Advertisement

Purpose:

Loss of bladder smooth muscle caveolae, which are membrane invaginations involved in signaling regulation, is associated with detrusor dysfunction. We investigated whether caveolar loss in bladder smooth muscle from SHR rats contributes to detrusor overactivity by dysregulating caveolar mediated signaling.

Materials and Methods:

Caveolar density and caveolin-1 protein expression were compared between SHR and WKY rats by ultrastructural and molecular analysis. The functional effects of caveolar depletion achieved by methyl-β-cyclodextrin on neurogenic and agonist induced contractions, and spontaneous activity in isolated bladder tissue were also compared between the strains. P2X1 receptor and caveolin-1 interaction was investigated by confocal microscopy, co-immunoprecipitation and proximity ligation assay.

Results:

Bladder smooth muscle caveolar density and caveolin-1 expression were decreased in SHR vs WKY rats. Responses to α-β-methylene adenosine triphosphate at baseline were lower in SHR than in WKY rats. Methyl-β-cyclodextrin significantly decreased α-β-methylene adenosine triphosphate responses in WKY rats but had less effect in SHR rats. Methyl-β-cyclodextrin decreased the amplitude of the purinergic component of neurally mediated contractions in each strain but had no effect on the cholinergic component. Bladder spontaneous activity was significantly higher in SHR than in WKY rats. Exposure to methyl-β-cyclodextrin or P2X1 receptor antagonist significantly increased spontaneous activity in WKY rats but had no effect in SHR rats. P2X1 receptor and caveolin-1 were co-localized and co-precipitated in bladder smooth muscle tissue.

Conclusions:

Caveolar depletion in WKY bladders results in a functional phenotype analogous to that of overactive SHR bladder. The intrinsically decreased caveolae in SHR rats causes loss of the caveolar mediated regulation of purinergic signaling and augmented spontaneous activity, conditions that may lead to detrusor overactivity.

References

  • 1 : A myogenic basis for the overactive bladder. Urology1997; 50: 57. Google Scholar
  • 2 : Structural basis of geriatric voiding dysfunction: II. Aging detrusor: normal versus impaired contractility. J Urol1993; 150: 1657. LinkGoogle Scholar
  • 3 : Role of plasmalemmal caveolae in signal transduction. Am J Physiol1998; 64: 749. Google Scholar
  • 4 : The biology of caveolae: lessons from caveolin knockout mice and implications for human disease. Mol Interv2003; 3: 445. Google Scholar
  • 5 : Smooth muscle caveolae differentially regulate specific agonist induced bladder contractions. Neurourol Urodyn2007; 26: 71. Google Scholar
  • 6 : Cholesterol depletion alters coronary artery myocyte Ca(2+) signaling in a stimulus-specific manner. Cell Calcium2010; 47: 84. Google Scholar
  • 7 : Loss of smooth muscle caveolae in the aging bladder. Neurourol Urodyn2012; 31: 586. Google Scholar
  • 8 : Alterations in caveolin expression and ultrastructure after bladder smooth muscle hypertrophy. J Urol2009; 182: 2497. LinkGoogle Scholar
  • 9 : Biochemical and functional correlates of an increased membrane density of caveolae in hypertrophic rat urinary bladder. Eur J Pharmacol2010; 649: 362. Google Scholar
  • 10 : Spinal and peripheral mechanisms contributing to hyperactive voiding in spontaneously hypertensive rats. Am J Physiol1998; 275: R136. Google Scholar
  • 11 : The spontaneously hypertensive rat: insight into the pathogenesis of irritative symptoms in benign prostatic hyperplasia and young anxious males. Exp Physiol1999; 84: 137. Google Scholar
  • 12 : Direct observation of individual endogenous protein complexes in situ by proximity ligation. Nat Methods2006; 3: 995. Google Scholar
  • 13 : Effects of gender, age and hypertension on beta-adrenergic receptor function in rat urinary bladder. Naunyn Schmiedebergs Arch Pharmacol2006; 373: 300. Google Scholar
  • 14 : Selection of a control rat for conscious Spontaneous Hypertensive rats in studies of detrusor overactivity on the basis of measurement of intra-abdominal pressures. Neurourol Urodyn2010; 29: 1338. Google Scholar
  • 15 : Urogenital alterations in aged male caveolin-1 knockout mice. J Urol2004; 171: 950. LinkGoogle Scholar
  • 16 : Differential regulation of nitric oxide synthases and their allosteric regulators in heart and vessels of hypertensive rats. Cardiovasc Res2003; 57: 456. Google Scholar
  • 17 : Extraction of membrane cholesterol disrupts caveolae and impairs serotonergic (5-HT2A) and histaminergic (H1) responses in bovine airway smooth muscle: role of Rho-kinase. Can J Physiol Pharmacol2009; 87: 180. Google Scholar
  • 18 : Human urinary bladder smooth muscle is dependent on membrane cholesterol for cholinergic activation. Eur J Pharmacol2010; 634: 142. Google Scholar
  • 19 : Postganglionic efferent transmission to the bladder and urethra. In: . Edited by . Yverdon, Switzerland: Harwood Academic Publishers1993: 142. chapt 10. Google Scholar
  • 20 : A role for muscarinic receptors or rho-kinase in hypertension associated rat bladder dysfunction?. J Urol2005; 173: 2178. LinkGoogle Scholar
  • 21 : P2X receptors and their role in female idiopathic detrusor instability. J Urol2002; 167: 157. LinkGoogle Scholar
  • 22 : Alterations in purinergic and cholinergic components of contractile responses of isolated detrusor contraction in a rat model of partial bladder outlet obstruction. BJU Int2006; 97: 372. Google Scholar
  • 23 : Biomechanical properties and innervation of the female caveolin-1-deficient detrusor. Br J Pharmacol2011; 162: 1156. Google Scholar
  • 24 : Loss of caveolin-1 expression is associated with disruption of muscarinic cholinergic activities in the urinary bladder. Neurochem Int2004; 45: 1185. Google Scholar
  • 25 : Identification of atropine-and P2X1 receptor antagonist-resistant, neurogenic contractions of the urinary bladder. J Neurosci2007; 27: 845. Google Scholar
  • 26 : Increased cholesterol decreases uterine activity: functional effects of cholesterol alteration in pregnant rat myometrium. Am J Physiol Cell Physiol2005; 288: C982. Google Scholar
  • 27 : Extracellular nucleotides affect pericyte-mediated regulation of rat in situ vasa recta diameter. Acta Physiol2011; 202: 241. Google Scholar
  • 28 : Spontaneous purinergic neurotransmission in the mouse urinary bladder. J Physiol2008; 586: 5743. Google Scholar
  • 29 : Disruption of lipid rafts inhibits P2X1 receptor-mediated currents and arterial vasoconstriction. J Biol Chem2005; 280: 30705. Google Scholar
  • 30 : UTP controls cell surface distribution and vasomotor activity of the human P2Y2 receptor through an epidermal growth factor receptor-transregulated mechanism. J Biol Chem2010; 285: 2940. Google Scholar

Division of Urology, Veterans Affairs Boston Healthcare System, Harvard Medical School, Boston, Massachusetts

Advertisement