Immunohistochemical localization of 3',5'-cyclic guanosine monophosphate in the canine proximal colon: Responses to nitric oxide and electrical stimulation of enteric inhibitory neurons

There is growing evidence that nitric oxide serves as a neurotransmitter released from enteric inhibitory nerves in the gastrointestinal tract. The distribution of nitric oxide synthase suggests that nitric oxide may also be a neurotransmitter within enteric ganglia. Since many actions of nitric oxi...

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Veröffentlicht in:Neuroscience 1993-09, Vol.56 (2), p.513-522
Hauptverfasser: Shuttleworth, C.W., Xue, C., Ward, S.M., De Vente, J., Sanders, K.M.
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De Vente, J.
Sanders, K.M.
description There is growing evidence that nitric oxide serves as a neurotransmitter released from enteric inhibitory nerves in the gastrointestinal tract. The distribution of nitric oxide synthase suggests that nitric oxide may also be a neurotransmitter within enteric ganglia. Since many actions of nitric oxide are mediated by stimulation of soluble guanylate cyclase and a subsequent increase in 3',5'-cyclic guanosine monophosphate (cGMP) concentration, targets for nitric oxide in the canine proximal colon were investigated by immunohistochemical localization of cGMP. In the presence of phosphodiesterase inhibitors (M&B 22948, 100 μM and 3-isobutyl-1-methyl-xanthine, 1 mM), exogenous nitric oxide and electrical field stimulation caused an accumulation of cGMP-like immunoreactivity in several cell-types including colonic smooth muscle cells. cGMP-like immunoreactivity was also observed in a subpopulation of neurons in both myenteric and submucosal ganglia. Sequential labeling with the NADPH diaphorase technique showed that 94% of neurons that responded to exogenous nitric oxide with an increase in cGMP-like immunoreactivity were NADPH diaphorase negative. None of the myenteric neurons that responded to electrical field stimulation with an increase in cGMP-like immunoreactivity were NADPH diaphorase positive, and only one submucosal neuron with cGMP-like immunoreactivity was also NADPH diaphorase positive. The electrical field-stimulated increase in cGMP-like immunoreactivity was blocked by nitroarginine (100 μM). An increase in cGMP-like immunoreactivity also occurred in interstitial cells located at the submucosal surface of the circular muscle layer. These cells are interposed between nerve varicosities and smooth muscle cells and may partially mediate neuromuscular transmission. Sodium nitroprusside and nitric oxide also caused an accumulation of cGMP-like immunoreactivity in smooth muscle cells of intramural arterioles and venules. The results of this study further support the role of nitric oxide as a neurotransmitter in colonie muscles, and provide support for the hypothesis that interstitial cells are functionally innervated by enteric inhibitory neurons. The data also suggest that nitric oxide may serve as a neurotransmitter in enteric ganglia.
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The distribution of nitric oxide synthase suggests that nitric oxide may also be a neurotransmitter within enteric ganglia. Since many actions of nitric oxide are mediated by stimulation of soluble guanylate cyclase and a subsequent increase in 3',5'-cyclic guanosine monophosphate (cGMP) concentration, targets for nitric oxide in the canine proximal colon were investigated by immunohistochemical localization of cGMP. In the presence of phosphodiesterase inhibitors (M&amp;B 22948, 100 μM and 3-isobutyl-1-methyl-xanthine, 1 mM), exogenous nitric oxide and electrical field stimulation caused an accumulation of cGMP-like immunoreactivity in several cell-types including colonic smooth muscle cells. cGMP-like immunoreactivity was also observed in a subpopulation of neurons in both myenteric and submucosal ganglia. Sequential labeling with the NADPH diaphorase technique showed that 94% of neurons that responded to exogenous nitric oxide with an increase in cGMP-like immunoreactivity were NADPH diaphorase negative. None of the myenteric neurons that responded to electrical field stimulation with an increase in cGMP-like immunoreactivity were NADPH diaphorase positive, and only one submucosal neuron with cGMP-like immunoreactivity was also NADPH diaphorase positive. The electrical field-stimulated increase in cGMP-like immunoreactivity was blocked by nitroarginine (100 μM). An increase in cGMP-like immunoreactivity also occurred in interstitial cells located at the submucosal surface of the circular muscle layer. These cells are interposed between nerve varicosities and smooth muscle cells and may partially mediate neuromuscular transmission. Sodium nitroprusside and nitric oxide also caused an accumulation of cGMP-like immunoreactivity in smooth muscle cells of intramural arterioles and venules. 