6533b834fe1ef96bd129cde6

RESEARCH PRODUCT

Fatty acid metabolism, pharmacological nutrients and hypertension.

J.-p. PoissonC. FoucherV. DardelMichel NarceMarie-claire DelachambreS. GermainJ.m. Frenoux

subject

Fatty Acid Desaturasesmedicine.medical_specialtyBiochemistrychemistry.chemical_compoundNutrientInternal medicineRats Inbred SHRmedicineAnimalsCYP2C8chemistry.chemical_classificationFatty acid metabolismFatty AcidsFatty acidGeneral MedicineEicosapentaenoic acidRatsEndocrinologyBlood pressurechemistryBiochemistryLiverDocosahexaenoic acidHypertensionFatty Acids UnsaturatedArachidonic acidEnergy Intake

description

Abstract The purpose of the present study was to investigate the effect of a concentrated preparation (EPA30) containing eicosapentaenoic acid (EPA. 20:5 n -3) and docosahexaenoic acid (DHA, 22:6 n -3) on the limiting desaturation steps of the polyunsaturated fatty acid biosynthesis in spontaneously hypertensive rats (SHR). Adult SHR were divided into two groups: one group received a standard diet, and the experimental group the standard diet including 0.8% of EPA30 for 9 weeks. Blood pressure was measured at the end of the diets. The desaturase activities and fatty acid composition were determined in isolated hepatocytes. The blood pressure did not decrease in the experimental group. The desaturated products of the n -6 family (gamma-linolenic acid, 18:3 n -6 and arachidonic acid, 20:4 n -6) were lowered in the EPA30 group, when their respective substrates (18:2 n -6 and 20:3 n -6) were increased. EPA and DHA were higher in the experimental group, Δ 6 n -3, Δ 6 n -6 and Δ 5 n -6 desaturase activities were depressed approximately 20% in the EPA 30 group. EPA30 being an active nutrient on the EFAs cascade, increasing the level of PG3 precursors and decreasing the level of PG2 precursors, favorable conditions have been established to reduce hypertension. The underlying mechanism related to the regulation of desaturase activities by these fatty nutrients remains to be elucidated.

10.1016/s0300-9084(97)81505-2https://pubmed.ncbi.nlm.nih.gov/9209710