Functional roles of bladder α1‐adrenoceptors in the activation of single‐unit primary bladder afferent activity in rats

Objectives To clarify the involvement of bladder α1‐adrenoceptors (α1‐ARs) in afferent pathways by investigating the effects of silodosin and BMY7378, selective α1A‐ or α1D‐AR antagonists, respectively, on single‐unit afferent nerve fibre activity (SAA) of the primary bladder afferent nerves and the...

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Veröffentlicht in:BJU international 2016-06, Vol.117 (6), p.993-1001
Hauptverfasser: Aizawa, Naoki, Sugiyama, Rino, Ichihara, Koji, Fujimura, Tetsuya, Fukuhara, Hiroshi, Homma, Yukio, Igawa, Yasuhiko
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container_end_page 1001
container_issue 6
container_start_page 993
container_title BJU international
container_volume 117
creator Aizawa, Naoki
Sugiyama, Rino
Ichihara, Koji
Fujimura, Tetsuya
Fukuhara, Hiroshi
Homma, Yukio
Igawa, Yasuhiko
description Objectives To clarify the involvement of bladder α1‐adrenoceptors (α1‐ARs) in afferent pathways by investigating the effects of silodosin and BMY7378, selective α1A‐ or α1D‐AR antagonists, respectively, on single‐unit afferent nerve fibre activity (SAA) of the primary bladder afferent nerves and their relationship with bladder microcontractions in rats. Materials and Methods A total of 63 female Sprague–Dawley rats were anaesthetized with urethane. The SAA of Aδ and C fibres generated from the left L6 dorsal roots was determined using electrical stimulation of the left pelvic nerve and bladder distension. After measuring baseline SAA during constant filling cystometry, the procedure was repeated with i.v. (0.3–30 μg/kg) or intravesical (10 μm) administration of each antagonist. In separate rats, the bladder was filled with saline until the intravesical pressure reached 30 cmH2O, and was kept under isovolumetric conditions, then the recording was performed with i.v.‐administered vehicle and silodosin (0.3 μg/kg). Results A total of Aδ fibres and 33 C fibres were isolated from 63 rats. The SAA of Aδ fibres, but not C fibres, were dose‐dependently decreased after both i.v. and intravesical administrations of each of the antagonists. In the experiments under bladder isovolumetric conditions, silodosin administration significantly decreased the SAA of Aδ fibres, but not C fibres, compared with vehicle administration. There were no significant effects on either the mean basal bladder pressure or microcontractions. Conclusion The present study suggests that both α1A‐ or α1D‐ARs in the rat bladder are involved in the activation of the bladder mechanosensory Aδ fibres during bladder filling, and that this activation may not be related to bladder microcontractions.
doi_str_mv 10.1111/bju.13313
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Materials and Methods A total of 63 female Sprague–Dawley rats were anaesthetized with urethane. The SAA of Aδ and C fibres generated from the left L6 dorsal roots was determined using electrical stimulation of the left pelvic nerve and bladder distension. After measuring baseline SAA during constant filling cystometry, the procedure was repeated with i.v. (0.3–30 μg/kg) or intravesical (10 μm) administration of each antagonist. In separate rats, the bladder was filled with saline until the intravesical pressure reached 30 cmH2O, and was kept under isovolumetric conditions, then the recording was performed with i.v.‐administered vehicle and silodosin (0.3 μg/kg). Results A total of Aδ fibres and 33 C fibres were isolated from 63 rats. The SAA of Aδ fibres, but not C fibres, were dose‐dependently decreased after both i.v. and intravesical administrations of each of the antagonists. In the experiments under bladder isovolumetric conditions, silodosin administration significantly decreased the SAA of Aδ fibres, but not C fibres, compared with vehicle administration. There were no significant effects on either the mean basal bladder pressure or microcontractions. Conclusion The present study suggests that both α1A‐ or α1D‐ARs in the rat bladder are involved in the activation of the bladder mechanosensory Aδ fibres during bladder filling, and that this activation may not be related to bladder microcontractions.