Evidence map›Paper›PMID 37551408›Full record

ArticleDrug design, development and therapy2023

Dispelling Dampness, Relieving Turbidity and Dredging Collaterals Decoction, Attenuates Potassium Oxonate-Induced Hyperuricemia in Rat Models.

Hai-Bo Liu, Min Yang, Wan Li, Ting Luo, Yang Wu, Xiang-Yu Huang, Yao-Lei Zhang, Tao Liu, Yong Luo

Abstract read
In one paragraph

Article in Drug design, development and therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
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  4. Frontiers in nutrition · 2025
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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

9 authors.

Hai-Bo Liu *Department of Biomedical Engineer, General Hospital of Western Theater Command, Chengdu, Sichuan, People's Republic of China.
Min Yang *Department of Traditional Chinese Medicine, General Hospital of Western Theater Command, Chengdu, Sichuan, People's Republic of China.
Wan LiDepartment of Traditional Chinese Medicine, General Hospital of Western Theater Command, Chengdu, Sichuan, People's Republic of China.
Ting LuoDepartment of Traditional Chinese Medicine, General Hospital of Western Theater Command, Chengdu, Sichuan, People's Republic of China.
Yang WuDepartment of Traditional Chinese Medicine, General Hospital of Western Theater Command, Chengdu, Sichuan, People's Republic of China.ORCID 0000-0002-9199-325X
Xiang-Yu HuangDepartment of Traditional Chinese Medicine, General Hospital of Western Theater Command, Chengdu, Sichuan, People's Republic of China.ORCID 0009-0005-0768-6863
Yao-Lei ZhangBasic Medical Laboratory, General Hospital of Western Theater Command, Chengdu, Sichuan, People's Republic of China.
Tao LiuDepartment of Traditional Chinese Medicine, General Hospital of Western Theater Command, Chengdu, Sichuan, People's Republic of China.
Yong Luo *Department of Traditional Chinese Medicine, General Hospital of Western Theater Command, Chengdu, Sichuan, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Dispelling dampness, relieving turbidity and dredging collaterals decoction (DED), is a traditional Chinese medicine used in the treatment of hyperuricemia. We aimed to explore the effect and mechanism of DED in the treatment of hyperuricemia. Methods: The effects of DED (9.48, 4.74, and 2.37 g/kg/d) on potassium oxonate (750 mg/kg/d)-induced hyperuricemia in rats were evaluated by serum uric acid (UA), creatinine (CRE), blood urea nitrogen (BUN), and renal pathological changes. Network pharmacology was used to identify the effective components and targets of DED, and the key targets and signaling pathways for its effects on hyperuricemia were screened. Molecular docking was used to predict the action of DED. H&E, immunohistochemistry, WB, and PCR were used to validate the network pharmacology results. Results: DED can effectively alleviate hyperuricemia, inhibit UA, CRE, BUN, and xanthine oxidase (XOD) activity, and reduce renal inflammatory cell infiltration and glomerular atrophy. The experiment identified 27 potential targets of DED for hyperuricemia, involving 9 components: wogonin, stigmasterol 3-O-beta-D-glucopyranoside, 3β-acetoxyatractylone, beta-sitosterol, stigmasterol, diosgenin, naringenin, astilbin, and quercetin. DED can relieve hyperuricemia mainly by inhibiting RAGE, HMGB1, IL17R, and phospho-TAK1, and by regulating the AGE-RAGE and IL-17 signaling pathways. Conclusion: DED can alleviate hyperuricemia by inhibiting XOD activity and suppressing renal cell apoptosis and inflammation via the AGE-RAGE signaling pathway and IL-17 signaling pathway. This study provides a theoretical basis for the clinical application of DED.

Indexed as

HyperuricemiaAnimalsInterleukin-17KidneyMolecular Docking SimulationOxonic AcidRatsUric AcidXanthine OxidaseInterleukin-17Oxonic Acidpotassium oxonateUric AcidXanthine Oxidasedispelling dampnessdredging collateralshyperuricemianetwork pharmacologyrelieving turbidity

Identifiers

PMID37551408
PMCPMC10404409

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.