Oxygen isotope fractionation in healthy subjects and in patients with COPD
Abstract We determined the oxygen isotope fractionation degree for oxygen utilized ( δU ) in expired alveolar gas relative to inspired air in patients with chronic obstructive lung disease (COPD) and, for comparison, in two groups of healthy subjects, old and young. In addition, we determined Δrel R...
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Veröffentlicht in: | Respiratory physiology & neurobiology 2007-08, Vol.157 (2), p.335-340 |
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description | Abstract We determined the oxygen isotope fractionation degree for oxygen utilized ( δU ) in expired alveolar gas relative to inspired air in patients with chronic obstructive lung disease (COPD) and, for comparison, in two groups of healthy subjects, old and young. In addition, we determined Δrel Rvent and Δrel Rtot . These determinants of δU (=Δrel Rtot − Δrel Rvent ) are related to the oxygen isotope fractionation which occurs in the first part of the O2 pathway by ventilation of alveolar gas (Δrel Rvent ) and by O2 transport and utilization in the rest of the O2 pathway from the alveolar space (Δrel Rtot ). Mean δU values for the three groups of subjects were close: 9.0, 9.0 and 9.9‰, respectively, with no significant differences between groups. Mean Δrel Rvent for patients with COPD was substantially larger than for young, healthy subjects, 4.0‰ versus 0.94‰, with P < 10−3 . This result indicates that the contribution of intrapulmonary gas transport by diffusion to Δrel Rvent is larger for patients with COPD than for young, healthy subjects. Mean Δrel Rtot for patients with COPD was also larger than for young, healthy subjects, 13.0‰ versus 10.84‰, but this difference was not significant ( P = 0.06). Further, Δrel Rtot was much larger than Δrel Rvent for all groups of subjects ( P < 10−7 ). |
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In addition, we determined Δrel Rvent and Δrel Rtot . These determinants of δU (=Δrel Rtot − Δrel Rvent ) are related to the oxygen isotope fractionation which occurs in the first part of the O2 pathway by ventilation of alveolar gas (Δrel Rvent ) and by O2 transport and utilization in the rest of the O2 pathway from the alveolar space (Δrel Rtot ). Mean δU values for the three groups of subjects were close: 9.0, 9.0 and 9.9‰, respectively, with no significant differences between groups. Mean Δrel Rvent for patients with COPD was substantially larger than for young, healthy subjects, 4.0‰ versus 0.94‰, with P < 10−3 . This result indicates that the contribution of intrapulmonary gas transport by diffusion to Δrel Rvent is larger for patients with COPD than for young, healthy subjects. Mean Δrel Rtot for patients with COPD was also larger than for young, healthy subjects, 13.0‰ versus 10.84‰, but this difference was not significant ( P = 0.06). Further, Δrel Rtot was much larger than Δrel Rvent for all groups of subjects ( P < 10−7 ).</description><identifier>ISSN: 1569-9048</identifier><identifier>EISSN: 1878-1519</identifier><identifier>DOI: 10.1016/j.resp.2006.12.011</identifier><identifier>PMID: 17291839</identifier><language>eng</language><publisher>Amsterdarm: Elsevier B.V</publisher><subject>Adult ; Age Factors ; Aged ; Ar and O 2 isotopes ; Biological and medical sciences ; Chemical Fractionation - methods ; Diffusion ; Fundamental and applied biological sciences. Psychology ; Gas exchange ; Humans ; Mammals ; Medical Education ; Middle Aged ; Oxygen - metabolism ; Oxygen Consumption - physiology ; Oxygen isotope fractionation ; Oxygen Isotopes - metabolism ; Oxygen uptake and transport ; Pulmonary Diffusing Capacity - physiology ; Pulmonary Disease, Chronic Obstructive - physiopathology ; Pulmonary/Respiratory ; Respiratory Function Tests - methods ; Vertebrates: respiratory system</subject><ispartof>Respiratory physiology & neurobiology, 2007-08, Vol.157 (2), p.335-340</ispartof><rights>Elsevier B.V.