Positron emission tomography with [18F]fluorodeoxyglucose to evaluate neutrophil kinetics during acute lung injury
Departments of 1 Radiology, 2 Internal Medicine, and 3 Surgery, Washington University School of Medicine, St. Louis, Missouri 63110 Submitted 23 September 2003 ; accepted in final form 27 November 2003 We measured neutrophil glucose uptake with positron emission tomographic imaging and [ 18 F]fluoro...
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creator | Chen, Delphine L Schuster, Daniel P |
description | Departments of 1 Radiology, 2 Internal Medicine, and 3 Surgery, Washington University School of Medicine, St. Louis, Missouri 63110
Submitted 23 September 2003
; accepted in final form 27 November 2003
We measured neutrophil glucose uptake with positron emission tomographic imaging and [ 18 F]fluorodeoxyglucose ([ 18 F]FDG-PET) in anesthetized dogs after intravenous oleic acid-induced acute lung injury (ALI; OA group, n = 6) or after low-dose intravenous endotoxin (known to activate neutrophils without causing lung injury) followed by OA (Etx + OA group, n = 7). The following two other groups were studied as controls: one that received no intervention ( n = 5) and a group treated with Etx only ( n = 6). PET imaging was performed 1.5 h after initiating experimental interventions. The rate of [ 3 H]deoxyglucose ([ 3 H]DG) uptake was also measured in vitro in cells recovered from bronchoalveolar lavage (BAL) performed after PET imaging. Circulating neutrophil counts fell significantly in animals treated with Etx but not in the other two groups. The rate of [ 18 F]FDG uptake, measured by the influx constant K i , was significantly elevated ( P < 0.05) in both Etx-treated groups (7.9 ± 2.6 x 10 -3 ml blood·ml lung -1 ·min -1 in the Etx group, 9.3 ± 4.8 x 10 -3 ml blood·ml lung -1 ·min -1 in the Etx + OA group) but not in the group treated only with OA (3.4 ± 0.8 x 10 -3 ml blood·ml lung -1 ·min -1 ) when compared with the normal control (1.6 ± 0.4 x 10 -3 ml blood·ml lung -1 ·min -1 ). [ 3 H]DG uptake was increased (73 ± 7%) in BAL neutrophils recovered from the Etx + OA group ( P < 0.05) but not in the OA group. K i and [ 3 H]DG uptake rates were linearly correlated ( R 2 = 0.65). We conclude that the rate of [ 18 F]FDG uptake in the lungs during ALI reflects the state of neutrophil activation. [ 18 F]FDG-PET imaging can detect pulmonary sequestration of activated neutrophils, despite the absence of alveolar neutrophilia. Thus [ 18 F]FDG-PET imaging may be a useful tool to study neutrophil kinetics during ALI.
radionuclide imaging; acute respiratory distress syndrome; fluorodeoxyglucose; dogs
Address for reprint requests and other correspondence: D. L. Chen, Campus Box 8225, Washington Univ. School of Medicine, 660 S. Euclid Ave., St. Louis, MO 63110 (E-mail: chend{at}mir.wustl.edu ). |
doi_str_mv | 10.1152/ajplung.00339.2003 |
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Submitted 23 September 2003
; accepted in final form 27 November 2003
We measured neutrophil glucose uptake with positron emission tomographic imaging and [ 18 F]fluorodeoxyglucose ([ 18 F]FDG-PET) in anesthetized dogs after intravenous oleic acid-induced acute lung injury (ALI; OA group, n = 6) or after low-dose intravenous endotoxin (known to activate neutrophils without causing lung injury) followed by OA (Etx + OA group, n = 7). The following two other groups were studied as controls: one that received no intervention ( n = 5) and a group treated with Etx only ( n = 6). PET imaging was performed 1.5 h after initiating experimental interventions. The rate of [ 3 H]deoxyglucose ([ 3 H]DG) uptake was also measured in vitro in cells recovered from bronchoalveolar lavage (BAL) performed after PET imaging. Circulating neutrophil counts fell significantly in animals treated with Etx but not in the other two groups. The rate of [ 18 F]FDG uptake, measured by the influx constant K i , was significantly elevated ( P < 0.05) in both Etx-treated groups (7.9 ± 2.6 x 10 -3 ml blood·ml lung -1 ·min -1 in the Etx group, 9.3 ± 4.8 x 10 -3 ml blood·ml lung -1 ·min -1 in the Etx + OA group) but not in the group treated only with OA (3.4 ± 0.8 x 10 -3 ml blood·ml lung -1 ·min -1 ) when compared with the normal control (1.6 ± 0.4 x 10 -3 ml blood·ml lung -1 ·min -1 ). [ 3 H]DG uptake was increased (73 ± 7%) in BAL neutrophils recovered from the Etx + OA group ( P < 0.05) but not in the OA group. K i and [ 3 H]DG uptake rates were linearly correlated ( R 2 = 0.65). We conclude that the rate of [ 18 F]FDG uptake in the lungs during ALI reflects the state of neutrophil activation. [ 18 F]FDG-PET imaging can detect pulmonary sequestration of activated neutrophils, despite the absence of alveolar neutrophilia. Thus [ 18 F]FDG-PET imaging may be a useful tool to study neutrophil kinetics during ALI.
