responding. Here we tested the effects of optogenetic vmPFC-PH circuit stimulation in male and female rats on social and motivational behaviors as well as physiological stress responses. Additionally, an intersectional genetic approach was used to knock down synaptobrevin in PH-projecting vmPFC neurons. Our collective results indicate that male vmPFC-PH circuitry promotes positive motivational valence and is both sufficient and necessary to reduce sympathetic-mediated stress responses. In females, the vmPFC-PH circuit does not affect social or preference behaviors but is sufficient and necessary to elevate neuroendocrine stress responses. Altogether, these data suggest cortical regulation of stress reactivity and behavior is mediated, in part, by projections to the hypothalamus that function in a sex-specific manner. Cold Spring Harbor Laboratory 2023-07-10 /pmc/articles/PMC10369879/ /pubmed/37502938 http://dx.doi.org/10.1101/2023.07.09.548297 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Schaeuble, Derek
Wallace, Tyler
Pace, Sebastian A.
Hentges, Shane T.
Myers, Brent
Sex-specific prefrontal-hypothalamic control of behavior and stress responding
title Sex-specific prefrontal-hypothalamic control of behavior and stress responding
title_full Sex-specific prefrontal-hypothalamic control of behavior and stress responding
title_fullStr Sex-specific prefrontal-hypothalamic control of behavior and stress responding
title_full_unstemmed Sex-specific prefrontal-hypothalamic control of behavior and stress responding
title_short Sex-specific prefrontal-hypothalamic control of behavior and stress responding
title_sort sex-specific prefrontal-hypothalamic control of behavior and stress responding
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10369879/
https://www.ncbi.nlm.nih.gov/pubmed/37502938
http://dx.doi.org/10.1101/2023.07.09.548297
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