Bajic Danica, Wiens Frank, Wintergerst Eva, Deyaert Stef, Baudot Aurélien, Abbeele Pieter Van den
DSM Nutritional Products Ltd., Wurmisweg 576, 4303 Kaiseraugst, Switzerland.
Cryptobiotix SA, Technologiepark-Zwijnaarde 82, 9052 Ghent, Belgium.
Metabolites. 2024 Apr 20;14(4):239. doi: 10.3390/metabo14040239.
Recent studies suggest that the dietary intake of human milk oligosaccharides (HMOs) provides health benefits from infancy up to adulthood. Thus far, beneficial changes in the adult gut microbiome have been observed at oral doses of 5-20 g/day of HMOs. Efficacy of lower doses has rarely been tested. We assessed four HMO molecular species-2'Fucosyllactose (2'FL), Lacto-N-neotetraose (LNnT), 3'Sialyllactose (3'SL), and 6'Sialyllactose (6'SL)-at predicted doses from 0.3 to 5 g/day for 6-year-old children and adults ( = 6 each), using ex vivo SIFR technology (Cryptobiotix, Ghent, Belgium). This technology employing bioreactor fermentation on fecal samples enables us to investigate microbial fermentation products that are intractable in vivo given their rapid absorption/consumption in the human gut. We found that HMOs significantly increased short-chain fatty acids (SCFAs), acetate, propionate (in children/adults), and butyrate (in adults) from predicted doses of 0.3-0.5 g/day onwards, with stronger effects as dosing increased. The fermentation of 6'SL had the greatest effect on propionate, LNnT most strongly increased butyrate, and 2'FL and 3'SL most strongly increased acetate. An untargeted metabolomic analysis revealed that HMOs enhanced immune-related metabolites beyond SCFAs, such as aromatic lactic acids (indole-3-lactic acid/3-phenyllactic acid) and 2-hydroxyisocaproic acid, as well as gut-brain-axis-related metabolites (γ-aminobutyric acid/3-hydroxybutyric acid/acetylcholine) and vitamins. The effects of low doses of HMOs potentially originate from the highly specific stimulation of keystone species belonging to, for example, the family, which had already significantly increased at doses of only 0.5 g/day LNnT (adults) and 1 g/day 2'FL (children/adults).
最近的研究表明,从婴儿期到成年期,饮食中摄入人乳寡糖(HMOs)都对健康有益。迄今为止,已观察到口服剂量为5-20克/天的HMOs会使成人肠道微生物群发生有益变化。较低剂量的功效很少得到测试。我们使用体外SIFR技术(比利时根特的Cryptobiotix公司),对6岁儿童和成人(各6人)预测剂量为0.3至5克/天的四种HMO分子种类——2'-岩藻糖基乳糖(2'FL)、N-新四糖(LNnT)、3'-唾液酸乳糖(3'SL)和6'-唾液酸乳糖(6'SL)进行了评估。这项利用粪便样本进行生物反应器发酵的技术,使我们能够研究那些因其在人体肠道中快速吸收/消耗而在体内难以处理的微生物发酵产物。我们发现,从预测剂量0.3-0.5克/天起,HMOs显著增加了短链脂肪酸(SCFAs)、乙酸盐、丙酸盐(儿童/成人)和丁酸盐(成人),且随着剂量增加效果增强。6'SL的发酵对丙酸盐的影响最大,LNnT最强烈地增加了丁酸盐,而2'FL和3'SL最强烈地增加了乙酸盐。非靶向代谢组学分析表明,HMOs除了增强SCFAs外,还增强了与免疫相关的代谢物,如芳香族乳酸(吲哚-3-乳酸/3-苯乳酸)和2-羟基异己酸,以及与肠脑轴相关的代谢物(γ-氨基丁酸/3-羟基丁酸/乙酰胆碱)和维生素。低剂量HMOs的作用可能源于对例如 科等关键物种的高度特异性刺激,在仅0.5克/天LNnT(成人)和1克/天2'FL(儿童/成人)的剂量下,这些关键物种就已显著增加。