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致肥胖的自助餐厅饮食会引起小鼠肠道微生物群的动态变化,降低肠肌间神经元兴奋性,并损害肠道收缩功能。

Obesogenic cafeteria diet induces dynamic changes in gut microbiota, reduces myenteric neuron excitability, and impairs gut contraction in mice.

作者信息

Ramírez-Maldonado Luis M, Guerrero-Castro Julio, Rodríguez-Mejía José L, Cárdenas-Conejo Yair, Bonales-Alatorre Edgar O, Valencia-Cruz Georgina, Anguiano-García Paulina T, Vega-Juárez Irving I, Dagnino-Acosta Adán, Ruvalcaba-Galindo Jessica, Valdez-Morales Eduardo E, Ochoa-Cortes Fernando, Barajas-Espinosa Alma, Guerrero-Alba Raquel, Liñán-Rico Andrómeda

机构信息

Centro Universitario de Investigaciones Biomédicas (CUIB), Universidad de Colima, Colima, México.

Laboratorio de Biología Sintética Estructural y Molecular, Universidad de Colima-Consejo Nacional de Humanidades, Ciencias y Tecnologías, Colima, México.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2025 Jan 1;328(1):G32-G48. doi: 10.1152/ajpgi.00198.2024. Epub 2024 Nov 5.

DOI:10.1152/ajpgi.00198.2024
PMID:39499253
Abstract

The cafeteria diet (CAF) is a superior diet model in animal experiments compared with the conventional high-fat diet (HFD), effectively inducing obesity, metabolic disturbances, and multi-organ damage. Nevertheless, its impact on gut microbiota composition during the progression of obesity, along with its repercussions on the enteric nervous system (ENS) and gastrointestinal motility has not been completely elucidated. To gain more insight into the effects of CAF diet in the gut, C57BL/6 mice were fed with CAF or a standard diet for 2 or 8 wk. CAF-fed mice experienced weight gain, disturbed glucose metabolism, dysregulated expression of colonic IL-6, IL-22, TNFα, and TPH1, and altered colon morphology, starting at . Fecal DNA was isolated and gut microbiota composition was monitored by sequencing the V3-V4 16S rRNA region. Sequence analysis revealed that and were specific biomarkers associated with CAF-feeding at , while and were prominent at . In addition, the impact of CAF diet on ENS was investigated (), where HuC/D+ neurons were measured and counted, and their biophysical properties were evaluated by patch clamp. Gut contractility was tested in whole-mount preparations. Myenteric neurons in CAF-fed mice exhibited reduced body size, incremented cell density, and decreased excitability. The amplitude and frequency of the rhythmic spontaneous contractions in the colon and ileum were affected by the CAF diet. Our findings demonstrate, for the first time, that CAF diet gradually changes the gut microbiota and promotes low-grade inflammation, impacting the functional properties of myenteric neurons and gut contractility in mice. The gut microbiota changes gradually following the consumption of CAF diet. An increase in and is a hallmark of dysbiosis at the early onset of gut inflammation and obesity. The CAF diet was effective in inducing intestinal low-grade inflammation and alterations in myenteric neuronal excitability in mice. CAF diet is a reliable strategy to study the interplay between gut dysbiosis and low-grade inflammation, in addition to the mechanisms underlying gastrointestinal dysmotility associated with obesity.

摘要

与传统高脂饮食(HFD)相比,自助餐厅饮食(CAF)在动物实验中是一种更优的饮食模式,能有效诱发肥胖、代谢紊乱和多器官损伤。然而,其在肥胖进展过程中对肠道微生物群组成的影响,以及对肠神经系统(ENS)和胃肠动力的影响尚未完全阐明。为了更深入了解CAF饮食对肠道的影响,将C57BL/6小鼠喂食CAF或标准饮食2周或8周。从第 周开始,喂食CAF的小鼠出现体重增加、葡萄糖代谢紊乱、结肠IL-6、IL-22、TNFα和TPH1表达失调,以及结肠形态改变。分离粪便DNA,并通过对V3-V4 16S rRNA区域进行测序来监测肠道微生物群组成。序列分析显示, 在 时是与CAF喂养相关的特定生物标志物,而 在 时较为突出。此外,研究了CAF饮食对ENS的影响( ),测量并计数HuC/D+神经元,并通过膜片钳评估其生物物理特性。在整装标本中测试肠道收缩性。喂食CAF的小鼠的肌间神经元表现出体积减小、细胞密度增加和兴奋性降低。CAF饮食影响结肠和回肠有节奏的自发收缩的幅度和频率。我们的研究结果首次表明,CAF饮食会逐渐改变肠道微生物群并促进低度炎症,影响小鼠肌间神经元的功能特性和肠道收缩性。食用CAF饮食后,肠道微生物群会逐渐发生变化。 和 的增加是肠道炎症和肥胖早期肠道菌群失调的标志。CAF饮食可有效诱导小鼠肠道低度炎症和肌间神经元兴奋性改变。CAF饮食是研究肠道菌群失调与低度炎症之间相互作用以及肥胖相关胃肠动力障碍潜在机制的可靠策略。

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引用本文的文献

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Am J Physiol Gastrointest Liver Physiol. 2025 Mar 1;328(3):G179-G181. doi: 10.1152/ajpgi.00391.2024. Epub 2025 Jan 28.