Increase in endotoxin-induced mucosal permeability is related to increased nitric oxide synthase activity using the Ussing chamber

OBJECTIVETo determine if nitric oxide production is associated with increased intestinal permeability after endotoxin challenge using the ex vivo Ussing chamber. SUBJECTSIleal mucosal membranes harvested from normal rats weighing 300 to 420 g. INTERVENTIONSEndotoxin (lipopolysaccharide), 1, 10, 100...

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Veröffentlicht in:Critical care medicine 1999-05, Vol.27 (5), p.880-886
Hauptverfasser: Mishima, Shiro, Xu, Dazhong, Deitch, Edwin A
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Xu, Dazhong
Deitch, Edwin A
description OBJECTIVETo determine if nitric oxide production is associated with increased intestinal permeability after endotoxin challenge using the ex vivo Ussing chamber. SUBJECTSIleal mucosal membranes harvested from normal rats weighing 300 to 420 g. INTERVENTIONSEndotoxin (lipopolysaccharide), 1, 10, 100 [micro sign]g/mL, or saline was placed on the serosal side of ileal mucosal membranes mounted in Ussing chambers after 10 Escherichia coli C-25 had been placed on the mucosal side of the ileal membranes (n = 6-7/group). In a second set of experiments, ileal membranes were exposed to 100 [micro sign]g/mL lipopolysaccharide with or without the addition of the nitric oxide synthase inhibitor, N at a concentration of 10 mM (n = 7-8/group). MAIN OUTCOME MEASUREBacterial translocation of E. coli C-25 from the mucosal to the serosal side of the ileal membrane was measured every hour during the 3-hr experimental period, as were serial measurements of the potential difference and resistance values of the ileal membranes. At the conclusion of the 3-hr period, the ileal membranes were harvested and levels of inducible nitric oxide synthase and constitutive nitric oxide synthase activity were measured. RESULTSThe incidence of E. coli C-25 passage across the ileal membranes mounted in the Ussing chambers was significantly increased in the ileal membranes exposed to 10 or 100 [micro sign]g/mL of lipopolysaccharide (71% and 86%, respectively) vs. the control membranes (0%) or the membranes exposed to 1 [micro sign]g/mL of lipopolysaccharide (0%) (p < .05). This increase in E. coli C-25 passage in the ileal membranes exposed to 10 or 100 [micro sign]g/mL of lipopolysaccharide was associated with a decrease in ileal membrane resistance and an increase in inducible nitric oxide synthase activity (p < .05). The addition of N protected against lipopolysaccharide-induced bacterial translocation and prevented the lipopolysaccharide-induced increase in ileal membrane inducible nitric oxide synthase activity. CONCLUSIONThese results indicate that lipopolysaccharide induction of increased ileal inducible nitric oxide synthase activity is necessary for lipopolysaccharide-induced E. coli C-25 translocation to occur in normal ileal mucosal membranes tested in the Ussing chamber system. (Crit Care Med 1999; 27:880-886)
doi_str_mv 10.1097/00003246-199905000-00018
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SUBJECTSIleal mucosal membranes harvested from normal rats weighing 300 to 420 g. INTERVENTIONSEndotoxin (lipopolysaccharide), 1, 10, 100 [micro sign]g/mL, or saline was placed on the serosal side of ileal mucosal membranes mounted in Ussing chambers after 10 Escherichia coli C-25 had been placed on the mucosal side of the ileal membranes (n = 6-7/group). In a second set of experiments, ileal membranes were exposed to 100 [micro sign]g/mL lipopolysaccharide with or without the addition of the nitric oxide synthase inhibitor, N at a concentration of 10 mM (n = 7-8/group). MAIN OUTCOME MEASUREBacterial translocation of E. coli C-25 from the mucosal to the serosal side of the ileal membrane was measured every hour during the 3-hr experimental period, as were serial measurements of the potential difference and resistance values of the ileal membranes. At the conclusion of the 3-hr period, the ileal membranes were harvested and levels of inducible nitric oxide synthase and constitutive nitric oxide