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3
*
Unité de Nutrition Lipidique, Institut National de la Recherche Agronomique, 21034 Dijon Cédex, France;
Laboratoire de Physiologie de la Nutrition, Université de Paris-Sud, 91405 Orsay, France; and
**
Laboratoire de Toxicologie Nutritionnelle, Institut National de la Recherche Agronomique, 21034 Dijon Cédex, France.
3To whom correspondence should be addressed.
Cyclic fatty acid monomers purified from a heated linseed oil were
given for 2 wk to adult rats as triacylglycerol at two dose levels,
i.e., 0.1 and 1 g/100 g diet, to determine their effect on some aspects
of lipid metabolism. Indirect evidence of a peroxisome
proliferatorlike effect was observed, as determined by an elevation
of some characteristic enzyme activities, such as peroxisomal
acyl-CoA oxidase, and the microsomal
- but also (
-1)-laurate
hydroxylase (CYP4A1 and CYP2E1, respectively). The dietary cyclic fatty
acids induced a coordinated regulation between the activities of the
lipogenic enzymes studied (
9-desaturase, phosphatidate
phosphohydrolase) and peroxisomal oxidation, but not with mitochondrial
ß-oxidation. The dose-dependent decrease of
9-desaturase
activity (P < 0.05) with cyclic fatty acid monomer
intake was accompanied by a similar decrease of the monounsaturated
fatty acid level in liver. The increase in the
-linolenic acid level
also suggested an increase in
6-desaturase activity with cyclic
fatty acid intake (P < 0.05). In addition, our
results strongly suggested that the altered liver levels of
eicosapentaenoic and arachidonic acids were due to the peroxisomal
retroconversion process in rats fed cyclic acids. Finally, an effect of
these cyclic compounds on the carbohydrate metabolism cannot be
disregarded because they decreased liver glycogen concentration. We
conclude that cyclic fatty acid monomers affect different aspects of
lipid metabolism, including a phenotypic peroxisome proliferator
response. This provides the ground for further studies investigating
the biochemical pathways that underlie the nutritional effect of such
molecules.
KEY WORDS: rats liver cyclic fatty acid monomer lipogenic enzymes peroxisome proliferator
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