Voltage-gated Na+ channel blockers reduce functional bladder capacity in the conscious spontaneously hypertensive rat
| Autor: | Malcolm J. Jugus, Stephen H. Eisennagel, Nicholas J. Laping, Kevin S. Thorneloe, Angela K. Clouse, Timothy D. Westfall |
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| Rok vydání: | 2011 |
| Předmět: |
medicine.medical_specialty
Urology Amitriptyline Mexiletine Lamotrigine Sodium Channels Spontaneously hypertensive rat Internal medicine Rats Inbred SHR Muscarinic acetylcholine receptor medicine Animals Channel blocker medicine.diagnostic_test business.industry Triazines Urinary Bladder Overactive Cystometry Carbamazepine Receptors Muscarinic Rats Urodynamics Endocrinology Female business medicine.drug Sodium Channel Blockers |
| Zdroj: | Urology. 79(6) |
| ISSN: | 1527-9995 |
| Popis: | Objective To evaluate the consequence of pharmacologic inhibition of voltage-gated Na+ channels (Nav) in the conscious rat, based on Nav having been implicated as modulators of rodent urodynamics using knockout as well as antisense oligodeoxynucleotide approaches. Methods The urodynamic response to standard Nav blockers, lamotrigine, amitriptyline, mexiletine, and carbamazepine were evaluated using conscious, continuous-filling cystometry in spontaneously hypertensive rats (SHRs). As a selectivity evaluation, the activity of the Nav blockers at muscarinic receptors was assessed via effect on carbachol-evoked bladder contractions. Results Lamotrigine, amitriptyline, mexiletine, and carbamazepine decreased peak micturition pressure, micturition interval, and void volume. These effects were markedly similar to observations with muscarinic antagonists. Therefore, we evaluated the selectivity of these agents against bladder muscarinic receptors. Lamotrigine, mexiletine, and carbamazepine had no effect on muscarinic bladder contractions, whereas amitriptyline displayed a robust antagonism of carbachol-induced contractility. Conclusion Three Nav blockers—lamotrigine, mexiletine, and carbamazepine—demonstrated a reduction in micturition pressure and functional bladder capacity, similar to previous observations with muscarinic antagonists. These 3 Nav blockers are free of muscarinic antagonism, consistent with their cystometric effects being mediated via their Nav blocking activities. The negative findings reported here with Nav blockers suggest that Nav channel blockade is unlikely to reflect an improved treatment strategy for bladder disorders over currently prescribed muscarinic antagonists. |
| Databáze: | OpenAIRE |
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