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本文引用的文献

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Fluoxetine effects on behavior and adult hippocampal neurogenesis in female C57BL/6J mice across the estrous cycle.氟西汀对发情周期内雌性 C57BL/6J 小鼠行为和成年海马神经发生的影响。
Psychopharmacology (Berl). 2020 May;237(5):1281-1290. doi: 10.1007/s00213-020-05456-5. Epub 2020 Jan 21.
2
Fighting Females: Neural and Behavioral Consequences of Social Defeat Stress in Female Mice.战斗女性:社会挫败应激对雌性小鼠的神经和行为后果。
Biol Psychiatry. 2019 Nov 1;86(9):657-668. doi: 10.1016/j.biopsych.2019.05.005. Epub 2019 May 13.
3
Are hormones a "female problem" for animal research?激素对于动物研究来说是“女性问题”吗?
Science. 2019 May 31;364(6443):825-826. doi: 10.1126/science.aaw7570.
4
A Novel Method for Chronic Social Defeat Stress in Female Mice.一种用于慢性社交挫败应激雌性小鼠的新方法。
Neuropsychopharmacology. 2018 May;43(6):1276-1283. doi: 10.1038/npp.2017.259. Epub 2017 Nov 1.
5
Establishment of a repeated social defeat stress model in female mice.建立雌性小鼠重复社会挫败应激模型。
Sci Rep. 2017 Oct 9;7(1):12838. doi: 10.1038/s41598-017-12811-8.
6
Vicarious Social Defeat Stress Induces Depression-Related Outcomes in Female Mice.替代性社交挫败应激诱导雌性小鼠产生抑郁相关结局。
Biol Psychiatry. 2018 Jan 1;83(1):9-17. doi: 10.1016/j.biopsych.2017.07.014. Epub 2017 Jul 29.
7
Hierarchical Status Predicts Behavioral Vulnerability and Nucleus Accumbens Metabolic Profile Following Chronic Social Defeat Stress.层级地位预测慢性社会挫败应激后行为易损性和伏隔核代谢特征。
Curr Biol. 2017 Jul 24;27(14):2202-2210.e4. doi: 10.1016/j.cub.2017.06.027. Epub 2017 Jul 14.
8
Female rats are not more variable than male rats: a meta-analysis of neuroscience studies.雌性大鼠并不比雄性大鼠更具变异性:神经科学研究的荟萃分析。
Biol Sex Differ. 2016 Jul 26;7:34. doi: 10.1186/s13293-016-0087-5. eCollection 2016.
9
Sex Differences in Nucleus Accumbens Transcriptome Profiles Associated with Susceptibility versus Resilience to Subchronic Variable Stress.伏隔核转录组图谱中的性别差异与对亚慢性可变应激的易感性和恢复力相关。
J Neurosci. 2015 Dec 16;35(50):16362-76. doi: 10.1523/JNEUROSCI.1392-15.2015.
10
Vicarious social defeat stress: Bridging the gap between physical and emotional stress.替代性社会挫败应激:弥合生理应激与情绪应激之间的差距。
J Neurosci Methods. 2016 Jan 30;258:94-103. doi: 10.1016/j.jneumeth.2015.10.012. Epub 2015 Nov 3.

慢性非歧视性社会挫败是一种有效的慢性应激范式,适用于雄性和雌性小鼠。

Chronic non-discriminatory social defeat is an effective chronic stress paradigm for both male and female mice.

机构信息

Department of Psychology, Behavioral and Systems Neuroscience Area, Rutgers, The State University of New Jersey, 152 Frelinghuysen Rd, Piscataway, NJ, 08854, USA.

Graduate Program in Neuroscience, Rutgers, The State University of New Jersey, New Brunswick, Piscataway, NJ, 08854, USA.

出版信息

Neuropsychopharmacology. 2019 Dec;44(13):2220-2229. doi: 10.1038/s41386-019-0520-7. Epub 2019 Sep 7.

DOI:10.1038/s41386-019-0520-7
PMID:31493767
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6898575/
Abstract

Stress-related mood disorders are more prevalent in females than males, yet preclinical chronic stress paradigms were developed in male rodents and are less effective in female rodents. Here we characterize a novel chronic non-discriminatory social defeat stress (CNSDS) paradigm that results in comparable stress effects in both sexes. Male and female C57BL/6J mice were simultaneously introduced into the home cage of resident CD-1 aggressors for 10 daily 5-min sessions. CD-1 aggressors attacked males and females indiscriminately, resulting in stress resilient and susceptible subpopulations in both sexes. CD-1 aggressors attacked C57BL/6J male intruders faster and more frequently than female intruders. However, CNSDS similarly induced negative valence behaviors in SUS mice of both sexes relative to RES and CNTRL mice. Furthermore, SUS male and female mice displayed similar increases in plasma corticosterone levels following CNSDS exposure relative to pre-stress exposure levels. The estrous cycle did not impact CD-1 attack behavior or negative valence behaviors. Thus, CNSDS induces chronic stress behavioral and neuroendocrine effects in both male and female C57BL/6J mice and allows direct comparisons between sexes. Adoption of this modified social defeat paradigm will help advance the initiative to include female rodents in preclinical chronic stress research.

摘要

应激相关情绪障碍在女性中比男性更为普遍,但临床前慢性应激模型是在雄性啮齿动物中开发的,对雌性啮齿动物的效果较差。在这里,我们描述了一种新的慢性非歧视性社会挫败应激(CNSDS)模型,该模型在两性中均产生可比的应激效应。雄性和雌性 C57BL/6J 小鼠同时被引入到 CD-1 攻击型常驻者的巢箱中进行 10 天的 5 分钟日常攻击。CD-1 攻击型常驻者会无差别地攻击雄性和雌性,从而导致两性中都有应激抗性和应激易感性亚群。CD-1 攻击型常驻者攻击 C57BL/6J 雄性入侵者的速度和频率都高于雌性入侵者。然而,与 RES 和 CNTRL 小鼠相比,CNSDS 同样会诱导 SUS 小鼠产生负性情绪行为,无论其性别如何。此外,与应激前暴露水平相比,SUS 雄性和雌性小鼠在 CNSDS 暴露后血浆皮质酮水平也有相似的升高。发情周期不会影响 CD-1 的攻击行为或负性情绪行为。因此,CNSDS 会在雄性和雌性 C57BL/6J 小鼠中引起慢性应激行为和神经内分泌效应,并允许对两性进行直接比较。采用这种改良的社会挫败模型将有助于推进将雌性啮齿动物纳入临床前慢性应激研究的倡议。