Hyposensitivity to nerve stimulation in portal hypertensive rats: role of nitric oxide
Portal hypertension goes along with vascular hyporeactivity, partly mediated by nitric oxide (NO). Interactions between the adrenergic nervous system and NO in portal hypertension are undetermined. We tested (1) whether superior mesenteric arterial beds of portal hypertensive rats have an altered se...
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Veröffentlicht in: | European journal of clinical investigation 1997-11, Vol.27 (11), p.902-907 |
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description | Portal hypertension goes along with vascular hyporeactivity, partly mediated by nitric oxide (NO). Interactions between the adrenergic nervous system and NO in portal hypertension are undetermined. We tested (1) whether superior mesenteric arterial beds of portal hypertensive rats have an altered sensitivity to periarterial nerve stimulation (PNS) and (2) the role of NO in modulating nerve‐stimulated responses. Vasopressor responses to PNS (Hz, 2–32) were similar in preparations of partial portal vein‐ligated (PVL, n = 12) and control (CON, n = 12) rats (60.0 ± 6.7 and 47.8 ± 6.1 cmH2O respectively) for 24 Hz (NS), but sensitivity of vessels of portal hypertensive animals displayed a significant right‐ward shift [Hz needed for 50% of maximal response (Hz50) being 15.5 ± 0.4 and 12.9 ± 0.6 for PVL and CON respectively, P |
doi_str_mv | 10.1046/j.1365-2362.1997.2110758.x |
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C. ; SUMANOVSKI, L. T. ; MOLL-KAUFMANN, C. ; STALDER, G. A.</creator><creatorcontrib>SIEBER, C. C. ; SUMANOVSKI, L. T. ; MOLL-KAUFMANN, C. ; STALDER, G. A.</creatorcontrib><description>Portal hypertension goes along with vascular hyporeactivity, partly mediated by nitric oxide (NO). Interactions between the adrenergic nervous system and NO in portal hypertension are undetermined. We tested (1) whether superior mesenteric arterial beds of portal hypertensive rats have an altered sensitivity to periarterial nerve stimulation (PNS) and (2) the role of NO in modulating nerve‐stimulated responses. Vasopressor responses to PNS (Hz, 2–32) were similar in preparations of partial portal vein‐ligated (PVL, n = 12) and control (CON, n = 12) rats (60.0 ± 6.7 and 47.8 ± 6.1 cmH2O respectively) for 24 Hz (NS), but sensitivity of vessels of portal hypertensive animals displayed a significant right‐ward shift [Hz needed for 50% of maximal response (Hz50) being 15.5 ± 0.4 and 12.9 ± 0.6 for PVL and CON respectively, P < 0.001]. NO formation inhibition by Nω‐nitro‐l‐arginine (10−4 mol L−1) significantly increased responses to PNS (P < 0.05), the absolute values for 24 Hz being 101.4 ± 11.7 cmH2O for PVL (n = 8) and 86.4 ± 11.4 cmH2O for CON (n = 7) (NS). NO formation inhibition reversed the hyposensitivity in preparations of PVL, Hz50 being 13.9 ± 0.5 and 13.2 ± 0.2 for PVL and CON respectively (NS). Adrenergic receptor antagonism with prazosin (10−7 mol L−1) and yohimbine (10−6 mol L−1) inhibited PNS‐mediated vasopressor reactivity (n = 6 per group, P < 0.001), confirming the nervous origin of vasoconstrictor responses. It is concluded that (1) portal hypertension goes along with a significant hyposensitivity to PNS and (2) this hyposensitivity is reversed by NO‐formation inhibition.</description><identifier>ISSN: 0014-2972</identifier><identifier>EISSN: 1365-2362</identifier><identifier>DOI: 10.1046/j.1365-2362.1997.2110758.x</identifier><identifier>PMID: 9395785</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Animals ; Biological and medical sciences ; Electric Stimulation ; Gastroenterology. Liver. Pancreas. Abdomen ; Hypertension, Portal - physiopathology ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Nitric oxide ; Nitric Oxide - physiology ; Nitroarginine - pharmacology ; Other diseases. Semiology ; periarterial nerve stimulation ; Peripheral Nerves - physiology ; portal hypertension ; Prazosin - pharmacology ; Rats ; Rats, Sprague-Dawley ; vascular reactivity ; Vasoconstriction - drug effects</subject><ispartof>European journal of clinical investigation, 1997-11, Vol.27 (11), p.902-907</ispartof><rights>Blackwell Science Ltd, Oxford</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4361-a917ea61cac0ba3df9ae92f4ad650da6e345c5b35436152bf43baf50d4a2021f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1365-2362.1997.2110758.