体温和神经功率谱对反复束缚应激反应的性别差异。

IF 2.6 4区 心理学 Q2 BEHAVIORAL SCIENCES Stress-The International Journal on the Biology of Stress Pub Date : 2024-01-01 Epub Date: 2024-02-28 DOI:10.1080/10253890.2024.2320780
I C Ravaglia, V Jasodanand, S Bhatnagar, L A Grafe
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引用次数: 0

摘要

重复压力与罹患创伤后应激障碍(PTSD)等精神疾病的风险增加有关,而创伤后应激障碍在女性中更为常见,但这种性别差异背后的神经生物学尚不清楚。创伤后应激障碍患者对重复压力的习惯化会受损,最近的临床前研究表明,雌性大鼠对重复压力的习惯化不如雄性大鼠充分,从而导致认知和睡眠受损。进一步的研究应考察重复应激后在体温和神经活动等其他相关指标上的性别差异。在这项研究中,我们分析了成年雄性和雌性大鼠在束缚期间以及应激后睡眠转换期间的核心体温和脑电图功率谱。我们发现,雄性大鼠的核心体温比雌性大鼠更能适应反复束缚。此外,我们还发现雌性大鼠在束缚的两天中平均β波段功率都高于雄性大鼠,这表明雌性大鼠的唤醒水平更高。最后,我们观察到,在束缚大鼠的第 1 天,雌性大鼠在睡眠转换期间的 delta 波段功率低于雄性大鼠,但在束缚大鼠的第 5 天,雌性大鼠的 delta 波段功率高于雄性大鼠。这表明,与雄性相比,雌性可能需要更长的时间来启动睡眠恢复。这些发现表明,男性和女性在反复应激后的生理和神经过程存在差异。了解两性压力反应的调节方式可以为压力相关疾病的个体化治疗提供启示。
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Sex differences in body temperature and neural power spectra in response to repeated restraint stress.

Repeated stress is associated with an increased risk of developing psychiatric illnesses such as post-traumatic stress disorder (PTSD), which is more common in women, yet the neurobiology behind this sex difference is unknown. Habituation to repeated stress is impaired in PTSD, and recent preclinical studies have shown that female rats do not habituate as fully as male rats to repeated stress, which leads to impairments in cognition and sleep. Further research should examine sex differences after repeated stress in other relevant measures, such as body temperature and neural activity. In this study, we analyzed core body temperature and EEG power spectra in adult male and female rats during restraint, as well as during sleep transitions following stress. We found that core body temperature of male rats habituated to repeated restraint more fully than female rats. Additionally, we found that females had a higher average beta band power than males on both days of restraint, indicating higher levels of arousal. Lastly, we observed that females had lower delta band power than males during sleep transitions on Day 1 of restraint, however, females demonstrated higher delta band power than males by Day 5 of restraint. This suggests that it may take females longer to initiate sleep recovery compared with males. These findings indicate that there are differences in the physiological and neural processes of males and females after repeated stress. Understanding the way that the stress response is regulated in both sexes can provide insight into individualized treatment for stress-related disorders.

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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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