产后匮乏的逆境会影响青春期特定性别的小脑适应和奖励行为。

IF 3.3 3区 心理学 Q1 BEHAVIORAL SCIENCES
Malabika Maulik , Kassandra Looschen , Colton Smith , Khyla Johnson , Alaina F. Carman , Cherishma Nagisetty , Katilyn Corriveau , Colin Salisbury , Kayla Deschepper , Madison Michels , Angela N. Henderson-Redmond , Daniel J. Morgan , Swarup Mitra
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引用次数: 0

摘要

以产后护理不善为表现形式的早期生活逆境是影响晚年行为的主要发育压力源。先前的研究表明,早期生活压力对神经行为异常的影响。具体而言,研究表明,有限的床上用品和筑巢材料会导致成年后的行为缺陷。然而,对LBN如何影响青春期的性别特异性神经行为适应的了解有限,青春期是一个易患精神疾病(包括物质使用障碍)的发育阶段。对LBN和应激幼稚的c57BL/6青少年雄性和雌性小鼠后代的一系列行为进行了测试,包括开阔场地、新物体识别、提升+迷宫、社会偏好和吗啡诱导的条件性位置偏好。与压力天真的小鼠相比,暴露于LBN的雄性小鼠在社会偏好方面存在显著的性别特异性缺陷,并且在吗啡诱导的条件位置偏好测试中,LBN雄性和雌性都对药物配对室有更高的偏好。这些行为缺陷伴随着男性小脑深核(DCN)中转录因子Klf9的性别特异性增加。此外,已知由Klf9转录调节的昼夜节律基因Bmal1的mRNA水平在DCN中降低。由于Bmal1最近与细胞外基质调节有关,我们检查了会阴神经网(PNN),并在雄性而非雌性LBN小鼠的DCN中观察到PNN耗竭。总的来说,我们对产后逆境如何影响小脑细胞外基质稳态提供了一个新的理解,可能是通过Klf9破坏昼夜节律轴,这可能是青春期性别特异性行为适应的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Postpartum scarcity-adversity inflicts sex-specific cerebellar adaptations and reward behaviors in adolescence

Postpartum scarcity-adversity inflicts sex-specific cerebellar adaptations and reward behaviors in adolescence

Early life adversity in the form of poor postnatal care is a major developmental stressor impacting behavior later in life. Previous studies have shown the impact of early life stress on neurobehavioral abnormalities. Specifically, research has demonstrated how limited bedding and nesting (LBN) materials can cause behavioral deficits in adulthood. There is, however, a limited understanding of how LBN influences sex-specific neurobehavioral adaptation in adolescence, a developmental stage susceptible to psychiatric diseases including substance use disorder. LBN and stress-naive c57BL/6 adolescent male and female mouse offspring were tested for a battery of behaviors including open field, novel object recognition, elevated plus maze, social preference, and morphine-induced conditioned place preference. There was a significant sex-specific deficit in social preference in male mice exposed to LBN compared to stress-naïve counterparts and both LBN males and females had a higher preference towards the drug-paired chamber in the morphine-induced conditioned place preference test. These behavioral deficits were concomitant with sex-specific increases in the transcription factor, Klf9 in the deep cerebellar nuclei (DCN) of males. Further, mRNA levels of the circadian gene Bmal1, which is known to be transcriptionally regulated by Klf9, were decreased in the DCN. Since Bmal1 has recently been implicated in extracellular matrix modulation, we examined perineuronal nets (PNN) and observed depleted PNN in the DCN of males but not female LBN mice. Overall, we provide a novel understanding of how postpartum adversity impinges on the cerebellar extracellular matrix homeostasis, likely, through disruption of the circadian axis by Klf9 that might underlie sex-specific behavioral adaptations in adolescence.

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来源期刊
CiteScore
6.40
自引率
2.80%
发文量
122
审稿时长
38 days
期刊介绍: Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.
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