Cargando…

Orchidectomy enhances the expression of endothelin-1 and ET(B) receptors in rat portal vein

Functional studies have shown that orchidectomy increases the effects of phenylephrine on rat portal veins, but that it is completely prevented in the presence of both ET(A) and ET(B) receptor antagonists. Although it suggests the involvement of endothelin-1 (ET-1), the local production of this vaso...

Descripción completa

Detalles Bibliográficos
Autores principales: Rossignoli, Patrícia de S., De Labio, Roger W., Payão, Spencer L. M., Pereira, Oduvaldo C. M., Chies, Agnaldo B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Society of Smooth Muscle Research 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137319/
https://www.ncbi.nlm.nih.gov/pubmed/26081371
http://dx.doi.org/10.1540/jsmr.50.85
Descripción
Sumario:Functional studies have shown that orchidectomy increases the effects of phenylephrine on rat portal veins, but that it is completely prevented in the presence of both ET(A) and ET(B) receptor antagonists. Although it suggests the involvement of endothelin-1 (ET-1), the local production of this vasoactive peptide has not been directly quantified in portal veins. Therefore, the aim of the present study was to verify if orchidectomy increases the local expression of ET-1 as well as ET(A) and ET(B) receptors in the rat portal vein. Indeed, the genic expression of ET-1, ET(A) and ET(B) receptors in rat portal veins taken from control (CONT), orchidectomized (ORX) and ORX plus testosterone-replacement therapy (ORX + T) animals were determined by Real Time RT-PCR. The results showed that orchidectomy induced a significant increment in genic expression of ET-1and ET(B) receptors in the rat portal veins, which was completely reversed by testosterone replacement treatment. In conclusion, the results suggest that orchidectomy increases the production of ET-1 in the rat portal vein and that, at least partially, it may be related to the previously reported elevation of responses to phenylephrine.