In vivo characterization of lung morphology and function in anesthetized free-breathing mice using micro-computed tomography
1 Imaging Research Laboratories, Robarts Research Institute, London, Ontario; 2 Lawson Health Research Institute, London, Ontario; and Departments of 3 Physiology and Pharmacology, 4 Medical Biophysics, and 5 Diagnostic Radiology and Nuclear Medicine, University of Western Ontario, London, Ontario,...
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Published in | Journal of applied physiology (1985) Vol. 102; no. 5; pp. 2046 - 2055 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Bethesda, MD
Am Physiological Soc
01.05.2007
American Physiological Society |
Subjects | |
Online Access | Get full text |
ISSN | 8750-7587 1522-1601 |
DOI | 10.1152/japplphysiol.00629.2006 |
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Abstract | 1 Imaging Research Laboratories, Robarts Research Institute, London, Ontario; 2 Lawson Health Research Institute, London, Ontario; and Departments of 3 Physiology and Pharmacology, 4 Medical Biophysics, and 5 Diagnostic Radiology and Nuclear Medicine, University of Western Ontario, London, Ontario, Canada
Submitted 3 June 2006
; accepted in final form 19 January 2007
Lung morphology and function in human subjects can be monitored with computed tomography (CT). Because many human respiratory diseases are routinely modeled in rodents, a means of monitoring the changes in the structure and function of the rodent lung is desired. High-resolution images of the rodent lung can be attained with specialized micro-CT equipment, which provides a means of monitoring rodent models of lung disease noninvasively with a clinically relevant method. Previous studies have shown respiratory-gated images of intubated and respirated mice. Although the image quality and resolution are sufficient in these studies to make quantitative measurements, these measurements of lung structure will depend on the settings of the ventilator and not on the respiratory mechanics of the individual animals. In addition, intubation and ventilation can have unnatural effects on the respiratory dynamics of the animal, because the airway pressure, tidal volume, and respiratory rate are selected by the operator. In these experiments, important information about the symptoms of the respiratory disease being studied may be missed because the respiration is forced to conform to the ventilator settings. In this study, we implement a method of respiratory-gated micro-CT for use with anesthetized free-breathing rodents. From the micro-CT images, quantitative analysis of the structure of the lungs of healthy unconscious mice was performed to obtain airway diameters, lung and airway volumes, and CT densities at end expiration and during inspiration. Because the animals were free breathing, we were able to calculate tidal volume (0.09 ± 0.03 ml) and functional residual capacity (0.16 ± 0.03 ml).
lung volume; airway diameter; tidal volume; functional residual capacity
Address for reprint requests and other correspondence: N. Ford, 100 Perth Dr., PO Box 5015, London, ON, Canada N6A5K8 (e-mail: nford{at}imaging.robarts.ca ) |
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AbstractList | Lung morphology and function in human subjects can be monitored with computed tomography (CT). Because many human respiratory diseases are routinely modeled in rodents, a means of monitoring the changes in the structure and function of the rodent lung is desired. High-resolution images of the rodent lung can be attained with specialized micro-CT equipment, which provides a means of monitoring rodent models of lung disease noninvasively with a clinically relevant method. Previous studies have shown respiratory-gated images of intubated and respirated mice. Although the image quality and resolution are sufficient in these studies to make quantitative measurements, these measurements of lung structure will depend on the settings of the ventilator and not on the respiratory mechanics of the individual animals. In addition, intubation and ventilation can have unnatural effects on the respiratory dynamics of the animal, because the airway pressure, tidal volume, and respiratory rate are selected by the operator. In these experiments, important information about the symptoms of the respiratory disease being studied may be missed because the respiration is forced to conform to the ventilator settings. In this study, we implement a method of respiratory-gated micro-CT for use with anesthetized free-breathing rodents. From the micro-CT images, quantitative analysis of the structure of the lungs of healthy unconscious mice was performed to obtain airway diameters, lung and airway volumes, and CT densities at end expiration and during inspiration. Because