4.7 Article

Short chain fatty acids exchange across the gut and liver in humans measured at surgery

期刊

CLINICAL NUTRITION
卷 28, 期 6, 页码 657-661

出版社

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.clnu.2009.05.011

关键词

Propionate; Butyrate; Acetate; Interorgan metabolism; Human

资金

  1. Netherlands Organisation for Health Research and Development

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Background & aims: Short chain fatty acids (SCFAs; acetate, propionate and butyrate) are important energy sources for colonocytes and are assumed to play a key role in gut health. Local effects of SCFAs have been investigated, but less is known about whole body metabolism of these SCFAs. The aim of the present study was to quantify the role of the gut and liver in interorgan exchange of SCFAs in humans in vivo. Methods: Twenty-two patients undergoing major upper abdominal surgery were studied. Blood was sampled from a radial artery, the portal and a hepatic vein. Portal, splanchnic and arterial blood flow was measured using intra-operative Duplex ultrasonography. SCFAs were measured on a liquid chromatography system combined with mass spectrometry. Results: SCFAs were released by the gut, 34.9 (9.1) mu mol kg bodyweight(-1) h(-1). SCFAs uptake by the liver was significant for propionate and butyrate; -5.6 (1.3) and -3.8 (1.6) mu mol kg bodyweight(-1) h(-1) (p = 0.0002 and p = 0.03) respectively and counterbalanced gut release. Liver uptake of acetate was not significant, -5.2 (6.6) mu mol kg bodyweight(-1) h(-1) (p = 0.434). Splanchnic (i.e., gut + liver) SCFAs release was significant for acetate and propionate, 17.3 (7.3) and 1.2 (0.4) mu mol kg bodyweight(-1) h(-1) (p = 0.027 and p = 0.0038), respectively. Splanchnic release of butyrate was not significantly different from zero (1.9 (1.2) mu mol kg bodyweight(-1) h(-1), p = 0.129). BMI and previous colonic resection did not affect gut release of SCFAs. Conclusion: This is the first in vivo study on the role of the gut and liver in SCFAs exchange in humans in vivo. It is shown that intestinal SCFAs release by the gut is equalled by hepatic uptake. (C) 2009 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.

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