早期生活中的逆境消除了小鼠主动与被动威胁反应的性别差异。

IF 2.6 4区 心理学 Q2 BEHAVIORAL SCIENCES Stress-The International Journal on the Biology of Stress Pub Date : 2023-11-01 DOI:10.1080/10253890.2023.2244598
Gabriela Manzano Nieves, Marilyn Bravo, Kevin G Bath
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引用次数: 0

摘要

早期生活逆境(ELA)增加了患焦虑症的风险(其特征是恐惧和回避行为加剧),女性患病理的可能性是男性的两倍。巴甫洛夫恐惧条件反射任务已被用于研究支持病理内表型的可能机制。在这些范式中,性别和ELA对行为反应性质的选择性影响的识别可能为了解应对习得性恐惧的应对策略提供一个独特的窗口,以指导更多的机制研究。这项研究的目的有两个:;首先,测试雄性和雌性小鼠是否使用不同的条件参数(低、中、高强度足部电击)对威胁学习采取了不同的应对策略。其次,测试有限寝具和筑巢(LBN)形式的ELA是否改变了小鼠对条件反射的行为反应。小鼠在三种不同的足部电击强度(0.35 mA;0.57 mA;0.7 mA)。在整个试验中测量了冰冻、飞镖和足震反应性。在条件作用过程中,在几乎所有测试的电击强度下,对照饲养的雌性小鼠表现出明显高于对照雄性的跳跃行为率。LBN饲养使雌性飞镖的比例降至雄性水平。因此,LBN形式的ELA显著减少了雌性小鼠主动与被动应对策略的募集,但通常不会改变雄性小鼠的反应。需要做更多的工作来理解这些行为效应的神经基础。这项工作的发现有可能揭示ELA如何影响区域大脑发育的轨迹,以及与病理学和可能的症状表现相关的行为内表型的性别选择风险。
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Early life adversity ablates sex differences in active versus passive threat responding in mice.

Early life adversity (ELA) heightens the risk for anxiety disorders (which are characterized by heightened fear and avoidance behaviors), with females being twice as likely as males to develop pathology. Pavlovian fear conditioning tasks have been used to study possible mechanisms supporting endophenotypes of pathology. Identification of sex and ELA selective effects on the nature of behavioral responding in these paradigms may provide a unique window into coping strategies in response to learned fear to guide more mechanistic studies. The goals of this study were two-fold; First, to test if male and female mice employed different coping strategies in response to threat learning using different conditioning parameters (low, medium, and high intensity foot shocks). Second, to test if ELA in the form of limited bedding and nesting (LBN) altered the behavioral response of mice to conditioning. Mice received 6 tone/foot-shock pairings at one of three different foot-shock intensities (0.35 mA; 0.57 mA; 0.7 mA). Freezing, darting, and foot-shock reactivity were measured across trials. During conditioning, control-reared female mice exhibited significantly higher rates of darting behavior compared to control males at nearly all shock intensities tested. LBN rearing decreased the proportion of darting females to levels observed in males. Thus, ELA in the form of LBN significantly diminished the recruitment of active versus passive coping strategies in female mice but did not generally change male responding. Additional work will be required to understand the neural basis of these behavioral effects. Findings extending from this work have the potential to shed light on how ELA impacts trajectories of regional brain development with implications for sex-selective risk for behavioral endophenotypes associated with pathology and possibly symptom presentation.

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来源期刊
CiteScore
5.60
自引率
0.00%
发文量
25
审稿时长
6-12 weeks
期刊介绍: The journal Stress aims to provide scientists involved in stress research with the possibility of reading a more integrated view of the field. Peer reviewed papers, invited reviews and short communications will deal with interdisciplinary aspects of stress in terms of: the mechanisms of stressful stimulation, including within and between individuals; the physiological and behavioural responses to stress, and their regulation, in both the short and long term; adaptive mechanisms, coping strategies and the pathological consequences of stress. Stress will publish the latest developments in physiology, neurobiology, molecular biology, genetics research, immunology, and behavioural studies as they impact on the understanding of stress and its adverse consequences and their amelioration. Specific approaches may include transgenic/knockout animals, developmental/programming studies, electrophysiology, histochemistry, neurochemistry, neuropharmacology, neuroanatomy, neuroimaging, endocrinology, autonomic physiology, immunology, chronic pain, ethological and other behavioural studies and clinical measures.
期刊最新文献
Inhibition of prefrontal cortex parvalbumin interneurons mitigates behavioral and physiological sequelae of chronic stress in male mice. Maternal prenatal distress exposure negatively associates with the stability of neonatal frontoparietal network. Decreased amygdala-sensorimotor connectivity mediates the association between prenatal stress and broad autism phenotype in young adults: Project Ice Storm. Accumbal μ-opioid receptors and salt taste-elicited hedonic responses in a rodent model of prenatal adversity, and their correlates using human functional genomics. Behavior, synaptic mitochondria, and microglia are differentially impacted by chronic adolescent stress and repeated endotoxin exposure in male and female rats.
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