synthase activity were measured. RESULTSThe incidence of E. coli C-25 passage across the ileal membranes mounted in the Ussing chambers was significantly increased in the ileal membranes exposed to 10 or 100 [micro sign]g/mL of lipopolysaccharide (71% and 86%, respectively) vs. the control membranes (0%) or the membranes exposed to 1 [micro sign]g/mL of lipopolysaccharide (0%) (p &lt; .05). This increase in E. coli C-25 passage in the ileal membranes exposed to 10 or 100 [micro sign]g/mL of lipopolysaccharide was associated with a decrease in ileal membrane resistance and an increase in inducible nitric oxide synthase activity (p &lt; .05). The addition of N protected against lipopolysaccharide-induced bacterial translocation and prevented the lipopolysaccharide-induced increase in ileal membrane inducible nitric oxide synthase activity. CONCLUSIONThese results indicate that lipopolysaccharide induction of increased ileal inducible nitric oxide synthase activity is necessary for lipopolysaccharide-induced E. coli C-25 translocation to occur in normal ileal mucosal membranes tested in the Ussing chamber system. (Crit Care Med 1999; 27:880-886)</description><identifier>ISSN: 0090-3493</identifier><identifier>EISSN: 1530-0293</identifier><identifier>DOI: 10.1097/00003246-199905000-00018</identifier><identifier>PMID: 10362408</identifier><identifier>CODEN: CCMDC7</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams &amp; Wilkins, Inc</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Bacterial Translocation - physiology ; Biological and medical sciences ; Cell Membrane Permeability - physiology ; Disease Models, Animal ; Emergency and intensive care: infection, septic shock ; Escherichia coli ; Ileum ; In Vitro Techniques ; Intensive care medicine ; Intestinal Mucosa - enzymology ; Intestinal Mucosa - microbiology ; Lipopolysaccharides - adverse effects ; Male ; Medical sciences ; Nitric Oxide Synthase - antagonists &amp; inhibitors ; Nitric Oxide Synthase - physiology ; omega-N-Methylarginine - pharmacology ; Rats ; Rats, Sprague-Dawley ; Time Factors</subject><ispartof>Critical care medicine, 1999-05, Vol.27 (5), p.880-886</ispartof><rights>1999 Lippincott Williams &amp; Wilkins, Inc.</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3858-8ccf5335da6b049c50fbb085ee8f1a5bf9d8dd85522560bdc48ae72629ab8a4e3</citedby><cites>FETCH-LOGICAL-c3858-8ccf5335da6b049c50fbb085ee8f1a5bf9d8dd85522560bdc48ae72629ab8a4e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,780,784,789,790,23930,23931,25140,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1850136$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10362408$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mishima, Shiro</creatorcontrib><creatorcontrib>Xu, Dazhong</creatorcontrib><creatorcontrib>Deitch, Edwin A</creatorcontrib><title>Increase in endotoxin-induced mucosal permeability is related to increased nitric oxide synthase activity using the Ussing chamber</title><title>Critical care medicine</title><addtitle>Crit Care Med</addtitle><description>OBJECTIVETo determine if nitric oxide production is associated with increased intestinal permeability after endotoxin challenge using the ex vivo Ussing chamber. SUBJECTSIleal mucosal membranes harvested from normal rats weighing 300 to 420 g. INTERVENTIONSEndotoxin (lipopolysaccharide), 1, 10, 100 [micro sign]g/mL, or saline was placed on the serosal side of ileal mucosal membranes mounted in Ussing chambers after 10 Escherichia coli C-25 had been placed on the mucosal side of the ileal membranes (n = 6-7/group). In a second set of experiments, ileal membranes were exposed to 100 [micro sign]g/mL lipopolysaccharide with or without the addition of the nitric oxide synthase inhibitor, N at a concentration of 10 mM (n = 7-8/group). MAIN OUTCOME MEASUREBacterial translocation of E. coli C-25 from the mucosal to the serosal side of the ileal membrane was measured every hour during the 3-hr experimental period, as were serial measurements of the potential difference and resistance values of the ileal membranes. At the conclusion of the 3-hr period, the ileal membranes were