radionuclide imaging; acute respiratory distress syndrome; fluorodeoxyglucose; dogs
Address for reprint requests and other correspondence: D. L. Chen, Campus Box 8225, Washington Univ. School of Medicine, 660 S. Euclid Ave., St. Louis, MO 63110 (E-mail: chend{at}mir.wustl.edu ).</description><identifier>ISSN: 1040-0605</identifier><identifier>EISSN: 1522-1504</identifier><identifier>DOI: 10.1152/ajplung.00339.2003</identifier><identifier>PMID: 14660487</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Blood Pressure ; Body Temperature ; Deoxyglucose - pharmacokinetics ; Dogs ; Fluorodeoxyglucose F18 ; Heart Rate ; Male ; Neutrophils - diagnostic imaging ; Neutrophils - immunology ; Oxygen - blood ; Radiopharmaceuticals ; Respiratory Distress Syndrome, Adult - diagnostic imaging ; Respiratory Distress Syndrome, Adult - immunology ; Tomography, Emission-Computed ; Tritium</subject><ispartof>American journal of physiology. Lung cellular and molecular physiology, 2004-04, Vol.286 (4), p.834-L840</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-b624029469a32771d80cf3ea0c9671c3209700d553bb8c1775c298bb53757a913</citedby><cites>FETCH-LOGICAL-c387t-b624029469a32771d80cf3ea0c9671c3209700d553bb8c1775c298bb53757a913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3039,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14660487$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Delphine L</creatorcontrib><creatorcontrib>Schuster, Daniel P</creatorcontrib><title>Positron emission tomography with [18F]fluorodeoxyglucose to evaluate neutrophil kinetics during acute lung injury</title><title>American journal of physiology. Lung cellular and molecular physiology</title><addtitle>Am J Physiol Lung Cell Mol Physiol</addtitle><description>Departments of 1 Radiology, 2 Internal Medicine, and 3 Surgery, Washington University School of Medicine, St. Louis, Missouri 63110
Submitted 23 September 2003
; accepted in final form 27 November 2003
We measured neutrophil glucose uptake with positron emission tomographic imaging and [ 18 F]fluorodeoxyglucose ([ 18 F]FDG-PET) in anesthetized dogs after intravenous oleic acid-induced acute lung injury (ALI; OA group, n = 6) or after low-dose intravenous endotoxin (known to activate neutrophils without causing lung injury) followed by OA (Etx + OA group, n = 7). The following two other groups were studied as controls: one that received no intervention ( n = 5) and a group treated with Etx only ( n = 6). PET imaging was performed 1.5 h after initiating experimental interventions. The rate of [ 3 H]deoxyglucose ([ 3 H]DG) uptake was also measured in vitro in cells recovered from bronchoalveolar lavage (BAL) performed after PET imaging. Circulating neutrophil counts fell significantly in animals treated with Etx but not in the other two groups. The rate of [ 18 F]FDG uptake, measured by the influx constant K i , was significantly elevated ( P < 0.05) in both Etx-treated groups (7.9 ± 2.6 x 10 -3 ml blood·ml lung -1 ·min -1 in the Etx group, 9.3 ± 4.8 x 10 -3 ml blood·ml lung -1 ·min -1 in the Etx + OA group) but not in the group treated only with OA (3.4 ± 0.8 x 10 -3 ml blood·ml lung -1 ·min -1 ) when compared with the normal control (1.6 ± 0.4 x 10 -3 ml blood·ml lung -1 ·min -1 ). [ 3 H]DG uptake was increased (73 ± 7%) in BAL neutrophils recovered from the Etx + OA group ( P < 0.05) but not in the OA group. K i and [ 3 H]DG uptake rates were linearly correlated ( R 2 = 0.65). We conclude that the rate of [ 18 F]FDG uptake in the lungs during ALI reflects the state of neutrophil activation. [ 18 F]FDG-PET imaging can detect pulmonary sequestration of activated neutrophils, despite the absence of alveolar neutrophilia. Thus [ 18 F]FDG-PET imaging may be a useful tool to study neutrophil kinetics during ALI.
