Randomised clinical study: inulin short-chain fatty acid esters for targeted delivery of short-chain fatty acids to the human colon.
Randomised clinical study: inulin short-chain fatty acid esters for targeted delivery of short-chain fatty acids to the human colon.
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DOI:
10.1111/apt.13749
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发表时间:
2016-10
影响因子:
7.6
通讯作者:
Morrison DJ
中科院分区:
文献类型:
--
作者:
Polyviou T;MacDougall K;Chambers ES;Viardot A;Psichas A;Jawaid S;Harris HC;Edwards CA;Simpson L;Murphy KG;Zac-Varghese SE;Blundell JE;Dhillo WS;Bloom SR;Frost GS;Preston T;Tedford MC;Morrison DJ
Short‐chain fatty acids (SCFA) produced through fermentation of nondigestible carbohydrates by the gut microbiota are associated with positive metabolic effects. However, well‐controlled trials are limited in humans. To develop a methodology to deliver SCFA directly to the colon, and to optimise colonic propionate delivery in humans, to determine its role in appetite regulation and food intake. Inulin SCFA esters were developed and tested as site‐specific delivery vehicles for SCFA to the proximal colon. Inulin propionate esters containing 0–61 wt% (IPE‐0–IPE‐61) propionate were assessed in vitro using batch faecal fermentations. In a randomised, controlled, crossover study, with inulin as control, ad libitum food intake (kcal) was compared after 7 days on IPE‐27 or IPE‐54 (10 g/day all treatments). Propionate release was determined using 13C‐labelled IPE variants. In vitro, IPE‐27–IPE‐54 wt% propionate resulted in a sevenfold increase in propionate production compared with inulin (P < 0.05). In vivo, IPE‐27 led to greater 13C recovery in breath CO 2 than IPE‐54 (64.9 vs. 24.9%, P = 0.001). IPE‐27 also led to a reduction in energy intake during the ad libitum test meal compared with both inulin (439.5 vs. 703.9 kcal, P = 0.025) and IPE‐54 (439.5 vs. 659.3 kcal, P = 0.025), whereas IPE‐54 was not significantly different from inulin control. IPE‐27 significantly reduced food intake suggesting colonic propionate plays a role in appetite regulation. Inulin short‐chain fatty acid esters provide a novel tool for probing the diet–gut microbiome–host metabolism axis in humans.
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影响因子:
6.9
作者:
Daud, Norlida M.;Ismail, Nurhafzan A.;Frost, Gary S.
通讯作者:
Frost, Gary S.
影响因子:
12.2
作者:
Morrison DJ;Preston T
通讯作者:
Preston T
影响因子:
3.7
作者:
Maurer, Jacoba M.;Schellekens, Reinout C. A.;Kosterink, Jos G. W.
通讯作者:
Kosterink, Jos G. W.
影响因子:
4.8
作者:
Brown, AJ;Goldsworthy, SM;Dowell, SJ
通讯作者:
Dowell, SJ
DOI:
10.1152/ajpgi.1998.275.6.g1415
发表时间:
1998-12-01
影响因子:
4.5
作者:
Cherbut, C;Ferrier, L;Galimiche, JP
通讯作者:
Galimiche, JP