TY - JOUR
T1 - Contrast medium-induced pulmonary vascular hyperpermeability
T2 - Is aggravated in a rat climacterium model
AU - Tominaga, Koji
AU - Kataoka, Yasufumi
AU - Sendo, Toshiaki
AU - Furuta, Wakako
AU - Niizeki, Midori
AU - Oishi, Ryozo
PY - 2001/3/24
Y1 - 2001/3/24
N2 - RATIONALE AND OBJECTIVES. To test whether climacterium influences adverse pulmonary reactions to contrast media, the authors investigated the effect of ioxaglate on pulmonary vascular permeability in ovariectomized rats as a climacterium model. METHODS. From 7 days after surgery, ovariectomized rats were treated with estradiol valerate or vehicle once per week for 3 weeks. At 28 days after surgery, ioxaglate, an ionic contrast medium, was intravenously injected at 1.5 mL/min in rats. Pulmonary vascular permeability was evaluated by measuring the amount of Evans blue dye in the lung tissue. RESULTS. Ioxaglate dose-dependently increased pulmonary vascular permeability in sham-operated and ovariectomized rats. Ovariectomized rats showed a 2.6-fold increased aggravation of vascular permeability by ioxaglate 4 g I/kg compared with sham-operated rats. Estradiol valerate (0.2-5.0 mg/kg) dose-dependently blocked ioxaglate-increased vascular permeability in ovariectomized rats. CONCLUSIONS. These findings suggest that climacterium is included, at least in part, in the risk factors for contrast-induced adverse pulmonary reactions, and this risk is lowered by estrogen replacement therapy.
AB - RATIONALE AND OBJECTIVES. To test whether climacterium influences adverse pulmonary reactions to contrast media, the authors investigated the effect of ioxaglate on pulmonary vascular permeability in ovariectomized rats as a climacterium model. METHODS. From 7 days after surgery, ovariectomized rats were treated with estradiol valerate or vehicle once per week for 3 weeks. At 28 days after surgery, ioxaglate, an ionic contrast medium, was intravenously injected at 1.5 mL/min in rats. Pulmonary vascular permeability was evaluated by measuring the amount of Evans blue dye in the lung tissue. RESULTS. Ioxaglate dose-dependently increased pulmonary vascular permeability in sham-operated and ovariectomized rats. Ovariectomized rats showed a 2.6-fold increased aggravation of vascular permeability by ioxaglate 4 g I/kg compared with sham-operated rats. Estradiol valerate (0.2-5.0 mg/kg) dose-dependently blocked ioxaglate-increased vascular permeability in ovariectomized rats. CONCLUSIONS. These findings suggest that climacterium is included, at least in part, in the risk factors for contrast-induced adverse pulmonary reactions, and this risk is lowered by estrogen replacement therapy.
KW - Contrast media
KW - Estradiol
KW - Pulmonary edema
KW - Rat climacterium model
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U2 - 10.1097/00004424-200103000-00001
DO - 10.1097/00004424-200103000-00001
M3 - Article
C2 - 11228576
AN - SCOPUS:0035094734
SN - 0020-9996
VL - 36
SP - 131
EP - 135
JO - Investigative Radiology
JF - Investigative Radiology
IS - 3
ER -