radionuclide imaging; acute respiratory distress syndrome; fluorodeoxyglucose; dogs
Address for reprint requests and other correspondence: D. L. Chen, Campus Box 8225, Washington Univ. School of Medicine, 660 S. Euclid Ave., St. Louis, MO 63110 (E-mail: chend{at}mir.wustl.edu ).</description><subject>Animals</subject><subject>Blood Pressure</subject><subject>Body Temperature</subject><subject>Deoxyglucose - pharmacokinetics</subject><subject>Dogs</subject><subject>Fluorodeoxyglucose F18</subject><subject>Heart Rate</subject><subject>Male</subject><subject>Neutrophils - diagnostic imaging</subject><subject>Neutrophils - immunology</subject><subject>Oxygen - blood</subject><subject>Radiopharmaceuticals</subject><subject>Respiratory Distress Syndrome, Adult - diagnostic imaging</subject><subject>Respiratory Distress Syndrome, Adult - immunology</subject><subject>Tomography, Emission-Computed</subject><subject>Tritium</subject><issn>1040-0605</issn><issn>1522-1504</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMFu1DAURS0EoqXwAyyQV-wyPNtxnCxRxQDSSGVRVghZjuMkHjxxsOO2-Xs8nam6YvWe5HOvng9C7wlsCOH0k9rPLk3DBoCxZkPzeIEu8wMtCIfyZd6hhAIq4BfoTYx7AOAA1Wt0QcqqgrIWlyj88NEuwU_YHGyMNi-LP_ghqHlc8b1dRvyL1NvfvUs--M74h3VwSftoMofNnXJJLQZPJuWSebQO_7GTWayOuEvBTgNWOmXgeCi20z6F9S161SsXzbvzvEI_t19ur78Vu5uv368_7wrNarEUbUVLoE1ZNYpRIUhXg-6ZUaCbShDNKDQCoOOctW2tiRBc06ZuW84EF6oh7Ap9PPXOwf9NJi4y_1Ab59RkfIpSEAGU8TqD9ATq4GMMppdzsAcVVklAHk3Ls2n5aFoeTefQh3N7ag-me46c1WagOQGjHcZ7G4zMRrNg54dVbpNzt-ZheWqmdSVLuatZKeeuz9ni_9mnY54z7B9lYqLT</recordid><startdate>20040401</startdate><enddate>20040401</enddate><creator>Chen, Delphine L</creator><creator>Schuster, Daniel P</creator><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>20040401</creationdate><title>Positron emission tomography with [18F]fluorodeoxyglucose to evaluate neutrophil kinetics during acute lung injury</title><author>Chen, Delphine L ; Schuster, Daniel P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-b624029469a32771d80cf3ea0c9671c3209700d553bb8c1775c298bb53757a913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Blood Pressure</topic><topic>Body Temperature</topic><topic>Deoxyglucose - pharmacokinetics</topic><topic>Dogs</topic><topic>Fluorodeoxyglucose F18</topic><topic>Heart Rate</topic><topic>Male</topic><topic>Neutrophils - diagnostic imaging</topic><topic>Neutrophils - immunology</topic><topic>Oxygen - blood</topic><topic>Radiopharmaceuticals</topic><topic>Respiratory Distress Syndrome, Adult - diagnostic imaging</topic><topic>Respiratory Distress Syndrome, Adult - immunology</topic><topic>Tomography, Emission-Computed</topic><topic>Tritium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Delphine L</creatorcontrib><creatorcontrib>Schuster, Daniel P</creatorcontrib><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>American journal of physiology. Lung cellular and molecular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Delphine L</au><au>Schuster, Daniel P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Positron emission tomography with [18F]fluorodeoxyglucose to evaluate neutrophil kinetics during acute lung injury</atitle><jtitle>American journal of physiology. Lung cellular and molecular physiology</jtitle><addtitle>Am J Physiol Lung Cell Mol Physiol</addtitle><date>2004-04-01</date><risdate>2004</risdate><volume>286</volume><issue>4</issue><spage>834</spage><epage>L840</epage><pages>834-L840</pages><issn>1040-0605</issn><eissn>1522-1504</eissn><abstract>Departments of 1 Radiology, 2 Internal Medicine, and 3 Surgery, Washington University School of Medicine, St. Louis, Missouri 63110
