Iontophoresis of Endothelin Receptor Antagonists in Rats and MenReportar como inadecuado




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Introduction

The treatment of scleroderma-related digital ulcers is challenging. The oral endothelin receptor antagonist ERA bosentan has been approved but it may induce liver toxicity. The objective of this study was to test whether ERAs bosentan and sitaxentan could be locally delivered using iontophoresis.

Methods

Cathodal and anodal iontophoresis of bosentan and sitaxentan were performed on anaesthetized rat hindquarters without and during endothelin-1 infusion. Skin blood flow was quantified using laser-Doppler imaging and cutaneous tolerability was assessed. Iontophoresis of sitaxentan 20 min, 20 or 100 µA was subsequently performed on the forearm skin of healthy men n = 5.

Results

In rats neither bosentan nor sitaxentan increased skin blood flux compared to NaCl. When simultaneously infusing endothelin-1, cathodal iontophoresis of sitaxentan increased skin blood flux compared to NaCl AUC0–20 were 44032.2±12277 and 14957.5±23818.8 %BL.s, respectively; P = 0.01. In humans, sitaxentan did not significantly increase skin blood flux as compared to NaCl. Iontophoresis of ERAs was well tolerated both in animals and humans.

Conclusions

This study shows that cathodal iontophoresis of sitaxentan but not bosentan partially reverses endothelin-induced skin vasoconstriction in rats, suggesting that sitaxentan diffuses into the dermis. However, sitaxentan does not influence basal skin microvascular tone in rats or in humans.



Autor: Matthieu Roustit , Sophie Blaise, Claire Arnaud, Marcin Hellmann, Claire Millet, Diane Godin-Ribuot, Boris Dufournet, Jean Bouton

Fuente: http://plos.srce.hr/



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