摘要
Endothelins (ETs) are vasoactive peptides evolutionary well conserved that exert their effects through two specific receptors (ETA and ETB) widely distributed in all vertebrates. In snakes, the presence and function of endothelins and their receptors are still scarcely described. We have recently demonstrated the presence of ETA and ETB2 receptors in the snake Bothrops jararaca (Bj). In the present work we showed that distinctively from Bj, the vascular contraction induced by endothelin in Oxyrhopus guibei (Og) snake is mediated only by ETA receptors. Selective ETB agonists (SRTX-c and IRL1620) and antagonists (IRL1038 and BQ788) were ineffective in Og preparations of isolated aorta. We also showed that ET-1 response on Og arterial blood pressure was monophasic hypertensive as opposed to biphasic (hypotension followed by hypertension) in Bj. Furthermore, we characterized the relaxing properties of endothelin receptor ETB1 in pre-contracted aorta preparations. We showed that IRL1620 induced relaxation of pre-contracted Bj aorta but was ineffective in relaxing Og preparations. IRL1620 relaxing effect on Bj aorta was abolished by l-NAME, indicating involvement of NO release, and was reduced by selective ETB antagonists. Our findings suggest that Og snake has a more primitive spectrum of ET receptors (only ETA receptor) than Bj (presence of ETA, ETB1 and ETB2 receptors).