# Botanical formulation HX110B ameliorates PPE-induced emphysema in mice via regulation of PPAR/RXR signaling pathway

**Authors:** Soojin Lee, Chang Hyung Lee, Jungkyu Lee, Yoonseon Jeong, Jong-Hyung Park, In-Jeong Nam, Doo Suk Lee, Hyun Myung Lee, Soo-Yeon Ahn, Eujung Kim, Seungyeon Jeong, Seung-Shin Yu, Wonwoo Lee

PMC · DOI: 10.1371/journal.pone.0305911 · PLOS ONE · 2024-07-25

## TL;DR

A botanical formulation called HX110B helps treat emphysema in mice by reducing inflammation and activating a key signaling pathway.

## Contribution

HX110B is shown to ameliorate PPE-induced emphysema via PPAR/RXR signaling, offering a novel therapeutic approach for COPD.

## Key findings

- HX110B improved alveolar wall and air space damage in emphysema mouse models.
- HX110B reduced pro-inflammatory mediators and increased lung protective factors.
- HX110B activates the PPAR-RXR signaling pathway in vitro.

## Abstract

Chronic obstructive pulmonary disease (COPD), an inflammatory lung disease, causes approximately 3 million deaths each year; however, its pathological mechanisms are not fully understood. In this study, we examined whether HX110B, a mixture of Taraxacum officinale, Dioscorea batatas, and Schizonepeta tenuifolia extracts, could suppress porcine pancreatic elastase (PPE)-induced emphysema in mice and its mechanism of action. The therapeutic efficacy of HX110B was tested using a PPE-induced emphysema mouse model and human bronchial epithelial cell line BEAS-2B. In vivo data showed that the alveolar wall and air space expansion damaged by PPE were improved by HX110B administration. HX110B also effectively suppresses the expression levels of pro-inflammatory mediators including IL-6, IL-1β, MIP-2, and iNOS, while stimulating the expression of lung protective factors such as IL-10, CC16, SP-D, and sRAGE. Moreover, HX110B improved the impaired OXPHOS subunit gene expression. In vitro analysis revealed that HX110B exerted its effects by activating the PPAR-RXR signaling pathways. Overall, our data demonstrated that HX110B could be a promising therapeutic option for COPD treatment.

## Linked entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569], IL1B (interleukin 1 beta) [NCBI Gene 3553], CXCL2 (C-X-C motif chemokine ligand 2) [NCBI Gene 2920], NOS2 (nitric oxide synthase 2) [NCBI Gene 4843], IL10 (interleukin 10) [NCBI Gene 3586], SCGB1A1 (secretoglobin family 1A member 1) [NCBI Gene 7356], HOXD13 (homeobox D13) [NCBI Gene 3239], AGER (advanced glycosylation end-product specific receptor) [NCBI Gene 177]
- **Diseases:** emphysema (MONDO:0004849), chronic obstructive pulmonary disease (MONDO:0005002), COPD (MONDO:0005002)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** SCGB1A1 (secretoglobin family 1A member 1) [NCBI Gene 7356] {aka CC10, CC16, CCPBP, CCSP, UGB, UP-1}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Cxcl2 (C-X-C motif chemokine ligand 2) [NCBI Gene 20310] {aka CINC-2a, GROb, Gro2, MIP-2, MIP-2a, Mgsa-b}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Nos2 (nitric oxide synthase 2, inducible) [NCBI Gene 18126] {aka MAC-NOS, NOS-II, Nos-2, Nos2a, i-NOS, iNOS}, SFTPD (surfactant protein D) [NCBI Gene 6441] {aka COLEC7, PSP-D, SFTP4, SP-D}, Ppara (peroxisome proliferator activated receptor alpha) [NCBI Gene 19013] {aka 4933429D07Rik, Nr1c1, PPAR-alpha, PPARalpha, Ppar}
- **Diseases:** COPD (MESH:D029424), inflammatory (MESH:D007249), deaths (MESH:D003643), emphysema (MESH:D004646), inflammatory lung disease (MESH:D008171)
- **Chemicals:** HX110B (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Taraxacum officinale (dandelion, species) [taxon 50225], Dioscorea polystachya (Chinese yam, species) [taxon 55575], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** BEAS-2B. — Homo sapiens (Human), Transformed cell line (CVCL_0168)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11271920/full.md

## References

112 references — full list in the complete paper: https://tomesphere.com/paper/PMC11271920/full.md

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Source: https://tomesphere.com/paper/PMC11271920