在接受过回肠造口术但身体健康的人中口服混合酶 Elevase® 后对大分子消化的急性生理影响--随机、双盲、安慰剂对照探索性研究

Shahneela Ali Manzer, Annie Simon, J. Colom, Ekaterina Khokhlova, Martin Buckley, C. Phipps, J. Deaton, K. Rea
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引用次数: 0

摘要

消化酶可选择性地降解蛋白质、碳水化合物和脂类;在进食时补充消化酶可加速复杂食物基质的分解,促进营养吸收,降低对食物的敏感性,并有助于治疗某些疾病。食物消化受多种内在和外在因素的影响,每个人的消化情况都不尽相同。这项研究采用了随机、交叉、安慰剂对照设计,每个参与者都是自己的对照组。这项事后分析调查了一种名为 Elevase® 的混合膳食酶补充剂对膳食大分子消化的影响,样本来自曾接受过小肠切除术并导致回肠造口的健康参与者(NCT04489810)。这是首次使用这种研究范式来评估酶补充后的体内膳食分解情况。可以说,与人工肠道消化模型、临床前动物模型或使用粪便分析的传统临床研究相比,这种技术能提供更优越的数据,因为它能在小肠原位实时获取样本,而小肠是营养吸收的主要场所。研究表明,4 小时后,Elevase® 能显著提高回肠样本中的单糖含量(主要是葡萄糖和果糖),这些样本取自不同日期相同饮食的同一人。此外,胆盐牛磺脱氧胆酸也有所增加,这表明宿主对混合酶诱导的大分子消化产生了生理反应。总之,这些研究结果表明,Elevase® 可以加速食物消化,并有可能增加膳食中的营养成分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute physiological effects on macromolecule digestion following oral ingestion of the enzyme blend Elevase® in individuals that had undergone an ileostomy, but were otherwise healthy—a randomized, double blinded, placebo-controlled exploratory study
Digestive enzymes can selectively degrade proteins, carbohydrates and lipids; and their supplementation alongside food may accelerate the breakdown of complex food matrices, facilitate greater nutrient absorption, decrease food sensitivities and aid in the management of certain disease states. Several intrinsic and extrinsic factors govern food digestion and for every individual this phenomenon is unique. This study was conducted as a randomized, crossover, placebo-controlled design where each participant served as their own control. This post-hoc analysis investigated the impact of a dietary enzyme supplementation blend known as Elevase® on dietary macromolecule digestion in samples from otherwise healthy participants that had previously undergone a small bowel resection, resulting in an ileostomy (NCT04489810). This is the first time this study-paradigm has been used for the assessment of in vivo dietary breakdown following enzyme supplementation. Arguably, this technique offers superior data when compared to that generated in artificial gut digestion models, preclinical animal models, or indeed conventional clinical studies using stool analyses, as it allows real-time access to samples in situ in the small intestine where the majority of nutritional absorption takes place. It was demonstrated that after 4 h, Elevase® significantly increased monosaccharide levels (predominantly glucose and fructose) in the ileostomy samples taken from the same individuals on the same diet on a different day. In addition, the bile salt taurohyodeoxycholic acid was also increased, suggesting a physiological host response to the macromolecule digestion induced by the enzymatic blend. Overall, these findings suggest Elevase® could accelerate food digestion and potentially increase nutrient availability from the diet.
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