Keratinocyte growth factor attenuates hydrostatic pulmonary edema in an isolated, perfused rat lung model
Details
Serval ID
serval:BIB_90D13CF08079
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Keratinocyte growth factor attenuates hydrostatic pulmonary edema in an isolated, perfused rat lung model
Journal
Am J Physiol Heart Circ Physiol
ISSN
0363-6135 (Print)
ISSN-L
0363-6135
Publication state
Published
Issued date
03/2001
Volume
280
Number
3
Pages
H1311-7
Language
english
Notes
Welsh, D A
Guery, B P
Deboisblanc, B P
Dobard, E P
Creusy, C
Mercante, D
Nelson, S
Summer, W R
Mason, C M
eng
Am J Physiol Heart Circ Physiol. 2001 Mar;280(3):H1311-7. doi: 10.1152/ajpheart.2001.280.3.H1311.
Guery, B P
Deboisblanc, B P
Dobard, E P
Creusy, C
Mercante, D
Nelson, S
Summer, W R
Mason, C M
eng
Am J Physiol Heart Circ Physiol. 2001 Mar;280(3):H1311-7. doi: 10.1152/ajpheart.2001.280.3.H1311.
Abstract
Hydrostatic pulmonary edema is a common complication of congestive heart failure, resulting in substantial morbidity and mortality. Keratinocyte growth factor (KGF) is a mitogen for type II alveolar epithelial and microvascular cells. We utilized the isolated perfused rat lung model to produce hydrostatic pulmonary edema by varying the left atrial and pulmonary capillary pressure. Pretreatment with KGF attenuated hydrostatic edema formation. This was demonstrated by lower wet-to-dry lung weight ratios, histological evidence of less alveolar edema formation, and reduced alveolar accumulation of intravascularly administered FITC-labeled large-molecular-weight dextran in rats pretreated with KGF. Thus KGF attenuates injury in this ex vivo model of hydrostatic pulmonary edema via mechanisms that prevent increases in alveolar-capillary permeability.
Keywords
Animals, Blood Pressure, Capillaries/physiology, Capillary Permeability/drug effects/physiology, Dextrans/pharmacokinetics, Fibroblast Growth Factor 7, Fibroblast Growth Factors/*pharmacology, Fluorescein-5-isothiocyanate/*analogs & derivatives/pharmacokinetics, Hydrostatic Pressure, In Vitro Techniques, Male, Organ Size, Perfusion, Pulmonary Alveoli/blood supply/pathology/*physiopathology, Pulmonary Circulation/physiology, Pulmonary Edema/*drug therapy/pathology/*physiopathology, Rats, Rats, Sprague-Dawley, Specific Pathogen-Free Organisms
Pubmed
Create date
29/04/2021 10:59
Last modification date
30/04/2021 6:38