Nitric Oxide Is Generated in Smooth Muscle Layer by Neurokinin A and Counteracts Constriction in Guinea Pig Airway

It has been reported that several bronchoconstrictors generate nitric oxide (NO), counteracting bronchoconstriction, and removal of bronchial epithelia reduces NO production. However, it has not been elucidated whether neurokinin A (NKA), a potent bronchoconstrictor liberated from nerve terminals, g...

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Veröffentlicht in:Nitric oxide 2001-10, Vol.5 (5), p.465-474
Hauptverfasser: Imasaki, Takao, Kobayashi, Hirosuke, Hataishi, Ryuji, Hayashi, Izumi, Tomita, Tomoyuki, Majima, Masataka
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container_end_page 474
container_issue 5
container_start_page 465
container_title Nitric oxide
container_volume 5
creator Imasaki, Takao
Kobayashi, Hirosuke
Hataishi, Ryuji
Hayashi, Izumi
Tomita, Tomoyuki
Majima, Masataka
description It has been reported that several bronchoconstrictors generate nitric oxide (NO), counteracting bronchoconstriction, and removal of bronchial epithelia reduces NO production. However, it has not been elucidated whether neurokinin A (NKA), a potent bronchoconstrictor liberated from nerve terminals, generates NO. Specific questions in this study were (1) does NKA also generate NO, (2) does NO counteract NKA-induced bronchoconstriction, and (3) does the NO generation require bronchial epithelial cells? In an in vivo study exogenous as well as endogenous (capsaicin-induced) NKA increased airway opening pressure (Pao) and the exhaled NO level, and both were inhibited by an antagonist selective for NK2 receptor (a receptor for NKA), SR48968. The exhaled NO level became negligible with an inhibitor of NO synthase (NOS) type 1-3 (NG-nitro-l-arginine methyl ester, l-NAME) with increased Pao, but not with a NOS type 2 inhibitor. In an in vitro study, NKA increased the nitrite/nitrate level in superfused fluid of tracheal segments. Removing smooth muscle reduced nitrite/nitrate in the fluid to negligible levels, while the level was unchanged with removal of the epithelia. Pretreatment with l-NAME enhanced the tension of epithelia-removed tracheal segments. These findings indicate that (1) NKA generates NO, (2) NO counteracts NKA-induced bronchoconstriction, and (3) NKA activates NOS in the muscle layer, independently of bronchial epithelia.
doi_str_mv 10.1006/niox.2001.0361
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However, it has not been elucidated whether neurokinin A (NKA), a potent bronchoconstrictor liberated from nerve terminals, generates NO. Specific questions in this study were (1) does NKA also generate NO, (2) does NO counteract NKA-induced bronchoconstriction, and (3) does the NO generation require bronchial epithelial cells? In an in vivo study exogenous as well as endogenous (capsaicin-induced) NKA increased airway opening pressure (Pao) and the exhaled NO level, and both were inhibited by an antagonist selective for NK2 receptor (a receptor for NKA), SR48968. The exhaled NO level became negligible with an inhibitor of NO synthase (NOS) type 1-3 (NG-nitro-l-arginine methyl ester, l-NAME) with increased Pao, but not with a NOS type 2 inhibitor. In an in vitro study, NKA increased the nitrite/nitrate level in superfused fluid of tracheal segments. Removing smooth muscle reduced nitrite/nitrate in the fluid to negligible levels, while the level was unchanged with removal of the epithelia. Pretreatment with l-NAME enhanced the tension of epithelia-removed tracheal segments. 