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Certain e-liquids and aromatic aldehyde flavoring agents were previously identified as inhibitors of microsomal recombinant CYP2A6, the primary nicotine-metabolizing enzyme. However, due to their reactive nature, aldehydes may react with cellular components before reaching CYP2A6 in the endoplasmic reticulum. To determine whether e-liquid flavoring agents inhibited CYP2A6 in a cellular system, we investigated their effects on CYP2A6 using BEAS-2B cells transduced to overexpress CYP2A6. We demonstrated that two e-liquids and three aldehyde flavoring agents (cinnamaldehyde, benzaldehyde, and ethyl vanillin) exhibited dose-dependent inhibition of cellular CYP2A6.
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Brett R. Winters
Cytokinetics (United States)
Phillip W. Clapp
University of North Carolina at Chapel Hill
Steven O. Simmons
Environmental Protection Agency
ACS Omega
University of North Carolina at Chapel Hill
Environmental Protection Agency
Research Triangle Park Foundation
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Winters et al. (Mon,) studied this question.
synapsesocial.com/papers/6a230378d6da8eab4757f565 — DOI: https://doi.org/10.1021/acsomega.2c08258
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