Evidence map›Paper›PMID 36960871›Full record

ArticleMolecular medicine reports2023

Mechanism of dioscin ameliorating renal fibrosis through NF‑κB signaling pathway‑mediated inflammatory response.

Yang Wang, Peng Liu, Guijie Ma, Chenguang Wu, Wenhui Zhu, Pengce Sun, Wenya Lu, Xinyu Yang, Yilun Zhang, Na Liu and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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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 4 institutions in 1 country.

Yang Wang *Renal Division, Department of Medicine, Heilongjiang Academy of Chinese Medicine Sciences, Harbin, Heilongjiang 150036, P.R. China.
Peng Liu *Shunyi Hospital, Beijing Hospital of Traditional Chinese Medicine, Shunyi, Beijing 101300, P.R. China.
Guijie MaRenal Division, Department of Medicine, Heilongjiang Academy of Chinese Medicine Sciences, Harbin, Heilongjiang 150036, P.R. China.
Chenguang WuRenal Division, Department of Medicine, Heilongjiang Academy of Chinese Medicine Sciences, Harbin, Heilongjiang 150036, P.R. China.
Wenhui ZhuRenal Division, Department of Medicine, Heilongjiang Academy of Chinese Medicine Sciences, Harbin, Heilongjiang 150036, P.R. China.
Pengce SunHeilongjiang University of Chinese Medicine, Harbin, Heilongjiang 150036, P.R. China.
Wenya LuRenal Division, Department of Medicine, Heilongjiang Academy of Chinese Medicine Sciences, Harbin, Heilongjiang 150036, P.R. China.
Xinyu YangRenal Division, Department of Medicine, Heilongjiang Academy of Chinese Medicine Sciences, Harbin, Heilongjiang 150036, P.R. China.
Yilun ZhangHeilongjiang University of Chinese Medicine, Harbin, Heilongjiang 150036, P.R. China.
Na LiuRenal Division, Department of Medicine, Heilongjiang Academy of Chinese Medicine Sciences, Harbin, Heilongjiang 150036, P.R. China.
Ping LiBeijing Key Lab for Immune‑Mediated Inflammatory Diseases, China‑Japan Friendship Hospital, Beijing 100029, P.R. China.
Heilongjiang Academy of Sciences · CNHeilongjiang University of Chinese Medicine · CNChina-Japan Friendship Hospital · CNShunyi Hospital of Beijing Traditional Chinese Medicine Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dioscin (DIS) is a natural compound derived from Chinese herbal medicine. In recent years, multiple studies have reported that DIS has immunoregulation, anti‑fibrosis, anti‑inflammation, anti‑viral and anti‑tumor effects. However, the mechanism by which DIS ameliorates renal fibrosis and inflammation remains to be elucidated. The aim of the present study was to investigate the role of DIS in renal fibrosis and inflammation and to explore its underlying mechanism. It used network pharmacology to predict the targets of DIS for the treatment of renal interstitial fibrosis. The present study was performed using unilateral ureteral obstruction mice and HK‑2 cells

Indexed as

Kidney DiseasesUreteral ObstructionAnimalsDiosgeninFibrosisInflammationKidneyMiceNF-kappa BNitrilesSignal TransductionSulfones3-(4-methylphenylsulfonyl)-2-propenenitriledioscinDiosgeninNF-kappa BNitrilesSulfonesdioscinNF‑κB p65 signaling pathwayrenal inflammationunilateral ureteral obstruction mice

Identifiers

PMID36960871
PMCPMC10073814
OpenAlexW4353080154

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.