鱼油通过GPR120-VEGFR3-MLCK途径促进乳结拉链,从而减少肠道脂肪吸收

IF 11.4 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Junfeng Wang, Liling Cai, Jinhao Liu, Fenglin Zhang, Gonghao Zhang, Haoyan Kang, Guo Ren, Lidong Yan, Yue Zhang, Zhe Pan, Shilong Liu, Canjun Zhu, Ruifan Wu, Lina Wang, Gang Shu, Qingyan Jiang, Songbo Wang
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引用次数: 0

摘要

饮食引起的肥胖可以通过减少肠道脂肪吸收来改善。富含n-3 PUFAs(如DHA和EPA)的鱼油已显示出减轻体重的希望。然而,鱼油在调节肠道脂肪吸收中的作用及其可能的潜在机制在很大程度上仍然未知。目的探讨鱼油抗肥胖作用的机制。方法用鱼油喂养小鼠,用DHA或EPA处理淋巴内皮细胞。评估肠道脂肪吸收、乳拉链样连接以及GPR120-VEGFR3-MLCK通路的参与情况。结果我们发现鱼油灌胃抑制肠道脂肪吸收,与小鼠空肠中乳拉链样连接比例升高和VEGFR3表达降低有关。同时,在饲喂hfd的小鼠中,抑制VEGFR3信号可以增强空肠乳中的拉链状连接,从而减少脂肪吸收,对抗肥胖。此外,DHA和EPA通过下调pa处理的LECs中VEGFR3信号传导,增加了拉链状连接的比例。然而,用VEGFC激活VEGFR3信号或用AH-7614抑制GPR120完全阻断了DHA和EPA诱导的拉链状连接的升高。此外,DHA和EPA以GPR120-VEGFR3依赖的方式抑制MLCK信号传导,抑制MLCK类似于DHA和EPA对拉链样连接的促进作用。这些体外结果表明,DHA和EPA通过GPR120-VEGFR3-MLCK信号通路增加了pa处理的LECs中拉链状连接的比例。最后,补充鱼油减少肠道脂肪吸收,促进乳拉链样连接,增强GPR120表达,抑制VEGFR3表达和MLCK信号。总的来说,这些发现首次表明鱼油通过GPR120-VEGFR3-MLCK途径促进乳结收缩,从而减少肠道脂肪吸收。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fish oil reduces intestinal fat absorption by promoting lacteal junction zippering via GPR120-VEGFR3-MLCK pathway

Fish oil reduces intestinal fat absorption by promoting lacteal junction zippering via GPR120-VEGFR3-MLCK pathway

Introduction

Diet-induced obesity can be improved by reducing intestinal fat absorption. Fish oil, enriched in n-3 PUFAs such as DHA and EPA, has shown promise in weight reduction. However, the role of fish oil in regulating intestinal fat absorption and the possible underlying mechanism remains largely unknown.

Objectives

The aim of this study was to understand the mechanism underlying the fish oil elicited anti-obesity effects.

Methods

HFD-fed mice were subjected to fish oil and lymphatic endothelial cells (LECs) were treated with DHA or EPA. The intestinal fat absorption, the lacteal zipper-like junctions, and the involvement of GPR120-VEGFR3-MLCK pathway were assessed.

Results

We found that fish oil gavage suppressed intestinal fat absorption associated with elevated proportion of lacteal zipper-like junctions and decreased expression of VEGFR3 in mice jejunum. Meanwhile, inhibition of VEGFR3 signaling in HFD-fed mice enhanced zipper-like junctions in jejunal lacteal to reduce fat absorption and combat obesity. In addition, DHA and EPA increased the proportion of zipper-like junctions via downregulation of VEGFR3 signaling in PA-treated LECs. However, activation of VEGFR3 signaling with VEGFC or inhibition of GPR120 with AH-7614 totally blocked the elevation of zipper-like junctions induced by DHA and EPA. Furthermore, DHA and EPA inhibited MLCK signaling in a GPR120-VEGFR3 dependent manner and inhibition of MLCK mimicked the promotive effects of DHA and EPA on zipper-like junctions. These in vitro results suggested that DHA and EPA increased the proportion of zipper-like junctions in PA-treated LECs through the GPR120-VEGFR3-MLCK signaling pathway. Finally, fish oil supplementation reduced intestinal fat absorption, promoted lacteal zipper-like junctions, enhanced GPR120 expression, inhibited VEGFR3 expression and MLCK signaling.

Conclusion

Overall, these findings showed for the first time that fish oil reduced intestinal fat absorption by promoting lacteal junctions zippering via GPR120-VEGFR3-MLCK pathway.
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来源期刊
Journal of Advanced Research
Journal of Advanced Research Multidisciplinary-Multidisciplinary
CiteScore
21.60
自引率
0.90%
发文量
280
审稿时长
12 weeks
期刊介绍: Journal of Advanced Research (J. Adv. Res.) is an applied/natural sciences, peer-reviewed journal that focuses on interdisciplinary research. The journal aims to contribute to applied research and knowledge worldwide through the publication of original and high-quality research articles in the fields of Medicine, Pharmaceutical Sciences, Dentistry, Physical Therapy, Veterinary Medicine, and Basic and Biological Sciences. The following abstracting and indexing services cover the Journal of Advanced Research: PubMed/Medline, Essential Science Indicators, Web of Science, Scopus, PubMed Central, PubMed, Science Citation Index Expanded, Directory of Open Access Journals (DOAJ), and INSPEC.
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