Evidence map›Paper›PMID 40950286›Full record

ArticleAmerican journal of translational research2025

NLBK alleviates airway remodeling in COPD by inhibiting RXRA-mediated transcription of PLA2G2A.

Teng Zhang, Fang Fang, Dan Wu, Guodong Wang

Abstract read
In one paragraph

Article in American journal of translational research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Teng ZhangAffiliated Mental Health Center & Hangzhou Seventh People's Hospital, Zhejiang University School of Medicine Hangzhou, Zhejiang, P. R. China.
Fang FangHangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University Hangzhou, Zhejiang, P. R. China.
Dan WuHangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University Hangzhou, Zhejiang, P. R. China.
Guodong WangHangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University Hangzhou, Zhejiang, P. R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesNourishing lung benefiting kidney granule (NLBK) is used to treat chronic obstructive pulmonary disease (COPD). However, the molecular mechanism underlying its therapeutic effect is still unclear. In this study, we elucidated the molecular mechanism by which NLBK alleviates airway reorganization in COPD.

methodsWe investigated the function of NLBK in regulating inflammatory reactions and endoplasmic reticulum stress (ERS) in mice with COPD. Through bioinformatics and network pharmacology analysis, we identified the main components and targets: Zhebeiresinol-nuclear receptors such as Retinol X receptor A (RXRA) and Phospholipase A2, group IIA (PLA2G2A). A rescue experiment was performed to confirm the relationship between Zhebeiresinol and PLA2G2A in alleviating COPD symptoms. Moreover, by conducting a series of experiments, we determined the transcriptional regulation of RXRA on PLA2G2A.

resultsNLBK significantly inhibited cigarette smoke exposure-induced inflammatory response, lung function injury, and ERS in COPD mice. Zhebeiresinol acted as an active ingredient of NLBK, which was found to mitigate the inflammatory response, lung function injury, and ERS in COPD mice through the silencing of PLA2G2A, the specific target of NLBK. Zhebeiresinol repressed the phosphorylation of RXRA and entry into the nucleus, which efficiently suppressed the transcription of PLA2G2A.

conclusionsNLBK can alleviate airway remodeling in COPD through the RXRA-PLA2G2A axis, providing a new mechanistic basis for the clinical application of NLBK.

Indexed as

Chronic obstructive pulmonary disease (COPD)phospholipase A2 group IIA (PLA2G2A)retinol X receptor A (RXRA)yangfei yishen granule (NLBK)zhebeiresinol

Identifiers

PMID40950286
PMCPMC12432733

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