Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Victor H. Avilés-Rosas"'
Autor:
Eduardo Rivera-Mancilla, Victor H. Avilés-Rosas, Guadalupe Manrique-Maldonado, Alain H. Altamirano-Espinoza, Belinda Villanueva-Castillo, Antoinette MaassenVanDenBrink, Carlos M. Villalón
Publikováno v:
The Journal of Headache and Pain, Vol 18, Iss 1, Pp 1-12 (2017)
Abstract Background Dihydroergotamine (DHE) is an acute antimigraine agent that displays affinity for dopamine D2-like receptors, serotonin 5-HT1/2 receptors and α1/α2-adrenoceptors. Since activation of vascular α1/α2-adrenoceptors results in sys
Externí odkaz:
https://doaj.org/article/4d842091c6ed4def9ddb5e122c8662c1
Autor:
Alain H. Altamirano-Espinoza, Carlos M. Villalón, Guadalupe Manrique-Maldonado, Eduardo Rivera-Mancilla, A. Maassen van den Brink, Victor H. Avilés-Rosas, Bruno A. Marichal-Cancino
Publikováno v:
British Journal of Pharmacology. 174:2001-2014
Background and purpose Olcegepant (BIBN4096BS) is a selective non-peptide CGRP receptor antagonist with acute antimigraine properties. Since systemic vascular tone is modulated by perivascular (primary sensory CGRPergic and sympathetic) nerves, this
Autor:
Carlos M. Villalón, Alain H. Altamirano-Espinoza, Eduardo Rivera-Mancilla, Victor H. Avilés-Rosas, Belinda Villanueva-Castillo, Antoinette MaassenVanDenBrink, Guadalupe Manrique-Maldonado
Publikováno v:
The Journal of Headache and Pain, Vol 18, Iss 1, Pp 1-12 (2017)
Journal of Headache and Pain, 18:104. Springer-Verlag Italia
Journal of Headache and Pain, 18:104. Springer-Verlag Italia
Background Dihydroergotamine (DHE) is an acute antimigraine agent that displays affinity for dopamine D2-like receptors, serotonin 5-HT1/2 receptors and α1/α2-adrenoceptors. Since activation of vascular α1/α2-adrenoceptors results in systemic vas
Autor:
Carlos M. Villalón, Victor H. Avilés-Rosas, Guadalupe Manrique-Maldonado, Eduardo Rivera-Mancilla, Alain H. Altamirano-Espinoza, Bruno A. Marichal-Cancino
Publikováno v:
European journal of pharmacology. 754
This study has investigated whether pharmacological activation of Gi/o coupled histamine H3/H4 receptors inhibits the rat vasodepressor sensory outflow. For this purpose, 100 male Wistar rats were pithed, artificially ventilated and pretreated (i.v.)