harvested and levels of inducible nitric oxide synthase and constitutive nitric oxide synthase activity were measured. RESULTSThe incidence of E. coli C-25 passage across the ileal membranes mounted in the Ussing chambers was significantly increased in the ileal membranes exposed to 10 or 100 [micro sign]g/mL of lipopolysaccharide (71% and 86%, respectively) vs. the control membranes (0%) or the membranes exposed to 1 [micro sign]g/mL of lipopolysaccharide (0%) (p &lt; .05). This increase in E. coli C-25 passage in the ileal membranes exposed to 10 or 100 [micro sign]g/mL of lipopolysaccharide was associated with a decrease in ileal membrane resistance and an increase in inducible nitric oxide synthase activity (p &lt; .05). The addition of N protected against lipopolysaccharide-induced bacterial translocation and prevented the lipopolysaccharide-induced increase in ileal membrane inducible nitric oxide synthase activity. CONCLUSIONThese results indicate that lipopolysaccharide induction of increased ileal inducible nitric oxide synthase activity is necessary for lipopolysaccharide-induced E. coli C-25 translocation to occur in normal ileal mucosal membranes tested in the Ussing chamber system. (Crit Care Med 1999; 27:880-886)</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Bacterial Translocation - physiology</subject><subject>Biological and medical sciences</subject><subject>Cell Membrane Permeability - physiology</subject><subject>Disease Models, Animal</subject><subject>Emergency and intensive care: infection, septic shock</subject><subject>Escherichia coli</subject><subject>Ileum</subject><subject>In Vitro Techniques</subject><subject>Intensive care medicine</subject><subject>Intestinal Mucosa - enzymology</subject><subject>Intestinal Mucosa - microbiology</subject><subject>Lipopolysaccharides - adverse effects</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Nitric Oxide Synthase - antagonists &amp; inhibitors</subject><subject>Nitric Oxide Synthase - physiology</subject><subject>omega-N-Methylarginine - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Time Factors</subject><issn>0090-3493</issn><issn>1530-0293</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU2PFCEQhonRuOPqXzAcjLdWaJoeOJqNH5ts4sU9k2qotlGaHoF2nau_XGZ7_LhIQqoq9bwvyQshlLNXnOn9a1aPaLu-4VprJuvU1MvVA7LjUtSh1eIh2TGmWSM6LS7Ik5y_VKKTe_GYXHAm-rZjakd-XkebEDJSHylGt5Tlh4-Nj2616Oi82iVDoAdMM8Lggy9H6jNNGKDUfVmqbjNwNPqSvKXVwCHNx1imky_Y4r-fZGv28TMtE9LbfN_aCeYB01PyaISQ8dm5XpLbd28_XX1obj6-v756c9NYoaRqlLWjFEI66AfWaSvZOAxMSUQ1cpDDqJ1yTknZtrJng7OdAty3fathUNChuCQvN99DWr6tmIuZfbYYAkRc1mx6rdiea1ZBtYE2LTknHM0h-RnS0XBmTvmb3_mbP_mb-_yr9Pn5jXWY0f0j3AKvwIszANlCGBNE6_NfTknGRV-xbsPullAw5a9hvcNkJoRQJvO_7xe_AFF0oBA</recordid><startdate>199905</startdate><enddate>199905</enddate><creator>Mishima, Shiro</creator><creator>Xu, Dazhong</creator><creator>Deitch, Edwin A</creator><general>Lippincott Williams &amp; Wilkins, Inc</general><general>Lippincott</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>199905</creationdate><title>Increase in endotoxin-induced mucosal permeability is related to increased nitric oxide synthase activity using the Ussing chamber</title><author>Mishima, Shiro ; Xu, Dazhong ; Deitch, Edwin A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3858-8ccf5335da6b049c50fbb085ee8f1a5bf9d8dd85522560bdc48ae72629ab8a4e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Bacterial Translocation - physiology</topic><topic>Biological and medical sciences</topic><topic>Cell Membrane Permeability - physiology</topic><topic>Disease Models, Animal</topic><topic>Emergency and intensive care: infection, septic shock</topic><topic>Escherichia coli</topic><topic>Ileum</topic><topic>In Vitro Techniques</topic><topic>Intensive care medicine</topic><topic>Intestinal Mucosa - enzymology</topic><topic>Intestinal Mucosa - microbiology</topic><topic>Lipopolysaccharides - adverse effects</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nitric Oxide Synthase - antagonists &amp; inhibitors</topic><topic>Nitric Oxide Synthase - physiology</topic><topic>omega-N-Methylarginine - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mishima, Shiro</creatorcontrib><creatorcontrib>Xu, Dazhong</creatorcontrib><creatorcontrib>Deitch, Edwin A</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>Critical care medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mishima, Shiro</au><au>Xu, Dazhong</au><au>Deitch, Edwin A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increase in endotoxin-induced mucosal permeability is related to increased nitric oxide synthase activity using the Ussing chamber</atitle><jtitle>Critical care medicine</jtitle><addtitle>Crit Care Med</addtitle><date>1999-05</date><risdate>1999</risdate><volume>27</volume><issue>5</issue><spage>880</spage><epage>886</epage><pages>880-886</pages><issn>0090-3493</issn><eissn>1530-0293</eissn><coden>CCMDC7</coden><abstract>OBJECTIVETo determine if nitric oxide production is associated with increased intestinal permeability after endotoxin challenge using the ex vivo Ussing chamber. SUBJECTSIleal mucosal membranes harvested from normal rats weighing 300 to 420 g. INTERVENTIONSEndotoxin (lipopolysaccharide), 1, 10, 100 [micro sign]g/mL, or saline was placed on the serosal side of ileal mucosal membranes mounted in Ussing chambers after 10 Escherichia coli C-25 had been placed on the mucosal side of the ileal membranes (n = 6-7/group). In a second set of experiments, ileal membranes were exposed to 100 [micro sign]g/mL lipopolysaccharide with or without the addition of the nitric oxide synthase inhibitor, N at a concentration of 10 mM (n = 7-8/group). MAIN OUTCOME MEASUREBacterial translocation of E. coli C-25 from the mucosal to the serosal side of the ileal membrane was measured every hour during the 3-hr experimental period, as were serial measurements of the potential difference and resistance values of the ileal membranes. At the conclusion of the 3-hr period, the ileal membranes were harvested and levels of inducible nitric oxide synthase and constitutive nitric oxide synthase activity were measured. RESULTSThe incidence of E. coli C-25 passage across the ileal membranes mounted in the Ussing chambers was significantly increased in the ileal membranes exposed to 10 or 100 [micro sign]g/mL of lipopolysaccharide (71% and 86%, respectively) vs. the control membranes (0%) or the membranes exposed to 1 [micro sign]g/mL of lipopolysaccharide (0%) (p &lt; .05). This increase in E. coli C-25 passage in the ileal membranes exposed to 10 or 100 [micro sign]g/mL of lipopolysaccharide was associated with a decrease in ileal membrane resistance and an increase in inducible nitric oxide synthase activity (p &lt; .05). The addition of N protected against lipopolysaccharide-induced bacterial translocation and prevented the lipopolysaccharide-induced increase in ileal membrane inducible nitric oxide synthase activity. CONCLUSIONThese results indicate that lipopolysaccharide induction of increased ileal inducible nitric oxide synthase activity is necessary for lipopolysaccharide-induced E. coli C-25 translocation to occur in normal ileal mucosal membranes tested in the Ussing chamber system. (Crit Care Med 1999; 27:880-886)</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams &amp; Wilkins, Inc</pub><pmid>10362408</pmid><doi>10.1097/00003246-199905000-00018</doi><tpages>7</tpages></addata></record>
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subjects Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Animals
Bacterial Translocation - physiology
Biological and medical sciences
Cell Membrane Permeability - physiology
Disease Models, Animal
Emergency and intensive care: infection, septic shock
Escherichia coli
Ileum
In Vitro Techniques
Intensive care medicine
Intestinal Mucosa - enzymology
Intestinal Mucosa - microbiology
Lipopolysaccharides - adverse effects
Male
Medical sciences
Nitric Oxide Synthase - antagonists & inhibitors
Nitric Oxide Synthase - physiology
omega-N-Methylarginine - pharmacology
Rats
Rats, Sprague-Dawley
Time Factors
title Increase in endotoxin-induced mucosal permeability is related to increased nitric oxide synthase activity using the Ussing chamber
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