首页> 外文期刊>Toxicological sciences: An official journal of the Society of Toxicology >An 8-Month Systems Toxicology Inhalation/Cessation Study in Apoe(-/-) Mice to Investigate Cardiovascular and Respiratory Exposure Effects of a Candidate Modified Risk Tobacco Product, THS 2.2, Compared With Conventional Cigarettes
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An 8-Month Systems Toxicology Inhalation/Cessation Study in Apoe(-/-) Mice to Investigate Cardiovascular and Respiratory Exposure Effects of a Candidate Modified Risk Tobacco Product, THS 2.2, Compared With Conventional Cigarettes

机译:在Apoe(-/-)小鼠中进行的为期8个月的系统毒理学吸入/戒断研究,以研究候选改良风险烟草产品THS 2.2与常规香烟相比的心血管和呼吸暴露效应

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摘要

Smoking cigarettes is a major risk factor in the development and progression of cardiovascular disease (CVD) and chronic obstructive pulmonary disease (COPD). Modified risk tobacco products (MRTPs) are being developed to reduce smoking-related health risks. The goal of this study was to investigate hallmarks of COPD and CVD over an 8-month period in apolipoprotein E-deficient mice exposed to conventional cigarette smoke (CS) or to the aerosol of a candidate MRTP, tobacco heating system (THS) 2.2. In addition to chronic exposure, cessation or switching to THS2.2 after 2 months of CS exposure was assessed. Engaging a systems toxicology approach, exposure effects were investigated using physiology and histology combined with transcriptomics, lipidomics, and proteomics. CS induced nasal epithelial hyperplasia and metaplasia, lung inflammation, and emphysematous changes (impaired pulmonary function and alveolar damage). Atherogenic effects of CS exposure included altered lipid profiles and aortic plaque formation. Exposure to THS2.2 aerosol (nicotine concentration matched to CS, 29.9mg/m(3)) neither induced lung inflammation or emphysema nor did it consistently change the lipid profile or enhance the plaque area. Cessation or switching to THS2.2 reversed the inflammatory responses and halted progression of initial emphysematous changes and the aortic plaque area. Biological processes, including senescence, inflammation, and proliferation, were significantly impacted by CS but not by THS2.2 aerosol. Both, cessation and switching to THS2.2 reduced these perturbations to almost sham exposure levels. In conclusion, in this mouse model cessation or switching to THS2.2 retarded the progression of CS-induced atherosclerotic and emphysematous changes, while THS2.2 aerosol alone had minimal adverse effects.
机译:吸烟是心血管疾病(CVD)和慢性阻塞性肺疾病(COPD)发生和发展的主要危险因素。正在开发改良风险烟草产品(MRTP),以减少与吸烟有关的健康风险。这项研究的目的是调查暴露于常规香烟烟雾(CS)或候选MRTP气雾剂,烟草加热系统(THS)2.2的载脂蛋白E缺陷型小鼠在8个月内的COPD和CVD的特征。除了慢性暴露,还评估了CS暴露2个月后的戒断或改用THS2.2。采用系统毒理学方法,结合生理学和组织学,结合转录组学,脂质组学和蛋白质组学,研究了暴露影响。 CS引起鼻上皮增生和化生,肺部炎症和气肿改变(肺功能受损和肺泡损伤)。 CS暴露的致动脉粥样硬化作用包括改变脂质分布和主动脉斑块形成。暴露于THS2.2气雾剂(烟碱浓度与CS匹配,为29.9mg / m(3))既不会引起肺部炎症或肺气肿,也不会持续改变脂质分布或增加斑块面积。停止或改用THS2.2可逆转炎症反应,并停止最初的气肿改变和主动脉斑块区域的进展。包括衰老,炎症和增殖在内的生物过程受CS影响很大,但不受THS2.2气溶胶影响。停止使用和切换到THS2.2都将这些干扰降低到几乎是假的暴露水平。总之,在该小鼠模型中,停止或切换至THS2.2可以延迟CS诱导的动脉粥样硬化和气肿变化的进程,而仅THS2.2气雾剂的不良反应最小。

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