Dexmedetomidine-induced contraction of isolated rat aorta is dependent on extracellular calcium concentration

BACKGROUND: Dexmedetomidine is a highly selective α(2)-adrenoceptor agonist that is widely used for sedation and analgesia during the perioperative period. Intravenous administration of dexmedetomidine induces transient hypertension due to vasoconstriction via the activation of the α(2)-adrenoceptor...

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Detalles Bibliográficos
Autores principales: Ok, Seong-Ho, Bae, Sung Il, Shim, Haeng Seon, Sohn, Ju-Tae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Anesthesiologists 2012
Materias:
Experimental Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460155/
https://www.ncbi.nlm.nih.gov/pubmed/23060983
http://dx.doi.org/10.4097/kjae.2012.63.3.253

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460155/
https://www.ncbi.nlm.nih.gov/pubmed/23060983
http://dx.doi.org/10.4097/kjae.2012.63.3.253

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