2010
DOI: 10.1016/j.urology.2010.05.012
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Loss of Muscarinic and Purinergic Receptors in Urinary Bladder of Rats With Hydrochloric Acid-induced Cystitis

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Cited by 10 publications
(10 citation statements)
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References 29 publications
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“…Robust eupnoeic phrenic activity was often difficult to re-establish, once lost. Furthermore it was difficult to traverse the ureto-bladder junction with the cannula preventing intravesical pressure recording so this approach was abandoned in favor of the more conventional pressure monitoring/infusion needle inserted into the bladder dome (Streng et al, 2004; Yoshida et al, 2010). …”
Section: Discussionmentioning
confidence: 99%
“…Robust eupnoeic phrenic activity was often difficult to re-establish, once lost. Furthermore it was difficult to traverse the ureto-bladder junction with the cannula preventing intravesical pressure recording so this approach was abandoned in favor of the more conventional pressure monitoring/infusion needle inserted into the bladder dome (Streng et al, 2004; Yoshida et al, 2010). …”
Section: Discussionmentioning
confidence: 99%
“…Release of ATP from urothelial cells with hypoosmotic mechanical stimulation was increased by over 600 % in inflamed bladder from cyclophosphamide-treated animals; BTX inhibited this release [626]. In rats with hydrochloric acidinduced cystitis, there was a loss of both muscarinic and purinergic receptors, although the in vivo release of ATP from mucosal cells was significantly enhanced, perhaps acting on P2X3 receptors on afferent fibres to contribute to urinary frequency and non-voiding contractions [738,740], as well as in cyclophosphamide-and protamine sulphate-induced cystitis [732]. A hyperosmolar model of OAB has been claimed to be less invasive and more physiological compared to the cyclophosphamide model [349].…”
Section: Detrusor Overactivitymentioning
confidence: 96%
“…P2X receptors (mainly P2X 1 ), expressed in mammalian bladders, are ATP-gated ion channels that contribute to urinary bladder functions (24,28). Several studies suggested that PPADS strongly suppresses P2X-purinoceptor-mediated contractions (25,31,32). α,β-meATP, an ATP analog, is a selective P2X receptor agonist and resistant to ATPase.…”
Section: Discussionmentioning
confidence: 99%