grant

Systematic identification of cardiotoxic e-cigarette flavorants

Organization UNIVERSITY OF LOUISVILLELocation LOUISVILLE, UNITED STATESPosted 22 Apr 2022Deadline 31 Mar 2027
NIHUS FederalResearch GrantFY202521+ years oldAction PotentialsAcuteAdultAdult HumanAdverse effectsAerosolsAffectAldehydesArrhythmiaAssayBioassayBiologicalBiological AssayBlood SerumBody TissuesCancersCardiacCardiac ArrhythmiaCardiac ChronotropismCardiac Electrophysiologic TechniquesCardiac Electrophysiological DiagnosticsCardiac Muscle CellsCardiac MyocytesCardiac ToxicityCardiocyteCardiotoxicCardiotoxicityCardiovascularCardiovascular Body SystemCardiovascular Organ SystemCardiovascular PhysiologyCardiovascular systemCessation of lifeChemicalsChronicCirculationConsciousConsciousnessConsumptionCyclicityDataDeathDependenceDevicesDoseDysfunctionECGEKGElectrocardiogramElectrocardiographyElectronic cigaretteElectrophysiologyElectrophysiology (science)Emerging Tobacco ProductsEquilibriumEvaluationExposure toFemaleFlavorantFlavoringFlavoring AgentsFood AdditivesFunctional disorderFutureHeartHeart ArrhythmiasHeart Muscle CellsHeart RateHeart VascularHeart myocyteHeatingHumanIn VitroIncidenceIndividualIngestionInhalationInhalingKnowledgeLinkLong-Term EffectsLungLung Respiratory SystemMalignant NeoplasmsMalignant TumorMarketingMiceMice MammalsModelingModern ManMonitorMurineMusNegative FindingNeurophysiology / ElectrophysiologyNicotineOral IngestionOutcomePathologicPathway interactionsPerformancePeriodicityPhysiopathologyPoliciesPrevalencePropanediolsPropylene GlycolsRegulationResearch PriorityRhythmicityRiskSafetySerumSmokerSmokingSolventsStructureSumTestingTissuesToxic effectToxicitiesToxicologyToxinVentricularVentricular ArrhythmiaWorkYouthYouth 10-21adulthoodaerosolizedair filterbalancebalance functionbiologiccardiac electrophysiologycardiac functioncardiomyocytecardiovascular functioncirculatory systemclinical predictorse-cige-cig aerosolse-cig liquidse-cig usee-cig usere-cig vapore-cigarettee-cigarette aerosolse-cigarette liquidse-cigarette usee-cigarette usere-cigarette vapore-juicee-liquidecigecig aerosolsecig liquidsecig useecig userecig vaporecigaretteecigarette aerosolsecigarette liquidsecigarette useecigarette userecigarette vaporejuiceelectronic cigarette aerosolelectronic cigarette useelectronic cigarette userelectronic cigarette vaporelectronic liquidelectrophysiologicaleliquidexperimentexperimental researchexperimental studyexperimentsexposure to nicotinefunction of the heartheart cellheart electrophysiologyheart functionhigh riskin vivoingestmalemalignancymanufactureneoplasm/cancernicotine exposurepathophysiologypathwayrespiratoryresponsestemsudden cardiac deathtobacco productstobacco regulatory sciencevegetable glycerinyouth age
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Full Description

Abstract
The use of e-cigarettes (e-cigs) has increased substantially since they were first introduced in 2003. E-cig

devices aerosolize e-liquids that typically consist of humectants with variable levels of nicotine and flavoring

chemicals. Although there are thousands of commercially available flavor mixtures, they routinely overlap in

individual flavor chemicals (flavorants), which are far fewer in number. Many of these flavorants belong to

common chemical classes and are generally recognized as safe for ingestion. However, their direct and indirect

cardiac effects following heating and inhalation, particularly in combination with nicotine, remain mostly unknown.

Direct exposure to nicotine alone distinctly affects the cardiac action potential waveform, potentially contributing

to the high incidence of arrhythmias and sudden cardiac death among smokers. Recent evidence also suggests

that nicotine in e-cigs may similarly promote adverse cardiac outcomes. Yet, the influence of flavorants on the

cardiac effects of e-cig aerosols remains untested. In our ongoing work, we found that exposure to nicotine-

containing e-cig aerosols of various flavors acutely and differentially altered the electrocardiogram (ECG) in mice,

variably inducing QT interval prolongation, increasing heart rate, and evoking arrhythmia. As well, two separate

e-liquids with the same characterizing flavorant consistently increased ventricular arrhythmias. Furthermore, we

observed in cardiomyocytes that treatment with several flavorants common to e-cigs directly altered contractility,

rhythmicity, and action potential duration. Nonetheless, it remains unknown how individual flavorants in e-cig

aerosols exert direct or indirect cardiac effects in vivo. Considering the growing popularity of e-cigarettes and

the urgent need for studying the in vivo toxicological profile of constituents in these products, we propose to test

the hypothesis that e-cigarette flavorants modify the effects of e-cig aerosol exposures on cardiac

electrophysiology, leading to arrhythmias and functional remodeling of the heart. To test this, we will

systematically identify both acute and long-term effects of flavorant exposure on cardiac electrophysiology using

a combination of state-of-the-art in vivo, in vitro, and ex vivo approaches. Specifically, we will: 1) Identify the

acute effects of flavored e-cig aerosol inhalation on cardiac electrophysiology in vivo, 2) Examine the

direct impact of flavorants on cardiac electrophysiology in vitro and ex vivo, and, 3) Elucidate deleterious

impacts of acute and chronic flavorant aerosol exposure on cardiac electrophysiology, structure, and

function. These studies, which are responsive to the research priorities of the FDA/CTP, will provide new data

showing how different flavor chemicals affect cardiac excitability and potentially promote arrhythmogenesis.

Such results would aid in formulating policies regulating the manufacture, distribution and marketing of flavored

e-cigarettes.

Grant Number: 5R01HL163818-04
NIH Institute/Center: NIH

Principal Investigator: Alex Carll

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