Reduction of endothelial permeability in vitro by cAMP and cGMP
Conference
·
· FASEB Journal (Federation of American Societies for Experimental Biology); (United States)
OSTI ID:5488209
- Albany Medical College, NY (United States)
The cAMP enhancing-vasodilator isoproterenol has been shown previously to decrease endothelial permeability in vitro. This effect may not be unique to cAMP-enhancing agents. The authors have shown that thrombin at a concentration of 2 pM, a level which relaxes aortic vessel strips in association with increased levels of cGMP, reduces endothelial permeability. In this study, the permeability effect of cAMP and cGMP analogues were assessed by measuring the clearance of {sup 125}I-albumin across bovine pulmonary artery endothelial cell monolayers. The experiments were divided into baseline and experimental periods so that each monolayer served as its own control. The cAMP and cGMP analogues, 8-bromo-cAMP (1 mM) and 8-bromo-cGMP (1 mM), decreased clearance form a vehicle control value of 1.3{+-}0.2 (mean {+-}SD of experimental/baseline clearance, n=15 cell monolayers) to 0.7{+-}0.2 and 1.0{+-}0.2, respectively, although cGMP did not decrease clearance from its own baseline value. Coincubation of these analogues with thrombin (0.1 uM) also decreased the thrombin-induced increase in albumin clearance from 2.2{+-}0.5 to 0.8{+-}0.2 (cAMP) and 1.5{+-}0.2 (cGMP). The data indicate that in vitro both cAMP and cGMP-enhancing vasodilators would reduce endothelial permeability and that cAMP-enhancing agents would be more effective.
- OSTI ID:
- 5488209
- Report Number(s):
- CONF-9004153--
- Conference Information:
- Journal Name: FASEB Journal (Federation of American Societies for Experimental Biology); (United States) Journal Volume: 4:3
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
550301* -- Cytology-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
ALBUMINS
AMP
ANIMAL CELLS
ANIMAL TISSUES
ANIMALS
AROMATICS
ARTERIES
AZAARENES
BIOLOGICAL EFFECTS
BLOOD COAGULATION FACTORS
BLOOD VESSELS
BODY
CARDIOVASCULAR AGENTS
CARDIOVASCULAR SYSTEM
CATTLE
COAGULANTS
DOMESTIC ANIMALS
DRUGS
ENDOTHELIUM
ENZYMES
GUANOSINE
HEMATOLOGIC AGENTS
HEMOSTATICS
HETEROCYCLIC COMPOUNDS
HYDROLASES
IN VITRO
LUNGS
MAMMALS
NUCLEOSIDES
NUCLEOTIDES
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANS
PEPTIDE HYDROLASES
PERMEABILITY
PROTEINS
PURINES
RESPIRATORY SYSTEM
RIBOSIDES
RUMINANTS
SERINE PROTEINASES
THROMBIN
TISSUES
VASODILATORS
VERTEBRATES
59 BASIC BIOLOGICAL SCIENCES
ALBUMINS
AMP
ANIMAL CELLS
ANIMAL TISSUES
ANIMALS
AROMATICS
ARTERIES
AZAARENES
BIOLOGICAL EFFECTS
BLOOD COAGULATION FACTORS
BLOOD VESSELS
BODY
CARDIOVASCULAR AGENTS
CARDIOVASCULAR SYSTEM
CATTLE
COAGULANTS
DOMESTIC ANIMALS
DRUGS
ENDOTHELIUM
ENZYMES
GUANOSINE
HEMATOLOGIC AGENTS
HEMOSTATICS
HETEROCYCLIC COMPOUNDS
HYDROLASES
IN VITRO
LUNGS
MAMMALS
NUCLEOSIDES
NUCLEOTIDES
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANS
PEPTIDE HYDROLASES
PERMEABILITY
PROTEINS
PURINES
RESPIRATORY SYSTEM
RIBOSIDES
RUMINANTS
SERINE PROTEINASES
THROMBIN
TISSUES
VASODILATORS
VERTEBRATES