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Chronic Exposure to Both Electronic and Conventional Cigarettes Alters Ileum and Colon Turnover, Immune Function, and Barrier Integrity in Mice

Journal of Xenobiotics 2024 5 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 55 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Madjid Djouina, Madjid Djouina, Madjid Djouina, Madjid Djouina, Madjid Djouina, Madjid Djouina, Anaïs Ollivier, Mathilde Body–Malapel Christophe Waxin, Christophe Waxin, Cécile Vignal, Ségolène Caboche, Laurent Dubuquoy, Mathilde Body–Malapel Christophe Waxin, Christophe Waxin, Gwenola Kervoaze, Ségolène Caboche, Gwenola Kervoaze, David Launay, Muriel Pichavant, Cécile Vignal, Mathilde Body–Malapel Christophe Waxin, Ségolène Caboche, Delphine Beury, Djamal Achour, David Hot, Céline Grare, Céline Grare, Delphine Beury, Delphine Beury, Cécile Vignal, David Hot, Laurent Dubuquoy, David Hot, Laurent Dubuquoy, David Launay, David Launay, Laurent Dubuquoy, Sébastien Anthérieu, Mathilde Body–Malapel Jean‐Marc Lo‐Guidice, Laurent Dubuquoy, Mathilde Body–Malapel Mathilde Body–Malapel David Launay, Cécile Vignal, Philippe Gosset, Mathilde Body–Malapel

Summary

Researchers compared the effects of e-cigarette aerosol and conventional cigarette smoke on mouse intestinal tissue over six months. They found that both exposures caused damage to the gut lining, reduced cell turnover, and impaired immune function in the ileum and colon. The study suggests that e-cigarettes, like traditional cigarettes, may negatively affect digestive health by disrupting the intestinal barrier.

Although the effects of cigarette smoke (CS) on the development of several intestinal diseases is well documented, the impact of e-cigarette aerosol (e-cig) on digestive health is largely unknown. To compare the effects of e-cig and CS on mouse ileum and colon, animals were chronically exposed for 6 months by nose-only inhalation to e-cig at 18 or 30 W power, or to 3R4F CS. Results showed that e-cig exposure decreased colon cell proliferation. Several other proliferative defects were observed in response to both e-cig and CS exposure, including up- and down-regulation of cyclin D1 protein levels in the ileum and colon, respectively. E-cig and CS exposure reduced myeloperoxidase activity in the ileum. In the colon, both exposures disrupted gene expression of cytokines and T cell transcription factors. For tight junction genes, ZO-1- and occludin-protein expression levels were reduced in the ileum and colon, respectively, by e-cig and CS exposure. The 16S sequencing of microbiota showed specific mild dysbiosis, according to the type of exposure. Overall, e-cig exposure led to altered proliferation, inflammation, and barrier function in both the ileum and colon, and therefore may be a gut hazard on par with conventional CS.

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