Micalis Institute, Institut National de la Recherche Agronomique (INRA), AgroParisTech, Université Paris-Saclay, Jouy-en-Josas, France.
Collège Doctoral, Sorbonne Université, Paris, France.
FASEB J. 2019 Jun;33(6):7126-7142. doi: 10.1096/fj.201801526RR. Epub 2019 Apr 2.
Current fructose consumption levels often overwhelm the intestinal capacity to absorb fructose. We investigated the impact of fructose malabsorption on intestinal endocrine function and addressed the role of the microbiota in this process. To answer this question, a mouse model of moderate fructose malabsorption [ketohexokinase mutant (KHK)] and wild-type (WT) littermate mice were used and received a 20%-fructose (KHK-F and WT-F) or 20%-glucose diet. Cholecystokinin () mRNA and protein expression in the ileum and cecum, as well as preproglucagon () and neurotensin () mRNA expression in the cecum, increased in KHK-F mice. In KHK-F mice, triple-label immunohistochemistry showed major up-regulation of CCK in enteroendocrine cells (EECs) that were glucagon-like peptide-1 (GLP-1)/Peptide YY (PYY) in the ileum and colon and GLP-1/PYY in the cecum. The cecal microbiota composition was drastically modified in the KHK-F in association with an increase in glucose, propionate, succinate, and lactate concentrations. Antibiotic treatment abolished fructose malabsorption-dependent induction of cecal mRNA expression and, in mouse GLUTag and human NCI-H716 cells, mRNA expression levels increased in response to propionate, both suggesting a microbiota-dependent process. Fructose reaching the lower intestine can modify the composition and metabolism of the microbiota, thereby stimulating the production of CCK from the EECs possibly in response to propionate.-Zhang, X., Grosfeld, A., Williams, E., Vasiliauskas, D., Barretto, S., Smith, L., Mariadassou, M., Philippe, C., Devime, F., Melchior, C., Gourcerol, G., Dourmap, N., Lapaque, N., Larraufie, P., Blottière, H. M., Herberden, C., Gerard, P., Rehfeld, J. F., Ferraris, R. P., Fritton, J. C., Ellero-Simatos, S., Douard, V. Fructose malabsorption induces cholecystokinin expression in the ileum and cecum by changing microbiota composition and metabolism.
目前,果糖的摄入量常常超过肠道吸收果糖的能力。我们研究了果糖吸收不良对肠道内分泌功能的影响,并探讨了微生物组在这一过程中的作用。为了回答这个问题,我们使用了一种中度果糖吸收不良的小鼠模型(己酮激酶突变体(KHK))和野生型(WT)同窝小鼠,并给予它们 20%果糖(KHK-F 和 WT-F)或 20%葡萄糖饮食。KHK-F 小鼠的回肠和盲肠中胆囊收缩素(CCK)mRNA 和蛋白表达增加,盲肠中前胰高血糖素(proglucagon)()和神经降压素(neurotensin)()mRNA 表达增加。在 KHK-F 小鼠中,三重免疫组织化学显示,在回肠和结肠中 GLP-1/肽 YY(PYY)和在盲肠中 GLP-1/PYY 的肠内分泌细胞(enteroendocrine cells,EECs)中 CCK 主要上调。KHK-F 小鼠的盲肠微生物组组成发生了巨大变化,与葡萄糖、丙酸盐、琥珀酸盐和乳酸浓度增加有关。抗生素治疗消除了果糖吸收不良依赖性诱导的盲肠 mRNA 表达,并且在小鼠 GLUTag 和人 NCI-H716 细胞中,丙酸盐可增加 mRNA 表达水平,这表明这是一种依赖微生物组的过程。到达下消化道的果糖可以改变微生物组的组成和代谢,从而可能通过丙酸盐刺激 EEC 产生 CCK。-Zhang, X., Grosfeld, A., Williams, E., Vasiliauskas, D., Barretto, S., Smith, L., Mariadassou, M., Philippe, C., Devime, F., Melchior, C., Gourcerol, G., Dourmap, N., Lapaque, N., Larraufie, P., Blottière, H. M., Herberden, C., Gerard, P., Rehfeld, J. F., Ferraris, R. P., Fritton, J. C., Ellero-Simatos, S., Douard, V. Fructose malabsorption induces cholecystokinin expression in the ileum and cecum by changing microbiota composition and metabolism.