the animals were free breathing, we were able to calculate tidal volume (0.09 +/- 0.03 ml) and functional residual capacity (0.16 +/- 0.03 ml).Lung morphology and function in human subjects can be monitored with computed tomography (CT). Because many human respiratory diseases are routinely modeled in rodents, a means of monitoring the changes in the structure and function of the rodent lung is desired. High-resolution images of the rodent lung can be attained with specialized micro-CT equipment, which provides a means of monitoring rodent models of lung disease noninvasively with a clinically relevant method. Previous studies have shown respiratory-gated images of intubated and respirated mice. Although the image quality and resolution are sufficient in these studies to make quantitative measurements, these measurements of lung structure will depend on the settings of the ventilator and not on the respiratory mechanics of the individual animals. In addition, intubation and ventilation can have unnatural effects on the respiratory dynamics of the animal, because the airway pressure, tidal volume, and respiratory rate are selected by the operator. In these experiments, important information about the symptoms of the respiratory disease being studied may be missed because the respiration is forced to conform to the ventilator settings. In this study, we implement a method of respiratory-gated micro-CT for use with anesthetized free-breathing rodents. From the micro-CT images, quantitative analysis of the structure of the lungs of healthy unconscious mice was performed to obtain airway diameters, lung and airway volumes, and CT densities at end expiration and during inspiration. Because the animals were free breathing, we were able to calculate tidal volume (0.09 +/- 0.03 ml) and functional residual capacity (0.16 +/- 0.03 ml). Lung morphology and function in human subjects can be monitored with computed tomography (CT). Because many human respiratory diseases are routinely modeled in rodents, a means of monitoring the changes in the structure and function of the rodent lung is desired. High-resolution images of the rodent lung can be attained with specialized micro-CT equipment, which provides a means of monitoring rodent models of lung disease noninvasively with a clinically relevant method. Previous studies have shown respiratory-gated images of intubated and respirated mice. Although the image quality and resolution are sufficient in these studies to make quantitative measurements, these measurements of lung structure will depend on the settings of the ventilator and not on the respiratory mechanics of the individual animals. In addition, intubation and ventilation can have unnatural effects on the respiratory dynamics of the animal, because the airway pressure, tidal volume, and respiratory rate are selected by the operator. In these experiments, important information about the symptoms of the respiratory disease being studied may be missed because the respiration is forced to conform to the ventilator settings. In this study, we implement a method of respiratory-gated micro-CT for use with anesthetized free-breathing rodents. From the micro-CT images, quantitative analysis of the structure of the lungs of healthy unconscious mice was performed to obtain airway diameters, lung and airway volumes, and CT densities at end expiration and during inspiration. Because the animals were free breathing, we were able to calculate tidal volume (0.09 plus or minus 0.03 ml) and functional residual capacity (0.16 plus or minus 0.03 ml). Lung morphology and function in human subjects can be monitored with computed tomography (CT). Because many human respiratory diseases are routinely modeled in rodents, a means of monitoring the changes in the structure and function of the rodent lung is desired. High-resolution images of the rodent lung can be attained with specialized micro-CT equipment, which provides a means of monitoring rodent models of lung disease noninvasively with a clinically relevant method. Previous studies have shown respiratory-gated images of intubated and respirated mice. Although the image quality and resolution are sufficient in these studies to make quantitative measurements, these measurements of lung structure will depend on the settings of the ventilator and not on the respiratory mechanics of the individual animals. In addition, intubation and ventilation can have unnatural effects on the respiratory dynamics of the animal, because the airway pressure, tidal volume, and respiratory rate are selected by the operator. In these experiments, important information about the symptoms of the respiratory disease being studied may be missed because the respiration is forced to conform to the ventilator settings. In this