# Toxic Effects of Ecigs Following Transition From Conventional Cigarettes

> **NIH NIH R01** · BAYLOR COLLEGE OF MEDICINE · 2020 · $447,532

## Abstract

The use of electronic cigarette (ecig), is gaining popularity among never and active smokers who are persuaded
by intense ad campaigns that brands their use as a healthy alternative to cigarette smoke. In addition to the well-
established noxious effects of cigarette smoke in the lungs, we have demonstrated that nano-sized carbon black
particles, generated by incomplete combustion of tobacco, activate antigen presenting cells and promotes
emphysema. Whether heated vaporized contents in ENDS (e.g. propylene glycol (PG), vegetable glycerol (VG)
with or without nicotine) is a safe alternative to cigarette smoking in active or former smokers, remains
unknown. We have developed a robust mouse model of conventional and electronic cigarette (ecig) exposure
and made several novel discoveries that provide unique insights into the toxicology of ecig in the lungs. We
have found that chronic inhalation of smoke, and ecig (with or without nicotine) elicits DNA adducts, and
results cellular changes in the lungs. Further, when mice are transitioned from cigarette smoke to ecig, there is a
significant suppression of lung innate mucosal immunity. In response to this RFA, we propose to use novel
toxicology approaches to identify biomarkers, as well as test cardiovascular and respiratory health effects of
ecig and its components to aid the FDA in formulating regulations applicable to the ENDS industry. To achieve
our goal, we have designed a preclinical model that closely simulates human behavior to explore how transition
from smoke to ecig could escalate their toxicity in the lungs. In addition, by tapping into an existing cohort of
smokers who participate in neurocognitive behavior studies at BCM, conduct ancillary studies to identify novel
biomarkers and determine whether ecig with and without nicotine alters innate immune function, and promote
serum cumulative inflammatory potentials. To accomplish our goal, we will examine lung DNA adducts,
metabolomics, lipidomics, and systemic innate immunity in mice exposed to chronic smoke and transitioned to
ecig. We will also examine the role of ecig with and without nicotine on systemic immunity and metabolomics
in human volunteers. We will test the following three specific aims: Aim 1: To examine the effects of
components of ecig in DNA adduct formation using a preclinical model of transition from chronic smoke
to ecig inhalation. Hypothesis: The ratio of PG/VG alters DNA adducts in the lungs. Aim 2: To identify toxic
cellular responses to ecig using a preclinical model of transition from chronic smoke to ecig inhalation.
Hypothesis: Chronic ecig exposure and/or transition to ecig in mice exposed to smoke alters endothelial and/or
immune cell responses. Aim 3: To identify toxic cellular responses to ecig using a cohort of active smokers
and ecig users. Hypothesis: Exposure to ecig alters endothelial and/or immune cell responses. Successful
completion of the proposed preclinical and human translational studies provides ...

## Key facts

- **NIH application ID:** 9982334
- **Project number:** 5R01ES029442-03
- **Recipient organization:** BAYLOR COLLEGE OF MEDICINE
- **Principal Investigator:** Farrah Kheradmand
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $447,532
- **Award type:** 5
- **Project period:** 2018-08-01 → 2023-07-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9982334

## Citation

> US National Institutes of Health, RePORTER application 9982334, Toxic Effects of Ecigs Following Transition From Conventional Cigarettes (5R01ES029442-03). Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/grant/nih/9982334. Licensed CC0.

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