</rights><rights>2007 Elsevier B.V.</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c390t-2e24fdc5b7ef48aa4767a32632c0d5516568d35664527b5cdcad81d06b0e35693</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S156990480700002X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18811360$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17291839$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Luijendijk, S.C.M</creatorcontrib><creatorcontrib>IJzerman, T.H</creatorcontrib><creatorcontrib>van der Grinten, C.P.M</creatorcontrib><title>Oxygen isotope fractionation in healthy subjects and in patients with COPD</title><title>Respiratory physiology & neurobiology</title><addtitle>Respir Physiol Neurobiol</addtitle><description>Abstract We determined the oxygen isotope fractionation degree for oxygen utilized ( δU ) in expired alveolar gas relative to inspired air in patients with chronic obstructive lung disease (COPD) and, for comparison, in two groups of healthy subjects, old and young. In addition, we determined Δrel Rvent and Δrel Rtot . These determinants of δU (=Δrel Rtot − Δrel Rvent ) are related to the oxygen isotope fractionation which occurs in the first part of the O2 pathway by ventilation of alveolar gas (Δrel Rvent ) and by O2 transport and utilization in the rest of the O2 pathway from the alveolar space (Δrel Rtot ). Mean δU values for the three groups of subjects were close: 9.0, 9.0 and 9.9‰, respectively, with no significant differences between groups. Mean Δrel Rvent for patients with COPD was substantially larger than for young, healthy subjects, 4.0‰ versus 0.94‰, with P < 10−3 . This result indicates that the contribution of intrapulmonary gas transport by diffusion to Δrel Rvent is larger for patients with COPD than for young, healthy subjects. Mean Δrel Rtot for patients with COPD was also larger than for young, healthy subjects, 13.0‰ versus 10.84‰, but this difference was not significant ( P = 0.06). Further, Δrel Rtot was much larger than Δrel Rvent for all groups of subjects ( P < 10−7 ).</description><subject>Adult</subject><subject>Age Factors</subject><subject>Aged</subject><subject>Ar and O 2 isotopes</subject><subject>Biological and medical sciences</subject><subject>Chemical Fractionation - methods</subject><subject>Diffusion</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gas exchange</subject><subject>Humans</subject><subject>Mammals</subject><subject>Medical Education</subject><subject>Middle Aged</subject><subject>Oxygen - metabolism</subject><subject>Oxygen Consumption - physiology</subject><subject>Oxygen isotope fractionation</subject><subject>Oxygen Isotopes - metabolism</subject><subject>Oxygen uptake and transport</subject><subject>Pulmonary Diffusing Capacity - physiology</subject><subject>Pulmonary Disease, Chronic Obstructive - physiopathology</subject><subject>Pulmonary/Respiratory</subject><subject>Respiratory Function Tests - methods</subject><subject>Vertebrates: respiratory system</subject><issn>1569-9048</issn><issn>1878-1519</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kVuL1DAYhoMo7kH_gBfSG71rzaE5FESQ0XV3WRhBBe9Cmnx1UjtpTVrd-femzMCCF-Yih4_n_RKeIPSC4IpgIt70VYQ0VRRjURFaYUIeoXOipCoJJ83jvOeiKRtcqzN0kVKPMZFEsqfojEjaEMWac3S7vT_8gFD4NM7jBEUXjZ39GMw6FT4UOzDDvDsUaWl7sHMqTHBrfcoEhHz-4-ddsdl-_vAMPenMkOD5ab1E364-ft1cl3fbTzeb93elZQ2eSwq07pzlrYSuVsbUUkjDqGDUYsc5EVwox7gQNaey5dZZ4xRxWLQYcrlhl-j1se8Ux18LpFnvfbIwDCbAuCQtMRdMYpFBegRtHFOK0Okp-r2JB02wXg3qXq8G9WpQE6qzwRx6eeq-tHtwD5GTsgy8OgEmWTNkYcH69MAplbsInLm3Rw6yi98eok42G7PgfMwitRv9_9_x7p-4HXzw-cafcIDUj0sM2bImOuWA_rL-9frVWOI86Hf2Fzd7o0w</recordid><startdate>20070801</startdate><enddate>20070801</enddate><creator>Luijendijk, S.C.M</creator><creator>IJzerman, T.H</creator><creator>van der Grinten, C.P.M</creator><general>Elsevier B.V</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>20070801</creationdate><title>Oxygen isotope fractionation in healthy subjects and in patients with COPD</title><author>Luijendijk, S.C.M ; IJzerman, T.H ; van der Grinten, C.P.