Inhibition of Microsomal Monooxygenases in Vitro by Aromatic Hydrocarbons

Author(s):  
K. Pyykkö
2019 ◽  
Vol 207 ◽  
pp. 43-51 ◽  
Author(s):  
Richard C. Kolanczyk ◽  
Jeffrey S. Denny ◽  
Barbara R. Sheedy ◽  
Patricia K. Schmieder ◽  
Mark A. Tapper

1994 ◽  
Vol 8 (2) ◽  
pp. 121-135 ◽  
Author(s):  
Patricia D.C. Brown-Woodman ◽  
William S. Webster ◽  
Kelvin Picker ◽  
Fazlul Huq

2019 ◽  
Vol 59 ◽  
pp. 281-291
Author(s):  
Myriam Coulet ◽  
Hélia Latado ◽  
Mireille Moser ◽  
Harrie Besselink ◽  
Matthew Tate ◽  
...  

Author(s):  
Lynn Crosby ◽  
Berran Yucesoy ◽  
Carmine Leggett ◽  
Zheng Tu ◽  
Steven A Belinsky ◽  
...  

Abstract There has been limited toxicity testing of cigarillos, including comparison to cigarettes. This study compared the smoke chemistry and the cytotoxic and genotoxic potential of 10 conventional cigarettes and 10 cigarillos based on the greatest market share. Whole smoke and total particulate matter (TPM) were generated using the Canadian Intense and International Organization for Standardization puffing protocols. Tobacco-specific nitrosamines, carbonyls, and polycyclic aromatic hydrocarbons were measured using gas chromatography-mass spectrometry. TPM smoke extracts were used for the in vitro assays. Cytotoxicity was assessed in human bronchial epithelial continuously cultured cell line cells using the neutral red uptake assay. Genotoxic potential was assessed using the micronucleus (human lung adenocarcinoma continuously cultured cell line cells), Ames, and thymidine kinase assays. TPM from all cigarillos tested was more cytotoxic than cigarettes. Micronucleus formation was significantly greater for cigarillos compared with cigarettes at the highest dose of TPM, with or without rat liver S9 fraction. In the Ames test +S9, both tobacco products exhibited significant dose-dependent increases in mutation frequency, indicating metabolic activation is required for genotoxicity. In the thymidine kinase assay +S9, cigarillos showed a significantly enhanced mutation frequency although both tobacco products were positive. The levels of all measured polycyclic aromatic hydrocarbons, tobacco-specific nitrosamines, and carbonyls (except acrolein) were significantly greater in cigarillos than cigarettes. The Canadian Intense puffing protocol demonstrated increased smoke constituent levels compared with International Organization for Standardization. Even though the gas vapor phase was not tested, the results of this study showed that under the tested conditions the investigated cigarillos showed greater toxicity than comparator cigarettes. This study found that there is significantly greater toxicity in the tested U.S. marketed cigarillos than cigarettes for tobacco constituent levels, cytotoxicity, and genotoxicity. These findings are important for understanding the human health toxicity from the use of cigarillos relative to cigarettes and for building upon knowledge regarding harm from cigarillos to inform risk mitigation strategies.


2003 ◽  
Vol 185 (16) ◽  
pp. 4755-4763 ◽  
Author(s):  
Antonia Rojas ◽  
Ana Segura ◽  
María Eugenia Guazzaroni ◽  
Wilson Terán ◽  
Ana Hurtado ◽  
...  

ABSTRACT The TtgGHI efflux pump of Pseudomonas putida DOT-T1E plays a key role in the innate and induced tolerance of this strain to aromatic hydrocarbons and antibiotics. The ttgGHI operon is expressed constitutively from two overlapping promoters in the absence of solvents and at a higher level in their presence, but not in response to antibiotics. Adjacent to the ttgGHI operon is the divergently transcribed ttgVW operon. In TtgV-deficient backgrounds, although not in a TtgW-deficient background, expression of the ttgGHI and ttgVW operons increased fourfold. This suggests that TtgV represses expression from the ttgG promoters and controls its own. TtgW plays no major role in the regulation of expression of these promoters. Primer extension revealed that the divergent ttgG and ttgV promoters overlap, and mobility shift assays indicated that TtgV binds to this region with high affinity. DNaseI footprint assays revealed that TtgV protected four DNA helical turns that include the −10 and −35 boxes of the ttgV and ttgG promoters.


1968 ◽  
Vol 64 (1) ◽  
pp. 81-86 ◽  
Author(s):  
MASAHIKO KODAMA ◽  
YUSAKU TAGASHIRA ◽  
CHIKAYOSHI NAGATA

2019 ◽  
Vol 246 ◽  
pp. 678-687 ◽  
Author(s):  
Sarah McCarrick ◽  
Virginia Cunha ◽  
Ondřej Zapletal ◽  
Jan Vondráček ◽  
Kristian Dreij

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