Spatial-temporal dynamics of pulmonary blood flow in the healthy human lung in response to altered Fi^sub O2
The temporal dynamics of blood flow in the human lung have been largely unexplored due to the lack of appropriate technology. Using the magnetic resonance imaging method of arterial spin labeling (ASL) with subject-gated breathing, we produced a dynamic series of flow-weighted images in a single sag...
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Veröffentlicht in: | Journal of applied physiology (1985) 2013-01, Vol.114 (1), p.107 |
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creator | Asadi, Amran K Cronin, Matthew V Sá, Rui Carlos Theilmann, Rebecca J Holverda, Sebastiaan Hopkins, Susan R Buxton, Richard B Prisk, G Kim |
description | The temporal dynamics of blood flow in the human lung have been largely unexplored due to the lack of appropriate technology. Using the magnetic resonance imaging method of arterial spin labeling (ASL) with subject-gated breathing, we produced a dynamic series of flow-weighted images in a single sagittal slice of the right lung with a spatial resolution of ~1 cm3 and a temporal resolution of ~10 s. The mean flow pattern determined from a set of reference images was removed to produce a time series of blood flow fluctuations. The fluctuation dispersion (FD), defined as the spatial standard deviation of each flow fluctuation map, was used to quantify the changes in distribution of flow in six healthy subjects in response to 100 breaths of hypoxia (FiO2 = 0.125) or hyperoxia (FiO2 = 1.0). Two reference frames were used in calculation, one determined from the initial set of images (FDglobal), and one determined from the mean of each corresponding baseline or challenge period (FDlocal). FDlocal thus represented changes in temporal variability as a result of intervention, whereas FDglobal encompasses both FDlocal and any generalized redistribution of flow associated with switching between two steady-state patterns. Hypoxic challenge resulted in a significant increase (96%, P < 0.001) in FDglobal from the normoxic control period and in FDlocal (46%, P = 0.0048), but there was no corresponding increase in spatial relative dispersion (spatial standard deviation of the images divided by the mean; 8%, not significant). There was a smaller increase in FDglobal in response to hyperoxia (47%, P = 0.0015) for the single slice, suggestive of a more general response of the pulmonary circulation to a change from normoxia to hyperoxia. These results clearly demonstrate a temporal change in the sampled distribution of pulmonary blood flow in response to hypoxia, which is not observed when considering only the relative dispersion of the spatial distribution. [PUBLICATION ABSTRACT] |
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Using the magnetic resonance imaging method of arterial spin labeling (ASL) with subject-gated breathing, we produced a dynamic series of flow-weighted images in a single sagittal slice of the right lung with a spatial resolution of ~1 cm3 and a temporal resolution of ~10 s. The mean flow pattern determined from a set of reference images was removed to produce a time series of blood flow fluctuations. The fluctuation dispersion (FD), defined as the spatial standard deviation of each flow fluctuation map, was used to quantify the changes in distribution of flow in six healthy subjects in response to 100 breaths of hypoxia (FiO2 = 0.125) or hyperoxia (FiO2 = 1.0). Two reference frames were used in calculation, one determined from the initial set of images (FDglobal), and one determined from the mean of each corresponding baseline or challenge period (FDlocal). FDlocal thus represented changes in temporal variability as a result of intervention, whereas FDglobal encompasses both FDlocal and any generalized redistribution of flow associated with switching between two steady-state patterns. Hypoxic challenge resulted in a significant increase (96%, P < 0.001) in FDglobal from the normoxic control period and in FDlocal (46%, P = 0.0048), but there was no corresponding increase in spatial relative dispersion (spatial standard deviation of the images divided by the mean; 8%, not significant). There was a smaller increase in FDglobal in response to hyperoxia (47%, P = 0.0015) for the single slice, suggestive of a more general response of the pulmonary circulation to a change from normoxia to hyperoxia. These results clearly demonstrate a temporal change in the sampled distribution of pulmonary blood flow in response to hypoxia, which is not observed when considering only the relative dispersion of the spatial distribution. 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Using the magnetic resonance imaging method of arterial spin labeling (ASL) with subject-gated breathing, we produced a dynamic series of flow-weighted images in a single sagittal slice of the right lung with a spatial resolution of ~1 cm3 and a temporal resolution of ~10 s. The mean flow pattern determined from a set of reference images was removed to produce a time series of blood flow fluctuations. The fluctuation dispersion (FD), defined as the spatial standard deviation of each flow fluctuation map, was used to quantify the changes in distribution of flow in six healthy subjects in response to 100 breaths of hypoxia (FiO2 = 0.125) or hyperoxia (FiO2 = 1.0). Two reference frames were used in calculation, one determined from the initial set of images (FDglobal), and one determined from the mean of each corresponding baseline or challenge period (FDlocal). FDlocal thus represented changes in temporal variability as a result of intervention, whereas FDglobal encompasses both FDlocal and any generalized redistribution of flow associated with switching between two steady-state patterns. Hypoxic challenge resulted in a significant increase (96%, P < 0.001) in FDglobal from the normoxic control period and in FDlocal (46%, P = 0.0048), but there was no corresponding increase in spatial relative dispersion (spatial standard deviation of the images divided by the mean; 8%, not significant). There was a smaller increase in FDglobal in response to hyperoxia (47%, P = 0.0015) for the single slice, suggestive of a more general response of the pulmonary circulation to a change from normoxia to hyperoxia. These results clearly demonstrate a temporal change in the sampled distribution of pulmonary blood flow in response to hypoxia, which is not observed when considering only the relative dispersion of the spatial distribution. 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Using the magnetic resonance imaging method of arterial spin labeling (ASL) with subject-gated breathing, we produced a dynamic series of flow-weighted images in a single sagittal slice of the right lung with a spatial resolution of ~1 cm3 and a temporal resolution of ~10 s. The mean flow pattern determined from a set of reference images was removed to produce a time series of blood flow fluctuations. The fluctuation dispersion (FD), defined as the spatial standard deviation of each flow fluctuation map, was used to quantify the changes in distribution of flow in six healthy subjects in response to 100 breaths of hypoxia (FiO2 = 0.125) or hyperoxia (FiO2 = 1.0). Two reference frames were used in calculation, one determined from the initial set of images (FDglobal), and one determined from the mean of each corresponding baseline or challenge period (FDlocal). FDlocal thus represented changes in temporal variability as a result of intervention, whereas FDglobal encompasses both FDlocal and any generalized redistribution of flow associated with switching between two steady-state patterns. Hypoxic challenge resulted in a significant increase (96%, P < 0.001) in FDglobal from the normoxic control period and in FDlocal (46%, P = 0.0048), but there was no corresponding increase in spatial relative dispersion (spatial standard deviation of the images divided by the mean; 8%, not significant). There was a smaller increase in FDglobal in response to hyperoxia (47%, P = 0.0015) for the single slice, suggestive of a more general response of the pulmonary circulation to a change from normoxia to hyperoxia. These results clearly demonstrate a temporal change in the sampled distribution of pulmonary blood flow in response to hypoxia, which is not observed when considering only the relative dispersion of the spatial distribution. 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source | American Physiological Society; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Blood Hypoxia Lungs NMR Nuclear magnetic resonance Oxygen |
title | Spatial-temporal dynamics of pulmonary blood flow in the healthy human lung in response to altered Fi^sub O2 |
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