In Vivo Angiographic Detection of Vascular Lesions in Apolipoprotein E-Knockout Mice Using a Synchrotron Radiation Microangiography System

Genetically modified hyperlipidemic mice provide important information on the pathogenesis of atherosclerosis, but most experimental designs are limited to in vitro or ex vivo examinations. The present study was designed to detect atherosclerotic lesions in situ in apolipoprotein E-knockout (apoE-KO...

Full description

Saved in:
Bibliographic Details
Published inCirculation Journal Vol. 66; no. 11; pp. 1057 - 1059
Main Authors Yamashita, Tomoya, Kawashima, Seinosuke, Ozaki, Masanori, Namiki, Masayuki, Shinohara, Masakazu, Inoue, Nobutaka, Hirata, Ken-ichi, Umetani, Keiji, Yokoyama, Mitsuhiro
Format Journal Article
LanguageEnglish
Published Kyoto The Japanese Circulation Society 2002
Japanese Circulation Society
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Genetically modified hyperlipidemic mice provide important information on the pathogenesis of atherosclerosis, but most experimental designs are limited to in vitro or ex vivo examinations. The present study was designed to detect atherosclerotic lesions in situ in apolipoprotein E-knockout (apoE-KO) mice using a newly developed angiography system, synchrotron radiation (SR) microangiography, which uses monochromatic SR as an X-ray source and a high definition camera or video system as a detector. Digital microangiography with 7 mm pixel sizes was carried out and atherosclerotic lesion in small arteries less than 500 μm in diameter were detected. Moreover, the coronary artery stenotic lesion of an apoE-KO mouse was detected in situ with the angiography system. The new SR microangiography system is a powerful tool for investigating atherosclerotic lesions in situ in genetically engineered mice and will promote the basic study of atherosclerotic disease. (Circ J 2002; 66: 1057 - 1059)
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1346-9843
1347-4820
DOI:10.1253/circj.66.1057