Vascular permeability and late radiation fibrosis in mouse lung
Description
It has been suggested that fibrosis which developed after irradiation is caused by increases in vascular permeability. Plasma proteins leak into irradiated tissue where fibrinogen may be converted into fibrin which is gradually replaced by fibrous tissue. Vascular and fibrotic changes in mouse lung were investigated after X irradiation of the right hemithorax. Blood volume and accumulation of extravascular proteins were measured using indium (111In)-labeled red cells, iodinated (131I) albumin, and iodinated (125I) fibrinogen. During the first few months after X rays, lung blood volume decreased to a plateau which depended on radiation dose (10-25 Gy). Small increases in extravascular albumin and fibrinogen occurred at 1-12 weeks after 10-25 Gy. Hydroxyproline per gram of dry irradiated lung was increased at 18 weeks after 15-25 Gy. Support for the hypothesis was that hydroxyproline per gram only increased after X-ray doses which caused marked extravasation of protein. There was no evidence, however, for deposition of 125I-fibrin or for a gradual increase in fibrosis corresponding to the prolonged excess of extravascular protein
Additional details
Publishing Information
- Journal Title
- Radiat. Res.
- Journal Volume
- 103
- Journal Issue
- 1
- Series
- Radiat. Res.
- Journal Page Range
- 60-76
- ISSN
- 0033-7587
- CODEN
- RAREA
Conference
- Title
- Radiation Research Society annual meeting.
- Dates
- 13-17 Apr 1986.
- Place
- Las Vegas, NV (USA).
INIS
- Country of Publication
- United States
- Country of Input or Organization
- United States
- INIS RN
- 17016384
- Subject category
- S63: RADIATION, THERMAL, AND OTHER ENVIRONMENTAL POLLUTANT EFFECTS ON LIVING ORGANISMS AND BIOLOGICAL MATERIALS; S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- ALBUMINS; BLOOD PLASMA; BLOOD VESSELS; COLLAGEN; DELAYED RADIATION EFFECTS; ERYTHROCYTES; FIBRINOGEN; FIBROSIS; INDIUM 111; IODINE 125; IODINE 131; LUNGS; MICE; PERMEABILITY; PROTEINS; RADIATION EFFECTS; TRACER TECHNIQUES; X RADIATION
- Descriptors DEC
- ANIMALS; BETA DECAY RADIOISOTOPES; BETA-MINUS DECAY RADIOISOTOPES; BIOLOGICAL EFFECTS; BIOLOGICAL MATERIALS; BIOLOGICAL RADIATION EFFECTS; BLOOD; BLOOD CELLS; BLOOD COAGULATION FACTORS; BODY; BODY FLUIDS; CARDIOVASCULAR SYSTEM; COAGULANTS; DAYS LIVING RADIOISOTOPES; DISEASES; DRUGS; ELECTROMAGNETIC RADIATION; ELECTRON CAPTURE RADIOISOTOPES; GLOBULINS; HEMATOLOGIC AGENTS; INDIUM ISOTOPES; INTERMEDIATE MASS NUCLEI; IODINE ISOTOPES; IONIZING RADIATIONS; ISOMERIC TRANSITION ISOTOPES; ISOTOPE APPLICATIONS; ISOTOPES; MAMMALS; MATERIALS; MINUTES LIVING RADIOISOTOPES; NUCLEI; ODD-EVEN NUCLEI; ORGANIC COMPOUNDS; ORGANS; PATHOLOGICAL CHANGES; RADIATIONS; RADIOISOTOPES; RESPIRATORY SYSTEM; RODENTS; SCLEROPROTEINS; VERTEBRATES
Optional Information
- Secondary number(s)
- CONF-860423--.