In vitro metabolism of rumenic acid in bovine liver slices.

Reprod Nutr Dev

INRA, Research Unit on Herbivores, Nutrients and Metabolisms Group, Saint-Genès-Champanelle, France.

Published: October 2005

AI Article Synopsis

  • Ruminant products are a key source of conjugated linoleic acid (CLA) for humans, but liver metabolism can affect its availability during fat mobilization.
  • An experiment compared the metabolism of rumenic acid (a type of CLA) and oleic acid in bovine liver slices, showing that rumenic acid uptake was significantly higher than that of oleic acid.
  • Most of the metabolized rumenic acid was converted into other compounds and preferentially incorporated into polar lipids, indicating its significant metabolic processing in the liver.

Article Abstract

Ruminant products are the major source of CLA for humans. However, during periods of fat mobilization, the liver might play an important role in CLA metabolism which would limit the availability of the latter for muscles and milk. In this context, rumenic acid (cis-9, trans-11 CLA) metabolism in the bovine liver (n = 5) was compared to that of oleic acid (n = 3) by using the in vitro liver slice method. Liver slices were incubated for 17 h in a medium containing 0.75 mM of FA mixture and 55 microM of either [1-(14)C] rumenic acid or [1-(14)C] oleic acid at 37 degrees C under an atmosphere of 95% O(2)-5% CO(2). Rumenic acid uptake by liver slices was twice (P = 0.009) that of oleic acid. Hepatic oxidation of both FA (> 50% of incorporated FA) led essentially to the production of acid-soluble products and to a lower extent to CO(2) production. Rumenic acid was partly converted (> 12% of incorporated rumenic acid) into conjugated C18:3. CLA and its conjugated derivatives were mainly esterified into polar lipids (71.7%), whereas oleic acid was preferentially esterified into neutral lipids (59.8%). Rumenic acid secretion as part of VLDL particles was very low and was one-fourth lower than that of oleic acid. In conclusion, rumenic acid was highly metabolized by bovine hepatocytes, especially by the oxidation pathway and by its conversion into conjugated C18:3 for which the biological properties need to be elucidated.

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Source
http://dx.doi.org/10.1051/rnd:2005039DOI Listing

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