Modulation of autonomic neuroeffector transmission by nitric oxide in guinea pig ileum

N G-monomethyl-L-arginine (L-NMMA), an inhibitor of nitric oxide synthesis, markedly enhanced tonic (“hump”) responses to transmural stimulatin in guinea pig ileum longitudinal muscle. The enhancement of the hump responses was probably due to a prejunctional effect on substance P-like neurotransmiss...

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Veröffentlicht in:Biochemical and biophysical research communications 1990-11, Vol.173 (1), p.106-110
Hauptverfasser: Gustafsson, Lars E., Wiklund, Claes U., Wikhund, N. Peter, Persson, Magnus G., Moncada, Salvador
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container_end_page 110
container_issue 1
container_start_page 106
container_title Biochemical and biophysical research communications
container_volume 173
creator Gustafsson, Lars E.
Wiklund, Claes U.
Wikhund, N. Peter
Persson, Magnus G.
Moncada, Salvador
description N G-monomethyl-L-arginine (L-NMMA), an inhibitor of nitric oxide synthesis, markedly enhanced tonic (“hump”) responses to transmural stimulatin in guinea pig ileum longitudinal muscle. The enhancement of the hump responses was probably due to a prejunctional effect on substance P-like neurotransmission, since the action of L-NMMA was exerted also in the presence of atropine, and since responses to substance P, a mimic of nerve stimulation, were unaffected by L-NMMA as were cholinergic twitch responses and the overflow of [ 3H]choline. Further in support, the hump responses were blocked by the substance P antagonist Spantide. All effects of L-NMMA were stereospecifically reversed by L-arginine. Endogenous nitric oxide thus selectively modulates peptidergic neurotransmission in the gut.
doi_str_mv 10.1016/S0006-291X(05)81028-9
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Peter</creatorcontrib><creatorcontrib>Persson, Magnus G.</creatorcontrib><creatorcontrib>Moncada, Salvador</creatorcontrib><title>Modulation of autonomic neuroeffector transmission by nitric oxide in guinea pig ileum</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>N G-monomethyl-L-arginine (L-NMMA), an inhibitor of nitric oxide synthesis, markedly enhanced tonic (“hump”) responses to transmural stimulatin in guinea pig ileum longitudinal muscle. The enhancement of the hump responses was probably due to a prejunctional effect on substance P-like neurotransmission, since the action of L-NMMA was exerted also in the presence of atropine, and since responses to substance P, a mimic of nerve stimulation, were unaffected by L-NMMA as were cholinergic twitch responses and the overflow of [ 3H]choline. Further in support, the hump responses were blocked by the substance P antagonist Spantide. All effects of L-NMMA were stereospecifically reversed by L-arginine. Endogenous nitric oxide thus selectively modulates peptidergic neurotransmission in the gut.</description><subject>Acetylcholine - metabolism</subject><subject>Animals</subject><subject>Arginine - analogs &amp; derivatives</subject><subject>Arginine - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Cell physiology</subject><subject>Choline - metabolism</subject><subject>Electric Stimulation</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Guinea Pigs</subject><subject>Ileum - drug effects</subject><subject>Ileum - innervation</subject><subject>Ileum - physiology</subject><subject>In Vitro Techniques</subject><subject>Isomerism</subject><subject>Kinetics</subject><subject>Male</subject><subject>Molecular and cellular biology</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle, Smooth - drug effects</subject><subject>Muscle, Smooth - innervation</subject><subject>Muscle, Smooth - physiology</subject><subject>Myenteric Plexus - drug effects</subject><subject>Myenteric Plexus - physiology</subject><subject>Neurotransmission</subject><subject>Nitric Oxide - metabolism</subject><subject>omega-N-Methylarginine</subject><subject>Substance P - pharmacology</subject><subject>Synaptic Transmission - drug effects</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v3CAQhlHVKt2k_QmRuLRqDk4HDDacqijql5Qqh36oN4TxEFHZsAW7Sv592OyqOeY0h3nmneGBkFMG5wxY9_47AHQN1-z3O5BnigFXjX5GNgw0NJyBeE42_5GX5LiUPwCMiU4fkSPW14gWNuTXtzSuk11CijR5atclxTQHRyOuOaH36JaU6ZJtLHMoZccNdzSGJVco3YYRaYj0Zg0RLd2GGxomXOdX5IW3U8HXh3pCfn76-OPyS3N1_fnr5cVV44TqlwZb3QGMQ6-kQg5KcC-Y1aJ3yDgfOseV5D13LRsG23PlFCLz2kvvbNsja0_I233uNqe_K5bF1CMdTpONmNZiVH2mEAqeBJlUUnK1S5R70OVUSkZvtjnMNt8ZBmYn3jyINzurBqR5EG90nTs9LFiHGcfHqb3p2n9z6Nvi7OSrUBfKI6bbTmjZVu7DnsOq7V_AbIoLGB2OIde_MGMKT1xyD-T1oCw</recordid><startdate>19901130</startdate><enddate>19901130</enddate><creator>Gustafsson, Lars E.</creator><creator>Wiklund, Claes U.</creator><creator>Wikhund, N. 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Peter ; Persson, Magnus G. ; Moncada, Salvador</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c487t-e39600db7858e20842f41a947ce122b6c285272c31bba728c8ee1f9f5fca37e13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Acetylcholine - metabolism</topic><topic>Animals</topic><topic>Arginine - analogs &amp; derivatives</topic><topic>Arginine - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Cell physiology</topic><topic>Choline - metabolism</topic><topic>Electric Stimulation</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. 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The enhancement of the hump responses was probably due to a prejunctional effect on substance P-like neurotransmission, since the action of L-NMMA was exerted also in the presence of atropine, and since responses to substance P, a mimic of nerve stimulation, were unaffected by L-NMMA as were cholinergic twitch responses and the overflow of [ 3H]choline. Further in support, the hump responses were blocked by the substance P antagonist Spantide. All effects of L-NMMA were stereospecifically reversed by L-arginine. Endogenous nitric oxide thus selectively modulates peptidergic neurotransmission in the gut.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>1701630</pmid><doi>10.1016/S0006-291X(05)81028-9</doi><tpages>5</tpages></addata></record>
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subjects Acetylcholine - metabolism
Animals
Arginine - analogs & derivatives
Arginine - pharmacology
Biological and medical sciences
Cell physiology
Choline - metabolism
Electric Stimulation
Female
Fundamental and applied biological sciences. Psychology
Guinea Pigs
Ileum - drug effects
Ileum - innervation
Ileum - physiology
In Vitro Techniques
Isomerism
Kinetics
Male
Molecular and cellular biology
Muscle Contraction - drug effects
Muscle, Smooth - drug effects
Muscle, Smooth - innervation
Muscle, Smooth - physiology
Myenteric Plexus - drug effects
Myenteric Plexus - physiology
Neurotransmission
Nitric Oxide - metabolism
omega-N-Methylarginine
Substance P - pharmacology
Synaptic Transmission - drug effects
title Modulation of autonomic neuroeffector transmission by nitric oxide in guinea pig ileum
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