HEPES BUFFER PERFUSATE ALTERS RABBIT LUNG ENDOTHELIAL PERMEABILITY

Douglas, GC; Swanson, JA; Kern, DF

HERO ID

5183213

Reference Type

Journal Article

Year

1993

Language

English

PMID

8226560

HERO ID 5183213
In Press No
Year 1993
Title HEPES BUFFER PERFUSATE ALTERS RABBIT LUNG ENDOTHELIAL PERMEABILITY
Authors Douglas, GC; Swanson, JA; Kern, DF
Journal Journal of Applied Physiology
Volume 75
Issue 3
Page Numbers 1423-1425
Abstract N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid (HEPES) has been shown to cause changes in cultured endothelial cells and smooth muscle function at concentrations from 5 to 25 mM. To determine whether HEPES also affects vascular permeability, the effects of two buffers, HEPES and phosphate, were compared in isolated perfused rabbit lungs. Hemodynamic parameters and vascular protein permeability-surface area products (PS) were measured after perfusion with the buffers. Endothelial permeability was measured for an anionic and a cationic albumin to assess the charge effects of the zwitterion buffer. With HEPES, there were no changes in vascular pressure or resistance but permeability was affected. Cationic albumin permeability increased with 12 mM HEPES (8.7phosphate-->30(12) mM HEPES x ml.min-1.g dry lung-1 x 10(-2)) as did the anionic albumin PS (2.7phosphate-->3.52(12) mM HEPES). The cationic PS returned to baseline (8.1(60) mM HEPES) at 60 mM HEPES, but the anionic PS did not change from the 12 mM HEPES (4.01(60) mM HEPES). In summary, we find that HEPES is not innocuous. Although hemodynamic parameters did not change, endothelial permeability was increased when HEPES was used at normal concentrations. Therefore, HEPES should be used with caution as a physiological buffer in perfused organ systems.
Doi 10.1152/jappl.1993.75.3.1423
Pmid 8226560
Wosid WOS:A1993LY89600055
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Keyword LUNG ENDOTHELIUM; ENDOTHELIAL PERMEABILITY; BUFFER SOLUTIONS