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Chronic hypoxia accelerates the progression of atherosclerosis in apolipoprotein E-knockout mice.
Authors:Daisuke Nakano  Tetsuya Hayashi  Naoko Tazawa  Chika Yamashita  Sakiko Inamoto  Nobuaki Okuda  Tatsuhiko Mori  Koichi Sohmiya  Yasushi Kitaura  Yoshikatsu Okada  Yasuo Matsumura
Affiliation:Department of Pharmacology, Osaka University of Pharmaceutical Sciences, Takatsuki, Japan.
Abstract:The aim of this study was to investigate the effect of chronic hypoxia on the development and progression of atherosclerosis in apolipoprotein E-knockout (apoE-KO) mice. Male and female apoE-KO mice (6 weeks old) and age- and sex-matched wild-type mice were kept under hypoxic conditions (10.0 +/- 0.5% O2) in a gas chamber or in room air for 3 weeks. Aortic atherosclerotic plaque was not observed in wild-type mice under normoxic or hypoxic conditions. In the apoE-KO mice, however, hypoxia induced proliferation of smooth muscle cells and plaque formation in the aorta, which were not observed under normoxic conditions. Although sexual dimorphism of the response to hypoxia was not observed, these hypoxia-induced atherogenic changes were accompanied by a significant increase of plasma low density lipoprotein (LDL) cholesterol and NADPH-dependent vascular superoxide (O2-) production. Furthermore, matrix metalloproteinase (MMP)-9 was activated in the aorta of apoE-KO mice. In conclusion, chronic hypoxia accelerated the development of atherosclerosis in apoE-KO mice, along with increased O2- production and activated MMP-9 in the aorta.
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