4.7 Article

Effect of 1-week treatment with erythropoietin on the vascular endothelial function in anaesthetized rabbits

Journal

BRITISH JOURNAL OF PHARMACOLOGY
Volume 133, Issue 3, Pages 395-405

Publisher

WILEY
DOI: 10.1038/sj.bjp.0704083

Keywords

erythropoietin; acetylcholine; haemoglobin; nitric oxide synthase; endothelium-dependent vasodilator

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1 Chronic administration of erythropoietin (EPO) is often associated with hypertension in animals and humans. The aim of this study was to estimate whether 1-week treatment with EPO can affect the vascular endothelial function. 2 Rabbits were given with EPO (400 iu kg(-1) s.c.) or saline each other day for 1 week. Hypotensive responses to intravenously given acetylcholine (ACh), endothelium-independent nitric oxide donors (NOC7, nitroprusside and nitroglycerin) and prostaglandin I-2 were tested before and after administration of N-G-nitro-L-arginine methyl ester (L-NAME). a specific nitric oxide synthase inhibitor, under pentobarbitone: anaesthesia. 3 Blood haemoglobin concentration in EPO group was significantly higher than that in control group, whereas baseline values of aortic pressure, heart rate and femoral vascular resistance were similar. The dose of ACh (172 ng kg (1)) requiring for a 15 mmHg hypotension from the baseline in EPO group was apparently higher than that (55 ng kg(-1)) in control group. On the contrary, hypotensive responses to NOC7, nitroprusside, nitroglycerin and prostaglandin I-2 were comparable between two groups. The extent of ACh-induced hypotension did not correlate with haemoglobin concentration. 4 L-NAME significantly inhibited the ACh-induced vasodilating response in control group but did not in EPO group. 5 In another set of rabbits, the same treatment with EPO also decreased vasodilating responses to carbachol, bradykinin and substance P besides ACh as compared with control group. 6 These results indicate that 1-week treatment with EPO selectively attenuates depressor responses to endothelium-dependent vasodilators in anaesthetized rabbits, most likely due to inhibition of endothelial nitric oxide synthase. British Journal of Pharmacology (2001).

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