食用推荐的麦麸谷物可显著提高健康志愿者的粪便丁酸盐水平,并减少体外炎症标志物

Madalina Neacsu, S. Anderson, Pola Verschoor, N. Vaughan, G. Horgan, T. Hulshof, S. Duncan, S. Duthie, W. Russell
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引用次数: 4

摘要

麦麸谷物是膳食纤维的重要来源。这项研究的目的是调查高摄入量(120克)富含纤维的早餐麦片(提供了英国政府一份纤维摄入量的指导方针,但比制造商推荐的摄入量高出三倍)与推荐的摄入量(40克,含有11克膳食纤维)相比,是否有额外的潜在健康益处。为了评估这一点,该研究在食用两份不同的富含纤维的谷物后,测定了人类粪便、尿液和血浆样本中的短链脂肪酸(SCFA)谱。体外观察了细胞因子(IL-1β)炎症刺激对人结肠成纤维细胞前列腺素生成的抑制作用。健康志愿者8名,年龄18-55岁;BMI (18-30 kg/m2)食用富含麦麸的“即食谷物”,包括高摄入量(120克)和推荐摄入量(40克)。在5小时干预期间和进食后约24小时,收集粪便、尿液和血浆样本。食用推荐量麦麸谷物后,粪便丁酸盐增幅最大(p<0.05),增幅超过两倍(从13.95±9.17 mM增加到31.63±20.53 mM),食用推荐量麦麸谷物后,粪便丁酸盐增幅无显著变化(从21.96±11.03 mM增加到22.9±12.69 mM)。方差分析还发现,在食用麸皮谷物24小时后,尿液中丁酸盐的份量大小(高与推荐)仅对食用效果有微弱影响(p = 0.046)。在志愿者的粪便样本中测定的粪便中SCFAs的生理营养相关浓度显示出显著的抗炎活性或个体粪便中SCFAs;乙酸(p<0.001)、丙酸(p<0.001)和丁酸(p<0.01),以及两者组合。血浆叶酸在食用两种麦麸后也有所增加,并且在食用高麦麸后3小时时间点显著(p = 0.037)。与高摄入量(120克)(从110.5毫米到117.64毫米)相比,摄入推荐量(40克)的麦麸谷物增加了总微生物SCFA水平(从96.88毫米到136.96毫米),这表明摄入高份量的麦麸谷物可能促进粪便膨胀效应,从而降低结肠SCFA水平。这些数据表明,食用推荐量的麦麸麦片足以促进微生物丁酸盐的形成,减少结肠炎症,增加人体血浆叶酸水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Consumption of a Recommended Serving of Wheat Bran Cereals Significantly Increases Human Faecal Butyrate Levels in Healthy Volunteers and Reduces Markers of Inflammation Ex Vivo
Wheat bran cereals are an important source of dietary fibre. The aim of the study was to investigate if a high intake (120 g) of fibre rich breakfast cereal (which delivers the UK Government guidelines for fibre intake in one serving but is three-fold higher than the manufacturers recommended serving) has additional potential health benefits compared to the recommended serving (40 g, containing 11 g of dietary fibre). To assess this, the study determined the short chain fatty acid (SCFA) profiles in human faecal, urine and plasma samples after consumption of two different servings of fibre-rich cereal. Inhibition of prostanoid production was measured (ex vivo) in human colonic fibroblast cells after cytokine (IL-1β) inflammation stimulation. Eight healthy volunteers, 18-55 years old; BMI (18-30 kg/m2) consumed the wheat bran-rich “ready to eat cereal”, at both the high (120 g) serving and recommended (40 g) serving. Faecal, urine and plasma samples were collected at baseline, throughout the five-hour intervention period and approximately 24 hours following consumption. Faecal butyrate showed the largest increase (p<0.05) of more than a two-fold change following the consumption of the recommended serving of wheat bran cereal (from 13.95 ± 9.17 to 31.63 ± 20.53 mM) and no significant change following the higher serving (from 21.96 ± 11.03 to 22.9 ± 12.69 mM). ANOVA analysis also found a weak serving effect (p = 0.046) of the portion size (high vs. recommended) only for butyrate in urine 24 hours after consumption of the bran cereal. The physiological nutritionally relevant concentrations of faecal SCFAs, as determined in the volunteers’ faecal samples showed significant anti-inflammatory activity or the individual faecal SCFAs; acetate (p<0.001), propionate (p<0.001) and butyrate (p<0.01), as well as in combination. Plasma folate was also increased after consumption of both wheat bran servings and was significant (p = 0.037) at the three-hour time point following consumption of the high wheat bran serving. The consumption of the recommended serving (40 g) of wheat bran cereal increased the total microbial SCFAs levels (from 96.88 to 136.96 mM) compared to the higher serving (120 g) (from 110.5 to 117.64 mM) suggesting that the intake of the higher portion size is likely to promote a faecal bulking effect and thereby decrease colonic SCFA levels. These data indicate that consumption of the recommended serving of wheat bran cereal serving would therefore be sufficient to promote microbial butyrate formation, reduce colonic inflammation and increase plasma folate levels in humans.
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