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成年大鼠单一延长应激的性别差异长期效应。

Sex-divergent long-term effects of single prolonged stress in adult rats.

机构信息

Dept. of Physiology and Pharmacology, Sapienza University of Rome, 00185 Rome, Italy; Neurobiology of Behavior Laboratory, Santa Lucia Foundation, 00143 Rome, Italy.

Dept. of Physiology and Pharmacology, Sapienza University of Rome, 00185 Rome, Italy.

出版信息

Behav Brain Res. 2021 Mar 5;401:113096. doi: 10.1016/j.bbr.2020.113096. Epub 2020 Dec 24.

Abstract

Single prolonged stress (SPS) is an experimental model that recapitulates in rodents some of the core symptoms of post-traumatic stress disorder (PTSD). Although women have a two-fold greater risk to develop PTSD, most preclinical studies have been carried out in males. Furthermore, the long-term effects of behavioral alterations induced by SPS have been rarely investigated. Here, we evaluated the long-term effects of SPS on PTSD-relevant behavioral domains in rats and whether these effects were sex-dependent. To this aim, separate cohorts of male and female adult rats were subjected to SPS and, 30 days later, long-term effects were assessed. We found that SPS exposure reduced locomotor activity in both sexes in an open field task. Males only showed increased anxiety-like behavior in the elevated plus maze and marble burying tests, enhanced acoustic startle response and impaired spatial memory retention while females were unaffected. SPS exposure did not alter auditory fear memory dynamics in males, but it did alter extinction retrieval in females. We provide the first evidence that SPS reproduces long-term emotional alterations in male, but not in female, rats which were observed 30 days following trauma exposure, thus resembling some of the hallmark symptoms of PTSD. Furthermore, our results show for the first time a long-term SPS-induced alteration of cued fear extinction in females. Our findings are relevant to future research on trauma-related disorders and may help develop sex-specific interventions to treat PTSD.

摘要

单一延长应激(SPS)是一种实验模型,可在啮齿动物中重现创伤后应激障碍(PTSD)的一些核心症状。尽管女性患 PTSD 的风险是男性的两倍,但大多数临床前研究都是在男性中进行的。此外,SPS 引起的行为改变的长期影响很少被研究。在这里,我们评估了 SPS 对大鼠 PTSD 相关行为领域的长期影响,以及这些影响是否存在性别依赖性。为此,我们将分开的雄性和雌性成年大鼠队列暴露于 SPS 中,30 天后评估长期影响。我们发现,SPS 暴露会降低雄性和雌性在开阔场任务中的运动活性。雄性仅在高架十字迷宫和大理石埋藏试验中表现出焦虑样行为增加,听觉惊吓反应增强和空间记忆保留受损,而雌性则不受影响。SPS 暴露不会改变雄性的听觉恐惧记忆动力学,但会改变雌性的消退检索。我们提供了第一个证据,证明 SPS 会在创伤后 30 天内重现雄性大鼠的长期情绪改变,但不会重现雌性大鼠的情绪改变,这类似于 PTSD 的一些标志性症状。此外,我们的结果首次表明,SPS 会长期引起雌性条件性恐惧消退的改变。我们的发现与创伤相关障碍的未来研究有关,并可能有助于开发针对 PTSD 的特定于性别的干预措施。

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