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Int J Mol Sci ; 21(3)2020 Jan 30.
Article in English | MEDLINE | ID: mdl-32019237

ABSTRACT

In humans, aging is associated with endothelial dysfunction and an increased risk of venous thromboembolism. Although intake of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) at a ratio of 6:1 by old rats improved the endothelial dysfunction in arteries, the impact on veins remains unclear. Eight-month-old male Wistar rats were either untreated or orally administered corn oil, EPA:DHA 1:1, or EPA:DHA 6:1 (500 mg/kg/d) for seven days. Vascular reactivity was studied by myography. In middle-aged femoral artery rings, acetylcholine caused a partial relaxation at low concentrations and a contractile response at high concentrations, whereas in the old femoral vein only a partial relaxation was observed. The EPA:DHA 6:1 treatment blunted the contractile response to acetylcholine in the middle-aged femoral artery and both EPA:DHA 6:1 and 1:1 increased the relaxation to acetylcholine in the old femoral vein. No such effects were observed with corn oil. Both the non-selective cyclooxygenase inhibitor indomethacin and the COX-1 inhibitor SC-560 increased the relaxation to acetylcholine in the middle-aged femoral artery whereas the COX-2 inhibitor NS-398 increased that in the middle-aged femoral vein. In conclusion, our results indicate that aging is associated with an endothelial dysfunction in the femoral artery and vein, which can be improved by EPA:DHA 6:1 treatment-most likely via a cyclooxygenase-dependent mechanism.


Subject(s)
Aging/pathology , Docosahexaenoic Acids/administration & dosage , Eicosapentaenoic Acid/administration & dosage , Endothelium, Vascular/drug effects , Femoral Artery/drug effects , Femoral Vein/drug effects , Prostaglandin-Endoperoxide Synthases/chemistry , Vascular Diseases/drug therapy , Administration, Oral , Animals , Cyclooxygenase Inhibitors/pharmacology , Endothelium, Vascular/metabolism , Endothelium, Vascular/pathology , Femoral Artery/metabolism , Femoral Artery/pathology , Femoral Vein/metabolism , Femoral Vein/pathology , Male , Rats , Rats, Wistar , Vascular Diseases/metabolism , Vascular Diseases/pathology
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