围产期暴露于聚苯乙烯纳米塑料通过微生物-肠-脑轴改变成年后代小鼠的社会情感行为。

IF 8.8 2区 医学 Q1 IMMUNOLOGY
Yi Guo , Mei Li , Xiaoyu Liu , Huiling Duo , Boya Huang , Hengtai Lu , Xiangyu Zhang , Xuzhe Li , Ye Zhao , Kaoqi Lian , Tengfei Liu , Yun Shi , Yuan Gao , Li Meng , Di Zhao , Li Song , Rui Jiang , Haishui Shi
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引用次数: 0

摘要

聚苯乙烯纳米塑料(PS-NPs)是普遍存在的环境污染物,已在人类和动物的各种组织中检测到,引起了对其潜在健康危害的重大关切。在早期发育阶段接触PS-NPs的长期后果仍然没有充分的特征。在这项研究中,我们建立了一个小鼠模型,研究围产期通过饮用水长期口服PS-NPs,重点阐明PS-NPs摄入对成年后代社会行为的影响及其潜在机制,特别是涉及肠脑轴的影响。我们的研究结果表明,围产期PS-NPs暴露会引起成年后代的抑郁样行为,社会支配地位降低,社会互动减少。此外,我们观察到海马神经元内树突棘密度的减少,以及成年后代海马神经元和突触的超微结构损伤。PS-NPs暴露还导致雄性和雌性小鼠肠道微生物群物种组成的丰富度和均匀性降低,成年雄性肠道生态失调尤为明显。此外,在雄性和雌性成年后代的海马中都检测到代谢物丰度和代谢途径的改变。值得注意的是,肠道微生物的相对丰度与海马代谢物之间存在显著相关性。这些结果为通过微生物-肠道-脑轴介导的早期PS-NPs暴露与成年社会行为之间的关系提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Perinatal exposure to polystyrene nanoplastics alters socioemotional behaviors via the microbiota–gut–brain axis in adult offspring mice

Perinatal exposure to polystyrene nanoplastics alters socioemotional behaviors via the microbiota–gut–brain axis in adult offspring mice
Polystyrene nanoplastics (PS-NPs), ubiquitous environmental contaminants, have been detected in various tissues of humans and animals, raising significant concerns regarding their potential health hazards. The long-term consequences of PS-NPs exposure during early developmental stages remain inadequately characterized. In this study, we established a murine model to investigate the chronic oral administration of PS-NPs via drinking water during the perinatal period, with a focus on elucidating the impact of PS-NPs ingestion on the social behaviors of adult offspring and the underlying mechanisms, particularly those involving the gut–brain axis. Our findings revealed that perinatal PS-NPs exposure elicited depression-like behaviors, diminished social dominance, and reduced social interactions in adult offspring. Additionally, we observed a decrease in dendritic spine density within hippocampal neurons, along with ultrastructural damage to hippocampal neurons and synapses in the adult offspring. PS-NPs exposure also led to a reduction in the richness and evenness of gut microbiota species composition in both male and female mice, with gut dysbiosis being particularly pronounced in adult males. Furthermore, alterations in metabolite abundance and metabolic pathways were detected in the hippocampus of both male and female adult offspring. Notably, a significant correlation was identified between the relative abundance of intestinal microorganisms and hippocampal metabolites. These results offer new insights into the association between early-life PS-NPs exposure and adult social behaviors, mediated through the microbiota–gut–brain axis.
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来源期刊
CiteScore
29.60
自引率
2.00%
发文量
290
审稿时长
28 days
期刊介绍: Established in 1987, Brain, Behavior, and Immunity proudly serves as the official journal of the Psychoneuroimmunology Research Society (PNIRS). This pioneering journal is dedicated to publishing peer-reviewed basic, experimental, and clinical studies that explore the intricate interactions among behavioral, neural, endocrine, and immune systems in both humans and animals. As an international and interdisciplinary platform, Brain, Behavior, and Immunity focuses on original research spanning neuroscience, immunology, integrative physiology, behavioral biology, psychiatry, psychology, and clinical medicine. The journal is inclusive of research conducted at various levels, including molecular, cellular, social, and whole organism perspectives. With a commitment to efficiency, the journal facilitates online submission and review, ensuring timely publication of experimental results. Manuscripts typically undergo peer review and are returned to authors within 30 days of submission. It's worth noting that Brain, Behavior, and Immunity, published eight times a year, does not impose submission fees or page charges, fostering an open and accessible platform for scientific discourse.
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