# Comparative Assessment of Acute Pulmonary Effects Induced by Heat-Not-Burn Tobacco Aerosol Inhalation in a Murine Model

**Authors:** Beong Ki Kim, Won Jin Yang, Ye Seul Seong, Yong Jun Choi, Hye Jung Park, Min Kwang Byun, Yoon Soo Chang, Jae Hwa Cho, Chi Young Kim

PMC · DOI: 10.3390/ijms26031135 · 2025-01-28

## TL;DR

This study compares the lung effects of heat-not-burn tobacco and traditional cigarettes in mice, finding changes in blood proteins that suggest nicotine-related immune activation.

## Contribution

The study identifies specific proteins linked to HnB smoke exposure and provides insights into nicotine's impact on immune pathways.

## Key findings

- Exposure to HnB smoke increased levels of proteins like Ccl20, Cxcl1, and Pdgfb in mice.
- Protein expression profiles differed between HnB and traditional cigarette smoke exposure.
- The findings suggest nicotine pathways are activated by HnB smoke exposure.

## Abstract

Tobacco smoking remains a major global health concern, causing preventable deaths and economic strain. Although new tobacco products such as heat-not-burn (HnB) are safer alternatives to traditional cigarettes, research on their associated risks remains limited. This study aimed to investigate the effects of HnB smoke exposure on the lungs compared to those of traditional cigarettes and the combined use of HnB and cigarettes using experiments with a mouse model. We quantitatively analyzed changes in the levels of 92 blood plasma proteins using the proximity extension assay method and observed significant changes in their levels in mice exposed to different smoke conditions; specifically, the levels of certain proteins, including Ccl20, Cxcl1, and Pdgfb, increased in the HnB smoke-exposed group, suggesting activation of nicotine pathways. Comparative analysis with traditional cigarette smoke-exposed mice further highlighted similarities and differences in their protein expression profiles. This study contributes to an improved understanding of the biological mechanisms underlying the harmful effects of alternative nicotine delivery systems and identifies potential biomarkers associated with the harmful effects of HnB smoke exposure. However, the precise impact of nicotine on the immune system may be influenced by various factors, necessitating further research.

## Linked entities

- **Genes:** CCL20 (C-C motif chemokine ligand 20) [NCBI Gene 6364], CXCL1 (C-X-C motif chemokine ligand 1) [NCBI Gene 2919], PDGFB (platelet derived growth factor subunit B) [NCBI Gene 5155]
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Ccl20 (C-C motif chemokine ligand 20) [NCBI Gene 20297] {aka CKb4, LARC, MIP-3A, MIP-3[a], MIP3A, ST38}, Pdgfb (platelet derived growth factor subunit B) [NCBI Gene 18591] {aka PDGF-2, PDGF-B, Sis, c-sis}, Cxcl1 (C-X-C motif chemokine ligand 1) [NCBI Gene 14825] {aka Fsp, Gro1, KC, Mgsa, N51, Scyb1}
- **Diseases:** smoking (MESH:D015208), Pulmonary (MESH:D008171), deaths (MESH:D003643)
- **Species:** Nicotiana tabacum (American tobacco, species) [taxon 4097], Mus musculus (house mouse, species) [taxon 10090]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11817633/full.md

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Source: https://tomesphere.com/paper/PMC11817633