Department of Food Science and Engineering, Institute of Food Safety and Nutrition, Guangdong Engineering Technology Center of Food Safety Molecular Rapid Detection, Jinan University, Guangzhou, China.
Department of Gastroenterology, The Sixth Affiliated Hospital, Sun Yat-sen University, China; Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, The Sixth Affiliated Hospital, Sun Yat-sen University, China.
Food Chem Toxicol. 2023 Oct;180:114009. doi: 10.1016/j.fct.2023.114009. Epub 2023 Aug 29.
Ulcerative colitis (UC) is believed to arise from an imbalance between the intestinal microbiota and mucosal immunity, leading to excessive intestinal inflammation. Modulating the gut microbial community through dietary components presents a valuable strategy in aiding the treatment of UC. In this study, esters formed by binding of well-known prebiotics, fructooligosaccharides (FOS), with short chain fatty acids (SCFAs) via both enzymatic and chemical methods were evaluated for their impact on the gut microbiota of UC patients. An in vitro human colonic fermentation model was employed to monitor changes in total carbohydrates and SCFAs production during the fermentation of these esters by microbiota from patients with active and remission UC. The results showed that pronounced abundance of [Ruminococcus]_gnavus_group, Escherichia_Shigella, Lachnoclostridium, Klebsiella and other potential pathogens were detected in the fecal samples from UC patients, with a milder condition observed during the remission phase. Significant higher levels of corresponding SCFA were observed in the groups with addition of FOS-SCFAs esters during fermentation. Butyrylated fructooligosaccharides (B-FOS) and propionylated fructooligosaccharides (P-FOS) by enzymatic synthesis successfully promoted the proliferation of Bifidobacterium and inhibited Clostridium_sensu_stricto_1 and Klebsiella. Overall, B-FOS and P-FOS exhibit promising potential for restoring intestinal homeostasis and alleviating intestinal inflammation in individuals with UC.
溃疡性结肠炎(UC)被认为是由于肠道微生物群和黏膜免疫之间的失衡导致过度的肠道炎症。通过饮食成分调节肠道微生物群落是一种有价值的策略,可以辅助治疗 UC。在这项研究中,通过酶法和化学法将众所周知的益生元果寡糖(FOS)与短链脂肪酸(SCFAs)结合形成的酯类,评估了它们对 UC 患者肠道微生物群的影响。采用体外人类结肠发酵模型来监测这些酯类在 UC 患者的活跃期和缓解期微生物群发酵过程中总碳水化合物和 SCFA 产生的变化。结果表明,在 UC 患者的粪便样本中检测到了 Ruminococcus_gnavus_group、Escherichia_Shigella、Lachnoclostridium、Klebsiella 和其他潜在病原体的大量丰度,在缓解期观察到的情况较轻。在添加 FOS-SCFAs 酯类的发酵过程中,观察到相应 SCFA 的水平显著升高。酶法合成的丁酸化果寡糖(B-FOS)和丙酸化果寡糖(P-FOS)成功促进了双歧杆菌的增殖,抑制了 Clostridium_sensu_stricto_1 和 Klebsiella。总体而言,B-FOS 和 P-FOS 具有恢复肠道内稳态和缓解 UC 患者肠道炎症的潜力。