The permeability coefficient of albumin of the isolated rat mesentery Modification by some mediators of inflammation, cyclic AMP and calcium

In order to study the mechanisms whereby mediators of inflammation exert their exudative effects, we used isolated rat mesentery placed as a separation membrane between the two compartments of a diffusion cell. In this experimental arrangement, the permeability coefficient of albumin ( P A) can be e...

Full description

Saved in:
Bibliographic Details
Published inBiochimica et biophysica acta Vol. 588; no. 2; pp. 219 - 231
Main Authors Kahn, André, Brachet, Etienne
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 03.12.1979
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:In order to study the mechanisms whereby mediators of inflammation exert their exudative effects, we used isolated rat mesentery placed as a separation membrane between the two compartments of a diffusion cell. In this experimental arrangement, the permeability coefficient of albumin ( P A) can be easily computed from the equilibration rate of 125I-labelled albumin added to one compartment. Histamine, bradykinin, serotonin and prostaglandins A 1, A 2, E 1, E 2, F 1α and F 2α all increased P A to some extent, the maximal values being approx. +60%. Dibutyryl-cyclic AMP, theophylline and isoproterenol also increased P A, thus suggesting involvement of cyclic AMP. Direct measurements of this nucleotide confirmed this hypothesis; furthermore, a linear relation between cyclic AMP levels and P A could be demonstrated. In contrast, cyclic GMP is probably not involved in the control of P A. Calcium-depleted tissues had a low P A (approx. 40% below controls), and did not respond to exogenous prostaglandin E 1. These results suggest that transmesenteric passage of albumin is at least partly controlled by cyclic AMP and intracellular Ca 2+ levels.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0304-4165
0006-3002
1872-8006
DOI:10.1016/0304-4165(79)90205-8