study, we implement a method of respiratory-gated micro-CT for use with anesthetized free-breathing rodents. From the micro-CT images, quantitative analysis of the structure of the lungs of healthy unconscious mice was performed to obtain airway diameters, lung and airway volumes, and CT densities at end expiration and during inspiration. Because the animals were free breathing, we were able to calculate tidal volume (0.09 +/- 0.03 ml) and functional residual capacity (0.16 +/- 0.03 ml). Lung morphology and function in human subjects can be monitored with computed tomography (CT). Because many human respiratory diseases are routinely modeled in rodents, a means of monitoring the changes in the structure and function of the rodent lung is desired. High-resolution images of the rodent lung can be attained with specialized micro-CT equipment, which provides a means of monitoring rodent models of lung disease noninvasively with a clinically relevant method. Previous studies have shown respiratory-gated images of intubated and respirated mice. Although the image quality and resolution are sufficient in these studies to make quantitative measurements, these measurements of lung structure will depend on the settings of the ventilator and not on the respiratory mechanics of the individual animals. In addition, intubation and ventilation can have unnatural effects on the respiratory dynamics of the animal, because the airway pressure, tidal volume, and respiratory rate are selected by the operator. In these experiments, important information about the symptoms of the respiratory disease being studied may be missed because the respiration is forced to conform to the ventilator settings. In this study, we implement a method of respiratory-gated micro-CT for use with anesthetized free-breathing rodents. From the micro- CT images, quantitative analysis of the structure of the lungs of healthy unconscious mice was performed to obtain airway diameters, lung and airway volumes, and CT densities at end expiration and during inspiration. Because the animals were free breathing, we were able to calculate tidal volume (0.09 ± 0.03 ml) and functional residual capacity (0.16 ± 0.03 ml). [PUBLICATION ABSTRACT] Lung morphology and function in human subjects can be monitored with computed tomography (CT). Because many human respiratory diseases are routinely modeled in rodents, a means of monitoring the changes in the structure and function of the rodent lung is desired. High-resolution images of the rodent lung can be attained with specialized micro-CT equipment, which provides a means of monitoring rodent models of lung disease noninvasively with a clinically relevant method. Previous studies have shown respiratory-gated images of intubated and respirated mice. Although the image quality and resolution are sufficient in these studies to make quantitative measurements, these measurements of lung structure will depend on the settings of the ventilator and not on the respiratory mechanics of the individual animals. In addition, intubation and ventilation can have unnatural effects on the respiratory dynamics of the animal, because the airway pressure, tidal volume, and respiratory rate are selected by the operator. In these experiments, important information about the symptoms of the respiratory disease being studied may be missed because the respiration is forced to conform to the ventilator settings. In this study, we implement a method of respiratory-gated micro-CT for use with anesthetized free-breathing rodents. From the micro-CT images, quantitative analysis of the structure of the lungs of healthy unconscious mice was performed to obtain airway diameters, lung and airway volumes, and CT densities at end expiration and during inspiration. Because the animals were free breathing, we were able to calculate tidal volume (0.09 ± 0.03 ml) and functional residual capacity (0.16 ± 0.03 ml). 1 Imaging Research Laboratories, Robarts Research Institute, London, Ontario; 2 Lawson Health Research Institute, London, Ontario; and Departments of 3 Physiology and Pharmacology, 4 Medical Biophysics, and 5 Diagnostic Radiology and Nuclear Medicine, University of Western Ontario, London, Ontario, Canada Submitted 3 June 2006 ; accepted in final form 19 January 2007 Lung morphology and function in human subjects can be monitored with computed tomography (CT). Because many human respiratory diseases are routinely modeled in rodents, a means of monitoring the changes in the structure and function of the rodent lung is desired. High-resolution images of the rodent lung can be attained with specialized micro-CT equipment, which provides a means of monitoring rodent models of lung disease noninvasively with a clinically relevant method. Previous studies have shown respiratory-gated