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Chronic Internal Exposure to Low Dose 137Cs Induces Positive Impact on the Stability of Atherosclerotic Plaques by Reducing Inflammation in ApoE-/- Mice

机译:慢性内部低剂量137Cs暴露通过减少ApoE-/-小鼠的炎症对动脉粥样硬化斑块的稳定性产生积极影响。

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摘要

After Chernobyl and Fukushima Daï Chi, two major nuclear accidents, large amounts of radionuclides were released in the environment, mostly caesium 137 (137Cs). Populations living in contaminated territories are chronically exposed to radionuclides by ingestion of contaminated food. However, questions still remain regarding the effects of low dose ionizing radiation exposure on the development and progression of cardiovascular diseases. We therefore investigated the effects of a chronic internal exposure to 137Cs on atherosclerosis in predisposed ApoE-/- mice. Mice were exposed daily to 0, 4, 20 or 100 kBq/l 137Cs in drinking water, corresponding to range of concentrations found in contaminated territories, for 6 or 9 months. We evaluated plaque size and phenotype, inflammatory profile, and oxidative stress status in different experimental groups. Results did not show any differences in atherosclerosis progression between mice exposed to 137Cs and unexposed controls. However, 137Cs exposed mice developed more stable plaques with decreased macrophage content, associated with reduced aortic expression of pro-inflammatory factors (CRP, TNFα, MCP-1, IFNγ) and adhesion molecules (ICAM-1, VCAM-1 and E-selectin). Lesions of mice exposed to 137Cs were also characterized by enhanced collagen and smooth muscle cell content, concurrent with reduced matrix metalloproteinase MMP8 and MMP13 expression. These results suggest that low dose chronic exposure of 137Cs in ApoE-/- mice enhances atherosclerotic lesion stability by inhibiting pro-inflammatory cytokine and MMP production, resulting in collagen-rich plaques with greater smooth muscle cell and less macrophage content.
机译:在切尔诺贝利核电站和福岛核电站事故之后,两起重大核事故导致环境中释放出大量放射性核素,其中大部分为铯137( 137 Cs)。生活在受污染领土上的人口通过摄入受污染的食物而长期暴露于放射性核素。然而,关于低剂量电离辐射暴露对心血管疾病发展和进展的影响仍然存在疑问。因此,我们研究了慢性内部暴露于 137 Cs对易感ApoE -/-小鼠动脉粥样硬化的影响。每天将小鼠暴露于0、4、20或100 kBq / l的 137 Cs饮用水中(对应于在受污染地区发现的浓度范围),持续6或9个月。我们评估了不同实验组的斑块大小和表型,炎性特征和氧化应激状态。结果表明,暴露于 137 Cs的小鼠与未暴露的对照组之间的动脉粥样硬化进展没有任何差异。然而,暴露于 137 Cs的小鼠的斑块更稳定,巨噬细胞含量降低,与促炎因子(CRP,TNFα,MCP-1,IFNγ)和粘附分子(ICAM-1)的主动脉表达降低有关,VCAM-1和E-selectin)。暴露于 137 Cs的小鼠皮损的特征还在于胶原蛋白和平滑肌细胞含量增加,同时基质金属蛋白酶MMP8和MMP13表达降低。这些结果表明,低剂量长期暴露于ApoE -/-小鼠中的 137 Cs可以通过抑制促炎性细胞因子和MMP的产生来增强动脉粥样硬化病变的稳定性,从而导致胶原蛋白丰富斑块具有更大的平滑肌细胞和更少的巨噬细胞含量。

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