Why the study?
Does aerosol extract from a tobacco heating system reduce cytotoxicity, inflammation, and effects on cell migration compared to combustible cigarettes in human endothelial and monocytic cells?
Does aerosol extract from a tobacco heating system reduce cytotoxicity, inflammation, and effects on cell migration compared to combustible cigarettes in human endothelial and monocytic cells?
Aerosol from a heat-not-burn tobacco product induced substantially less cytotoxicity, inflammation, and disruption of endothelial and monocyte function in vitro compared to combustible cigarette smoke.
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Heated tobacco extracts show lower in vitro endothelial toxicity than combustible cigarettes; hypothesis-generating and should not yet inform clinical practice.
Reduction of harmful constituents by heating rather than combusting tobacco is a promising new approach to reduce harmful effects associated with cigarette smoking. We investigated the effect from a new candidate modified risk tobacco product, the tobacco heating system (THS) 2.2, on the migratory behavior of monocytes in comparison with combustible 3R4F reference cigarettes. The monocytic cell line (THP-1) and human coronary arterial endothelial cells (HCAECs) were used to analyze chemotaxis and transendothelial migration (TEM). To assess the influence of aerosol extract from THS2.2 and smoke extract from 3R4F on toxicity and inflammation, flow cytometry and ELISA assays were performed. The results show that treatment of THP-1 cells with extract from 3R4F or THS2.2 induced concentration-dependent increases in cytotoxicity and inflammation. The inhibitory effects of THS2.2 extract for chemotaxis and TEM were ∼18 times less effective compared to 3R4F extract. Furthermore, extract from 3R4F or THS2.2 induced concentration-dependent decreases in the integrity of HCAEC monolayer. For all examined endpoints, the extract from 3R4F showed more than one order of magnitude stronger effects than that from THS2.2 extract. These data indicate the potential of a heat not burn tobacco product to reduce the risk for cardiovascular disease compared to combustible cigarettes.
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Toorn et al. (2015) studied this question.
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