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However, it has not been elucidated whether neurokinin A (NKA), a potent bronchoconstrictor liberated from nerve terminals, generates NO. Specific questions in this study were (1) does NKA also generate NO, (2) does NO counteract NKA-induced bronchoconstriction, and (3) does the NO generation require bronchial epithelial cells? In an in vivo study exogenous as well as endogenous (capsaicin-induced) NKA increased airway opening pressure (Pao) and the exhaled NO level, and both were inhibited by an antagonist selective for NK2 receptor (a receptor for NKA), SR48968. The exhaled NO level became negligible with an inhibitor of NO synthase (NOS) type 1-3 (NG-nitro-l-arginine methyl ester, l-NAME) with increased Pao, but not with a NOS type 2 inhibitor. In an in vitro study, NKA increased the nitrite/nitrate level in superfused fluid of tracheal segments. Removing smooth muscle reduced nitrite/nitrate in the fluid to negligible levels, while the level was unchanged with removal of the epithelia. Pretreatment with l-NAME enhanced the tension of epithelia-removed tracheal segments. 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inhibitors</subject><subject>Nitric Oxide Synthase - metabolism</subject><subject>Nitric Oxide Synthase Type I</subject><subject>Nitric Oxide Synthase Type II</subject><subject>Nitric Oxide Synthase Type III</subject><subject>Nitrites - metabolism</subject><subject>Piperidines - pharmacology</subject><subject>Receptors, Neurokinin-2 - agonists</subject><subject>Receptors, Neurokinin-2 - antagonists &amp; inhibitors</subject><subject>tachykinin</subject><subject>Trachea - physiology</subject><issn>1089-8603</issn><issn>1089-8611</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1PAjEQQBujUUSvHk1P3sB-sNtyJESRBMFEPTfddtAqtNp2Ff69u4HoydPM4c1L5iF0QUmfElJeexc2fUYI7RNe0gPUoUQOe7Kk9PB3J_wEnab0RggZcFkeoxNKCymKknZQnLscncGLjbOApwlPwEPUGSx2Hj-uQ8iv-L5OZgV4prcQcbXFc6hjeHe-IUZYe4vHofa5OTM5NbtPrTK74FvHpHYeNH5wL3jk4rfenqGjpV4lON_PLnq-vXka3_Vmi8l0PJr1DB-Q3DPUaCkYsNKWhlXaikFVCFkJPhRUc2BDIcuKWaM5I1xLDZYVmvABM7YoBOVddLXzfsTwWUPKau2SgdVKewh1UoJRIeWQNWB_B5oYUoqwVB_RrXXcKkpUW1m1lVVbWbWVm4PLvbmu1mD_8H3WBpA7AJr_vhxElYwDb8C6CCYrG9x_7h_5RYwX</recordid><startdate>20011001</startdate><enddate>20011001</enddate><creator>Imasaki, Takao</creator><creator>Kobayashi, Hirosuke</creator><creator>Hataishi, Ryuji</creator><creator>Hayashi, Izumi</creator><creator>Tomita, Tomoyuki</creator><creator>Majima, Masataka</creator><general>Elsevier Inc</general><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>20011001</creationdate><title>Nitric Oxide Is Generated in Smooth Muscle Layer by Neurokinin A and Counteracts Constriction in Guinea Pig Airway</title><author>Imasaki, Takao ; Kobayashi, Hirosuke ; Hataishi, Ryuji ; Hayashi, Izumi ; Tomita, Tomoyuki ; Majima, Masataka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-c1ca872e26d6c2bad74b578b73971a3e29786b2dca3203a8aed25a0342cd55713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Airway Resistance - drug effects</topic><topic>Animals</topic><topic>asthma</topic><topic>Benzamides - pharmacology</topic><topic>bronchial smooth muscle</topic><topic>Bronchoconstriction - drug effects</topic><topic>capsaicin</topic><topic>Capsaicin - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Epithelial Cells - physiology</topic><topic>Guanidines - pharmacology</topic><topic>Guinea Pigs</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Muscle, Smooth - drug effects</topic><topic>Muscle, Smooth - metabolism</topic><topic>Neurokinin A - pharmacology</topic><topic>NG-Nitroarginine Methyl Ester - pharmacology</topic><topic>Nitrates - metabolism</topic><topic>nitric oxide</topic><topic>Nitric Oxide - biosynthesis</topic><topic>Nitric Oxide Synthase - antagonists &amp; inhibitors</topic><topic>Nitric Oxide Synthase - metabolism</topic><topic>Nitric Oxide Synthase Type I</topic><topic>Nitric Oxide Synthase Type II</topic><topic>Nitric Oxide Synthase Type III</topic><topic>Nitrites - metabolism</topic><topic>Piperidines - pharmacology</topic><topic>Receptors, Neurokinin-2 - agonists</topic><topic>Receptors, Neurokinin-2 - antagonists &amp; inhibitors</topic><topic>tachykinin</topic><topic>Trachea - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Imasaki, Takao</creatorcontrib><creatorcontrib>Kobayashi, Hirosuke</creatorcontrib><creatorcontrib>Hataishi, Ryuji</creatorcontrib><creatorcontrib>Hayashi, Izumi</creatorcontrib><creatorcontrib>Tomita, Tomoyuki</creatorcontrib><creatorcontrib>Majima, Masataka</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>Nitric oxide</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Imasaki, Takao</au><au>Kobayashi, Hirosuke</au><au>Hataishi, Ryuji</au><au>Hayashi, Izumi</au><au>Tomita, Tomoyuki</au><au>Majima, Masataka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nitric Oxide Is Generated in Smooth Muscle Layer by Neurokinin A and Counteracts Constriction in Guinea Pig Airway</atitle><jtitle>Nitric oxide</jtitle><addtitle>Nitric Oxide</addtitle><date>2001-10-01</date><risdate>2001</risdate><volume>5</volume><issue>5</issue><spage>465</spage><epage>474</epage><pages>465-474</pages><issn>1089-8603</issn><eissn>1089-8611</eissn><abstract>It has been reported that several bronchoconstrictors generate nitric oxide (NO), counteracting bronchoconstriction, and removal of bronchial epithelia reduces NO production. However, it has not been elucidated whether neurokinin A (NKA), a potent bronchoconstrictor liberated from nerve terminals, generates NO. Specific questions in this study were (1) does NKA also generate NO, (2) does NO counteract NKA-induced bronchoconstriction, and (3) does the NO generation require bronchial epithelial cells? In an in vivo study exogenous as well as endogenous (capsaicin-induced) NKA increased airway opening pressure (Pao) and the exhaled NO level, and both were inhibited by an antagonist selective for NK2 receptor (a receptor for NKA), SR48968. The exhaled NO level became negligible with an inhibitor of NO synthase (NOS) type 1-3 (NG-nitro-l-arginine methyl ester, l-NAME) with increased Pao, but not with a NOS type 2 inhibitor. In an in vitro study, NKA increased the nitrite/nitrate level in superfused fluid of tracheal segments. Removing smooth muscle reduced nitrite/nitrate in the fluid to negligible levels, while the level was unchanged with removal of the epithelia. Pretreatment with l-NAME enhanced the tension of epithelia-removed tracheal segments. These findings indicate that (1) NKA generates NO, (2) NO counteracts NKA-induced bronchoconstriction, and (3) NKA activates NOS in the muscle layer, independently of bronchial epithelia.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11587561</pmid><doi>10.1006/niox.2001.0361</doi><tpages>10</tpages></addata></record>
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subjects Airway Resistance - drug effects
Animals
asthma
Benzamides - pharmacology
bronchial smooth muscle
Bronchoconstriction - drug effects
capsaicin
Capsaicin - pharmacology
Dose-Response Relationship, Drug
Enzyme Inhibitors - pharmacology
Epithelial Cells - physiology
Guanidines - pharmacology
Guinea Pigs
In Vitro Techniques
Male
Muscle, Smooth - drug effects
Muscle, Smooth - metabolism
Neurokinin A - pharmacology
NG-Nitroarginine Methyl Ester - pharmacology
Nitrates - metabolism
nitric oxide
Nitric Oxide - biosynthesis
Nitric Oxide Synthase - antagonists & inhibitors
Nitric Oxide Synthase - metabolism
Nitric Oxide Synthase Type I
Nitric Oxide Synthase Type II
Nitric Oxide Synthase Type III
Nitrites - metabolism
Piperidines - pharmacology
Receptors, Neurokinin-2 - agonists
Receptors, Neurokinin-2 - antagonists & inhibitors
tachykinin
Trachea - physiology
title Nitric Oxide Is Generated in Smooth Muscle Layer by Neurokinin A and Counteracts Constriction in Guinea Pig Airway
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