4.5 Article

Vascular endothelial function is impaired by aerosol from a single IQOS HeatStick to the same extent as by cigarette smoke

期刊

TOBACCO CONTROL
卷 27, 期 -, 页码 S13-S19

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/tobaccocontrol-2018-054325

关键词

non-cigarette tobacco products; electronic nicotine delivery devices; harm reduction; nicotine; smoking caused disease

资金

  1. National Heart, Lung, and Blood Institute at the National Institutes of Health (NIH) [R01HL120062]
  2. US Food and Drug Administration Center for Tobacco Products (FDA CTP)
  3. California Tobacco-Related Disease Research Program [25IR-0030]
  4. National Cancer Institute at the NIH [P50CA180890]
  5. National Institute on Drug Abuse at the NIH [P30 DA012393]
  6. FDA CTP [P50CA180890]

向作者/读者索取更多资源

Background Heated tobacco products (also called 'heat-not-burn' products) heat tobacco at temperatures below that of combustion, causing nicotine and other compounds to aerosolise. One such product, IQOS from Philip Morris International, is being marketed internationally with claims of harm reduction. We sought to determine whether exposure to IQOS aerosol impairs arterial flow-mediated dilation (FMD), a measure of vascular endothelial function that is impaired by tobacco smoke. Methods We exposed anaesthetised rats (n=8/group) via nose cone to IQOS aerosol from single HeatSticks, mainstream smoke from single Marlboro Red cigarettes or clean air for a series of consecutive 30 s cycles over 1.5-5 min. Each cycle consisted of 15 or 5 s of exposure followed by removal from the nose cone. We measured pre-exposure and postexposure FMD, and postexposure serum nicotine and cotinine. Results FMD was impaired comparably by ten 15 s exposures and ten 5 s exposures to IQOS aerosol and to cigarette smoke, but not by clean air. Serum nicotine levels were similar to plasma levels after humans have smoked one cigarette, confirming that exposure conditions had real-world relevance. Postexposure nicotine levels were similar to 4.5-fold higher in rats exposed to IQOS than to cigarettes, despite nicotine being measured in the IQOS aerosol at similar to 63% the amount measured in smoke. When IQOS exposure was briefer, leading to comparable serum nicotine levels to the cigarette group, FMD was still comparably impaired. Conclusions Acute exposures to IQOS aerosol impairs FMD in rats. IQOS use does not necessarily avoid the adverse cardiovascular effects of smoking cigarettes.

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