Exploring the Cellular Impact of Size-Segregated Cigarette Aerosols: Insights into Indoor Particulate Matter Toxicity and Potential Therapeutic Interventions.
Yu-Xin ShenPe-Shuen LeeChia C WangMing-Chu TengJhih-Hong HuangHsiu-Fang FanPublished in: Chemical research in toxicology (2024)
Exposure to anthropogenic aerosols has been associated with a variety of adverse health effects, increased morbidity, and premature death. Although cigarette smoke poses one of the most significant public health threats, the cellular toxicity of particulate matter contained in cigarette smoke has not been systematically interrogated in a size-segregated manner. In this study, we employed a refined particle size classification to collect cigarette aerosols, enabling a comprehensive assessment and comparison of the impacts exerted by cigarette aerosol extract (CAE) on SH-SY5Y, HEK293T, and A549 cells. Exposure to CAE reduced cell viability in a dose-dependent manner, with organic components having a greater impact and SH-SY5Y cells displaying lower tolerance compared to HEK293T and A549 cells. Moreover, CAE was found to cause increased oxidative stress, mitochondrial dysfunction, and increased levels of apoptosis, pyroptosis, and autophagy, leading to increased cell death. Furthermore, we found that rutin, a phytocompound with antioxidant potential, could reduce intracellular reactive oxygen species and protect against CAE-triggered cell death. These findings underscore the therapeutic potential of antioxidant drugs in mitigating the adverse effects of cigarette aerosol exposure for better public health outcomes.
Keyphrases
- oxidative stress
- cell cycle arrest
- particulate matter
- cell death
- induced apoptosis
- air pollution
- public health
- endoplasmic reticulum stress
- water soluble
- reactive oxygen species
- pi k akt
- healthcare
- diabetic rats
- dna damage
- signaling pathway
- smoking cessation
- ischemia reperfusion injury
- mental health
- machine learning
- anti inflammatory
- heat shock
- drug induced
- human health
- clinical evaluation
- health risk
- heat shock protein
- heat stress