Selective α1A-blocker improves bladder storage function in rats via suppression of C-fiber afferent activity

Purpose In the present study, we used animal models to investigate whether the selective α 1A -blocker silodosin exerts inhibitory effects on detrusor overactivity by modulating C-fiber afferent activity. Methods To desensitize C-fiber afferents, 0.3 mg/kg of resiniferatoxin (RTX) was subcutaneously...

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Veröffentlicht in:World journal of urology 2010-10, Vol.28 (5), p.609-614
Hauptverfasser: Yokoyama, Osamu, Ito, Hideaki, Aoki, Yoshitaka, Oyama, Nobuyuki, Miwa, Yoshiji, Akino, Hironobu
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container_issue 5
container_start_page 609
container_title World journal of urology
container_volume 28
creator Yokoyama, Osamu
Ito, Hideaki
Aoki, Yoshitaka
Oyama, Nobuyuki
Miwa, Yoshiji
Akino, Hironobu
description Purpose In the present study, we used animal models to investigate whether the selective α 1A -blocker silodosin exerts inhibitory effects on detrusor overactivity by modulating C-fiber afferent activity. Methods To desensitize C-fiber afferents, 0.3 mg/kg of resiniferatoxin (RTX) was subcutaneously injected into some female Sprague–Dawley rats 2 days before creation of each model. (1) Left middle cerebral artery occlusion was performed to create a cerebral infarction (CI) model (CI rats). The effects of intravenous (i.v.) and intrathecal (i.t.) administrations of silodosin on cystometrography parameters were evaluated in conscious rats. (2) Rhythmic bladder pressure was recorded in rats under urethane anesthesia. Prostaglandin (PG) E 2 (0.4 mg/mL) was continuously administered intraurethrally, and the effects of intra-arterial (i.a.) silodosin on the micturition reflex (MR) were investigated. Results (1) Silodosin (i.v.) dose-dependently increased bladder capacity (BC) in CI rats without decreasing bladder contraction pressure, but had no effects on BC in RTX-CI rats. Silodosin (i.t.) markedly increased BC in CI rats, but not in RTX-CI rats. (2) After intraurethral administration of PGE 2 , the bladder contraction interval (BCI) was markedly reduced in non-RTX rats, but unchanged in RTX rats. Silodosin (i.a.) significantly prolonged BCI in non-RTX rats receiving intraurethral PGE 2 . Conclusions These results suggest that the α 1A -AR subtype activates C-fiber afferents, and that consequently α 1A -blockade can improve bladder storage function.
doi_str_mv 10.1007/s00345-009-0481-2
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Methods To desensitize C-fiber afferents, 0.3 mg/kg of resiniferatoxin (RTX) was subcutaneously injected into some female Sprague–Dawley rats 2 days before creation of each model. (1) Left middle cerebral artery occlusion was performed to create a cerebral infarction (CI) model (CI rats). The effects of intravenous (i.v.) and intrathecal (i.t.) administrations of silodosin on cystometrography parameters were evaluated in conscious rats. (2) Rhythmic bladder pressure was recorded in rats under urethane anesthesia. Prostaglandin (PG) E 2 (0.4 mg/mL) was continuously administered intraurethrally, and the effects of intra-arterial (i.a.) silodosin on the micturition reflex (MR) were investigated. Results (1) Silodosin (i.v.) dose-dependently increased bladder capacity (BC) in CI rats without decreasing bladder contraction pressure, but had no effects on BC in RTX-CI rats. Silodosin (i.t.) markedly increased BC in CI rats, but not in RTX-CI rats. (2) After intraurethral administration of PGE 2 , the bladder contraction interval (BCI) was markedly reduced in non-RTX rats, but unchanged in RTX rats. Silodosin (i.a.) significantly prolonged BCI in non-RTX rats receiving intraurethral PGE 2 . 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(2) After intraurethral administration of PGE 2 , the bladder contraction interval (BCI) was markedly reduced in non-RTX rats, but unchanged in RTX rats. Silodosin (i.a.) significantly prolonged BCI in non-RTX rats receiving intraurethral PGE 2 . Conclusions These results suggest that the α 1A -AR subtype activates C-fiber afferents, and that consequently α 1A -blockade can improve bladder storage function.