Exercise-induced metabolite Lac-Phe ameliorates colitis by inhibiting M1 macrophage polarization via the suppression of the NF-κB signaling pathway.

IF 7.1 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Runfeng Yu, Chi Zhang, Ming Yuan, Shubiao Ye, Tuo Hu, Shaopeng Chen, Guanzhan Liang, Jiaqi Liu, Haoxian Ke, Junfeng Huang, Ping Lan, Xiaosheng He, Xianrui Wu
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Abstract

Background and aims: Although the anti-inflammatory benefits of exercise are well-documented, the specific mechanisms responsible for these advantages remain uncertain. N-lactoyl-phenylalanine (Lac-Phe), a major metabolite produced during exercise, is synthesized through the condensation of lactic acid and phenylalanine, catalyzed by the CNDP2. However, the potential anti-inflammatory properties of Lac-Phe remain poorly understood. This study aimed to investigate the anti-inflammatory effects of Lac-Phe in the context of inflammatory bowel disease (IBD) and to examine the underlying mechanisms.

Methods: The levels of Lac-Phe were measured in both IBD patients and mice utilizing ELISA kits. The anti-inflammatory effects of Lac-Phe were demonstrated through colitis models. The impacts of Lac-Phe on macrophage polarization and the associated mechanisms were determined by flow cytometry, qPCR, RNA sequencing, Western blotting, and immunofluorescence.

Results: Our study revealed a reduction in plasma Lac-Phe content in IBD patients, in conjunction with a decrease in the expression of CNDP2 in the colon, which exhibited a negative correlation with disease activity scores. Exercise mitigated DSS-induced colitis in mice by elevating plasma Lac-Phe levels and inhibiting the polarization of M1 macrophages. Mechanistically, Lac-Phe impedes the movement of p65 protein from the cytoplasm into the nucleus, consequently suppressing the activation of the NF-κB signaling pathway and macrophage M1 polarization. Furthermore, the supplementation of phenylalanine, a substrate of Lac-Phe, was observed to enhance the generation of Lac-Phe and to exert a protective effect in the murine colitis model.

Conclusion: Our results suggest that exercise can induce the production of Lac-Phe, which plays a preventive role against DSS-induced colitis in mice. Lac-Phe mitigates colitis through inhibition of the polarization of M1 macrophage. Adjusting macrophage polarization with Lac-Phe and phenylalanine supplementation may offer a potential therapeutic strategy for managing IBD.

运动诱导的代谢物Lac-Phe通过抑制NF-κB信号通路抑制M1巨噬细胞极化来改善结肠炎。
背景和目的:尽管运动的抗炎作用已被充分证明,但产生这些优势的具体机制仍不确定。n -乳酸-苯丙氨酸(Lac-Phe)是运动过程中产生的主要代谢物,由乳酸和苯丙氨酸缩合合成,CNDP2催化。然而,Lac-Phe潜在的抗炎特性仍然知之甚少。本研究旨在探讨Lac-Phe在炎症性肠病(IBD)中的抗炎作用,并探讨其潜在机制。方法:采用酶联免疫吸附试验(ELISA)检测小鼠和IBD患者血清Lac-Phe水平。通过结肠炎模型验证Lac-Phe的抗炎作用。通过流式细胞术、qPCR、RNA测序、Western blotting和免疫荧光等方法检测Lac-Phe对巨噬细胞极化的影响及其相关机制。结果:我们的研究显示,IBD患者血浆Lac-Phe含量降低,同时结肠CNDP2表达降低,这与疾病活动度评分呈负相关。运动通过提高血浆Lac-Phe水平和抑制M1巨噬细胞的极化来减轻dss诱导的小鼠结肠炎。在机制上,Lac-Phe阻碍p65蛋白从细胞质进入细胞核,从而抑制NF-κB信号通路的激活和巨噬细胞M1极化。此外,补充苯丙氨酸(Lac-Phe的底物)可以促进Lac-Phe的生成,并在小鼠结肠炎模型中发挥保护作用。结论:运动可诱导Lac-Phe的产生,对dss诱导的小鼠结肠炎具有预防作用。Lac-Phe通过抑制M1巨噬细胞的极化来减轻结肠炎。通过补充Lac-Phe和苯丙氨酸调节巨噬细胞极化可能为控制IBD提供潜在的治疗策略。
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来源期刊
CiteScore
13.00
自引率
2.80%
发文量
246
审稿时长
42 days
期刊介绍: "Cell and Molecular Gastroenterology and Hepatology (CMGH)" is a journal dedicated to advancing the understanding of digestive biology through impactful research that spans the spectrum of normal gastrointestinal, hepatic, and pancreatic functions, as well as their pathologies. The journal's mission is to publish high-quality, hypothesis-driven studies that offer mechanistic novelty and are methodologically robust, covering a wide range of themes in gastroenterology, hepatology, and pancreatology. CMGH reports on the latest scientific advances in cell biology, immunology, physiology, microbiology, genetics, and neurobiology related to gastrointestinal, hepatobiliary, and pancreatic health and disease. The research published in CMGH is designed to address significant questions in the field, utilizing a variety of experimental approaches, including in vitro models, patient-derived tissues or cells, and animal models. This multifaceted approach enables the journal to contribute to both fundamental discoveries and their translation into clinical applications, ultimately aiming to improve patient care and treatment outcomes in digestive health.
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