British Journal of Pharmacology · 2008 · 51 citations · 42 references
MedicinePharmacologyUrologyBiochemical PharmacologyMolecular PharmacologyPharmacodynamicsBladder DysfunctionDetrusor ActivityDetrusor Muscle FunctionDetrusor OveractivityOveractive BladderPharmacology Of Nitrous OxideDetrusor Muscarinic Receptor FunctionFunctional AssaysMuscarinic AgonistsMuscarinic Receptor PharmacologyMuscarinic Receptor SubtypesMuscarinic ReceptorsNitric OxideReceptors
BACKGROUND AND PURPOSE: Overactive bladder is a complex and widely prevalent condition, but little is known about its physiopathology. We have carried out morphological, biochemical and functional assays to investigate the effects of long-term nitric oxide (NO) deficiency on muscarinic receptor and beta-adrenoceptor modulation leading to overactivity of rat detrusor muscle. EXPERIMENTAL APPROACH: Male Wistar rats received N(omega)-nitro-L-arginine methyl ester (L-NAME) in drinking water for 7-30 days. Functional responses to muscarinic and beta-adrenoceptor agonists were measured in detrusor smooth muscle (DSM) strips in Krebs-Henseleit solution. Measurements of [(3)H]inositol phosphate, NO synthase (NOS) activity, [(3)H]quinuclidinyl benzilate ([(3)H]QNB) binding and bladder morphology were also performed. KEY RESULTS: Long-term L-NAME treatment significantly increased carbachol-induced DSM contractile responses after 15 and 30 days; relaxing responses to the beta(3)-adrenoceptor agonist BRL 37-344 were significantly reduced at 30 days. Constitutive NOS activity in bladder was reduced by 86% after 7 days and maintained up to 30 days of L-NAME treatment. Carbachol increased sixfold the [(3)H]inositol phosphate in bladder tissue from rats treated with L-NAME. [(3)H]QNB was bound with an apparent K(D) twofold higher in bladder membranes after L-NAME treatment compared with that in control. No morphological alterations in DSM were found. CONCLUSIONS AND IMPLICATIONS: Long-term NO deficiency increased rat DSM contractile responses to a muscarinic agonist, accompanied by significantly enhanced K(D) values for muscarinic receptors and [(3)H]inositol phosphate accumulation in bladder. This supersensitivity for muscarinic agonists along with reductions of beta(3)-adrenoceptor-mediated relaxations indicated that overactive DSM resulted from chronic NO deficiency.
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Prevalence and burden of overactive bladder in the United States
Walter F. Stewart, J. Van Rooyen, Geoffrey W. Cundiff et al. · World Journal of Urology · 2003 · 2.3K citations · Full text
Medicine, Internal Medicine, Urology +13
Chronic inhibition of nitric oxide synthesis. A new model of arterial hypertension.
Miriam O. Ribeiro, Edson Antunes, Gilberto De Nucci et al. · Hypertension · 1992 · 794 citations · Full text
Medicine, Cardiology, Pharmacology +16