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Impaired Excitatory Neurotransmission in the Urinary Bladder from the Obese Zucker Rat: Role of Cannabinoid Receptors

Metabolic syndrome (MS) is a known risk factor for lower urinary tract symptoms. This study investigates whether functional and expression changes of cannabinoid CB(1) and CB(2) receptors are involved in the bladder dysfunction in an obese rat model with insulin resistance. Bladder samples from obes...

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Detalles Bibliográficos
Autores principales: Blaha, Igor, Recio, Paz, Martínez, María Pilar, López-Oliva, María Elvira, Ribeiro, Ana S. F., Agis-Torres, Ángel, Martínez, Ana Cristina, Benedito, Sara, García-Sacristán, Albino, Fernandes, Vítor S., Hernández, Medardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902197/
https://www.ncbi.nlm.nih.gov/pubmed/27285468
http://dx.doi.org/10.1371/journal.pone.0157424
Descripción
Sumario:Metabolic syndrome (MS) is a known risk factor for lower urinary tract symptoms. This study investigates whether functional and expression changes of cannabinoid CB(1) and CB(2) receptors are involved in the bladder dysfunction in an obese rat model with insulin resistance. Bladder samples from obese Zucker rat (OZR) and their respective controls lean Zucker rat (LZR) were processed for immunohistochemistry and western blot for studying the cannabinoid receptors expression. Detrusor smooth muscle (DSM) strips from LZR and OZR were also mounted in myographs for isometric force recordings. Neuronal and smooth muscle CB(1) and CB(2) receptor expression and the nerve fiber density was diminished in the OZR bladder. Electrical field stimulation (EFS) and acetylcholine (ACh) induced frequency- and concentration-dependent contractions of LZR and OZR DSM. ACh contractile responses were similar in LZR and OZR. EFS-elicited contractions, however, were reduced in OZR bladder. Cannabinoid receptor agonists and antagonists failed to modify the DSM basal tension in LZR and OZR In LZR bladder, EFS responses were inhibited by ACEA and SER-601, CB(1) and CB(2) receptor agonists, respectively, these effects being reversed by ACEA plus the CB(1) antagonist, AM-251 or SER-601 plus the CB(2) antagonist, AM-630. In OZR bladder, the inhibitory action of ACEA on nerve-evoked contractions was diminished, whereas that SER-601 did not change EFS responses. These results suggest that a diminished function and expression of neuronal cannabinoid CB(1) and CB(2) receptors, as well as a lower nerve fiber density is involved in the impaired excitatory neurotransmission of the urinary bladder from the OZR.