Sex Differences in the Neuroadaptations of Reward-related Circuits in Response to Subchronic Variable Stress. (15th April 2018)
- Record Type:
- Journal Article
- Title:
- Sex Differences in the Neuroadaptations of Reward-related Circuits in Response to Subchronic Variable Stress. (15th April 2018)
- Main Title:
- Sex Differences in the Neuroadaptations of Reward-related Circuits in Response to Subchronic Variable Stress
- Authors:
- Zhang, Song
Zhang, Hongxing
Ku, Stacy M.
Juarez, Barbara
Morel, Carole
Tzavaras, Nikos
Montgomery, Sarah
Hodes, Georgia E.
Brancato, Anna
Russo, Scott J.
Cao, Jun-Li
Han, Ming-Hu - Abstract:
- Highlights: We replicated that SCVS induced a depressed susceptible phenotype in female but not male mice. The firing activity of LHb-VTA circuit neurons was dramatically increased selectively in female mice that underwent SCVS. VTA dopamine neurons and LC-VTA circuit did not display firing differences between stressed and control mice in both sexes. Abstract: Women are twice as likely to be diagnosed with major depressive disorder. However, fewer studies in rodent models of depression have used female animals, leading to a relative lack of understanding of the female brain's response to stress, especially at a neural circuit level. In this study, we utilized a 6-day subchronic variable stress (SCVS) mouse model and measured novelty suppressed feeding as behavioral criteria to evaluate susceptibility to SCVS in male and female mice. First, we showed that SCVS induced a decrease in latency to eat (susceptible phenotype) in female mice, but not in males (resilient phenotype). After determining behavioral phenotypes, we investigated the firing activities of dopamine (DA) neurons in the ventral tegmental area (VTA), as well as the neurons that project from lateral habenula (LHb) to the VTA and from locus coeruleus (LC) to the VTA. Utilizing retrograding lumafluor fluorescent tracers and electrophysiology techniques, we performed cell type- and circuit-specific measures of neuronal firing rates. Our data show that SCVS significantly increased the firing rate of LHb-VTA circuitHighlights: We replicated that SCVS induced a depressed susceptible phenotype in female but not male mice. The firing activity of LHb-VTA circuit neurons was dramatically increased selectively in female mice that underwent SCVS. VTA dopamine neurons and LC-VTA circuit did not display firing differences between stressed and control mice in both sexes. Abstract: Women are twice as likely to be diagnosed with major depressive disorder. However, fewer studies in rodent models of depression have used female animals, leading to a relative lack of understanding of the female brain's response to stress, especially at a neural circuit level. In this study, we utilized a 6-day subchronic variable stress (SCVS) mouse model and measured novelty suppressed feeding as behavioral criteria to evaluate susceptibility to SCVS in male and female mice. First, we showed that SCVS induced a decrease in latency to eat (susceptible phenotype) in female mice, but not in males (resilient phenotype). After determining behavioral phenotypes, we investigated the firing activities of dopamine (DA) neurons in the ventral tegmental area (VTA), as well as the neurons that project from lateral habenula (LHb) to the VTA and from locus coeruleus (LC) to the VTA. Utilizing retrograding lumafluor fluorescent tracers and electrophysiology techniques, we performed cell type- and circuit-specific measures of neuronal firing rates. Our data show that SCVS significantly increased the firing rate of LHb-VTA circuit neurons in female mice when compared to that of their female controls, an effect that was absent in SCVS-exposed males. Interestingly, SCVS did not induce significant firing alterations in VTA DA neurons and LC-VTA circuit neurons in either female mice or male mice when compared to their stress-naïve controls. Overall, our data show sex differences in the LHb-VTA circuit responses to SCVS, and implicates a potential role of this projection in mediating vulnerability of female mice to stress-induced depression. … (more)
- Is Part Of:
- Neuroscience. Volume 376(2018)
- Journal:
- Neuroscience
- Issue:
- Volume 376(2018)
- Issue Display:
- Volume 376, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 376
- Issue:
- 2018
- Issue Sort Value:
- 2018-0376-2018-0000
- Page Start:
- 108
- Page End:
- 116
- Publication Date:
- 2018-04-15
- Subjects:
- aCSF artificial cerebrospinal fluid -- CMS chronic mild stress -- CRF corticotropin-releasing factor -- DA dopamine -- DBS deep-brain stimulation -- LC locus coeruleus -- LH learned helplessness -- LHb lateral habenula -- MHb medial habenula -- NAc nucleus accumbens -- NE norepinephrine -- NSF novelty suppressed feeding -- RSDS repeated social defeat stress -- SCVS subchronic variable stress -- VTA ventral tegmental area
sex difference -- major depression -- neuronal activity -- ventral tegmental area -- lateral habenula -- locus coeruleus
Neurochemistry -- Periodicals
Neurophysiology -- Periodicals
Neurology -- Periodicals
Neurochimie -- Périodiques
Neurophysiologie -- Périodiques
Neurochemistry
Neurophysiology
Electronic journals
Periodicals
Electronic journals
612.8 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03064522 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/03064522 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/03064522 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neuroscience.2018.02.021 ↗
- Languages:
- English
- ISSNs:
- 0306-4522
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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