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Direct EPR Detection of Nitric Oxide in Mice Infected with the Pathogenic Mycobacterium Mycobacterium tuberculosis
It has been shown that treatment of mice preinfected with Mycobacterium tuberculosis with spin NO traps (iron complexes with diethyldithiocarbamate) enables detection of large amounts of NO in internal organs 2 and 4 weeks after infection (up to 55–57 μmol/kg of wet lung tissue accumulated with spin...
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Published in: | Applied magnetic resonance 2010-03, Vol.38 (1), p.95-104 |
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creator | Vanin, Anatoly F. Selitskaya, Raisa P. Serezhenkov, Vladimir A. Mozhokina, Galina N. |
description | It has been shown that treatment of mice preinfected with
Mycobacterium tuberculosis
with spin NO traps (iron complexes with diethyldithiocarbamate) enables detection of large amounts of NO in internal organs 2 and 4 weeks after infection (up to 55–57 μmol/kg of wet lung tissue accumulated with spin NO traps during 30 min). The animals were infected with the drug-sensitive laboratory strain H37Rv and a clinical isolate nonrespondent to antituberculous drugs (the multidrug-resistant strain of
M. tuberculosis
) obtained from a patient with an active form of tuberculosis. Two weeks after infection with the multidrug-resistant strain, the NO level in the lungs, spleen, liver and kidney increased sharply concurrently with slight lesions of lung tissue. A reverse correlation, i.e., low level of NO in the lungs and other internal organs and extensive injury of lung tissue, was established for H37Rv-infected mice. Four weeks after infection, NO production in the lungs increased dramatically for both
M. tuberculosis
strains resulting in 80–84% damage of lung tissue. The lesion is suggested to be due to the development of defense mechanisms in
M. tuberculosis
counteracting NO effects. |
doi_str_mv | 10.1007/s00723-009-0038-y |
format | article |
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Mycobacterium tuberculosis
with spin NO traps (iron complexes with diethyldithiocarbamate) enables detection of large amounts of NO in internal organs 2 and 4 weeks after infection (up to 55–57 μmol/kg of wet lung tissue accumulated with spin NO traps during 30 min). The animals were infected with the drug-sensitive laboratory strain H37Rv and a clinical isolate nonrespondent to antituberculous drugs (the multidrug-resistant strain of
M. tuberculosis
) obtained from a patient with an active form of tuberculosis. Two weeks after infection with the multidrug-resistant strain, the NO level in the lungs, spleen, liver and kidney increased sharply concurrently with slight lesions of lung tissue. A reverse correlation, i.e., low level of NO in the lungs and other internal organs and extensive injury of lung tissue, was established for H37Rv-infected mice. Four weeks after infection, NO production in the lungs increased dramatically for both
M. tuberculosis
strains resulting in 80–84% damage of lung tissue. The lesion is suggested to be due to the development of defense mechanisms in
M. tuberculosis
counteracting NO effects.</description><identifier>ISSN: 0937-9347</identifier><identifier>EISSN: 1613-7507</identifier><identifier>DOI: 10.1007/s00723-009-0038-y</identifier><identifier>PMID: 20208978</identifier><language>eng</language><publisher>Vienna: Springer Vienna</publisher><subject>Animals ; Atoms and Molecules in Strong Fields ; Bioaccumulation ; Drug resistance ; Experiments ; Hemoglobin ; Immunocompetence ; Infections ; Laser Matter Interaction ; Lesions ; Liver ; Localization ; Low level ; Lungs ; Multidrug resistant organisms ; Neutrophils ; Nitric oxide ; Organic Chemistry ; Organs ; Pathogens ; Physical Chemistry ; Physics ; Physics and Astronomy ; Pneumonia ; Solid State Physics ; Spectroscopy/Spectrometry ; Spleen ; Tuberculosis</subject><ispartof>Applied magnetic resonance, 2010-03, Vol.38 (1), p.95-104</ispartof><rights>The Author(s) 2009</rights><rights>The Author(s) 2009. This work is published under http://creativecommons.org/licenses/by-nc/2.