Staff Publications

Staff Publications

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    'Staff publications' is the digital repository of Wageningen University & Research

    'Staff publications' contains references to publications authored by Wageningen University staff from 1976 onward.

    Publications authored by the staff of the Research Institutes are available from 1995 onwards.

    Full text documents are added when available. The database is updated daily and currently holds about 240,000 items, of which 72,000 in open access.

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Record number 562803
Title Butyrate induces oxidative metabolism of other mitochondrial substrates in colonocytes
Author(s) Bekebrede, Anna; Gerrits, W.J.J.; Deuren, Thirza van; Keijer, J.; Boer, V.C.J. de
Source In: Wias Annual Conference 2020 WIAS - p. 54 - 54.
Department(s) Human and Animal Physiology
WIAS
Animal Nutrition
VLAG
Publication type Abstract in scientific journal or proceedings
Publication year 2020
Abstract Butyrate, a short chain fatty acid, is considered important for gut health due to its role as primary energy source for colonocytes. However, high butyrate levels may bedetrimental for intestinal cells, because of a limited capacity to oxidize butyrate. As aresult, butyrate could accumulate intracellularly and cause damage, possibly via inhibition of histone deacetylases. Since butyrate levels in the colon fluctuate and are driven largely by dietary intake, it is important to understand the fate of butyrate in the colon. We now investigated the metabolic consequences of long and short-term butyrate exposure both in vitro using human and pig cells and in vivo in pigs. In cultured cells (HT29, Caco-2 and HCT-116), acute exposure to butyrate increased oxygen consumption,as has also been observed by other researchers. However, a simultaneous decrease in extracellular acidification was observed, indicating that glycolysis was inhibited. Furthermore, oxygen consumption did not increase in response to butyrate when no glucose was present in the medium. Taken together, these results lead usto believe that butyrate itself was not responsible for the observed oxygen consumption.Instead, butyrate stimulated pyruvate flux towards the mitochondria. Indeed,blocking of the mitochondrial pyruvate carrier likewise inhibited increased oxygen consumption upon butyrate treatment. Long-term exposure to butyrate (72 hours)decreased mitochondrial bio energetics of high-glucose cultured HT29 cells, while not significantly affecting low-glucose cultured cells. We therefore hypothesize that the observed increased pyruvate flux in high-glucose HT29 may lead to increased reactive oxygen species formation, which leads to decreased mitochondrial function in the long run. Similar to the high-glucose HT29 cells exposed to butyrate for 72h, freshly isolated colon cells from pigs fed a fibre diet also showed a decrease in metabolic function. This indicates that increased butyrate concentrations may also negatively impact metabolic function under physiological conditions.
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