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Psychology</subject><subject>Ganglia, Autonomic - drug effects</subject><subject>IBMX</subject><subject>Intestine. Mesentery</subject><subject>KRB</subject><subject>Krebs-Ringer bicarbonate solution</subject><subject>Litric oxide synthase-like immunoreactivity</subject><subject>Male</subject><subject>NADPH</subject><subject>nitric oxide</subject><subject>Nitric Oxide - pharmacology</subject><subject>nitric oxide synthase</subject><subject>Nitroprusside - pharmacology</subject><subject>NOS</subject><subject>NOS-LI</subject><subject>PBS</subject><subject>phosphate buffered saline</subject><subject>Purinones - pharmacology</subject><subject>Second Messenger Systems</subject><subject>SNP</subject><subject>sodium nitroprusside</subject><subject>TEM</subject><subject>transmission electron microscopy</subject><subject>Vertebrates: digestive system</subject><subject>β-nicotinamide adenine dinucleotide phosphate</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kd2K1DAcxYMo67j6Bgq5EFfBaj6apvVCkMWPhYUB0euQpP_aSJvUJBXHN_PtTJ1hLs1FAjm_nCTnIPSYkleU0OY14aSpasHY846_6AgXpNrfQTvaSl5JUdd30e6M3EcPUvpOyhA1v0AXUpCa0XaH_tzM8-rD6FIOdoTZWT3hKZTZ_dbZBY_DgPnVS3FV2YOdnMXfVu1Dch7wHHxYxpCWUWfAzuM8Arbab9oSwy83Fy8bpuDf4M-QluATJJwD9i7H4lSIHrD2PYYJ7LZV-JTdvE7nq8Fn2FjnR2dcDvGAPayxWD1E9wY9JXh0Wi_R1w_vv1x_qm73H2-u391WVhCeKwq0MUZ0vRw0A6HlQJoBDCe2ZQ3rDdSGFYl3pKspsZQb20pmNBii7QA9v0TPjr7lSz9WSFnNLlmYJu0hrEnJhkhJJClgfQRtDClFGNQSSwTxoChRW2Nqq0NtdaiOq3-NqX059uTkv5oZ-vOhU0VFf3rSdSoBDVF769IZq9tGdIQV7O0Rg5LFTwdRJevAW-hdLOGqPrj_v-MvgSy4Gw</recordid><startdate>19930901</startdate><enddate>19930901</enddate><creator>Shuttleworth, C.W.</creator><creator>Xue, C.</creator><creator>Ward, S.M.</creator><creator>De Vente, J.</creator><creator>Sanders, K.M.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><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>19930901</creationdate><title>Immunohistochemical localization of 3',5'-cyclic guanosine monophosphate in the canine proximal colon: Responses to nitric oxide and electrical stimulation of enteric inhibitory neurons</title><author>Shuttleworth, C.W. ; Xue, C. ; Ward, S.M. ; De Vente, J. ; Sanders, K.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-1e16bb59d7fa2e5a7f06feb30c8262dbe4b27fa3909410c13bc872baeb0acfed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>1-Methyl-3-isobutylxanthine - pharmacology</topic><topic>3',5'-cyclic guanosine monophosphate</topic><topic>3',5'-cyclic guanosine monophosphate-like immunoreactivity</topic><topic>3',5'-Cyclic-GMP Phosphodiesterases - antagonists &amp; inhibitors</topic><topic>3-isobutyl-1-methyl-xanthine</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>cGMP</topic><topic>cGMP-LI</topic><topic>Colon - chemistry</topic><topic>Colon - drug effects</topic><topic>Colon - physiology</topic><topic>Cyclic GMP - analysis</topic><topic>Cyclic GMP - physiology</topic><topic>Dogs</topic><topic>EFS</topic><topic>Electric Stimulation</topic><topic>electrical field stimulation</topic><topic>Enteric Nervous System - drug effects</topic><topic>Enteric Nervous System - physiology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Ganglia, Autonomic - drug effects</topic><topic>IBMX</topic><topic>Intestine. Mesentery</topic><topic>KRB</topic><topic>Krebs-Ringer bicarbonate solution</topic><topic>Litric oxide synthase-like immunoreactivity</topic><topic>Male</topic><topic>NADPH</topic><topic>nitric oxide</topic><topic>Nitric Oxide - pharmacology</topic><topic>nitric oxide synthase</topic><topic>Nitroprusside - pharmacology</topic><topic>NOS</topic><topic>NOS-LI</topic><topic>PBS</topic><topic>phosphate buffered saline</topic><topic>Purinones - pharmacology</topic><topic>Second Messenger Systems</topic><topic>SNP</topic><topic>sodium nitroprusside</topic><topic>TEM</topic><topic>transmission electron microscopy</topic><topic>Vertebrates: digestive system</topic><topic>β-nicotinamide adenine dinucleotide phosphate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shuttleworth, C.W.</creatorcontrib><creatorcontrib>Xue, C.</creatorcontrib><creatorcontrib>Ward, S.M.</creatorcontrib><creatorcontrib>De Vente, J.</creatorcontrib><creatorcontrib>Sanders, K.M.