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-e4f1aea149bc00f0c5e69a3a60dad54c9f99b64b029bc36edbfaafc885aa7dfe3</citedby><cites>FETCH-LOGICAL-c470t-e4f1aea149bc00f0c5e69a3a60dad54c9f99b64b029bc36edbfaafc885aa7dfe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20208978$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vanin, Anatoly F.</creatorcontrib><creatorcontrib>Selitskaya, Raisa P.</creatorcontrib><creatorcontrib>Serezhenkov, Vladimir A.</creatorcontrib><creatorcontrib>Mozhokina, Galina N.</creatorcontrib><title>Direct EPR Detection of Nitric Oxide in Mice Infected with the Pathogenic Mycobacterium Mycobacterium tuberculosis</title><title>Applied magnetic resonance</title><addtitle>Appl Magn Reson</addtitle><addtitle>Appl Magn Reson</addtitle><description>It has been shown that treatment of mice preinfected with
Mycobacterium tuberculosis
with spin NO traps (iron complexes with diethyldithiocarbamate) enables detection of large amounts of NO in internal organs 2 and 4 weeks after infection (up to 55–57 μmol/kg of wet lung tissue accumulated with spin NO traps during 30 min). The animals were infected with the drug-sensitive laboratory strain H37Rv and a clinical isolate nonrespondent to antituberculous drugs (the multidrug-resistant strain of
M. tuberculosis
) obtained from a patient with an active form of tuberculosis. Two weeks after infection with the multidrug-resistant strain, the NO level in the lungs, spleen, liver and kidney increased sharply concurrently with slight lesions of lung tissue. A reverse correlation, i.e., low level of NO in the lungs and other internal organs and extensive injury of lung tissue, was established for H37Rv-infected mice. Four weeks after infection, NO production in the lungs increased dramatically for both
M. tuberculosis
strains resulting in 80–84% damage of lung tissue. The lesion is suggested to be due to the development of defense mechanisms in
M. tuberculosis
counteracting NO effects.</description><subject>Animals</subject><subject>Atoms and Molecules in Strong Fields</subject><subject>Bioaccumulation</subject><subject>Drug resistance</subject><subject>Experiments</subject><subject>Hemoglobin</subject><subject>Immunocompetence</subject><subject>Infections</subject><subject>Laser Matter Interaction</subject><subject>Lesions</subject><subject>Liver</subject><subject>Localization</subject><subject>Low level</subject><subject>Lungs</subject><subject>Multidrug resistant organisms</subject><subject>Neutrophils</subject><subject>Nitric oxide</subject><subject>Organic Chemistry</subject><subject>Organs</subject><subject>Pathogens</subject><subject>Physical Chemistry</subject><subject>Physics</subject><subject>Physics and Astronomy</subject><subject>Pneumonia</subject><subject>Solid State Physics</subject><subject>Spectroscopy/Spectrometry</subject><subject>Spleen</subject><subject>Tuberculosis</subject><issn>0937-9347</issn><issn>1613-7507</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp1kUFvFSEUhYnR2Gf1B7gxJG7cjF5gZoCNiWmrNmltY3RNGObyHs28oQKjvn8vzatVm7gALjnfPXBzCHnO4DUDkG9y3bhoAHRdQjW7B2TFeiYa2YF8SFaghWy0aOUBeZLzFQDrFJOPyQEHDkpLtSLpOCR0hZ5cfqbHWGoZ4kyjp59CScHRi59hRBpmeh4c0tPZVwJH-iOUDS0bpJe2bOIa54qe71wcbJVTWLb3bmUZMLllijnkp-SRt1PGZ7fnIfn6_uTL0cfm7OLD6dG7s8a1EkqDrWcWLWv14AA8uA57bYXtYbRj1zrttR76dgBeAdHjOHhrvVOqs1aOHsUhebv3vV6GLY4O55LsZK5T2Nq0M9EG868yh41Zx--GK973QleDV7cGKX5bMBezDdnhNNkZ45INU53uNNdcVvTlPfQqLmmu4xmumdSqY6KvFNtTLsWcE_q7zzAwN4mafaKmJmpuEjW72vPi7ynuOn5HWAG-B3KV5jWmP0__3_UXgVGv4A</recordid><startdate>20100301</startdate><enddate>20100301</enddate><creator>Vanin, Anatoly F.</creator><creator>Selitskaya, Raisa P.</creator><creator>Serezhenkov, Vladimir A.</creator><creator>Mozhokina, Galina N.