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 |
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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 |
format | Article |
fullrecord | <record><control><sourceid>pubmed_sprin</sourceid><recordid>TN_cdi_pubmed_primary_19834713</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>19834713</sourcerecordid><originalsourceid>FETCH-LOGICAL-p982-2d3293381d3ebba4e0c986cac06b354f3dca7406add6779b4ccf65bad4d5004d3</originalsourceid><addsrcrecordid>eNo1kEtOwzAQhi0EoqVwADbIFzCMH4mTZVXxkiqxoHvLr1QpeclOKvVYXIQz4aiwGumff2b--RC6p_BIAeRTBOAiIwAlAVFQwi7QkgrOSSFZfomWIJkgoiz4At3EeACgMofsGi1o0oSkfInaT994O9ZHj3--6ZqYprdfPuC6HUJ_9BGbRjuXhDj2Qe89rqYu2fsO1x0Oeoz4WGscp2EIPsZZ7yu8IVVt0oyuKh98N2I9X6jH0y26qnQT_d1fXaHdy_Nu80a2H6_vm_WWDGXBCHOclZwX1HFvjBYebFnkVlvIDc9ExZ3VUkCeguVSlkZYW-WZ0U64DEA4vkIP57XDZFrv1BDqVoeT-n87GdjZEFOr2_ugDv0UuhRJUVAzW3VmqxJbNbNVjP8CMBRs0w</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Selective α1A-blocker improves bladder storage function in rats via suppression of C-fiber afferent activity</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Yokoyama, Osamu ; Ito, Hideaki ; Aoki, Yoshitaka ; Oyama, Nobuyuki ; Miwa, Yoshiji ; Akino, Hironobu</creator><creatorcontrib>Yokoyama, Osamu ; Ito, Hideaki ; Aoki, Yoshitaka ; Oyama, Nobuyuki ; Miwa, Yoshiji ; Akino, Hironobu</creatorcontrib><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.</description><identifier>ISSN: 0724-4983</identifier><identifier>EISSN: 1433-8726</identifier><identifier>DOI: 10.1007/s00345-009-0481-2</identifier><identifier>PMID: 19834713</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>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</subject><ispartof>World journal of urology, 2010-10, Vol.28 (5), p.609-614</ispartof><rights>Springer-Verlag 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-p982-2d3293381d3ebba4e0c986cac06b354f3dca7406add6779b4ccf65bad4d5004d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00345-009-0481-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00345-009-0481-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19834713$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yokoyama, Osamu</creatorcontrib><creatorcontrib>Ito, Hideaki</creatorcontrib><creatorcontrib>Aoki, Yoshitaka</creatorcontrib><creatorcontrib>Oyama, Nobuyuki</creatorcontrib><creatorcontrib>Miwa, Yoshiji</creatorcontrib><creatorcontrib>Akino, Hironobu</creatorcontrib><title>Selective α1A-blocker improves bladder storage function in rats via suppression of C-fiber afferent activity</title><title>World journal of urology</title><addtitle>World J Urol</addtitle><addtitle>World J Urol</addtitle><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.</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 & 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 ; Ito, Hideaki ; Aoki, Yoshitaka ; Oyama, Nobuyuki ; Miwa, Yoshiji ; Akino, Hironobu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p982-2d3293381d3ebba4e0c986cac06b354f3dca7406add6779b4ccf65bad4d5004d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adrenergic alpha-1 Receptor Antagonists - pharmacology</topic><topic>Adrenergic alpha-1 Receptor Antagonists - therapeutic use</topic><topic>Afferent Pathways - drug effects</topic><topic>Afferent Pathways - physiology</topic><topic>Animals</topic><topic>Cerebral Infarction - complications</topic><topic>Dinoprostone - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Indoles - pharmacology</topic><topic>Indoles - therapeutic use</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Models, Animal</topic><topic>Nephrology</topic><topic>Nerve Fibers, Unmyelinated - drug effects</topic><topic>Nerve Fibers, Unmyelinated - physiology</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Adrenergic, alpha-1 - drug effects</topic><topic>Receptors, Adrenergic, alpha-1 - physiology</topic><topic>Urinary Bladder - drug effects</topic><topic>Urinary Bladder - physiology</topic><topic>Urinary Bladder, Overactive - drug therapy</topic><topic>Urinary Bladder, Overactive - etiology</topic><topic>Urinary Bladder, Overactive - physiopathology</topic><topic>Urination - drug effects</topic><topic>Urination - physiology</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yokoyama, Osamu</creatorcontrib><creatorcontrib>Ito, Hideaki</creatorcontrib><creatorcontrib>Aoki, Yoshitaka</creatorcontrib><creatorcontrib>Oyama, Nobuyuki</creatorcontrib><creatorcontrib>Miwa, Yoshiji</creatorcontrib><creatorcontrib>Akino, Hironobu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>World journal of urology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yokoyama, Osamu</au><au>Ito, Hideaki</au><au>Aoki, Yoshitaka</au><au>Oyama, Nobuyuki</au><au>Miwa, Yoshiji</au><au>Akino, Hironobu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selective α1A-blocker improves bladder storage function in rats via suppression of C-fiber afferent activity</atitle><jtitle>World journal of urology</jtitle><stitle>World J Urol</stitle><addtitle>World J Urol</addtitle><date>2010-10</date><risdate>2010</risdate><volume>28</volume><issue>5</issue><spage>609</spage><epage>614</epage><pages>609-614</pages><issn>0724-4983</issn><eissn>1433-8726</eissn><abstract>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.</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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issn | 0724-4983 1433-8726 |
language | eng |
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source | MEDLINE; SpringerLink Journals - AutoHoldings |
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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