</creatorcontrib><collection>Pascal-Francis</collection><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>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shuttleworth, C.W.</au><au>Xue, C.</au><au>Ward, S.M.</au><au>De Vente, J.</au><au>Sanders, K.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunohistochemical localization of 3',5'-cyclic guanosine monophosphate in the canine proximal colon: Responses to nitric oxide and electrical stimulation of enteric inhibitory neurons</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>1993-09-01</date><risdate>1993</risdate><volume>56</volume><issue>2</issue><spage>513</spage><epage>522</epage><pages>513-522</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>There is growing evidence that nitric oxide serves as a neurotransmitter released from enteric inhibitory nerves in the gastrointestinal tract. The distribution of nitric oxide synthase suggests that nitric oxide may also be a neurotransmitter within enteric ganglia. Since many actions of nitric oxide are mediated by stimulation of soluble guanylate cyclase and a subsequent increase in 3',5'-cyclic guanosine monophosphate (cGMP) concentration, targets for nitric oxide in the canine proximal colon were investigated by immunohistochemical localization of cGMP. In the presence of phosphodiesterase inhibitors (M&amp;B 22948, 100 μM and 3-isobutyl-1-methyl-xanthine, 1 mM), exogenous nitric oxide and electrical field stimulation caused an accumulation of cGMP-like immunoreactivity in several cell-types including colonic smooth muscle cells. cGMP-like immunoreactivity was also observed in a subpopulation of neurons in both myenteric and submucosal ganglia. Sequential labeling with the NADPH diaphorase technique showed that 94% of neurons that responded to exogenous nitric oxide with an increase in cGMP-like immunoreactivity were NADPH diaphorase negative. None of the myenteric neurons that responded to electrical field stimulation with an increase in cGMP-like immunoreactivity were NADPH diaphorase positive, and only one submucosal neuron with cGMP-like immunoreactivity was also NADPH diaphorase positive. The electrical field-stimulated increase in cGMP-like immunoreactivity was blocked by nitroarginine (100 μM). An increase in cGMP-like immunoreactivity also occurred in interstitial cells located at the submucosal surface of the circular muscle layer. These cells are interposed between nerve varicosities and smooth muscle cells and may partially mediate neuromuscular transmission. Sodium nitroprusside and nitric oxide also caused an accumulation of cGMP-like immunoreactivity in smooth muscle cells of intramural arterioles and venules. The results of this study further support the role of nitric oxide as a neurotransmitter in colonie muscles, and provide support for the hypothesis that interstitial cells are functionally innervated by enteric inhibitory neurons. The data also suggest that nitric oxide may serve as a neurotransmitter in enteric ganglia.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>7504218</pmid><doi>10.1016/0306-4522(93)90350-O</doi><tpages>10</tpages></addata></record>
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identifier ISSN: 0306-4522
ispartof Neuroscience, 1993-09, Vol.56 (2), p.513-522
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subjects 1-Methyl-3-isobutylxanthine - pharmacology
3',5'-cyclic guanosine monophosphate
3',5'-cyclic guanosine monophosphate-like immunoreactivity
3',5'-Cyclic-GMP Phosphodiesterases - antagonists & inhibitors
3-isobutyl-1-methyl-xanthine
Animals
Biological and medical sciences
cGMP
cGMP-LI
Colon - chemistry
Colon - drug effects
Colon - physiology
Cyclic GMP - analysis
Cyclic GMP - physiology
Dogs
EFS
Electric Stimulation
electrical field stimulation
Enteric Nervous System - drug effects
Enteric Nervous System - physiology
Female
Fundamental and applied biological sciences. Psychology
Ganglia, Autonomic - drug effects
IBMX
Intestine. Mesentery
KRB
Krebs-Ringer bicarbonate solution
Litric oxide synthase-like immunoreactivity
Male
NADPH
nitric oxide
Nitric Oxide - pharmacology
nitric oxide synthase
Nitroprusside - pharmacology
NOS
NOS-LI
PBS
phosphate buffered saline
Purinones - pharmacology
Second Messenger Systems
SNP
sodium nitroprusside
TEM
transmission electron microscopy
Vertebrates: digestive system
β-nicotinamide adenine dinucleotide phosphate
title Immunohistochemical localization of 3',5'-cyclic guanosine monophosphate in the canine proximal colon: Responses to nitric oxide and electrical stimulation of enteric inhibitory neurons
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