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Denney, K.

Publications and source records attributed to Denney, K..

2 recordsLinked to original sources

Male and Female Mice Are Similarly Susceptible to Chronic Nondiscriminatory Social Defeat Stress Despite Differences in Attack Frequency from Aggressor

RationaleMood disorders are often precipitated by chronic stress and can result in an inability to adapt to the environment and increased vulnerability to challenging experiences. While diagnoses of mood disorders are diagnosed twice as frequently in women than in men, most preclinical chronic social defeat stress mouse models exclude females due to decreased aggression toward female intruders. ObjectivesWe previously reported that the chronic non-discriminatory social defeat stress (CNSDS) paradigm is effective in both sexes, allowing for comparisons between male and female mice. We aimed to improve the screening protocol to identify CD-1 aggressors for use in CNSDS and the method for determining susceptibility to CNSDS. Finally, we aimed to determine whether susceptibility to CNSDS correlated with impaired performance in a satiety- based outcome devaluation task. MethodsWe analyzed CNSDS screening and social defeat sessions to determine appropriate parameters for selecting CD-1 aggressors and investigated aggressions toward male and female intruder mice. We also investigated CNSDS effects on a reward valuation task. ResultsWe observed that despite receiving fewer attacks, female mice are equally susceptible to CNSDS as males and that CNSDS abolished satiety-based outcome devaluation in susceptible male and female mice, but not in resilient male and female mice. ConclusionsThese data suggest that CNSDS-defined susceptible and resilient phenotypes extend to reward behaviors.

neuroscience↗

Chronic social instability stress differentially affects the behavior and the transcriptome of the anterodorsal bed nucleus of the stria terminalis between male and female mice

Abstract Stress is comprised of systemic/physiological and processive/social factors, with social stressors requiring higher limbic processing. Sex is an important aspect of stress research as men and women show differing responses to stress and mood disorder development. We investigated how social stress affects the bed nucleus of the stria terminalis (BNST) and how sex may contribute. We used a chronic social instability stress (CSIS) paradigm to stress male and female mice for approximately 7 weeks. Afterwards, one cohort was used for avoidance behavior testing using the open field test, the elevated plus maze, the light/dark box emergence test, and the novelty suppressed feeding test. A second cohort was used for bulk RNA-sequencing of the anterodorsal (ad)BNST. A third cohort of CRH Cre+/Ai14 reporter mice were used for patch clamp electrophysiology in the adBNST. CSIS caused the females to be less avoidant, while the males became more avoidant. Low estrogen state in the females caused them to be less avoidant than in a high estrogen state. In the adBNST, we found major transcriptomic differences between the males and females. Males increased expression in more genes related to the RNA and protein processing whereas the females upregulated genes related to synaptic transmission. The transcriptome in the males is more sensitive to the stress than the females. Finally, CSIS caused adBNST CRH neurons to be hyperpolarized and have lower input resistance in males. In summary, social stress is differentially regulated between males and females, which may relate to the development of stress-related behavioral changes.

neuroscience↗