Key result
Clinically relevant concentrations of hydroxyethyl starch, dextran, and gelatin significantly reduced both NO-induced and NO-/prostacyclin-independent endothelium-dependent relaxation in porcine coronary arteries (p<0.05).
Why the study?
Do colloids like hydroxyethyl starch, dextran, and gelatin reduce endothelium-dependent relaxation in porcine coronary arteries?
Do colloids like hydroxyethyl starch, dextran, and gelatin reduce endothelium-dependent relaxation in porcine coronary arteries?
Answers are grounded in this paper and cite their sources.
Clinically relevant concentrations of hydroxyethyl starch, dextran, and gelatin significantly impair endothelium-dependent relaxation in porcine coronary arteries.
BACKGROUND: In a pilot study we could show that hydroxyethyl starch (HES) induced a significant reduction of endothelium-dependent relaxation (EDR) and the endothelium-derived hyperpolarizing factor (EDHF). In this follow-up study we investigated whether this effect of HES was dose-dependent and whether it could be replicated with other colloids like dextran (DX) and gelatin (GL). METHODS: Rings of fresh porcine coronary arteries were consecutively tested with or without HES, DX or GL (5, 10, or 20 mg/ml). Indomethacin was added in all measurements to eliminate prostacyclin effects. Prostaglandin F₂α was used for contraction and bradykinin (BK, 10⁻¹⁰ to 10⁻⁵ M) for inducing EDR. After blocking nitric oxide (NO) by N-nitro-L-arginine (L-NNA), the experiments were repeated to assess the EDHF-mediated relaxation response to BK. RESULTS: HES induced a reduction in EDR for the BK concentrations of 10⁻⁸ and 10⁻⁷ M (n = 10; p < 0.05). After NO blockage with L-NNA, the relaxation response was reduced especially for the BK concentrations of 10⁻⁶ and 10⁻⁵ M (p < 0.05). GL showed a reduction in EDR with or without NO blockage with L-NNA especially for the BK concentrations of 10⁻⁶ and 10⁻⁵ M (n = 14; p < 0.05). DX induced a significant reduction in EDR for the BK concentrations of 10⁻⁷ and 10⁻⁶ M (n = 12; p < 0.05). After NO blockage with L-NNA, the relaxation response was reduced especially for the BK concentrations of 10⁻⁶ and 10⁻⁵ M (p < 0.05). CONCLUSION: For clinically relevant concentrations of HES, DX and GL a significant reduction in both NO-induced and NO-/prostacyclin-independent EDR can be found in epicardial coronary arteries of the pig.
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Dagtekin et al. (2010) studied Porcine coronary arteries (ex vivo). Hydroxyethyl starch (HES), dextran (DX), and gelatin (GL) vs. Without HES, DX or GL was evaluated on Endothelium-dependent relaxation (EDR) and EDHF-mediated relaxation response to bradykinin (p=<0.05). Clinically relevant concentrations of hydroxyethyl starch, dextran, and gelatin significantly reduced both NO-induced and NO-/prostacyclin-independent endothelium-dependent relaxation in porcine coronary arteries (p<0.05).
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