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. 1982 Oct;70(4):724–731. doi: 10.1172/JCI110668

Hepatic Uptake of Bile Acids in Man

FASTING AND POSTPRANDIAL CONCENTRATIONS OF INDIVIDUAL BILE ACIDS IN PORTAL VENOUS AND SYSTEMIC BLOOD SERUM

Bo Angelin 1,2,3, Ingemar Björkhem 1,2,3, Kurt Einarsson 1,2,3, Staffan Ewerth 1,2,3
PMCID: PMC370280  PMID: 7119112

Abstract

This investigation was undertaken in order to (a) characterize the postprandial inflow of individual bile acids to the liver and (b) determine if peripheral venous bile acid levels always adequately reflect the portal venous concentration, or if saturation of hepatic bile acid uptake can occur under physiological conditions. In five patients with uncomplicated cholesterol gallstone disease, the umbilical cord was cannulated during cholecystectomy, and a catheter was left in the left portal branch for 5 to 7 d. The serum concentrations of cholic acid, chenodeoxycholic acid, and deoxycholic acid in portal venous and systemic circulation were then determined at intervals of 15 to 30 min before and after a standardized meal. A highly accurate and specific gas chromatographic/mass spectrometric technique was used.

The sum of the fasting concentrations of the three bile acids averaged 14.04±4.13 μmol/liter in portal venous serum, and 2.44±0.31 μmol/liter in peripheral venous serum. The estimated hepatic fractional uptake of cholic acid was ∼90%, and those of chenodeoxycholic acid and deoxycholic acid were 70-80%. This resulted in an enrichment of systemic bile acids in the dihydroxy bile acid species. In response to a standardized meal, portal venous bile acid concentrations increased two- to sixfold, with a peak seen 15-60 min after the meal. The maximum postprandial portal venous bile acid concentration averaged 43.04±6.12 μmol/liter, and the corresponding concentration in peripheral serum was 5.22±0.74 μmol/liter. The estimated fractional uptakes of the individual bile acids were not affected by the increased inflow to the liver. The peripheral venous concentrations of individual as well as total bile acids were well correlated with those in portal venous serum.

The results (a) give a quantitation of postprandial bile acid inflow to the liver and (b) indicate that the hepatic uptake system for bile acids in healthy man cannot be saturated during maximal inflow of endogenous bile acids. Measurement of peripheral serum bile acids can thus give important information on the status of the enterohepatic circulation.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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