Evidence map›Paper›PMID 36147321›Full record

ArticleFrontiers in pharmacology2022

Jian-Ti-Kang-Yi decoction alleviates poly(I:C)-induced pneumonia by inhibiting inflammatory response, reducing oxidative stress, and modulating host metabolism.

Huantian Cui, Yuming Wang, Bolun Yu, Yulin Wu, Gaijun Zhang, Junli Guo, Junyu Luo, Qin Li, Xiaojuan Li, Wenju He and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

13 authors at 9 institutions in 1 country.

Huantian CuiShandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, China.
Yuming WangGraduate School, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Bolun YuGraduate School, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Yulin WuTianjin Medical University Cancer Institute and Hospital, Tianjin, China.
Gaijun ZhangGraduate School, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Junli GuoHebei Hospital of Traditional Chinese Medicine, Hebei, China.
Junyu LuoYunnan Provincial Hospital of Chinese Medicine, Kunming, Yunnan, China.
Qin LiYunnan Provincial Hospital of Chinese Medicine, Kunming, Yunnan, China.
Xiaojuan LiJiaxing Hospital of Traditional Chinese Medicine, Jiaxing, Zhejiang, China.
Wenju HeTianjin First Central Hospital, Tianjin, China.
Weibo WenYunnan Provincial Hospital of Chinese Medicine, Kunming, Yunnan, China.
Jiabao LiaoJiaxing Hospital of Traditional Chinese Medicine, Jiaxing, Zhejiang, China.
Dongqiang WangTianjin First Central Hospital, Tianjin, China.
Tianjin University of Traditional Chinese Medicine · CNFirst Hospital of Jiaxing · CNYunnan Provincial Hospital of Traditional Chinese Medicine · CNHospital of Hebei Province · CNShandong University · CNTianjin First Center Hospital · CNTianjin Medical University · CNTianjin Medical University Cancer Institute and Hospital · CNYunnan University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Jian-Ti-Kang-Yi decoction (JTKY) is widely used in the treatment of COVID-19. However, the protective mechanisms of JTKY against pneumonia remain unknown. In this study, polyinosinic-polycytidylic acid (poly(I:C)), a mimic of viral dsRNA, was used to induce pneumonia in mice; the therapeutic effects of JTKY on poly(I:C)-induced pneumonia model mice were evaluated. In addition, the anti-inflammatory and anti-oxidative potentials of JTKY were also investigated. Lastly, the metabolic regulatory effects of JTKY in poly(I:C)-induced pneumonia model mice were studied using untargeted metabolomics. Our results showed that JTKY treatment decreased the wet-to-dry ratio in the lung tissue, total protein concentration, and total cell count of the bronchoalveolar lavage fluid (BALF). Hematoxylin and Eosin (HE) and Masson staining indicated that the JTKY treatment alleviated the pathological changes and decreased the fibrotic contents in the lungs. JTKY treatment also decreased the expression of pro-inflammatory cytokines [interleukin (IL)-1β, IL-6, and tumor necrosis factor-alpha (TNF-α)] and increased the levels of immunomodulatory cytokines (IL-4 and IL-10) in the BALF and serum. Flow cytometry analysis showed that the JTKY treatment lowered the ratio of CD86

Indexed as

antiinflammatory effectanti-oxidative effectJian-Ti-Kang-Yi decoctionpoly(I:C)-induced pneumoniauntargeted metabolomics

Identifiers

PMID36147321
PMCPMC9486163
OpenAlexW4294741483

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.