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-2e24fdc5b7ef48aa4767a32632c0d5516568d35664527b5cdcad81d06b0e35693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Age Factors</topic><topic>Aged</topic><topic>Ar and O 2 isotopes</topic><topic>Biological and medical sciences</topic><topic>Chemical Fractionation - methods</topic><topic>Diffusion</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gas exchange</topic><topic>Humans</topic><topic>Mammals</topic><topic>Medical Education</topic><topic>Middle Aged</topic><topic>Oxygen - metabolism</topic><topic>Oxygen Consumption - physiology</topic><topic>Oxygen isotope fractionation</topic><topic>Oxygen Isotopes - metabolism</topic><topic>Oxygen uptake and transport</topic><topic>Pulmonary Diffusing Capacity - physiology</topic><topic>Pulmonary Disease, Chronic Obstructive - physiopathology</topic><topic>Pulmonary/Respiratory</topic><topic>Respiratory Function Tests - methods</topic><topic>Vertebrates: respiratory system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luijendijk, S.C.M</creatorcontrib><creatorcontrib>IJzerman, T.H</creatorcontrib><creatorcontrib>van der Grinten, C.P.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>Respiratory physiology & neurobiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luijendijk, S.C.M</au><au>IJzerman, T.H</au><au>van der Grinten, C.P.M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oxygen isotope fractionation in healthy subjects and in patients with COPD</atitle><jtitle>Respiratory physiology & neurobiology</jtitle><addtitle>Respir Physiol Neurobiol</addtitle><date>2007-08-01</date><risdate>2007</risdate><volume>157</volume><issue>2</issue><spage>335</spage><epage>340</epage><pages>335-340</pages><issn>1569-9048</issn><eissn>1878-1519</eissn><abstract>Abstract We determined the oxygen isotope fractionation degree for oxygen utilized ( δU ) in expired alveolar gas relative to inspired air in patients with chronic obstructive lung disease (COPD) and, for comparison, in two groups of healthy subjects, old and young. In addition, we determined Δrel Rvent and Δrel Rtot . These determinants of δU (=Δrel Rtot − Δrel Rvent ) are related to the oxygen isotope fractionation which occurs in the first part of the O2 pathway by ventilation of alveolar gas (Δrel Rvent ) and by O2 transport and utilization in the rest of the O2 pathway from the alveolar space (Δrel Rtot ). Mean δU values for the three groups of subjects were close: 9.0, 9.0 and 9.9‰, respectively, with no significant differences between groups. Mean Δrel Rvent for patients with COPD was substantially larger than for young, healthy subjects, 4.0‰ versus 0.94‰, with P < 10−3 . This result indicates that the contribution of intrapulmonary gas transport by diffusion to Δrel Rvent is larger for patients with COPD than for young, healthy subjects. Mean Δrel Rtot for patients with COPD was also larger than for young, healthy subjects, 13.0‰ versus 10.84‰, but this difference was not significant ( P = 0.06). Further, Δrel Rtot was much larger than Δrel Rvent for all groups of subjects ( P < 10−7 ).</abstract><cop>Amsterdarm</cop><pub>Elsevier B.V</pub><pmid>17291839</pmid><doi>10.1016/j.resp.2006.12.011</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Age Factors Aged Ar and O 2 isotopes Biological and medical sciences Chemical Fractionation - methods Diffusion Fundamental and applied biological sciences. Psychology Gas exchange Humans Mammals Medical Education Middle Aged Oxygen - metabolism Oxygen Consumption - physiology Oxygen isotope fractionation Oxygen Isotopes - metabolism Oxygen uptake and transport Pulmonary Diffusing Capacity - physiology Pulmonary Disease, Chronic Obstructive - physiopathology Pulmonary/Respiratory Respiratory Function Tests - methods Vertebrates: respiratory system |
title | Oxygen isotope fractionation in healthy subjects and in patients with COPD |
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