Evidence map›Paper›PMID 37362920›Full record

ArticleFrontiers in microbiology2023

Qing-Kai-Ling oral liquid alleviated pneumonia via regulation of intestinal flora and metabolites in rats.

Hongying Chen, Siju Li, Biyan Pan, Kun Liu, Hansheng Yu, Chong Ma, Huiyuan Qi, Yuefeng Zhang, Xinyi Huang, Dongsheng Ouyang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Hongying Chen *Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Siju Li *School of Pharmaceutical Sciences, Sun Yat-sen University, Shenzhen, China.
Biyan PanGuangzhou Baiyunshan Mingxing Pharmaceutical Company Limited, Guangzhou, China.
Kun LiuSchool of Pharmaceutical Sciences, Sun Yat-sen University, Shenzhen, China.
Hansheng YuSchool of Pharmaceutical Sciences, Sun Yat-sen University, Shenzhen, China.
Chong MaSchool of Pharmaceutical Sciences, Sun Yat-sen University, Shenzhen, China.
Huiyuan QiSchool of Pharmaceutical Sciences, Sun Yat-sen University, Shenzhen, China.
Yuefeng ZhangSchool of Pharmaceutical Sciences, Sun Yat-sen University, Shenzhen, China.
Xinyi HuangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Dongsheng OuyangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Zhiyong XieSchool of Pharmaceutical Sciences, Sun Yat-sen University, Shenzhen, China.
Sun Yat-sen University · CNPharmacoGenetics (China) · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Qing-Kai-Ling (QKL) oral liquid, evolving from a classical Chinese formula known as An-Gong-Niu-Huang pills, is a well-established treatment for pneumonia with its mechanism remaining muddled. Studies have shown that the regulation of both intestinal flora and host-microbiota co-metabolism may contribute to preventing and treating pneumonia. The study aimed to investigate the potential mechanism by which QKL alleviates pneumonia from the perspective of 'microbiota-metabolites-host' interaction. Methods: We evaluated the therapeutic effects of QKL on lipopolysaccharide (LPS)-induced pneumonia rats. To explore the protective mechanism of QKL treatment, a multi-omics analysis that included 16S rDNA sequencing for disclosing the key intestinal flora, the fecal metabolome to discover the differential metabolites, and whole transcriptome sequencing of lung tissue to obtain the differentially expressed genes was carried out. Then, a Spearman correlation was employed to investigate the association between the intestinal flora, the fecal metabolome and inflammation-related indices. Results: The study demonstrated that pneumonia symptoms were significantly attenuated in QKL-treated rats, including decreased TNF-α, NO levels and increased SOD level. Furthermore, QKL was effective in alleviating pneumonia and provided protection equivalent to that of the positive drug dexamethasone. Compared with the Model group, QKL treatment significantly increased the richness and αlpha diversity of intestinal flora, and restored multiple intestinal genera (e.g., Conclusion: Our findings indicated that QKL could potentially modulate intestinal flora dysbiosis, improve host-microbiota co-metabolism dysregulation and regulate gene expression in the lungs, thereby mitigating LPS-induced pneumonia in rats. The study may provide new ideas for the clinical application and further development of QKL.

Indexed as

intestinal florametabolomemulti-omicspneumoniaQing-Kai-Lingtranscriptome

Identifiers

PMID37362920
PMCPMC10288885
OpenAlexW4380089786

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.