Late maternal separation provides resilience to chronic variable stress-induced anxiety- and depressive-like behaviours in male but not female mice.

IF 3 4区 医学 Q2 PSYCHIATRY World Journal of Biological Psychiatry Pub Date : 2024-09-01 Epub Date: 2024-08-18 DOI:10.1080/15622975.2024.2390411
Rajesh Kumar Ojha, Shweta Dongre, Padmasana Singh, Raj Kamal Srivastava
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Abstract

Maternal separation can have long-lasting effects on an individual's susceptibility to stress later in life. Maternal separation during the postnatal period is a commonly used paradigm in rodents to investigate the effects of early life stress on neurobehavioural changes and stress responsiveness. However, maternal separation during stress hyporesponsive and responsive periods of postnatal development may differ in its effects on stress resilience. Therefore, we hypothesised that late maternal separation (LMS) from postnatal day 10 to 21 in mice may have different effect on resilience than early maternal separation during the first week of postnatal life. Our results suggested that male LMS mice are more resilient to chronic variable stress (CVS)-induced anxiety and depressive-like behaviour as confirmed by the open field, light-dark field, elevated plus maze, sucrose preference and tail suspension tests. In contrast, female LMS mice were equally resilient as non-LMS female mice. We found increased expression of NPY, NPY1R, NPY2R, NPFFR1, and NPFFR2 in the hypothalamus of male LMS mice whereas the opposite effect was observed in the hippocampus. LMS in male and female mice did not affect circulating corticosterone levels in response to psychological or physiological stressors. Thus, LMS renders male mice resilient to CVS-induced neurobehavioural disorders in adulthood.

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晚期母体分离可使雄性小鼠(而非雌性小鼠)对慢性可变应激诱发的焦虑和抑郁行为产生恢复力。
母体分离会对个体日后的应激易感性产生长期影响。在啮齿类动物中,产后母体分离是研究早期生活压力对神经行为变化和压力反应性影响的常用范例。然而,在产后发育的应激低反应期和应激反应期母体分离对应激恢复力的影响可能有所不同。因此,我们假设,小鼠出生后第10至21天的晚期母体分离(LMS)与出生后第一周的早期母体分离对恢复力的影响可能不同。我们的研究结果表明,雄性LMS小鼠对慢性可变应激(CVS)诱发的焦虑和抑郁样行为有更强的恢复能力,这在开放场、光-暗场、高架加迷宫、蔗糖偏好和尾悬试验中得到了证实。相比之下,LMS雌性小鼠与非LMS雌性小鼠具有同样的适应能力。我们发现雄性 LMS 小鼠下丘脑中 NPY、NPY1R、NPY2R、NPFFR1 和 NPFFR2 的表达增加,而海马中的表达则相反。雄性和雌性小鼠的 LMS 不会影响循环中皮质酮水平对心理或生理压力的反应。因此,LMS可使雄性小鼠在成年后对CVS诱导的神经行为紊乱具有抵抗力。
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来源期刊
CiteScore
7.00
自引率
3.20%
发文量
73
审稿时长
6-12 weeks
期刊介绍: The aim of The World Journal of Biological Psychiatry is to increase the worldwide communication of knowledge in clinical and basic research on biological psychiatry. Its target audience is thus clinical psychiatrists, educators, scientists and students interested in biological psychiatry. The composition of The World Journal of Biological Psychiatry , with its diverse categories that allow communication of a great variety of information, ensures that it is of interest to a wide range of readers. The World Journal of Biological Psychiatry is a major clinically oriented journal on biological psychiatry. The opportunity to educate (through critical review papers, treatment guidelines and consensus reports), publish original work and observations (original papers and brief reports) and to express personal opinions (Letters to the Editor) makes The World Journal of Biological Psychiatry an extremely important medium in the field of biological psychiatry all over the world.
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