Electronic nicotine delivery systems (ENDS) are a rapidly growing global epidemic among adolescents and young adults. Unlike other ENDS such as e-cigarettes, e-hookahs are used through traditional water-pipes, allowing the vapor-containing nicotine, propylene glycol, glycerin, and flavorings-to pass through a water-filled basin, potentially altering the vapor, before it is inhaled through the user's mouth. Contributing to e-hookahs popularity is the belief that the flavored smoke is detoxified as it passes through the water-filled basin, rendering e-hookah a safer tobacco alternative. However, an e-hookahs deliver flavored nicotine by creating a vapor of fine particles and volatile organic compounds that could induce vascular toxicity. While e-hookah vaping acutely reduces endothelial function, the specific role of nicotine and the mechanisms by which it may impairs endothelial function remain understudied. The objective of this project is to investigate the specific role of nicotine in mediating the acute effects of e-hookah vaping on endothelial dysfunction.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
33
Participants will be invited to vape a 30-minute session of e-hookah containing nicotine
Participants will be invited to vape a 30-minute session of e-hookah without containing nicotine
University of California, Los Angeles
Los Angeles, California, United States
Flow-Mediated Dilation (FMD)
Using ultrasound, FMD of the brachial artery induced by reactive hyperemia, was used to measure endothelium-dependent vasodilator function. Outcome variable reflecting FMD (brachial artery diameter) was recorded for 45 seconds and resumed 30 seconds before cuff deflation and continuously for 2 minutes after deflation to obtain true peak vasodilatory response.
Time frame: Changes pre- and post- the 30-minute smoking or vaping exposure sessions
Acetylcholine-stimulated nitric oxide production
Human umbilical vein endothelial cells were cultured with subjects' serum sampled before and after the vaping sessions and acetylcholine-stimulated nitric oxide production was assessed
Time frame: Changes pre- and post- the 30-minute smoking or vaping exposure sessions
Basal reactive oxygen species bioactivity
Human umbilical vein endothelial cells were cultured with participants' serum sampled before and after the vaping sessions and basal reactive oxygen species bioactivity was assessed
Time frame: Changes pre- and post- the 30-minute smoking or vaping exposure sessions
Fibrinogen levels
Plasma fibrinogen
Time frame: Changes pre- and post- the 30-minute smoking or vaping exposure sessions
Heme oxygenase-1 assay
Heme oxygenase-1 concentration assay
Time frame: Changes pre- and post- the 30-minute smoking or vaping exposure sessions
paraoxonase-1 activity
paraoxonase-1 activity
Time frame: Changes pre- and post- the 30-minute smoking or vaping exposure sessions
HDL protection assay
HDL protection assay, reflecting the ability of HDL to inhibit oxidation to LDL
Time frame: Changes pre- and post- the 30-minute smoking or vaping exposure sessions
Nicotine levels
Plasma nicotine
Time frame: Changes pre- and post- the 30-minute smoking or vaping exposure sessions
Carbon monoxide levels
Exhaled carbon monoxide levels
Time frame: Changes pre- and post- the 30-minute smoking or vaping exposure sessions
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