Cannabis vaping elicits transcriptomic and metabolomic changes in inflammatory, oxidative stress and cancer pathways in human bronchial epithelial cells.

Maddison T Arlen, Stephanie J Patterson, Michelle K Page, Rui Liu, Vincenza Caruana, Emily T Wilson, Stéphane A Laporte, Maciej L Goniewicz, Cory S Harris, David H Eidelman, Carolyn J Baglole
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Abstract

The increasing shift from cannabis smoking to cannabis vaping is largely driven by the perception that vaping to form an aerosol represents a safer alternative to smoking and is a form of consumption appealing to youth. Herein, we compared the chemical composition and receptor-mediated activity of cannabis smoke extract (CaSE) to cannabis vaping extract (CaVE) along with the biological response in human bronchial epithelial cells. Chemical analysis using HPLC and GC/MS revealed that cannabis vaping aerosol contained fewer toxicants than smoke; CaSE and CaVE contained teratogens, carcinogens, and respiratory toxicants. A bioluminescence resonance energy transfer (BRET)-based biosensor detected the receptor-mediated activity of the extracts, primarily driven by Δ9-THC concentration. RNA- sequencing showed both CaSE and CaVE induced similar transcriptional responses, significantly upregulating genes within pathways related to inflammation, cancer, and cellular stress. This was paralleled by downregulation of pathways related to lipid synthesis and metabolism similarly from both CaSE and CaVE. Targeted metabolomics revealed significant changes in metabolites involved in lipid and membrane metabolism, energy production, nucleotide/DNA/RNA pathways, and oxidative stress response, suggesting potential impairment of lung epithelial cell repair and function. Additionally, the upregulation of 5-hydroxymethylcytosine (5hmC) indicates epigenetic changes potentially contributing to inflammation, oxidative stress, and an increased risk of cancer. These findings challenge the notion that cannabis vaping is risk-free, highlighting an urgent need for comprehensive research into its respiratory health effects. This comparison of cannabis consumption methods offers insights that could inform public health policies and raise consumer awareness regarding the potential risks of inhaling cannabis aerosol.

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吸食大麻会引起人类支气管上皮细胞炎症、氧化应激和癌症通路的转录组学和代谢组学变化。
越来越多的人从吸食大麻转向吸食大麻电子烟,主要是因为人们认为,吸食大麻形成气溶胶是一种比吸烟更安全的选择,是一种吸引年轻人的消费方式。在此,我们比较了大麻烟提取物(CaSE)和大麻蒸汽提取物(CaVE)的化学成分和受体介导的活性以及人类支气管上皮细胞的生物学反应。HPLC和GC/MS化学分析表明,大麻雾化气雾剂的有毒物质含量低于烟雾;CaSE和CaVE含有致畸物、致癌物和呼吸毒性物质。基于生物发光共振能量转移(BRET)的生物传感器检测了提取物的受体介导活性,主要由Δ9-THC浓度驱动。RNA测序显示,CaSE和CaVE诱导了相似的转录反应,显著上调了炎症、癌症和细胞应激相关通路中的基因。这与CaSE和CaVE中与脂质合成和代谢相关的通路下调相似。靶向代谢组学显示,参与脂质和膜代谢、能量产生、核苷酸/DNA/RNA通路和氧化应激反应的代谢物发生了显著变化,提示肺上皮细胞修复和功能可能受损。此外,5-羟甲基胞嘧啶(5hmC)的上调表明表观遗传变化可能导致炎症、氧化应激和癌症风险增加。这些发现挑战了吸食大麻没有风险的观念,强调了对其呼吸健康影响进行全面研究的迫切需要。这种大麻消费方法的比较提供了见解,可以为公共卫生政策提供信息,并提高消费者对吸入大麻气雾剂潜在风险的认识。
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来源期刊
CiteScore
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.
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