丁酰化淀粉增加结肠丁酸盐浓度,但对身体活跃的健康个体的免疫力影响有限。

IF 3.5 4区 医学 Q2 IMMUNOLOGY Exercise Immunology Review Pub Date : 2013-01-01
Nicholas P West, Claus T Christophersen, David B Pyne, Allan W Cripps, Michael A Conlon, David L Topping, Seungha Kang, Chris S McSweeney, Peter A Fricker, Daniel Aguirre, Julie M Clarke
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引用次数: 0

摘要

背景:丁酸盐输送到大肠可积极调节共生菌群,增强免疫力。目的:探讨通过摄入丁基化高直链玉米淀粉(HAMSB)提高大肠丁酸盐浓度对健康活动者粪便生化、微生物群及免疫指标的影响。设计:男性和女性志愿者被随机分配服用两剂20 g HAMSB (n = 23;年龄37.9±7.8岁;平均+/- SD)或低直链玉米淀粉(LAMS) (n = 18;年龄36.9 = 9.5岁),每日2次,连用28天。于第0、10和28天采集样本,评估粪便细菌群、粪便生化、血清细胞因子和唾液抗菌蛋白。结果:HAMSB导致粪便游离量相对增加(45%;12 - 86%;意思是;90%置信区间;P = 0.02),结合(950%;563 - 1564%;P < 0.01)、总丁酸(260%;174 - 373%;P < 0.01)和粪便丙酸(41%;12 - 77%;P = 0.02),从第0天到第28天。HAMSB还与相对1.6倍(1.2- 2.0倍;P < 0.01)和2.5倍(1.4 ~ 4.4倍;P = 0.01)升高血浆IL-10和tnf - α,但未改变其他免疫指标。粪便中的霉变单胞杆菌增加了81倍(28- 237倍);P < 0.01)和F. prausnitzii(2.1 ~ 12倍;P < 0.01)。结论:在健康的活跃个体中补充HAMSB可促进细菌的生长,从而改善肠道健康,对血浆细胞因子的影响有限。
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Butyrylated starch increases colonic butyrate concentration but has limited effects on immunity in healthy physically active individuals.

Background: Butyrate delivery to the large bowel may positively modulate commensal microbiota and enhance immunity.

Objective: To determine the effects of increasing large bowel butyrate concentration through ingestion of butyrylated high amylose maize starch (HAMSB) on faecal biochemistry and microbiota, and markers of immunity in healthy active individuals.

Design: Male and female volunteers were assigned randomly to consume either two doses of 20 g HAMSB (n = 23; age 37.9 +/- 7.8 y; mean +/- SD) or a low amylose maize starch (LAMS) (n = 18; age 36.9 = 9.5 y) twice daily for 28 days. Samples were collected on days 0, 10 and 28 for assessment of faecal bacterial groups, faecal biochemistry, serum cytokines and salivary antimicrobial proteins.

Results: HAMSB led to relative increases in faecal free (45%; 12-86%; mean; 90% confidence interval; P = 0.02), bound (950%; 563-1564%; P < 0.01) and total butyrate (260%; 174-373%; P < 0.01) and faecal propionate (41%; 12-77%; P = 0.02) from day 0 to day 28 compared to LAMS. HAMSB was also associated with a relative 1.6-fold (1.2- to 2.0-fold; P < 0.01) and 2.5-fold (1.4- to 4.4-fold; P = 0.01) increase in plasma IL-10 and TNF-alpha but did not alter other indices of immunity. There were relative greater increases in faecal P. distasonis (81-fold (28- to 237-fold; P < 0.01) and F. prausnitzii (5.1-fold (2.1- to 12-fold; P < 0.01) in the HAMSB group.

Conclusions: HAMSB supplementation in healthy active individuals promotes the growth of bacteria that may improve bowel health and has only limited effects on plasma cytokines.

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来源期刊
Exercise Immunology Review
Exercise Immunology Review 医学-免疫学
CiteScore
16.00
自引率
0.00%
发文量
7
期刊介绍: Exercise Immunology Review (EIR) serves as the official publication of the International Society of Exercise and Immunology and the German Society of Sports Medicine and Prevention. It is dedicated to advancing knowledge in all areas of immunology relevant to acute exercise and regular physical activity. EIR publishes review articles and papers containing new, original data along with extensive review-like discussions. Recognizing the diverse disciplines contributing to the understanding of immune function, the journal adopts an interdisciplinary approach, facilitating the dissemination of research findings from fields such as exercise sciences, medicine, immunology, physiology, behavioral science, endocrinology, pharmacology, and psychology.
期刊最新文献
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