Journal
NEUROUROLOGY AND URODYNAMICS
Volume 33, Issue 8, Pages 1251-1258Publisher
WILEY-BLACKWELL
DOI: 10.1002/nau.22482
Keywords
cannabinoid receptor; endocannabinoid system; mitogen-activated protein kinase; urinary bladder
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AimsTo study micturition and bladder overactivity in female rats after chronic treatment with the fatty acid amide hydrolase (FAAH) inhibitor oleoyl ethyl amide (OEtA). MethodsSprague-Dawley rats received daily subcutaneous injections of OEtA (0.3mg/kg), or vehicle for 2 weeks. Cystometries, organ bath studies, Western blot, and immunofluorescence were then used. Expressions of FAAH, cannabinoid 1 and 2 receptors (CB1 and CB2), mitogen-activated protein kinase (MAPK), vesicular acetyl choline-transporter protein (VAChT), and calcitonin gene-related peptide (CGRP) were evaluated. ResultsAt baseline, OEtA-treated rats had higher values (P<0.05) of micturition intervals (MI) and volumes (MV), bladder capacity (BC), threshold pressure, and flow pressure than vehicle controls. Intravesical PGE(2) reduced MI, MV, and BC, and increased basal pressure and the area under the curve in all rats. However, these urodynamic parameters were altered less by intravesical PGE(2) in OEtA-treated rats (P<0.05 vs. vehicle controls). Compared to vehicle controls, detrusor from OEtA-treated rats had larger contractions to carbachol at 10-0.1 mu M, but no difference in E-max was recorded. FAAH, CB1, CB2, VAChT, or CGRP was similarly expressed in bladders from all rats. In separate experiments, intravesical OEtA increased mucosal expression of phosphorylated MAPK. ConclusionsChronic FAAH inhibition altered sensory urodynamic parameters and reduced bladder overactivity. Even if it cannot be excluded that OEtA may act on central nervous sensory pathways to contribute to these effects, the presence of FAAH and CB receptors in the bladder and activation of intracellular signals for CB receptors by intravesical OEtA suggest a local role for FAAH in micturition control. Neurourol. Urodynam. 33:1251-1258, 2014. (c) 2013 Wiley Periodicals, Inc.
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