Western diet promotes endometriotic lesion growth in mice and induces depletion of Akkermansia muciniphila in intestinal microbiota.

IF 7 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Guillaume Parpex, Benoît Chassaing, Mathilde Bourdon, Pietro Santulli, Ludivine Doridot, Marine Thomas, Frédéric Batteux, Sandrine Chouzenoux, Charles Chapron, Carole Nicco, Louis Marcellin
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Abstract

Background: Endometriosis, affecting 10% of women in their reproductive years, remains poorly understood. Both individual and environmental unexplained factors are implicated in this heterogenous condition. This study aims to examine the influence of a Western diet on endometriosis lesion development in mice and to uncover the mechanisms involved.

Methods: Mice were fed either a control diet or a Western diet (high in fatty acids and low in fiber) for 4 weeks. Endometriosis was then surgically induced, and lesion development was monitored by ultrasound. After 7 weeks, the mice were sacrificed for analysis of lesion characteristics through RT-qPCR, immunohistochemistry, and flow cytometry. Additionally, the intestinal microbiota was assessed using 16S rRNA gene sequencing.

Results: Mice on the Western diet developed lesions that were significantly twice as large compared to those on the control diet. These lesions exhibited greater fibrosis and proliferation, alongside enhanced macrophage activity and leptin pathway expression. Changes in the intestinal microbiota were significantly noted after endometriosis induction, regardless of diet. Notably, mice on the Western diet with the most substantial lesions showed a loss of Akkermansia Muciniphila in their intestinal microbiota.

Conclusions: A Western diet significantly exacerbates lesion size in a mouse model of endometriosis, accompanied by metabolic and immune alterations. The onset of endometriosis also leads to substantial shifts in intestinal microbiota, suggesting a potential link between diet, intestinal health, and endometriosis development.

西式饮食会促进小鼠子宫内膜异位症病灶的生长,并诱导肠道微生物群中 Akkermansia muciniphila 的消耗。
背景:子宫内膜异位症影响着 10%的育龄妇女,但人们对这种疾病的了解仍然很少。个体因素和环境因素都与这种异质性疾病有关。本研究旨在探讨西方饮食对小鼠子宫内膜异位症病变发展的影响,并揭示其中的机制:方法:用对照组饮食或西式饮食(高脂肪酸、低纤维)喂养小鼠 4 周。然后通过手术诱发子宫内膜异位症,并通过超声波监测病灶的发展。7 周后,小鼠被处死,通过 RT-qPCR、免疫组化和流式细胞术分析病变特征。此外,还使用 16S rRNA 基因测序评估了肠道微生物群:结果:摄入西式饮食的小鼠发生的病变明显比摄入对照饮食的小鼠大两倍。这些病变表现出更大的纤维化和增生,同时巨噬细胞活性和瘦素通路表达也增强了。子宫内膜异位症诱导后,肠道微生物群发生了显著变化,与饮食无关。值得注意的是,采用西式饮食的小鼠病变最严重,其肠道微生物群中的Akkermansia Muciniphila数量减少:结论:在子宫内膜异位症小鼠模型中,西式饮食会明显加剧病灶的大小,并伴有代谢和免疫改变。子宫内膜异位症的发生也会导致肠道微生物群发生重大变化,这表明饮食、肠道健康和子宫内膜异位症的发展之间存在潜在联系。
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来源期刊
BMC Medicine
BMC Medicine 医学-医学:内科
CiteScore
13.10
自引率
1.10%
发文量
435
审稿时长
4-8 weeks
期刊介绍: BMC Medicine is an open access, transparent peer-reviewed general medical journal. It is the flagship journal of the BMC series and publishes outstanding and influential research in various areas including clinical practice, translational medicine, medical and health advances, public health, global health, policy, and general topics of interest to the biomedical and sociomedical professional communities. In addition to research articles, the journal also publishes stimulating debates, reviews, unique forum articles, and concise tutorials. All articles published in BMC Medicine are included in various databases such as Biological Abstracts, BIOSIS, CAS, Citebase, Current contents, DOAJ, Embase, MEDLINE, PubMed, Science Citation Index Expanded, OAIster, SCImago, Scopus, SOCOLAR, and Zetoc.
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