Submitted 23 September 2003
; accepted in final form 27 November 2003
We measured neutrophil glucose uptake with positron emission tomographic imaging and [ 18 F]fluorodeoxyglucose ([ 18 F]FDG-PET) in anesthetized dogs after intravenous oleic acid-induced acute lung injury (ALI; OA group, n = 6) or after low-dose intravenous endotoxin (known to activate neutrophils without causing lung injury) followed by OA (Etx + OA group, n = 7). The following two other groups were studied as controls: one that received no intervention ( n = 5) and a group treated with Etx only ( n = 6). PET imaging was performed 1.5 h after initiating experimental interventions. The rate of [ 3 H]deoxyglucose ([ 3 H]DG) uptake was also measured in vitro in cells recovered from bronchoalveolar lavage (BAL) performed after PET imaging. Circulating neutrophil counts fell significantly in animals treated with Etx but not in the other two groups. The rate of [ 18 F]FDG uptake, measured by the influx constant K i , was significantly elevated ( P < 0.05) in both Etx-treated groups (7.9 ± 2.6 x 10 -3 ml blood·ml lung -1 ·min -1 in the Etx group, 9.3 ± 4.8 x 10 -3 ml blood·ml lung -1 ·min -1 in the Etx + OA group) but not in the group treated only with OA (3.4 ± 0.8 x 10 -3 ml blood·ml lung -1 ·min -1 ) when compared with the normal control (1.6 ± 0.4 x 10 -3 ml blood·ml lung -1 ·min -1 ). [ 3 H]DG uptake was increased (73 ± 7%) in BAL neutrophils recovered from the Etx + OA group ( P < 0.05) but not in the OA group. K i and [ 3 H]DG uptake rates were linearly correlated ( R 2 = 0.65). We conclude that the rate of [ 18 F]FDG uptake in the lungs during ALI reflects the state of neutrophil activation. [ 18 F]FDG-PET imaging can detect pulmonary sequestration of activated neutrophils, despite the absence of alveolar neutrophilia. Thus [ 18 F]FDG-PET imaging may be a useful tool to study neutrophil kinetics during ALI.
radionuclide imaging; acute respiratory distress syndrome; fluorodeoxyglucose; dogs
Address for reprint requests and other correspondence: D. L. Chen, Campus Box 8225, Washington Univ. School of Medicine, 660 S. Euclid Ave., St. Louis, MO 63110 (E-mail: chend{at}mir.wustl.edu ).</abstract><cop>United States</cop><pmid>14660487</pmid><doi>10.1152/ajplung.00339.2003</doi></addata></record> |
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subjects | Animals Blood Pressure Body Temperature Deoxyglucose - pharmacokinetics Dogs Fluorodeoxyglucose F18 Heart Rate Male Neutrophils - diagnostic imaging Neutrophils - immunology Oxygen - blood Radiopharmaceuticals Respiratory Distress Syndrome, Adult - diagnostic imaging Respiratory Distress Syndrome, Adult - immunology Tomography, Emission-Computed Tritium |
title | Positron emission tomography with [18F]fluorodeoxyglucose to evaluate neutrophil kinetics during acute lung injury |
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