</description><identifier>ISSN: 1464-4096</identifier><identifier>EISSN: 1464-410X</identifier><identifier>DOI: 10.1111/bju.13313</identifier><identifier>PMID: 26332379</identifier><language>eng</language><publisher>England</publisher><subject>Adrenergic beta-1 Receptor Agonists - pharmacology ; Adrenergic beta-1 Receptor Antagonists - pharmacology ; adrenergic α‐1 receptor antagonists ; afferent ; Animals ; Female ; Muscle Contraction - drug effects ; Nerve Fibers, Unmyelinated - drug effects ; Neurons, Afferent - drug effects ; Neurons, Afferent - physiology ; Rats ; Rats, Sprague-Dawley ; Receptors, Adrenergic, beta-1 - physiology ; Sprague–Dawley rats ; urinary bladder ; Urinary Bladder - drug effects ; Urinary Bladder - innervation ; Urinary Bladder - physiology</subject><ispartof>BJU international, 2016-06, Vol.117 (6), p.993-1001</ispartof><rights>2015 The Authors BJU International © 2015 BJU International Published by John Wiley &amp; Sons Ltd</rights><rights>2015 The Authors BJU International © 2015 BJU International Published by John Wiley &amp; Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3063-9ae6e805b43f7267e6c1996440e19de09d8a46034f0e9266ffd3e434bc6ddd673</citedby><cites>FETCH-LOGICAL-c3063-9ae6e805b43f7267e6c1996440e19de09d8a46034f0e9266ffd3e434bc6ddd673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fbju.13313$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fbju.13313$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26332379$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aizawa, Naoki</creatorcontrib><creatorcontrib>Sugiyama, Rino</creatorcontrib><creatorcontrib>Ichihara, Koji</creatorcontrib><creatorcontrib>Fujimura, Tetsuya</creatorcontrib><creatorcontrib>Fukuhara, Hiroshi</creatorcontrib><creatorcontrib>Homma, Yukio</creatorcontrib><creatorcontrib>Igawa, Yasuhiko</creatorcontrib><title>Functional roles of bladder α1‐adrenoceptors in the activation of single‐unit primary bladder afferent activity in rats</title><title>BJU international</title><addtitle>BJU Int</addtitle><description>Objectives To clarify the involvement of bladder α1‐adrenoceptors (α1‐ARs) in afferent pathways by investigating the effects of silodosin and BMY7378, selective α1A‐ or α1D‐AR antagonists, respectively, on single‐unit afferent nerve fibre activity (SAA) of the primary bladder afferent nerves and their relationship with bladder microcontractions in rats. Materials and Methods A total of 63 female Sprague–Dawley rats were anaesthetized with urethane. The SAA of Aδ and C fibres generated from the left L6 dorsal roots was determined using electrical stimulation of the left pelvic nerve and bladder distension. After measuring baseline SAA during constant filling cystometry, the procedure was repeated with i.v. (0.3–30 μg/kg) or intravesical (10 μm) administration of each antagonist. In separate rats, the bladder was filled with saline until the intravesical pressure reached 30 cmH2O, and was kept under isovolumetric conditions, then the recording was performed with i.v.‐administered vehicle and silodosin (0.3 μg/kg). Results A total of Aδ fibres and 33 C fibres were isolated from 63 rats. The SAA of Aδ fibres, but not C fibres, were dose‐dependently decreased after both i.v. and intravesical administrations of each of the antagonists. In the experiments under bladder isovolumetric conditions, silodosin administration significantly decreased the SAA of Aδ fibres, but not C fibres, compared with vehicle administration. There were no significant effects on either the mean basal bladder pressure or microcontractions. Conclusion The present study suggests that both α1A‐ or α1D‐ARs in the rat bladder are involved in the activation of the bladder mechanosensory Aδ fibres during bladder filling, and that this activation may not be related to bladder microcontractions.</description><subject>Adrenergic beta-1 Receptor Agonists - pharmacology</subject><subject>Adrenergic beta-1 Receptor Antagonists - pharmacology</subject><subject>adrenergic α‐1 receptor antagonists</subject><subject>afferent</subject><subject>Animals</subject><subject>Female</subject><subject>Muscle Contraction - drug effects</subject><subject>Nerve Fibers, Unmyelinated - drug effects</subject><subject>Neurons, Afferent - drug effects</subject><subject>Neurons, Afferent - physiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Adrenergic, beta-1 - physiology</subject><subject>Sprague–Dawley rats</subject><subject>urinary bladder</subject><subject>Urinary Bladder - drug effects</subject><subject>Urinary Bladder - innervation</subject><subject>Urinary Bladder - physiology</subject><issn>1464-4096</issn><issn>1464-410X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1OwzAQRi0EoqWw4AIoS1iktWPXiZdQUX5UiQ2V2EVOPAZXaVLsBFSJBUfgKlyEQ3ASHNKyYzYeWe970nwIHRM8JH5G2aIZEkoJ3UF9wjgLGcEPu9sdC95DB84tMPYffLyPehGnNKKx6KO3aVPmtalKWQS2KsAFlQ6yQioFNvj6JN_vH1JZKKscVnVlXWDKoH6CQPrQi2yDbcCZ8rEAzzalqYOVNUtp138aqTV4Rd2FTL1uJVbW7hDtaVk4ONq8AzSfXt5PrsPZ3dXN5HwW5hRzGgoJHBI8zhjVccRj4DkRgjOGgQgFWKhEMo4p0xhExLnWigKjLMu5UorHdIBOO-_KVs8NuDpdGpdDUcgSqsalJE4EZr6QxKNnHZrbyjkLOt1ckxKctmWnvuz0t2zPnmy0TbYE9Udu2_XAqANeTQHr_03pxe28U_4A5fyNUQ</recordid><startdate>201606</startdate><enddate>201606</enddate><creator>Aizawa, Naoki</creator><creator>Sugiyama, Rino</creator><creator>Ichihara, Koji</creator><creator>Fujimura, Tetsuya</creator><creator>Fukuhara, Hiroshi</creator><creator>Homma, Yukio</creator><creator>Igawa, Yasuhiko</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201606</creationdate><title>Functional