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Production rates and metabolism of short-chain fatty acids in the colon and whole body using stable isotopes

Published online by Cambridge University Press:  05 March 2007

Etienne Pouteau*
Affiliation:
Nestle Research Center, Nestec Ltd, PO Box 44, Vers-Chez-Les-Blanc, 1000 Lausanne 26, Switzerland
Patrick Nguyen
Affiliation:
Unite de Nutrition et Alimentation, Ecole Nationale Veterinaire de Nantes, Nantes, France
Olivier Ballèvre
Affiliation:
Nestle Research Center, Nestec Ltd, PO Box 44, Vers-Chez-Les-Blanc, 1000 Lausanne 26, Switzerland
Michel Krempf
Affiliation:
Centre de Recherche en Nutrition Humaine, Groupe Metabolisme, Nantes, France
*
*Corresponding author: Dr Etienne Pouteau, fax +4121 785 85 44, [email protected]
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Abstract

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Short-chain fatty acids (SCFA; mainly acetate, propionate and butyrate) are largely produced in non-ruminants during the colonic bacterial fermentation of non-digestible carbohydrates. These intestinal exogenous SCFA pass in part through the splanchnic bed and reach the peripheral bloodstream, mixing with the endogenous circulating SCFA. The whole-body turnover of SCFA is thus composed of an endogenous peripheral turnover and an exogenous production that depends on dietary intake of non-digestible carbohydrates. In the present work methods were developed for determining the SCFA turnover in animals and in human subjects using stable isotopes. The original studies performed to determine endogenous and exogenous metabolism of SCFA in animals and in human subjects are summarised. Using intravenous infusion of 13C-labelled SCFA the whole-body turnover of acetate, propionate and butyrate was assessed in rats in a fasted state. The endogenous turnover of acetate and its oxidation were determined in healthy human subjects in the post-absorptive state, using intravenous infusion of[l-13C]acetate. Intragastric tracer infusions were performed to evaluate the splanchnic first-pass retention of acetate in adults. Finally, an original model was developed in healthy human subjects using intravenous infusion of[l-13C]acetate to determine in vivo the true colonic acetate production after ingestion of a non-digestible disaccharide. These present studies using stable isotopes provide the basis for a novel strategy to evaluate in vivo, in human subjects, the production of SCFA in the large intestine.

Type
Session: Short-chain fatty acids
Copyright
Copyright © The Nutrition Society 2003

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