Key result
Chronic hypoxia accelerates aortic atherosclerotic plaque formation and smooth muscle cell proliferation in apoE-KO mice.
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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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Nakano et al. (2005) studied Atherosclerosis. Chronic hypoxia vs. Room air (normoxia) was evaluated on Aortic atherosclerotic plaque formation and smooth muscle cell proliferation. Chronic hypoxia accelerated aortic atherosclerotic plaque formation and smooth muscle cell proliferation in 6-week-old apoE-KO mice compared with normoxia.
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