Sex differences in social stress
Sex differences in social stress
批准号:
7990375
负责人:
BRIAN C TRAINOR
金额:
$22.95万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-05-01 至 2012-04-30
关键词:
AcuteAffectAffectiveAggressive behaviorAgreementAnhedoniaAnimal ModelAntidepressive AgentsAnxietyAnxiety DisordersBehaviorBehavioralBiological ModelsBiologyBrainBrain-Derived Neurotrophic FactorCaliforniaChronicChronic stressComplexCorticosteroneDataDevelopmentDoseEstrous CycleExhibitsFemaleGonadal HormonesHippocampus (Brain)HumanIndividualLaboratoriesMajor Depressive DisorderMeasuresMediatingMental DepressionModelingMood DisordersMusNeurotransmittersNucleus AccumbensPeromyscusPharmaceutical PreparationsPlayPopulationProceduresReportingRewardsRodentRoleSelective Serotonin Reuptake InhibitorSerotoninSex CharacteristicsSourceStagingStimulusStressTestingVentral Tegmental AreaWithdrawalWomanWorkdentate gyrusinsightinterestmalemenmesolimbic systemmouse modelneurobiological mechanismnovelpublic health relevanceresearch studyresponsesexsocialsocial stress
中文摘要
描述(申请人提供):严重抑郁症影响超过10%的美国人口。有几种治疗方案可供选择,但许多人对治疗、药物治疗或两者兼而有之没有反应。尽管人们一致认为5-羟色胺等神经递质是重要的,但很明显,导致抑郁的机制比简单的5-羟色胺功能缺陷要复杂得多。抑郁症的一个重要特征是,女性患抑郁症的可能性几乎是男性的两倍。焦虑症在女性中也更普遍。然而,由于各种原因,大多数研究抑郁症相关神经生物学机制的动物模型都集中在男性身上。事实上,迫切需要开发模型系统,在模型系统中可以研究与抑郁和焦虑有关的行为,无论男女(Wizemann和Pardue2001)。慢性温和应激程序可以应用于雄性和雌性啮齿类动物,这种模式会导致快感丧失(对有益的刺激失去兴趣)。然而,一些实验室报告说,在复制慢性温和应激对行为的影响方面存在困难。相比之下,社会压力(从属)范式在世界各地的实验室小组中产生了可重复的结果。社交压力会导致明显的行为变化,包括快感缺失和社交回避(或退缩)的显着增加。社会压力的行为效应可以通过慢性但不是急性的抗抑郁药物治疗来逆转。这是相关的,因为慢性但不是急性抗抑郁治疗在治疗人类情感障碍方面是有效的。绝大多数使用社会压力的研究都集中在男性身上。这是因为在大多数种类的啮齿动物中,雌性攻击性是最小的,所以很难利用雌性内部的攻击性来制造社会压力。相比之下,加州雌性老鼠(Permyscus CalforNicus)具有攻击性,因为雄性和雌性都在保卫领土。此外,初步数据显示,在居民-入侵者攻击测试中,女性比男性对皮质酮的反应更大。对特发性抑郁症的洞察,我们希望它将有助于测试机制。尽管我们的模型可能不会提供与应激诱导的抑郁相关的假设。这项申请建议使用加州老鼠独特的生物学来检查神经生物学机制中的性别差异,这些机制介导了社会压力对情感行为的影响。
公共卫生相关性:情感障碍更有可能发生在女性身上,但大多数老鼠模型都专注于雄性,部分原因是后勤问题。我们建议使用社会压力范式来研究加州雄性和雌性小鼠的社交退缩和快感缺乏。我们将研究社会压力对行为和脑源性神经营养因子表达的影响。
英文摘要
DESCRIPTION (provided by applicant): Major depression affects more than 10 percent of the US population. There are several treatment options available, but many individuals do not respond to therapy, medication or both. Despite agreement that neurotransmitters such as serotonin are important, it is clear that the mechanisms contributing to depression are considerably more complex than a simple deficit of serotonin function. One important feature of depression is that women are almost twice as likely as men to be affected by depression. Anxiety disorders are also more prevalent in women. For a variety of reasons however, most animal models examining neurobiological mechanisms related to depression focus on males. Indeed, there is an urgent need for the development of model systems in which behaviors related to depression and anxiety can be studied in both sexes (Wizemann and Pardue 2001). The chronic mild stress procedure can be applied in both male and female rodents, and this paradigm induces anhedonia (loss of interest in a rewarding stimulus). However, some laboratories have reported difficulty in replicating the effects of chronic mild stress on behavior. In contrast, the social stress (subordination) paradigm produces repeatable results in laboratory groups around the world. Social stress induces pronounced behavioral changes including anhedonia and a marked increase in social avoidance (or withdrawal). The behavioral effects of social stress are reversed by chronic, but not acute, antidepressant treatment. This is relevant because chronic, but not acute antidepressant treatment is effective in treating affective disorders in humans. The overwhelming majority of studies using social stress have focused on males. This is because in most species of rodents, female aggression is minimal, so it is difficult to create social stress using intra-female aggression. In contrast, female California mice (Peromyscus californicus) are aggressive, as males and females defend territories. In addition, preliminary data show that females have larger corticosterone responses than males during resident-intruder aggression tests. Insights into idiopathic depression, we expect it will be useful for testing mechanistic. Although our model may not provide hypotheses related to stress-induced depression. This application proposes to use the unique biology of the California mouse to examine sex differences in neurobiological mechanisms that mediate the effects of social stress on affective behaviors.
PUBLIC HEALTH RELEVANCE: Affective disorders are more likely to occur in women, yet most mouse models focus on males in part due to logistical issues. We propose to use the social stress paradigm to examine social withdrawal and anhedonia in male and female California mice. We will examine the effects of social stress on behavior and expression of brain derived neurotrophic factor.
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会议论文
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