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Methods to Evaluate Cytotoxicity and Immunosuppression of Combustible Tobacco Product Preparations
Published on: January 10, 2015
A global toxicogenomic analysis investigating the mechanistic differences between tobacco and marijuana smoke
Rebecca M Maertens1, Paul A White, Andrew Williams
1Environmental Health Science and Research Bureau, Healthy Environments and Consumer Safety Branch, Health Canada, Ottawa, ON, Canada. rebecca.maertens@hc-sc.gc.ca
Abstract:
Like tobacco smoking, habitual marijuana smoking causes numerous adverse pulmonary effects. However, the mechanisms of action involved, especially as compared to tobacco smoke, are still unclear. To uncover putative modes of action, this study employed a toxicogenomics approach to compare the toxicological pathways perturbed following exposure to marijuana and tobacco smoke condensate in vitro. Condensates of mainstream smoke from hand-rolled tobacco and marijuana cigarettes were similarly prepared using identical smoking conditions. Murine lung epithelial cells were exposed to low, medium and high concentrations of the smoke condensates for 6h. RNA was extracted immediately or after a 4h recovery period and hybridized to mouse whole genome microarrays. Tobacco smoke condensate (TSC) exposure was associated with changes in xenobiotic metabolism, oxidative stress, inflammation, and DNA damage response. These same pathways were also significantly affected following marijuana smoke condensate (MSC) exposure. Although the effects of the condensates were largely similar, dose-response analysis indicates that the MSC is substantially more potent than TSC. In addition, steroid biosynthesis, apoptosis, and inflammation pathways were more significantly affected following MSC exposure, whereas M phase cell cycle pathways were more significantly affected following TSC exposure. MSC exposure also appeared to elicit more severe oxidative stress than TSC exposure, which may account for the greater cytotoxicity of MSC. This study shows that in general MSC impacts many of the same molecular processes as TSC. However, subtle pathway differences can provide insight into the differential toxicities of the two complex mixtures.
Insights
Habitual marijuana smoking causes adverse pulmonary effects, similar to tobacco smoking. This study reveals marijuana smoke condensate is more potent, impacting steroid biosynthesis and apoptosis pathways more significantly.
Area of Science:
- Pulmonary toxicology
- Molecular biology
- Toxicogenomics
Background:
- Habitual marijuana smoking, like tobacco smoking, leads to adverse pulmonary effects.
- The precise mechanisms underlying marijuana smoke's pulmonary toxicity, especially in comparison to tobacco smoke, remain largely unelucidated.
Purpose of the Study:
- To compare the toxicological pathways affected by marijuana smoke condensate (MSC) and tobacco smoke condensate (TSC) using a toxicogenomics approach.
- To elucidate the differential mechanisms of action between marijuana and tobacco smoke in pulmonary epithelial cells.
Main Methods:
- Preparation of condensates from hand-rolled marijuana and tobacco cigarettes under identical smoking conditions.
- In vitro exposure of murine lung epithelial cells to varying concentrations of MSC and TSC for 6 hours.
- RNA extraction and whole-genome microarray hybridization after immediate or delayed recovery periods.
Main Results:
- Both MSC and TSC exposure affected pathways including xenobiotic metabolism, oxidative stress, inflammation, and DNA damage response.
- MSC demonstrated greater potency than TSC, with more significant impacts on steroid biosynthesis, apoptosis, and inflammation pathways.
- MSC exposure induced more severe oxidative stress, correlating with higher cytotoxicity compared to TSC.
Conclusions:
- Marijuana smoke condensate impacts many molecular processes similarly to tobacco smoke condensate.
- Subtle differences in pathway perturbations, particularly MSC's potent effects on steroid biosynthesis and apoptosis, offer insights into differential pulmonary toxicities.
- MSC exhibits higher potency and cytotoxicity than TSC, likely due to more severe oxidative stress induction.
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