images of intubated and respirated mice. Although the image quality and resolution are sufficient in these studies to make quantitative measurements, these measurements of lung structure will depend on the settings of the ventilator and not on the respiratory mechanics of the individual animals. In addition, intubation and ventilation can have unnatural effects on the respiratory dynamics of the animal, because the airway pressure, tidal volume, and respiratory rate are selected by the operator. In these experiments, important information about the symptoms of the respiratory disease being studied may be missed because the respiration is forced to conform to the ventilator settings. In this study, we implement a method of respiratory-gated micro-CT for use with anesthetized free-breathing rodents. From the micro-CT images, quantitative analysis of the structure of the lungs of healthy unconscious mice was performed to obtain airway diameters, lung and airway volumes, and CT densities at end expiration and during inspiration. Because the animals were free breathing, we were able to calculate tidal volume (0.09 ± 0.03 ml) and functional residual capacity (0.16 ± 0.03 ml). lung volume; airway diameter; tidal volume; functional residual capacity Address for reprint requests and other correspondence: N. Ford, 100 Perth Dr., PO Box 5015, London, ON, Canada N6A5K8 (e-mail: nford{at}imaging.robarts.ca ) |
Author | Holdsworth, D. W Veldhuizen, R. A. W Drangova, M Ford, N. L Martin, E. L Lewis, J. F |
Author_xml | – sequence: 1 fullname: Ford, N. L – sequence: 2 fullname: Martin, E. L – sequence: 3 fullname: Lewis, J. F – sequence: 4 fullname: Veldhuizen, R. A. W – sequence: 5 fullname: Drangova, M – sequence: 6 fullname: Holdsworth, D. W |
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Cites_doi | 10.1164/ajrccm.162.supplement_2.ras-2 10.1152/ajplung.00141.2003 10.1152/physiolgenomics.2001.4.3.215 10.1111/j.1651-2227.1980.tb07328.x 10.1088/0031-9155/50/7/005 10.1097/01.rli.0000138134.89050.a5 10.1152/jappl.1999.87.6.2362 10.1097/01.rli.0000160070.67270.05 10.1186/1465-9921-4-2 10.1118/1.2198941 10.1080/09553008114550731 10.1152/jappl.1999.86.1.16 10.1038/nm1101 10.1097/00004424-199904000-00008 10.1162/153535004773861723 10.1088/0967-3334/14/2/009 10.1016/j.acra.2004.05.019 10.1118/1.598974 10.1172/JCI200112067 10.1164/rccm.200503-343OC 10.1364/JOSAA.1.000612 10.1016/j.media.2005.12.002 10.1088/0031-9155/49/17/023 10.2460/ajvr.1992.53.7.1218 10.1002/mrm.20251 10.1128/AEM.24.5.812-818.1972 10.1118/1.1617353 10.1088/0031-9155/51/5/003 10.1117/12.534769 10.1016/0360-3016(95)02078-0 10.1146/annurev.ns.07.120157.001031 10.1016/S0167-7799(02)02004-8 10.1016/j.compbiomed.2005.05.004 10.1118/1.1812604 10.1148/radiology.197.3.7480750 10.1183/09031936.03.00026403 10.1152/japplphysiol.00624.2003 10.1152/jappl.1985.58.3.954 10.1118/1.2013007 10.1378/chest.99.6.1357 10.1088/0031-9155/51/4/002 10.1152/japplphysiol.00706.2002 10.1118/1.1870152 10.1080/09553000110104614 10.1016/S0720-048X(00)00301-6 10.1016/S0033-8389(22)01199-X 10.1097/00004728-199511000-00016 10.1002/mrm.20400 10.1109/TSMC.1979.4310076 10.1152/jappl.2001.91.2.811 10.1016/j.media.2004.06.017 10.1259/0007-1285-30-349-40 10.1007/s00134-002-1618-6 10.1007/s001340051340 10.1148/radiol.2331031340 10.1259/0007-1285-58-687-225 10.1152/jappl.2001.90.5.1631 10.1152/jappl.2000.88.3.939 |
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Keywords | airway diameter Rodentia Tidal volume Respiratory system Functional residual capacity Characterization Respiratory tract Lung volume In vivo Vertebrata Mammalia Lung function Mouse Morphology Tomography Respiration Diameter |
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Snippet | 1 Imaging Research Laboratories, Robarts Research Institute, London, Ontario; 2 Lawson Health Research Institute, London, Ontario; and Departments of 3... Lung morphology and function in human subjects can be monitored with computed tomography (CT). Because many human respiratory diseases are routinely modeled in... |
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SubjectTerms | Airway management Anesthesia Animals Biological and medical sciences Computed tomography Correlation analysis Functional Residual Capacity Fundamental and applied biological sciences. Psychology Image Processing, Computer-Assisted Imaging, Three-Dimensional Lung - anatomy & histology Lung - diagnostic imaging Lung - physiology Lung Volume Measurements Lungs Male Mice Mice, Inbred C57BL Respiration Respiratory diseases Rodents Tidal Volume Tomography Tomography, X-Ray Computed - methods |
Title | In vivo characterization of lung morphology and function in anesthetized free-breathing mice using micro-computed tomography |
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