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The effect of HDL on endothelial function was evaluated using aorta rings of New Zealand rabbits in an isolated organ bath as previously described [60]. Aorta rings were incubated with HDL to a final concentration of 50 mg/dL of cholesterol in Krebs solution (118.1 mM NaCl, 4.7 mM KCl, 1.2 mM MgSO4, 1.20 mM KH2PO4, 2.5 mM CaCl2, 25.0 mM NaHCO3, and 11.1 mM glucose at pH 7.4), continuously bubbled with 95% O2 and 5% CO2, at 37 °C, 1 h prior to the test. After an equilibrium period, aorta rings were precontracted with 3 × 10−4 M phenylephrine. The endothelium-mediated relaxation (vasodilation) was evaluated using a dose–response curve to acetylcholine (5 × 10−9–8 × 10−7 M). Contractions were measured isometrically with an FT−03 Grass Force Displacement Transducer and recorded on a Grass Polygraph (Model 7D, Grass Medical Instruments, Quincy, MA, USA). All experiments were run in duplicate, and vasodilation of aorta rings was expressed as the percentage of pre-contraction with phenylephrine.

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