Evidence map›Paper›PMID 30832523›Full record

ArticleThe Journal of international medical research2019

Modified Chuanhu anti-gout mixture, a traditional Chinese medicine, protects against potassium oxonate-induced hyperuricemia and renal dysfunction in mice.

Wenjun You, Jie Wang, Yaowu Zou, Kui Che, Xu Hou, Honghua Fei, Yangang Wang

Open access · goldAbstract read
In one paragraph

Article in The Journal of international medical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Research progress on microRNA in gout.Frontiers in pharmacology · 2022
    Review
  6. Review
  7. Review
  8. Investigation of the Effects and Mechanisms ofEvidence-based complementary and alternative medicine : eCAM · 2020
    Article
  9. 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

7 authors at 3 institutions in 1 country.

Wenjun You1 Department of Endocrinology, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Jie Wang1 Department of Endocrinology, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Yaowu Zou3 Department of Endocrinology, Heze Hospital of Traditional Chinese Medicine, Heze, Shandong, China.
Kui Che1 Department of Endocrinology, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Xu Hou1 Department of Endocrinology, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Honghua Fei4 Department of Endocrinology, Rizhao First People's Hospital, Rizhao, Shandong, China.
Yangang Wang1 Department of Endocrinology, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.ORCID https://orcid.org/0000-0002-5367-0425
Qingdao University · CNHeze Municipal Hospital · CNPeople’s Hospital of Rizhao · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAcute gout is a painful, inflammatory arthritis that features a rapidly escalating inflammatory response resulting from the formation of monosodium urate crystals in the affected joint space. Previously, we found that Chuanhu anti-gout mixture (CAGM) had similar effects as colchicine against gout in the clinic. Subsequently, to improve its effectiveness and efficacy, we modified the original formulation of CAGM. The current study evaluated the effectiveness of the modified formulation in mice.

methodsPotassium oxonate (PO) was used to establish a mouse model of hyperuricemia. Plasma levels of uric acid and creatine were determined using the respective test kits. Hepatic xanthine oxidase (XOD) expression was examined by enzyme-linked immunosorbent assay. To explore the underlying mechanism, renal urate transporter 1 (URAT1) mRNA levels were evaluated by quantitative real-time PCR. Allopurinol and benzbromarone were used as reference drugs.

resultsThe original CAGM and its modified high-dose formulation significantly reduced serum uric acid and creatine levels in hyperuricemic mice. In addition, the CAGM-treated groups displayed lower mRNA levels of hepatic XOD and renal URAT1.

conclusionsCAGM and its modified formulation significantly ameliorated PO-induced hyperuricemia in mice, which might be partially attributable to reductions of hepatic XOD and renal URAT1 levels.

Indexed as

AnimalsCreatinineDrugs, Chinese HerbalHyperuricemiaKidneyMaleMiceOrganic Anion TransportersOrganic Cation Transport ProteinsOxonic AcidProtective AgentsRNA, MessengerUric AcidXanthine OxidaseCreatinineDrugs, Chinese HerbalOrganic Anion TransportersOrganic Cation Transport ProteinsOxonic Acidpotassium oxonateProtective AgentsRNA, MessengerSLC22A12 protein, humanUric AcidXanthine OxidaseChuanhu anti-gout mixturehyperuricemiarenal dysfunctiontraditional Chinese medicineurate transporter 1xanthine oxidase

Identifiers

PMID30832523
PMCPMC6567774
OpenAlexW2919497976

What OpenQuestion holds

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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 OpenQuestion graph.