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1365-2362.1997.2110758.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2053816$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9395785$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SIEBER, C. C.</creatorcontrib><creatorcontrib>SUMANOVSKI, L. T.</creatorcontrib><creatorcontrib>MOLL-KAUFMANN, C.</creatorcontrib><creatorcontrib>STALDER, G. A.</creatorcontrib><title>Hyposensitivity to nerve stimulation in portal hypertensive rats: role of nitric oxide</title><title>European journal of clinical investigation</title><addtitle>European Journal of Clinical Investigation</addtitle><description>Portal hypertension goes along with vascular hyporeactivity, partly mediated by nitric oxide (NO). Interactions between the adrenergic nervous system and NO in portal hypertension are undetermined. We tested (1) whether superior mesenteric arterial beds of portal hypertensive rats have an altered sensitivity to periarterial nerve stimulation (PNS) and (2) the role of NO in modulating nerve‐stimulated responses. Vasopressor responses to PNS (Hz, 2–32) were similar in preparations of partial portal vein‐ligated (PVL, n = 12) and control (CON, n = 12) rats (60.0 ± 6.7 and 47.8 ± 6.1 cmH2O respectively) for 24 Hz (NS), but sensitivity of vessels of portal hypertensive animals displayed a significant right‐ward shift [Hz needed for 50% of maximal response (Hz50) being 15.5 ± 0.4 and 12.9 ± 0.6 for PVL and CON respectively, P < 0.001]. NO formation inhibition by Nω‐nitro‐l‐arginine (10−4 mol L−1) significantly increased responses to PNS (P < 0.05), the absolute values for 24 Hz being 101.4 ± 11.7 cmH2O for PVL (n = 8) and 86.4 ± 11.4 cmH2O for CON (n = 7) (NS). NO formation inhibition reversed the hyposensitivity in preparations of PVL, Hz50 being 13.9 ± 0.5 and 13.2 ± 0.2 for PVL and CON respectively (NS). Adrenergic receptor antagonism with prazosin (10−7 mol L−1) and yohimbine (10−6 mol L−1) inhibited PNS‐mediated vasopressor reactivity (n = 6 per group, P < 0.001), confirming the nervous origin of vasoconstrictor responses. It is concluded that (1) portal hypertension goes along with a significant hyposensitivity to PNS and (2) this hyposensitivity is reversed by NO‐formation inhibition.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Electric Stimulation</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Hypertension, Portal - physiopathology</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - physiology</subject><subject>Nitroarginine - pharmacology</subject><subject>Other diseases. Semiology</subject><subject>periarterial nerve stimulation</subject><subject>Peripheral Nerves - physiology</subject><subject>portal hypertension</subject><subject>Prazosin - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>vascular reactivity</subject><subject>Vasoconstriction - drug effects</subject><issn>0014-2972</issn><issn>1365-2362</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkM1q3DAURkVpSKdpH6EgSunOrn4s2cqiEKbJJBCSTdosxbUsU009litp0vHbx2bM7Lu6iO_c74qD0GdKckoK-W2bUy5FxrhkOVWqzBmlpBRVfniDVqfoLVoRQouMqZK9Q-9j3BJCKsrZOTpXXImyEiv063YcfLR9dMm9uDTi5HFvw4vFMbndvoPkfI9djwcfEnT49zjYkGZ-QgKkeImD7yz2Le5dCs5gf3CN_YDOWuii_bjMC_Tz5vppfZvdP27u1lf3mSm4pBkoWlqQ1IAhNfCmVWAVawtopCANSMsLYUTNxUwLVrcFr6GdogIYYbTlF-jrsXcI_u_exqR3LhrbddBbv4-6VIUkrFITeHkETfAxBtvqIbgdhFFTomepeqtnc3o2p2epepGqD9Pyp-XKvt7Z5rS6WJzyL0sO0UDXBuiNiyeMEcErKifs-xH75zo7_scH9PX6bnpMBdmxwMVkD6cCCH-0LHkp9PPDRv94LplYb6qp6BUkmaM8</recordid><startdate>199711</startdate><enddate>199711</enddate><creator>SIEBER, C. C.</creator><creator>SUMANOVSKI, L. T.</creator><creator>MOLL-KAUFMANN, C.</creator><creator>STALDER, G. A.</creator><general>Blackwell Science Ltd</general><general>Blackwell</general><scope>BSCLL</scope><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>199711</creationdate><title>Hyposensitivity to nerve stimulation in portal hypertensive rats: role of nitric oxide</title><author>SIEBER, C. C. ; SUMANOVSKI, L. T. ; MOLL-KAUFMANN, C. ; STALDER, G. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4361-a917ea61cac0ba3df9ae92f4ad650da6e345c5b35436152bf43baf50d4a2021f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Electric Stimulation</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Hypertension, Portal - physiopathology</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - physiology</topic><topic>Nitroarginine - pharmacology</topic><topic>Other diseases. Semiology</topic><topic>periarterial nerve stimulation</topic><topic>Peripheral Nerves - physiology</topic><topic>portal hypertension</topic><topic>Prazosin - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>vascular reactivity</topic><topic>Vasoconstriction - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SIEBER, C. C.</creatorcontrib><creatorcontrib>SUMANOVSKI, L. T.</creatorcontrib><creatorcontrib>MOLL-KAUFMANN, C.</creatorcontrib><creatorcontrib>STALDER, G. A.</creatorcontrib><collection>Istex</collection><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>European journal of clinical investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SIEBER, C. C.</au><au>SUMANOVSKI, L. T.</au><au>MOLL-KAUFMANN, C.</au><au>STALDER, G. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hyposensitivity to nerve stimulation in portal hypertensive rats: role of nitric oxide</atitle><jtitle>European journal of clinical investigation</jtitle><addtitle>European Journal of Clinical Investigation</addtitle><date>1997-11</date><risdate>1997</risdate><volume>27</volume><issue>11</issue><spage>902</spage><epage>907</epage><pages>902-907</pages><issn>0014-2972</issn><eissn>1365-2362</eissn><abstract>Portal hypertension goes along with vascular hyporeactivity, partly mediated by nitric oxide (NO). Interactions between the adrenergic nervous system and NO in portal hypertension are undetermined. We tested (1) whether superior mesenteric arterial beds of portal hypertensive rats have an altered sensitivity to periarterial nerve stimulation (PNS) and (2) the role of NO in modulating nerve‐stimulated responses. Vasopressor responses to PNS (Hz, 2–32) were similar in preparations of partial portal vein‐ligated (PVL, n = 12) and control (CON, n = 12) rats (60.0 ± 6.7 and 47.8 ± 6.1 cmH2O respectively) for 24 Hz (NS), but sensitivity of vessels of portal hypertensive animals displayed a significant right‐ward shift [Hz needed for 50% of maximal response (Hz50) being 15.5 ± 0.4 and 12.9 ± 0.6 for PVL and CON respectively, P < 0.001]. NO formation inhibition by Nω‐nitro‐l‐arginine (10−4 mol L−1) significantly increased responses to PNS (P < 0.05), the absolute values for 24 Hz being 101.4 ± 11.7 cmH2O for PVL (n = 8) and 86.4 ± 11.4 cmH2O for CON (n = 7) (NS). NO formation inhibition reversed the hyposensitivity in preparations of PVL, Hz50 being 13.9 ± 0.5 and 13.2 ± 0.2 for PVL and CON respectively (NS). Adrenergic receptor antagonism with prazosin (10−7 mol L−1) and yohimbine (10−6 mol L−1) inhibited PNS‐mediated vasopressor reactivity (n = 6 per group, P < 0.001), confirming the nervous origin of vasoconstrictor responses. It is concluded that (1) portal hypertension goes along with a significant hyposensitivity to PNS and (2) this hyposensitivity is reversed by NO‐formation inhibition.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>9395785</pmid><doi>10.1046/j.1365-2362.1997.2110758.x</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Electric Stimulation Gastroenterology. Liver. Pancreas. Abdomen Hypertension, Portal - physiopathology Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical sciences Nitric oxide Nitric Oxide - physiology Nitroarginine - pharmacology Other diseases. Semiology periarterial nerve stimulation Peripheral Nerves - physiology portal hypertension Prazosin - pharmacology Rats Rats, Sprague-Dawley vascular reactivity Vasoconstriction - drug effects |
title | Hyposensitivity to nerve stimulation in portal hypertensive rats: role of nitric oxide |
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