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Reduced Chronic Toxicity and Carcinogenicity in A/J Mice in Response to Life-Time Exposure to Aerosol From a Heated Tobacco Product Compared With Cigarette Smoke
We conducted an inhalation study, in accordance with Organisation for Economic Co-operation and Development Test Guideline 453, exposing A/J mice to tobacco heating system (THS) 2.2 aerosol or 3R4F reference cigarette smoke (CS) for up to 18 months to evaluate chronic toxicity and carcinogenicity. A...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7657344/ https://www.ncbi.nlm.nih.gov/pubmed/32780830 http://dx.doi.org/10.1093/toxsci/kfaa131 |
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author | Wong, Ee Tsin Luettich, Karsta Krishnan, Subash Wong, Sin Kei Lim, Wei Ting Yeo, Demetrius Büttner, Ansgar Leroy, Patrice Vuillaume, Grégory Boué, Stéphanie Hoeng, Julia Vanscheeuwijck, Patrick Peitsch, Manuel C |
author_facet | Wong, Ee Tsin Luettich, Karsta Krishnan, Subash Wong, Sin Kei Lim, Wei Ting Yeo, Demetrius Büttner, Ansgar Leroy, Patrice Vuillaume, Grégory Boué, Stéphanie Hoeng, Julia Vanscheeuwijck, Patrick Peitsch, Manuel C |
author_sort | Wong, Ee Tsin |
collection | PubMed |
description | We conducted an inhalation study, in accordance with Organisation for Economic Co-operation and Development Test Guideline 453, exposing A/J mice to tobacco heating system (THS) 2.2 aerosol or 3R4F reference cigarette smoke (CS) for up to 18 months to evaluate chronic toxicity and carcinogenicity. All exposed mice showed lower thymus and spleen weight, blood lymphocyte counts, and serum lipid concentrations than sham mice, most likely because of stress and/or nicotine effects. Unlike THS 2.2 aerosol-exposed mice, CS-exposed mice showed increased heart weight, changes in red blood cell profiles and serum liver function parameters. Similarly, increased pulmonary inflammation, altered lung function, and emphysematous changes were observed only in CS-exposed mice. Histopathological changes in other respiratory tract organs were significantly lower in the THS 2.2 aerosol-exposed groups than in the CS-exposed group. Chronic exposure to THS 2.2 aerosol also did not increase the incidence or multiplicity of bronchioloalveolar adenomas or carcinomas relative to sham, whereas CS exposure did. Male THS 2.2 aerosol-exposed mice had a lower survival rate than sham mice, related to an increased incidence of urogenital issues that appears to be related to congenital factors rather than test item exposure. The lower impact of THS 2.2 aerosol exposure on tumor development and chronic toxicity is consistent with the significantly reduced levels of harmful and potentially harmful constituents in THS 2.2 aerosol relative to CS. The totality of the evidence from this study further supports the risk reduction potential of THS 2.2 for lung diseases in comparison with cigarettes. |
format | Online Article Text |
id | pubmed-7657344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76573442020-11-17 Reduced Chronic Toxicity and Carcinogenicity in A/J Mice in Response to Life-Time Exposure to Aerosol From a Heated Tobacco Product Compared With Cigarette Smoke Wong, Ee Tsin Luettich, Karsta Krishnan, Subash Wong, Sin Kei Lim, Wei Ting Yeo, Demetrius Büttner, Ansgar Leroy, Patrice Vuillaume, Grégory Boué, Stéphanie Hoeng, Julia Vanscheeuwijck, Patrick Peitsch, Manuel C Toxicol Sci Carcinogenesis We conducted an inhalation study, in accordance with Organisation for Economic Co-operation and Development Test Guideline 453, exposing A/J mice to tobacco heating system (THS) 2.2 aerosol or 3R4F reference cigarette smoke (CS) for up to 18 months to evaluate chronic toxicity and carcinogenicity. All exposed mice showed lower thymus and spleen weight, blood lymphocyte counts, and serum lipid concentrations than sham mice, most likely because of stress and/or nicotine effects. Unlike THS 2.2 aerosol-exposed mice, CS-exposed mice showed increased heart weight, changes in red blood cell profiles and serum liver function parameters. Similarly, increased pulmonary inflammation, altered lung function, and emphysematous changes were observed only in CS-exposed mice. Histopathological changes in other respiratory tract organs were significantly lower in the THS 2.2 aerosol-exposed groups than in the CS-exposed group. Chronic exposure to THS 2.2 aerosol also did not increase the incidence or multiplicity of bronchioloalveolar adenomas or carcinomas relative to sham, whereas CS exposure did. Male THS 2.2 aerosol-exposed mice had a lower survival rate than sham mice, related to an increased incidence of urogenital issues that appears to be related to congenital factors rather than test item exposure. The lower impact of THS 2.2 aerosol exposure on tumor development and chronic toxicity is consistent with the significantly reduced levels of harmful and potentially harmful constituents in THS 2.2 aerosol relative to CS. The totality of the evidence from this study further supports the risk reduction potential of THS 2.2 for lung diseases in comparison with cigarettes. Oxford University Press 2020-08-11 /pmc/articles/PMC7657344/ /pubmed/32780830 http://dx.doi.org/10.1093/toxsci/kfaa131 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society of Toxicology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Carcinogenesis Wong, Ee Tsin Luettich, Karsta Krishnan, Subash Wong, Sin Kei Lim, Wei Ting Yeo, Demetrius Büttner, Ansgar Leroy, Patrice Vuillaume, Grégory Boué, Stéphanie Hoeng, Julia Vanscheeuwijck, Patrick Peitsch, Manuel C Reduced Chronic Toxicity and Carcinogenicity in A/J Mice in Response to Life-Time Exposure to Aerosol From a Heated Tobacco Product Compared With Cigarette Smoke |
title | Reduced Chronic Toxicity and Carcinogenicity in A/J Mice in Response to Life-Time Exposure to Aerosol From a Heated Tobacco Product Compared With Cigarette Smoke |
title_full | Reduced Chronic Toxicity and Carcinogenicity in A/J Mice in Response to Life-Time Exposure to Aerosol From a Heated Tobacco Product Compared With Cigarette Smoke |
title_fullStr | Reduced Chronic Toxicity and Carcinogenicity in A/J Mice in Response to Life-Time Exposure to Aerosol From a Heated Tobacco Product Compared With Cigarette Smoke |
title_full_unstemmed | Reduced Chronic Toxicity and Carcinogenicity in A/J Mice in Response to Life-Time Exposure to Aerosol From a Heated Tobacco Product Compared With Cigarette Smoke |
title_short | Reduced Chronic Toxicity and Carcinogenicity in A/J Mice in Response to Life-Time Exposure to Aerosol From a Heated Tobacco Product Compared With Cigarette Smoke |
title_sort | reduced chronic toxicity and carcinogenicity in a/j mice in response to life-time exposure to aerosol from a heated tobacco product compared with cigarette smoke |
topic | Carcinogenesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7657344/ https://www.ncbi.nlm.nih.gov/pubmed/32780830 http://dx.doi.org/10.1093/toxsci/kfaa131 |
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