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基于代谢组学的电子烟急性暴露小鼠安全性评价

Metabolomics-based safety evaluation of acute exposure to electronic cigarettes in mice.

机构信息

Department of Toxicology and Sanitary Chemistry, School of Public Health, Capital Medical University, Beijing 100069, PR China; Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, PR China.

Department of Toxicology and Sanitary Chemistry, School of Public Health, Capital Medical University, Beijing 100069, PR China; Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, PR China.

出版信息

Sci Total Environ. 2022 Sep 15;839:156392. doi: 10.1016/j.scitotenv.2022.156392. Epub 2022 May 31.

Abstract

INTRODUCTION

A growing number of epidemiological evidence reveals that electronic cigarettes (E-cigs) were associated with pneumonia, hypertension and atherosclerosis, but the toxicological evaluation and mechanism of E-cigs were largely unknown.

OBJECTIVE

Our study was aimed to explore the adverse effects on organs and metabolomics changes in C57BL/6J mice after acute exposure to E-cigs.

METHODS AND RESULTS

Hematoxylin and eosin (H&E) staining found pathological changes in tissues after acute exposure to E-cigs, such as inflammatory cell infiltration, nuclear pyknosis, and intercellular interstitial enlargement. E-cigs could increase apoptosis-positive cells in a time-dependent way using Terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling (TUNEL) assay. Oxidative damage indicators of reactive oxygen species (ROS), malondialdehyde (MDA) and 4-hydroxynonena (4-HNE) were also elevated after E-cigs exposure. There was an increasing trend of total glycerol and cholesterol in serum, while the glucose and liver enzymes including alanine aminotransferase (ALT), aspartate transaminase (AST), gamma-glutamyltranspeptidase (γ-GT) had no significant change compared to that of control. Further, Q Exactive high field (HF) mass spectrometer was used to conduct metabolomics, which revealed that differential metabolites including l-carnitine, Capryloyl glycine, etc. Trend analysis showed the type of compounds that change over time. Pathway enrichment analysis indicated that E-cigs affected 24 metabolic pathways, which were mainly regulated amino acid metabolism, further affected the tricarboxylic acid (TCA) cycle. Additionally, metabolites-diseases network analysis found that the type 2 diabetes mellitus, propionic acidemia, defect in long-chain fatty acids transport and lung cancer may be related to E-cigs exposure.

CONCLUSIONS

Our findings provided important clues for metabolites biomarkers of E-cigs acute exposure and are beneficial for disease prevention.

摘要

简介

越来越多的流行病学证据表明,电子烟(E-cigs)与肺炎、高血压和动脉粥样硬化有关,但电子烟的毒理学评估和机制在很大程度上尚不清楚。

目的

本研究旨在探讨 C57BL/6J 小鼠急性暴露于电子烟后对器官的不良影响和代谢组学变化。

方法和结果

苏木精和伊红(H&E)染色发现组织在急性暴露于电子烟后发生了病理变化,如炎症细胞浸润、核固缩和细胞间间质增大。使用末端脱氧核苷酸转移酶介导的 dUTP-生物素缺口末端标记(TUNEL)检测,电子烟可以时间依赖性地增加凋亡阳性细胞。氧化应激标志物活性氧(ROS)、丙二醛(MDA)和 4-羟基壬烯酸(4-HNE)在电子烟暴露后也升高。血清中总甘油和胆固醇呈上升趋势,而葡萄糖和丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)、γ-谷氨酰转肽酶(γ-GT)等肝酶与对照组相比无明显变化。此外,使用 Q Exactive 高场(HF)质谱仪进行代谢组学分析,结果表明包括 l-肉碱、癸酰甘氨酸等在内的差异代谢物。趋势分析显示随时间变化的化合物类型。途径富集分析表明,电子烟影响 24 种代谢途径,主要调节氨基酸代谢,进一步影响三羧酸(TCA)循环。此外,代谢物-疾病网络分析发现,2 型糖尿病、丙酸血症、长链脂肪酸转运缺陷和肺癌可能与电子烟暴露有关。

结论

本研究结果为电子烟急性暴露的代谢物生物标志物提供了重要线索,有利于疾病预防。

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