1. Academic Validation
  2. Oxidant-increased endothelial permeability: prevention with phosphodiesterase inhibition vs. cAMP production

Oxidant-increased endothelial permeability: prevention with phosphodiesterase inhibition vs. cAMP production

  • J Appl Physiol (1985). 2000 Mar;88(3):835-42. doi: 10.1152/jappl.2000.88.3.835.
G B Waypa 1 C A Morton P A Vincent J R Mahoney Jr W K Johnston 3rd F L Minnear
Affiliations

Affiliation

  • 1 Vascular Biology Research Group and Department of Physiology and Cell Biology, Albany Medical College, Albany, New York 12208-3479, USA.
Abstract

The present objective was to determine whether hydrogen peroxide (H(2)O(2)) increases transvascular albumin clearance and lung weight in an isolated rat lung and whether posttreatment with cAMP-enhancing agents can prevent these increases. Transvascular albumin clearance was assessed by (125)I-labeled albumin clearance ((125)I-albumin flux/perfusate concentration of (125)I-albumin) at a given fluid filtration. Nonlinear regression analysis of transvascular albumin clearance vs. fluid filtration yielded values for the permeability-surface area product (PS) and the reflection coefficient (sigma). H(2)O(2) decreased sigma from a control value of 0.93 to 0.38, did not change PS, and increased lung weight. Posttreatment with isoproterenol, a beta(2)-adrenergic-receptor agonist, reduced the H(2)O(2)-induced decrease in sigma to 0.65 and augmented the increase in lung weight. Posttreatment with CP-80633, a phosphodiesterase 4 inhibitor, further reduced the H(2)O(2)-induced decrease in sigma to 0.79 and blocked the rise in lung weight. In the presence of isoproterenol or CP-80633, H(2)O(2) increased PS. Therefore, H(2)O(2) increased the convective and diffusive clearances of albumin across an intact pulmonary vasculature. Furthermore, inhibition of cAMP metabolism more effectively attenuated the H(2)O(2)-induced increases in convective albumin clearance and lung weight as compared with stimulation of cAMP production.

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