A 90-day OECD TG 413 rat inhalation study with systems toxicology endpoints demonstrates reduced exposure effects of the aerosol from the carbon heated tobacco product version 1.2 (CHTP1.2) compared with cigarette smoke. II. Systems toxicology assessment

被引:14
|
作者
Titz, Bjoern [1 ]
Kogel, Ulrike [1 ]
Martin, Florian [1 ]
Schlage, Walter K. [2 ]
Xiang, Yang [1 ]
Nury, Catherine [1 ]
Dijon, Sophie [1 ]
Baumer, Karine [1 ]
Peric, Dariusz [1 ]
Bornand, David [1 ]
Dulize, Remi [1 ]
Phillips, Blaine [3 ]
Leroy, Patrice [1 ]
Vuillaume, Gregory [1 ]
Lebrun, Stefan [1 ]
Elamin, Ashraf [1 ]
Guedj, Emmanuel [1 ]
Trivedi, Keyur [1 ]
Ivanov, Nikolai, V [1 ]
Vanscheeuwijck, Patrick [1 ]
Peitsch, Manuel C. [1 ]
Hoeng, Julia [1 ]
机构
[1] Philip Morris Prod SA, PMI R&D, Quai Jeanrenaud 5, CH-2000 Neuchatel, Switzerland
[2] Max Baermann Str 21, D-51429 Bergisch Gladbach, Germany
[3] Philip Morris Int Res Labs Pte Ltd, PMI R&D, Sci Pk 2, Singapore, Singapore
关键词
Modified risk tobacco product; Systems toxicology; Transcriptomics; Proteomics; Lipidomics; Subchronic inhalation toxicity; PITUITARY-ADRENAL AXIS; SPRAGUE-DAWLEY RATS; PART; CHEMICAL-COMPOSITION; LUNG INFLAMMATION; OXIDATIVE STRESS; NETWORK MODEL; HPA AXIS; NICOTINE; TOXICITY;
D O I
10.1016/j.fct.2018.02.058
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Modified risk tobacco products (MRTPs) have the potential to reduce smoking-related health risks. The Carbon Heated Tobacco Product 1.2 (CHTP1.2) is a potential MRTP that uses a pressed carbon heat source to generate an aerosol by heating tobacco. Here, we report the results from the systems toxicology arm of a 90-day rat inhalation study (OECD test guideline 413) to assess the effects of CHTP1.2 aerosol compared with cigarette smoke (CS). Transcriptomics, proteomics, and lipidomics analyses complemented the standard endpoints. In the respiratory nasal epithelium, CS induced an adaptive tissue and inflammatory response, which was much weaker after CHTP1.2 aerosol exposure, mostly limited to the highest CHTP1.2 concentration (at twice the 3R4F CS concentration: 50 vs. 23 mu g nicotine/L), in female rats. In the lungs, the effects of CS exposure included inflammatory and cellular stress responses, which were absent or much lower after CHTP1.2 aerosol exposure. Outside of the respiratory tract, CS and CHTP1.2 aerosol induced effects that were previously associated with exposure to any nicotine-containing aerosol, e.g., lower lipid concentrations in serum. Overall, this systems toxicology analysis complements and confirms the results from classical toxicological endpoints and further suggests potentially reduced respiratory health risks of CHTP1.2. 1.
引用
收藏
页码:284 / 301
页数:18
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