Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1987 Oct;28(10):1221-7.
doi: 10.1136/gut.28.10.1221.

Short chain fatty acids in human large intestine, portal, hepatic and venous blood

Affiliations

Short chain fatty acids in human large intestine, portal, hepatic and venous blood

J H Cummings et al. Gut. 1987 Oct.

Abstract

Evidence for the occurrence of microbial breakdown of carbohydrate in the human colon has been sought by measuring short chain fatty acid (SCFA) concentrations in the contents of all regions of the large intestine and in portal, hepatic and peripheral venous blood obtained at autopsy of sudden death victims within four hours of death. Total SCFA concentration (mmol/kg) was low in the terminal ileum at 13 +/- 6 but high in all regions of the colon ranging from 131 +/- 9 in the caecum to 80 +/- 11 in the descending colon. The presence of branched chain fatty acids was also noted. A significant trend from high to low concentrations was found on passing distally from caecum to descending colon. pH also changed with region from 5.6 +/- 0.2 in the caecum to 6.6 +/- 0.1 in the descending colon. pH and SCFA concentrations were inversely related. Total SCFA (mumol/l) in blood was, portal 375 +/- 70, hepatic 148 +/- 42 and peripheral 79 +/- 22. In all samples acetate was the principal anion but molar ratios of the three principal SCFA changed on going from colonic contents to portal blood to hepatic vein indicating greater uptake of butyrate by the colonic epithelium and propionate by the liver. These data indicate that substantial carbohydrate, and possibly protein, fermentation is occurring in the human large intestine, principally in the caecum and ascending colon and that the large bowel may have a greater role to play in digestion than has previously been ascribed to it.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Am J Clin Nutr. 1987 Feb;45(2):423-31 - PubMed
    1. J Gen Microbiol. 1986 Jun;132(6):1647-56 - PubMed
    1. Gastroenterology. 1966 Sep;51(3):383-9 - PubMed
    1. Ann N Y Acad Sci. 1968 Feb 26;150(1):75-81 - PubMed
    1. Acta Pathol Microbiol Scand. 1968;72(2):313-29 - PubMed

Publication types

LinkOut - more resources