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长期接触三手烟可能通过线粒体功能障碍加速生物衰老:来自人群和动物研究的证据。

Long-term exposure to third-hand smoke could accelerate biological aging via mitochondrial dysfunction: Evidence from population and animal studies.

机构信息

Department of Nutrition and Food Hygiene, School of Public Health, Key Laboratory of Precision Nutrition and Health, Ministry of Education, Harbin Medical University, 157 Baojian Road, Harbin, Heilongjiang 150081, China.

Department of Respiratory and Critical Care Medicine, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai 519000, China.

出版信息

J Hazard Mater. 2024 Dec 5;480:136061. doi: 10.1016/j.jhazmat.2024.136061. Epub 2024 Oct 4.

Abstract

The relationship between third-hand smoke (THS) exposure and lifespan remains inadequately explored. Our study sought to clarify the effects of THS on aging and lifespan. In this pursuit, our cross-sectional analysis assessed hematological aging markers in 986 non-smokers and examined lifespan alterations using a Drosophila model. THS exposure levels were quantified through survey metrics consistent with the Global Adult Tobacco Survey. The findings revealed that THS exposure significantly accelerated biological aging, with exposed individuals exhibiting an average increase in biological age of 3.04 years compared to their unexposed counterparts (p < 0.05). Correspondingly, the Drosophila model reflected these outcomes, showing a reduction in lifespan by 16.07 days (p < 0.01). Proteomic analyses identified MRPL2 as a pivotal protein in THS-induced aging, linking its expression to mitochondrial dysfunction and oxidative stress. Further metabolomic profiling highlighted disruptions in energy metabolism pathways. Follow-up in vitro experiments confirmed the role of MRPL2 in the aging processes at the cellular level. Overall, our results indicate that THS exposure is a significant accelerant of aging, providing new perspectives on the health consequences of environmental smoke residues.

摘要

三手烟(THS)暴露与寿命之间的关系尚未得到充分探讨。本研究旨在阐明 THS 对衰老和寿命的影响。为此,我们的横断面分析评估了 986 名不吸烟者的血液学衰老标志物,并使用果蝇模型研究了寿命变化。THS 暴露水平通过与全球成人烟草调查一致的调查指标进行量化。研究结果表明,THS 暴露显著加速了生物衰老,暴露组个体的生物年龄平均增加了 3.04 岁,与未暴露组相比(p<0.05)。相应地,果蝇模型反映了这些结果,寿命缩短了 16.07 天(p<0.01)。蛋白质组学分析确定 MRPL2 是 THS 诱导衰老的关键蛋白,其表达与线粒体功能障碍和氧化应激有关。进一步的代谢组学分析突出了能量代谢途径的紊乱。后续的体外实验证实了 MRPL2 在细胞水平衰老过程中的作用。总体而言,我们的研究结果表明,THS 暴露是衰老的一个重要加速因素,为环境烟草残留对健康的影响提供了新的视角。

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