Total protein level as a determinant of lung vasculature permeability was determined in BALF using the Bradford method (BPAK kit).
This article demonstrate the capacity of the Bradford Protein Assay Kit from OZ Biosciences to efficiently measure the total protein concentration in BALF of rats.article reference: Cell Biochem Biophys. 2014 Apr 24.
Plasma-Derived Human C1-Esterase Inhibitor Does Not Prevent Mechanical Ventilation-Induced Pulmonary Complement Activation in a Rat Model of Streptococcus pneumoniae Pneumonia.
de Beer FM, Aslami H, Hoeksma J, van Mierlo G, Wouters D, Zeerleder S, Roelofs JJ, Juffermans NP, Schultz MJ, Lagrand WK.
Abstract
Mechanical
ventilation has the potential to cause lung injury, and the role of
complement activation herein is uncertain. We hypothesized that
inhibition of the complement cascade by administration of plasma-derived human C1-esterase inhibitor
(C1-INH) prevents ventilation-induced pulmonary complement activation,
and as such attenuates lung inflammation and lung injury in a rat model
of Streptococcus pneumoniae pneumonia. Forty hours after intratracheal
challenge with S. pneumoniae causing pneumonia rats were subjected to
ventilation with lower tidal volumes and positive end-expiratory
pressure (PEEP) or high tidal volumes without PEEP, after an intravenous
bolus of C1-INH (200 U/kg) or placebo (saline). After 4 h of
ventilation blood, broncho-alveolar lavage fluid and lung tissue were
collected. Non-ventilated rats with S. pneumoniae pneumonia served as
controls. While ventilation with lower tidal volumes and PEEP slightly
amplified pneumonia-induced complement activation in the lungs,
ventilation with higher tidal volumes without PEEP augmented local
complement activation more strongly. Systemic pre-treatment with C1-INH,
however, failed to alter ventilation-induced complement activation with
both ventilation strategies. In accordance, lung inflammation and lung
injury were not affected by pre-treatment with C1-INH, neither in rats
ventilated with lower tidal volumes and PEEP, nor rats ventilated with
high tidal volumes without PEEP. Ventilation augments pulmonary
complement activation in a rat model of S. pneumoniae pneumonia.
Systemic administration of C1-INH, however, does not attenuate
ventilation-induced complement activation, lung inflammation, and lung
injury.
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