Key result
Heated tobacco extracts impair cardiomyocyte viability and beating rate less than combustible cigarettes.
Why the study?
The direct effects of heated tobacco products on cardiomyocytes remain unclear despite their increased use and perceived lower toxicity compared with combustible cigarettes.
Do nicotine- and tar-free cigarette smoke extracts from heated tobacco products reduce cell viability and spontaneous beating rate in cultured neonatal rat ventricular myocytes compared to combustible cigarettes?
Do nicotine- and tar-free cigarette smoke extracts from heated tobacco products reduce cell viability and spontaneous beating rate in cultured neonatal rat ventricular myocytes compared to combustible cigarettes?
Heated tobacco products exhibit direct cardiomyocyte toxicity similar to combustible cigarettes, raising concerns regarding their cardiac safety.
HTP extracts induce direct cardiomyocyte toxicity similar to combustible cigarettes; hypothesis-generating for product-specific mechanisms, with human relevance untested.
Smoking of combustible cigarettes is a risk factor for cardiovascular disease. Heated tobacco products (HTPs) have recently increased in use due to their perceived lower toxicity compared with combustible cigarettes, yet their direct effects on cardiomyocytes remain unclear. In the present study, we compared the effects of nicotine- and tar-free cigarette smoke extracts (CSE) from two HTPs (‘HTP-1’ and ‘HTP-2’) and a combustible reference cigarette (RF) on cultured neonatal rat ventricular myocyte. All CSEs reduced cell viability and the spontaneous beating rate, with toxicity ranked as RF > HTP-2 > HTP-1. HTP-2 and RF also induced intracellular Ca 2+ -overload, contractile dysfunction, and mitochondrial reactive oxygen species production, whereas HTP-1 did not. Mitochondrial respiration and ATP production were suppressed by all CSEs, while glycolysis was upregulated only by HTP-2 and RF, indicating different metabolic alterations. Acrolein, a shared toxicant in all products, also reduced cell viability, suggesting its involvement in CSE-induced cardiotoxicity. In summary, we revealed that HTPs, like combustible cigarettes, exhibit direct cardiomyocyte toxicity, but the underlying mechanisms appear to differ between different cigarette products with regard to abnormal Ca 2+ regulation and metabolic inhibition. These findings raise concern regarding the cardiac safety of HTPs.
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Yasuda et al. (2025) studied Cultured neonatal rat ventricular myocytes. Cigarette smoke extracts from heated tobacco products (HTP-1 and HTP-2) vs. Combustible reference cigarette (RF) was evaluated on Cell viability and spontaneous beating rate. Cigarette smoke extracts from heated tobacco products reduced cell viability and spontaneous beating rate in cultured cardiomyocytes, with toxicity ranked as combustible cigarettes > HTP-2 > HTP-1.
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