Literature DB >> 17615101

Sporadic coordinated shifts of regional ventilation and perfusion in juvenile pigs with normal gas exchange.

H Thomas Robertson1, Blazej Neradilek, Nayak L Polissar, Robb W Glenny.   

Abstract

Repeated high-resolution measurements of both regional pulmonary ventilation and regional blood flow (r ) have revealed that approximately 6 to 10% of the summed spatial and temporal heterogeneity can be attributed to spontaneous temporal variability. To test the hypothesis that the spontaneous temporal shifts of r and r are coordinated, 12 anaesthetized juvenile pigs had pairs of colours of aerosol and intravenous fluorescent microspheres (FMS) administered simultaneously at 20 min intervals to mark r and r . The animals were killed, the lungs inflated, air-dried and cut into approximately 2 cm(3) cubes. The concentrations of FMS colours from each cube, representing r and r at every 20 min interval, were measured with a fluorescence spectrophotometer. The correlation between per-piece temporal shifts in r and r , calculated as the mean within-piece covariance, was positive (P < 0.001) for every temporally adjacent pair of measurements in every animal, although there were large differences in the magnitude of the mean temporal covariance among animals. The individual cubes with the most positive temporal covariance across all measurement periods usually demonstrated a large single-interval coordinated shift of r and r , with average temporal covariance observed at the other intervals. The largest between-interval shifts in r and r included equal proportions of coordinated increases and coordinated decreases. High-resolution measurements of r and r acquired over 20 min intervals reveal that the overall positive correlation between temporal changes in r and r is driven by relatively infrequent large-magnitude changes within small regions of the lung.

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Year:  2007        PMID: 17615101      PMCID: PMC2277043          DOI: 10.1113/jphysiol.2007.136358

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  25 in total

1.  Effect of posture on regional gas exchange in pigs.

Authors:  William A Altemeier; Steve McKinney; Melissa Krueger; Robb W Glenny
Journal:  J Appl Physiol (1985)       Date:  2004-08-06

2.  Gravity is a minor determinant of pulmonary blood flow distribution.

Authors:  R W Glenny; W J Lamm; R K Albert; H T Robertson
Journal:  J Appl Physiol (1985)       Date:  1991-08

3.  Relative contribution of gravity to pulmonary perfusion heterogeneity.

Authors:  R W Glenny; L Polissar; H T Robertson
Journal:  J Appl Physiol (1985)       Date:  1991-12

4.  Pulmonary gas-exchange analysis by using simultaneous deposition of aerosolized and injected microspheres.

Authors:  W A Altemeier; H T Robertson; R W Glenny
Journal:  J Appl Physiol (1985)       Date:  1998-12

5.  High-resolution maps of regional ventilation utilizing inhaled fluorescent microspheres.

Authors:  H T Robertson; R W Glenny; D Stanford; L M McInnes; D L Luchtel; D Covert
Journal:  J Appl Physiol (1985)       Date:  1997-03

6.  Temporal heterogeneity of regional pulmonary perfusion is spatially clustered.

Authors:  R W Glenny; N L Polissar; S McKinney; H T Robertson
Journal:  J Appl Physiol (1985)       Date:  1995-09

Review 7.  Neuroepithelial bodies as airway oxygen sensors.

Authors:  E Cutz; A Jackson
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9.  Validation of fluorescent-labeled microspheres for measurement of regional organ perfusion.

Authors:  R W Glenny; S Bernard; M Brinkley
Journal:  J Appl Physiol (1985)       Date:  1993-05

10.  Effects of inspired carbon dioxide on ventilation-perfusion matching in normoxia, hypoxia, and hyperoxia.

Authors:  E R Swenson; H T Robertson; M P Hlastala
Journal:  Am J Respir Crit Care Med       Date:  1994-06       Impact factor: 21.405

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Authors:  H Thomas Robertson; Richard B Buxton
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Authors:  Amran K Asadi; Matthew V Cronin; Rui Carlos Sá; Rebecca J Theilmann; Sebastiaan Holverda; Susan R Hopkins; Richard B Buxton; G Kim Prisk
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4.  Extent to which pulmonary vascular responses to PCO2 and PO2 play a functional role within the healthy human lung.

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