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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Veröffentlicht in:American journal of physiology. Lung cellular and molecular physiology 2004-04, Vol.286 (4), p.834-L840
Hauptverfasser: Chen, Delphine L, Schuster, Daniel P
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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 ).
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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 &lt; 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 &lt; 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. 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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 &lt; 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 &lt; 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 &lt; 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 &lt; 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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