Literature DB >> 14532354

Signal transduction underlying carbachol-induced contraction of rat urinary bladder. I. Phospholipases and Ca2+ sources.

Tim Schneider1, Peter Hein, Martin C Michel.   

Abstract

We have reexamined the muscarinic receptor subtype mediating carbachol-induced contraction of rat urinary bladder and investigated the role of phospholipase (PL)C, D, and A2 and of intra- and extracellular Ca2+ sources in this effect. Based on the nonsubtype-selective tolterodine, the highly M2 receptor-selective (R)-4-[2-[3-(4-methoxy-benzoylamino)-benzyl]-piperidin-1-ylmethyl]-piperidine-1-carboxylic acid amide (Ro-320-6206), and the highly M3 receptor-selective darifenacin and 3-(1-carbamoyl-1,1-diphenylmethyl)-1-(4-methoxyphenylethyl)pyrrolidine (APP), contraction occurs via M3 receptors. Carbachol stimulated inositol phosphate formation in rat bladder slices, and this was abolished by the phospholipase C inhibitor 1-(6-[([17beta]-3-methoxyestra-1,3,5[10]-trien-17-yl)-amino]hexyl)-1H-pyrrole-2,5-dione (U 73,122; 10 microM). Nevertheless, U 73,122 (1-10 microM) did not significantly affect carbachol-stimulated bladder contraction. Carbachol had only little effect on PLD activity in bladder slices, but the PLD inhibitor butan-1-ol, relative to its negative control butan-2-ol (0.3% each), caused detectable inhibition of carbachol-induced bladder contraction. The cytosolic PLA2 inhibitor arachidonyltrifluoromethyl ketone weakly inhibited carbachol-induced contraction at a concentration of 300 microM, but the cyclooxygenase inhibitor indomethacin (1-10 microM) remained without effect. The Ca2+ entry blocker nifedipine (10-100 nM) almost completely inhibited carbachol-induced bladder contraction. In contrast, 1-[beta-[3-(4-methoxyphenyl)propoxy]-4-methoxyphenethyl]-1H-imidazole HCl (SKF 96,365; 10 microM), an inhibitor of store-operated Ca2+ channels, caused little inhibition. We conclude that carbachol-induced contraction of rat bladder largely depends on Ca2+ entry through nifedipine-sensitive channels and, perhaps, PLD, PLA2, and store-operated Ca2+ channels, whereas cyclooxygenase and, surprisingly, also PLC are not involved to a relevant extent.

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Year:  2003        PMID: 14532354     DOI: 10.1124/jpet.103.058248

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  25 in total

1.  Regulation of bladder muscarinic receptor subtypes by experimental pathologies.

Authors:  M R Ruggieri; A S Braverman
Journal:  Auton Autacoid Pharmacol       Date:  2006-07

2.  Age-dependent contribution of Rho kinase in carbachol-induced contraction of human detrusor smooth muscle in vitro.

Authors:  Timo Kirschstein; Chris Protzel; Katrin Porath; Tina Sellmann; Rüdiger Köhling; Oliver W Hakenberg
Journal:  Acta Pharmacol Sin       Date:  2013-10-14       Impact factor: 6.150

3.  A possible role of the cholinergic and purinergic receptor interaction in the regulation of the rat urinary bladder function.

Authors:  Ágnes Jenes; Ferenc Ruzsnavszky; Andrea Telek; Gyula P Szigeti; László Csernoch
Journal:  J Muscle Res Cell Motil       Date:  2012-02-28       Impact factor: 2.698

Review 4.  Interstitial cells: regulators of smooth muscle function.

Authors:  Kenton M Sanders; Sean M Ward; Sang Don Koh
Journal:  Physiol Rev       Date:  2014-07       Impact factor: 37.312

5.  Nerve-released acetylcholine contracts urinary bladder smooth muscle by inducing action potentials independently of IP3-mediated calcium release.

Authors:  Bernhard Nausch; Thomas J Heppner; Mark T Nelson
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2010-06-23       Impact factor: 3.619

Review 6.  Big-conductance Ca2+-activated K+ channels in physiological and pathophysiological urinary bladder smooth muscle cells.

Authors:  Shankar P Parajuli; Yun-Min Zheng; Robert Levin; Yong-Xiao Wang
Journal:  Channels (Austin)       Date:  2016-04-21       Impact factor: 2.581

7.  Propiverine and metabolites: differences in binding to muscarinic receptors and in functional models of detrusor contraction.

Authors:  Melinda Wuest; Anke Weiss; Magali Waelbroeck; Manfred Braeter; Lutz-Ullrich Kelly; Oliver W Hakenberg; Ursula Ravens
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2006-10-20       Impact factor: 3.000

8.  Normalization of organ bath contraction data for tissue specimen size: does one approach fit all?

Authors:  Betul R Erdogan; Irem Karaomerlioglu; Zeynep E Yesilyurt; Nihal Ozturk; A Elif Muderrisoglu; Martin C Michel; Ebru Arioglu-Inan
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2019-09-11       Impact factor: 3.000

9.  Activation of muscarinic M3 receptors inhibits large-conductance voltage- and Ca2+-activated K+ channels in rat urinary bladder smooth muscle cells.

Authors:  Shankar P Parajuli; Georgi V Petkov
Journal:  Am J Physiol Cell Physiol       Date:  2013-05-22       Impact factor: 4.249

10.  Actions of two main metabolites of propiverine (M-1 and M-2) on voltage-dependent L-type Ca2+ currents and Ca2+ transients in murine urinary bladder myocytes.

Authors:  Hai-Lei Zhu; Keith L Brain; Manami Aishima; Atsushi Shibata; John S Young; Katsuo Sueishi; Noriyoshi Teramoto
Journal:  J Pharmacol Exp Ther       Date:  2007-10-10       Impact factor: 4.030

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