roles of bladder α1‐adrenoceptors in the activation of single‐unit primary bladder afferent activity in rats</title><author>Aizawa, Naoki ; Sugiyama, Rino ; Ichihara, Koji ; Fujimura, Tetsuya ; Fukuhara, Hiroshi ; Homma, Yukio ; Igawa, Yasuhiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3063-9ae6e805b43f7267e6c1996440e19de09d8a46034f0e9266ffd3e434bc6ddd673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adrenergic beta-1 Receptor Agonists - pharmacology</topic><topic>Adrenergic beta-1 Receptor Antagonists - pharmacology</topic><topic>adrenergic α‐1 receptor antagonists</topic><topic>afferent</topic><topic>Animals</topic><topic>Female</topic><topic>Muscle Contraction - drug effects</topic><topic>Nerve Fibers, Unmyelinated - drug effects</topic><topic>Neurons, Afferent - drug effects</topic><topic>Neurons, Afferent - physiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Adrenergic, beta-1 - physiology</topic><topic>Sprague–Dawley rats</topic><topic>urinary bladder</topic><topic>Urinary Bladder - drug effects</topic><topic>Urinary Bladder - innervation</topic><topic>Urinary Bladder - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aizawa, Naoki</creatorcontrib><creatorcontrib>Sugiyama, Rino</creatorcontrib><creatorcontrib>Ichihara, Koji</creatorcontrib><creatorcontrib>Fujimura, Tetsuya</creatorcontrib><creatorcontrib>Fukuhara, Hiroshi</creatorcontrib><creatorcontrib>Homma, Yukio</creatorcontrib><creatorcontrib>Igawa, Yasuhiko</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>BJU international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aizawa, Naoki</au><au>Sugiyama, Rino</au><au>Ichihara, Koji</au><au>Fujimura, Tetsuya</au><au>Fukuhara, Hiroshi</au><au>Homma, Yukio</au><au>Igawa, Yasuhiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional roles of bladder α1‐adrenoceptors in the activation of single‐unit primary bladder afferent activity in rats</atitle><jtitle>BJU international</jtitle><addtitle>BJU Int</addtitle><date>2016-06</date><risdate>2016</risdate><volume>117</volume><issue>6</issue><spage>993</spage><epage>1001</epage><pages>993-1001</pages><issn>1464-4096</issn><eissn>1464-410X</eissn><abstract>Objectives To clarify the involvement of bladder α1‐adrenoceptors (α1‐ARs) in afferent pathways by investigating the effects of silodosin and BMY7378, selective α1A‐ or α1D‐AR antagonists, respectively, on single‐unit afferent nerve fibre activity (SAA) of the primary bladder afferent nerves and their relationship with bladder microcontractions in rats. Materials and Methods A total of 63 female Sprague–Dawley rats were anaesthetized with urethane. The SAA of Aδ and C fibres generated from the left L6 dorsal roots was determined using electrical stimulation of the left pelvic nerve and bladder distension. After measuring baseline SAA during constant filling cystometry, the procedure was repeated with i.v. (0.3–30 μg/kg) or intravesical (10 μm) administration of each antagonist. In separate rats, the bladder was filled with saline until the intravesical pressure reached 30 cmH2O, and was kept under isovolumetric conditions, then the recording was performed with i.v.‐administered vehicle and silodosin (0.3 μg/kg). Results A total of Aδ fibres and 33 C fibres were isolated from 63 rats. The SAA of Aδ fibres, but not C fibres, were dose‐dependently decreased after both i.v. and intravesical administrations of each of the antagonists. In the experiments under bladder isovolumetric conditions, silodosin administration significantly decreased the SAA of Aδ fibres, but not C fibres, compared with vehicle administration. There were no significant effects on either the mean basal bladder pressure or microcontractions. Conclusion The present study suggests that both α1A‐ or α1D‐ARs in the rat bladder are involved in the activation of the bladder mechanosensory Aδ fibres during bladder filling, and that this activation may not be related to bladder microcontractions.</abstract><cop>England</cop><pmid>26332379</pmid><doi>10.1111/bju.13313</doi><tpages>9</tpages></addata></record>
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subjects Adrenergic beta-1 Receptor Agonists - pharmacology
Adrenergic beta-1 Receptor Antagonists - pharmacology
adrenergic α‐1 receptor antagonists
afferent
Animals
Female
Muscle Contraction - drug effects
Nerve Fibers, Unmyelinated - drug effects
Neurons, Afferent - drug effects
Neurons, Afferent - physiology
Rats
Rats, Sprague-Dawley
Receptors, Adrenergic, beta-1 - physiology
Sprague–Dawley rats
urinary bladder
Urinary Bladder - drug effects
Urinary Bladder - innervation
Urinary Bladder - physiology
title Functional roles of bladder α1‐adrenoceptors in the activation of single‐unit primary bladder afferent activity in rats
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