Fara Agustina, Hernández Hernández Oswaldo, Palacios Jorge, Montilla Antonia, Zárate Gabriela
Laboratorio de Ecofisiología Tecnológica, CERELA-CONICET, San Miguel de Tucumán, Argentina.
Grupo de Química y Funcionalidad de Carbohidratos y Derivados, Instituto de Investigación en Ciencias de la Alimentación (CIAL) (CSIC-UAM), Madrid, Spain.
J Sci Food Agric. 2024 Aug 30;104(11):6769-6777. doi: 10.1002/jsfa.13504. Epub 2024 Apr 12.
The general assumption that prebiotics reach the colon without any alterations has been challenged. Some in vitro and in vivo studies have demonstrated that 'non-digestible' oligosaccharides are digested to different degrees depending on their structural composition. In the present study, we compared different methods aiming to assess the digestibility of oligosaccharides synthesized by β-galactosidase (β-gal) of Lactobacillus delbruecki subsp. bulgaricus CRL450 (CRL450-β-gal) from lactose, lactulose and lactitol.
In the simulated gastrointestinal fluid method, no changes were observed. However, the oligosaccharides synthesized by CRL450-β-gal were partially hydrolyzed in vitro, depending on their structure and composition, with rat small intestinal extract (RSIE) and small intestinal brush-border membrane vesicles (BBMV) from pig. Digestion of some oligosaccharides increased when mixtures were fed to C57BL/6 mice used as in vivo model; however, lactulose-oligosaccharides were the most resistant to the physiological conditions of mice. In general β (1→6) linked products showed higher resistance compared to β (1→3) oligosaccharides.
In vitro digestion methods, without disaccharidases, may underestimate the importance of carbohydrates hydrolysis in the small intestine. Although BVMM and RSIE digestion assays are appropriate in vitro methods for these studies, in vivo studies remain the most reliable for understanding what actually happens in the digestion of oligosaccharides. © 2024 The Authors. Journal of The Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.
益生元未经任何改变即可到达结肠这一普遍假设受到了挑战。一些体外和体内研究表明,“不可消化”的寡糖会根据其结构组成被不同程度地消化。在本研究中,我们比较了旨在评估德氏乳杆菌保加利亚亚种CRL450(CRL450-β-半乳糖苷酶)从乳糖、乳果糖和乳糖醇合成的寡糖消化率的不同方法。
在模拟胃肠液方法中,未观察到变化。然而,CRL450-β-半乳糖苷酶合成的寡糖在体外会被部分水解,这取决于其结构和组成,水解过程使用大鼠小肠提取物(RSIE)和猪的小肠刷状缘膜囊泡(BBMV)。当将混合物喂给作为体内模型的C57BL/6小鼠时,一些寡糖的消化增加;然而,乳果糖寡糖对小鼠的生理条件最具抗性。一般来说,与β(1→3)寡糖相比,β(1→6)连接的产物表现出更高的抗性。
没有二糖酶的体外消化方法可能会低估小肠中碳水化合物水解的重要性。尽管BBMV和RSIE消化试验是适用于这些研究的体外方法,但体内研究对于了解寡糖消化过程中实际发生的情况仍然是最可靠的。© 2024作者。《食品与农业科学杂志》由约翰·威利父子有限公司代表化学工业协会出版。