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Particle-induced pulmonary acute phase response may be the causal link between particle inhalation and cardiovascular disease

机译:颗粒物引起的肺急性期反应可能是颗粒物吸入与心血管疾病之间的因果关系

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Inhalation of ambient and workplace particulate air pollution is associated with increased risk of cardiovascular disease. One proposed mechanism for this association is that pulmonary inflammation induces a hepatic acute phase response, which increases risk of cardiovascular disease. Induction of the acute phase response is intimately linked to risk of cardiovascular disease as shown in both epidemiological and animal studies. Indeed, blood levels of acute phase proteins, such as C-reactive protein and serum amyloid A, are independent predictors of risk of cardiovascular disease in prospective epidemiological studies. In this review, we present and review emerging evidence that inhalation of particles (e.g., air diesel exhaust particles and nanoparticles) induces a pulmonary acute phase response, and propose that this induction constitutes the causal link between particle inhalation and risk of cardiovascular disease. Increased levels of acute phase mRNA and proteins in lung tissues, bronchoalveolar lavage fluid and plasma clearly indicate pulmonary acute phase response following pulmonary deposition of different kinds of particles including diesel exhaust particles, nanoparticles, and carbon nanotubes. The pulmonary acute phase response is dose-dependent and long lasting. Conversely, the hepatic acute phase response is reduced relative to lung or entirely absent. We also provide evidence that pulmonary inflammation, as measured by neutrophil influx, is a predictor of the acute phase response and that the total surface area of deposited particles correlates with the pulmonary acute phase response. We discuss the implications of these findings in relation to occupational exposure to nanoparticles. WIREs Nanomed Nanobiotechnol 2014, 6:517–531. doi: 10.1002/wnan.1279 For further resources related to this article, please visit the WIREs website. Conflict of interest: The authors have declared no conflicts of interest for this article.
机译:吸入周围和工作场所的颗粒物空气污染会增加患心血管疾病的风险。这种关联的一种建议机制是,肺部炎症会诱发肝急性期反应,从而增加患心血管疾病的风险。流行病学和动物研究均表明,急性期反应的诱导与心血管疾病的风险密切相关。实际上,在前瞻性流行病学研究中,急性期蛋白(例如C反应蛋白和血清淀粉样蛋白A)的血液水平是心血管疾病风险的独立预测因子。在这篇综述中,我们提出并综述了新兴的证据,即吸入颗粒(例如,空气柴油机排气颗粒和纳米颗粒)会引起肺部急性期反应,并提出这种诱导作用构成了颗粒吸入与心血管疾病风险之间的因果关系。肺组织,支气管肺泡灌洗液和血浆中急性期mRNA和蛋白质水平的增加清楚地表明,在肺部沉积了包括柴油机尾气颗粒,纳米颗粒和碳纳米管在内的各种颗粒后,肺部急性期反应明显。肺急性期反应是剂量依赖性的并且持续时间长。相反,肝急性期反应相对于肺减少或完全不存在。我们还提供了证据,即通过嗜中性粒细胞流入测量的肺部炎症是急性期反应的预测指标,并且沉积颗粒的总表面积与肺部急性期反应相关。我们讨论这些发现与职业性接触纳米颗粒的关系。电线Nanomed Nanobiotechnol 2014,6:517–531。电话:10.1002 / wnan.1279有关本文的更多资源,请访问WIREs网站。利益冲突:作者在本文中没有任何利益冲突。

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