</description><subject>Adrenergic alpha-1 Receptor Antagonists - pharmacology</subject><subject>Adrenergic alpha-1 Receptor Antagonists - therapeutic use</subject><subject>Afferent Pathways - drug effects</subject><subject>Afferent Pathways - physiology</subject><subject>Animals</subject><subject>Cerebral Infarction - complications</subject><subject>Dinoprostone - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Indoles - pharmacology</subject><subject>Indoles - therapeutic use</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Models, Animal</subject><subject>Nephrology</subject><subject>Nerve Fibers, Unmyelinated - drug effects</subject><subject>Nerve Fibers, Unmyelinated - physiology</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Adrenergic, alpha-1 - drug effects</subject><subject>Receptors, Adrenergic, alpha-1 - physiology</subject><subject>Urinary Bladder - drug effects</subject><subject>Urinary Bladder - physiology</subject><subject>Urinary Bladder, Overactive - drug therapy</subject><subject>Urinary Bladder, Overactive - etiology</subject><subject>Urinary Bladder, Overactive - physiopathology</subject><subject>Urination - drug effects</subject><subject>Urination - physiology</subject><subject>Urology</subject><issn>0724-4983</issn><issn>1433-8726</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kEtOwzAQhi0EoqVwADbIFzCMH4mTZVXxkiqxoHvLr1QpeclOKvVYXIQz4aiwGumff2b--RC6p_BIAeRTBOAiIwAlAVFQwi7QkgrOSSFZfomWIJkgoiz4At3EeACgMofsGi1o0oSkfInaT994O9ZHj3--6ZqYprdfPuC6HUJ_9BGbRjuXhDj2Qe89rqYu2fsO1x0Oeoz4WGscp2EIPsZZ7yu8IVVt0oyuKh98N2I9X6jH0y26qnQT_d1fXaHdy_Nu80a2H6_vm_WWDGXBCHOclZwX1HFvjBYebFnkVlvIDc9ExZ3VUkCeguVSlkZYW-WZ0U64DEA4vkIP57XDZFrv1BDqVoeT-n87GdjZEFOr2_ugDv0UuhRJUVAzW3VmqxJbNbNVjP8CMBRs0w</recordid><startdate>201010</startdate><enddate>201010</enddate><creator>Yokoyama, Osamu</creator><creator>Ito, Hideaki</creator><creator>Aoki, Yoshitaka</creator><creator>Oyama, Nobuyuki</creator><creator>Miwa, Yoshiji</creator><creator>Akino, Hironobu</creator><general>Springer-Verlag</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>201010</creationdate><title>Selective α1A-blocker improves bladder storage function in rats via suppression of C-fiber afferent activity</title><author>Yokoyama, Osamu ; 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Methods To desensitize C-fiber afferents, 0.3 mg/kg of resiniferatoxin (RTX) was subcutaneously injected into some female Sprague–Dawley rats 2 days before creation of each model. (1) Left middle cerebral artery occlusion was performed to create a cerebral infarction (CI) model (CI rats). The effects of intravenous (i.v.) and intrathecal (i.t.) administrations of silodosin on cystometrography parameters were evaluated in conscious rats. (2) Rhythmic bladder pressure was recorded in rats under urethane anesthesia. Prostaglandin (PG) E 2 (0.4 mg/mL) was continuously administered intraurethrally, and the effects of intra-arterial (i.a.) silodosin on the micturition reflex (MR) were investigated. Results (1) Silodosin (i.v.) dose-dependently increased bladder capacity (BC) in CI rats without decreasing bladder contraction pressure, but had no effects on BC in RTX-CI rats. Silodosin (i.t.) markedly increased BC in CI rats, but not in RTX-CI rats. (2) After intraurethral administration of PGE 2 , the bladder contraction interval (BCI) was markedly reduced in non-RTX rats, but unchanged in RTX rats. Silodosin (i.a.) significantly prolonged BCI in non-RTX rats receiving intraurethral PGE 2 . Conclusions These results suggest that the α 1A -AR subtype activates C-fiber afferents, and that consequently α 1A -blockade can improve bladder storage function.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>19834713</pmid><doi>10.1007/s00345-009-0481-2</doi><tpages>6</tpages></addata></record>
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subjects Adrenergic alpha-1 Receptor Antagonists - pharmacology
Adrenergic alpha-1 Receptor Antagonists - therapeutic use
Afferent Pathways - drug effects
Afferent Pathways - physiology
Animals
Cerebral Infarction - complications
Dinoprostone - pharmacology
Dose-Response Relationship, Drug
Female
Indoles - pharmacology
Indoles - therapeutic use
Medicine
Medicine & Public Health
Models, Animal
Nephrology
Nerve Fibers, Unmyelinated - drug effects
Nerve Fibers, Unmyelinated - physiology
Oncology
Original Article
Rats
Rats, Sprague-Dawley
Receptors, Adrenergic, alpha-1 - drug effects
Receptors, Adrenergic, alpha-1 - physiology
Urinary Bladder - drug effects
Urinary Bladder - physiology
Urinary Bladder, Overactive - drug therapy
Urinary Bladder, Overactive - etiology
Urinary Bladder, Overactive - physiopathology
Urination - drug effects
Urination - physiology
Urology
title Selective α1A-blocker improves bladder storage function in rats via suppression of C-fiber afferent activity
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