Proceedings of the National Academy of Sciences · 2008 · 518 citations · 40 references
Life SciencesNutritional SciencesPharmacologyFood ChemistryLipid BiochemistryMembrane BiochemistryEssential Fatty AcidsFatty Acid MetabolismLipid ChemistryLipid MetabolismLipids In FoodsMembrane Lipid CompositionAdenylyl Cyclase RegulationBlood PressureDietary Fatty AcidsFatty AcidsMembrane Fatty Acid CompositionOleic Acid ContentPhenolic CompoundsVegetable Oils
Olive oil consumption is associated with lower blood pressure, a benefit often attributed to its minor constituents. The study aims to demonstrate that olive oil’s hypotensive effect is driven by its high oleic acid content. The authors propose that increased oleic acid in cell membranes alters lipid phase behavior, modulating G‑protein signaling to reduce blood pressure. They found that only oleic acid, not its analogues or low‑oleic soybean oil, lowered blood pressure, confirming oleic acid’s specific regulatory role.
Numerous studies have shown that high olive oil intake reduces blood pressure (BP). These positive effects of olive oil have frequently been ascribed to its minor components, such as α-tocopherol, polyphenols, and other phenolic compounds that are not present in other oils. However, in this study we demonstrate that the hypotensive effect of olive oil is caused by its high oleic acid (OA) content (≈70–80%). We propose that olive oil intake increases OA levels in membranes, which regulates membrane lipid structure (H II phase propensity) in such a way as to control G protein-mediated signaling, causing a reduction in BP. This effect is in part caused by its regulatory action on G protein-associated cascades that regulate adenylyl cyclase and phospholipase C. In turn, the OA analogues, elaidic and stearic acids, had no hypotensive activity, indicating that the molecular mechanisms that link membrane lipid structure and BP regulation are very specific. Similarly, soybean oil (with low OA content) did not reduce BP. This study demonstrates that olive oil induces its hypotensive effects through the action of OA.
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