母体口服丙酸钠补充剂可恢复肠道完整性,减轻应激诱导的后代代谢和行为结果。

IF 5.8 1区 医学 Q1 PSYCHIATRY
Anastasia Bagaev, Debpali Sur, Oryan Agranyoni, Naamah Pe'er, Brajesh Kumar Savita, Beatriz Gonçalves Silva Rocha, Panayotis K Thanos, Shiri Navon-Venezia, Albert Pinhasov
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引用次数: 0

摘要

母亲依恋是后代出生后发育的关键决定因素,显著影响其晚年的代谢和行为模式。我们之前的研究表明,应激易感、社会顺从(Sub)小鼠在肠道生理上表现出显著的破坏,包括微生物组组成扭曲、结肠丙酸水平降低和肠道通透性增加。这些改变加剧了慢性炎症,导致代谢失衡,减少了产妇护理。在这项研究中,我们发现亚坝的细菌多样性和粪便丙酸水平显著降低。为了研究母体肠道完整性是否可以减轻后代的不良结局,我们从产后第0天(PD)开始,直到断奶(PD21),通过饮用水向子坝口服丙酸钠(SP)。补充SP显著改善了母性护理,反映在更快的幼崽检索时间和更好的筑巢。有益效果在两个月大的雄性后代中尤为明显,表现出焦虑样行为的减少,社交能力的改善和短期记忆的增强,同时特定肠道细菌(Roseburia和Shuttleworthia属)的丰度增加。此外,雄性后代表现出显著的代谢改善,包括附睾白色脂肪组织(eWAT)质量减少,脂肪细胞直径减少,eWAT mRNA表达增加GPR43和PPAR-γ。此外,补充SP增加结肠长度与结肠GPR43、PPAR-γ和Claudin-7 mRNA表达增加有关,这突出了丙酸盐在紧密连接调节和炎症中的重要性。重要的是,这些积极的结果表现出显著的性别依赖差异,雄性后代反应强烈,而雌性在母体补充SP后表现出最小的行为或代谢改善。总的来说,我们的研究结果强调,通过恢复母鼠肠道上皮屏障的完整性,可以减轻后代先天应激易感性相关的代谢和行为改变,强调了母体肠道环境的关键作用,并展示了对肠道微生物群靶向干预的明确性别特异性反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Maternal oral sodium propionate supplementation restores gut integrity and mitigates stress-induced metabolic and behavioral outcomes in offspring.

Maternal attachment is a critical determinant of offspring's postnatal development, significantly influencing their later-life metabolic and behavioral patterns. We previously showed that stress-vulnerable, socially submissive (Sub) mice exhibit significant disruptions in gut physiology including distorted microbiome composition, lower colonic propionate levels, and increased gut permeability. These alterations exacerbated chronic inflammation, caused metabolic imbalances and reduced maternal care. In this study, we revealed a significant reduction in bacterial diversity and fecal propionate levels in Sub dams. To investigate whether maternal gut integrity could mitigate adverse offspring outcomes, we provided oral sodium propionate (SP) supplementation to Sub dams via drinking water from postpartum day (PD) 0, until weaning (PD21). SP supplementation notably improved maternal care, reflected by faster pup retrieval times and better nesting. Beneficial effects were particularly pronounced in two-month-old male offspring, demonstrating decreased anxiety-like behavior, improved sociability and enhanced short-term memory accompanied by increased abundance of specific gut bacteria (Roseburia, and Shuttleworthia genus). Additionally, male offspring exhibited significant metabolic improvements, including reduced epididymal white adipose tissue (eWAT) mass, decreased adipocyte diameter accompanied by increased eWAT mRNA expression of GPR43 and PPAR-γ. Moreover, SP supplementation increased colon length linked with increased colonic mRNA expression of GPR43, PPAR-γ and Claudin-7, highlighting the importance of propionate in tight junction regulation and inflammation. Importantly, these positive outcomes exhibited notable sex-dependent differences, with male offspring responding robustly, whereas females showed minimal behavioral or metabolic improvements following maternal SP supplementation. Overall, our findings emphasize that innate stress vulnerability-related metabolic and behavioral alterations in offspring can be mitigated by restoring the dams' gut epithelial barrier integrity, highlighting the critical role of the maternal gut environment and demonstrating clear sex-specific responses to gut microbiota-targeted interventions.

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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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