</creator><general>Springer Vienna</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>88I</scope><scope>8FE</scope><scope>8FG</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>M2P</scope><scope>P5Z</scope><scope>P62</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20100301</creationdate><title>Direct EPR Detection of Nitric Oxide in Mice Infected with the Pathogenic Mycobacterium Mycobacterium tuberculosis</title><author>Vanin, Anatoly F. ; Selitskaya, Raisa P. ; Serezhenkov, Vladimir A. ; Mozhokina, Galina N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-e4f1aea149bc00f0c5e69a3a60dad54c9f99b64b029bc36edbfaafc885aa7dfe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Atoms and Molecules in Strong Fields</topic><topic>Bioaccumulation</topic><topic>Drug resistance</topic><topic>Experiments</topic><topic>Hemoglobin</topic><topic>Immunocompetence</topic><topic>Infections</topic><topic>Laser Matter Interaction</topic><topic>Lesions</topic><topic>Liver</topic><topic>Localization</topic><topic>Low level</topic><topic>Lungs</topic><topic>Multidrug resistant organisms</topic><topic>Neutrophils</topic><topic>Nitric oxide</topic><topic>Organic Chemistry</topic><topic>Organs</topic><topic>Pathogens</topic><topic>Physical Chemistry</topic><topic>Physics</topic><topic>Physics and Astronomy</topic><topic>Pneumonia</topic><topic>Solid State Physics</topic><topic>Spectroscopy/Spectrometry</topic><topic>Spleen</topic><topic>Tuberculosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vanin, Anatoly F.</creatorcontrib><creatorcontrib>Selitskaya, Raisa P.</creatorcontrib><creatorcontrib>Serezhenkov, Vladimir A.</creatorcontrib><creatorcontrib>Mozhokina, Galina N.</creatorcontrib><collection>SpringerOpen</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>Science Database</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Applied magnetic resonance</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vanin, Anatoly F.</au><au>Selitskaya, Raisa P.</au><au>Serezhenkov, Vladimir A.</au><au>Mozhokina, Galina N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Direct EPR Detection of Nitric Oxide in Mice Infected with the Pathogenic Mycobacterium Mycobacterium tuberculosis</atitle><jtitle>Applied magnetic resonance</jtitle><stitle>Appl Magn Reson</stitle><addtitle>Appl Magn Reson</addtitle><date>2010-03-01</date><risdate>2010</risdate><volume>38</volume><issue>1</issue><spage>95</spage><epage>104</epage><pages>95-104</pages><issn>0937-9347</issn><eissn>1613-7507</eissn><abstract>It has been shown that treatment of mice preinfected with
Mycobacterium tuberculosis
with spin NO traps (iron complexes with diethyldithiocarbamate) enables detection of large amounts of NO in internal organs 2 and 4 weeks after infection (up to 55–57 μmol/kg of wet lung tissue accumulated with spin NO traps during 30 min). The animals were infected with the drug-sensitive laboratory strain H37Rv and a clinical isolate nonrespondent to antituberculous drugs (the multidrug-resistant strain of
M. tuberculosis
) obtained from a patient with an active form of tuberculosis. Two weeks after infection with the multidrug-resistant strain, the NO level in the lungs, spleen, liver and kidney increased sharply concurrently with slight lesions of lung tissue. A reverse correlation, i.e., low level of NO in the lungs and other internal organs and extensive injury of lung tissue, was established for H37Rv-infected mice. Four weeks after infection, NO production in the lungs increased dramatically for both
M. tuberculosis
strains resulting in 80–84% damage of lung tissue. The lesion is suggested to be due to the development of defense mechanisms in
M. tuberculosis
counteracting NO effects.</abstract><cop>Vienna</cop><pub>Springer Vienna</pub><pmid>20208978</pmid><doi>10.1007/s00723-009-0038-y</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Atoms and Molecules in Strong Fields Bioaccumulation Drug resistance Experiments Hemoglobin Immunocompetence Infections Laser Matter Interaction Lesions Liver Localization Low level Lungs Multidrug resistant organisms Neutrophils Nitric oxide Organic Chemistry Organs Pathogens Physical Chemistry Physics Physics and Astronomy Pneumonia Solid State Physics Spectroscopy/Spectrometry Spleen Tuberculosis |
title | Direct EPR Detection of Nitric Oxide in Mice Infected with the Pathogenic Mycobacterium Mycobacterium tuberculosis |
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