Evidence map›Paper›PMID 28302963›Full record

ArticleExperimental animals2017

Potassium oxonate induces acute hyperuricemia in the tree shrew (tupaia belangeri chinensis).

Dong-Hong Tang, You-Song Ye, Chen-Yun Wang, Zhe-Li Li, Hong Zheng, Kai-Li Ma

Open access · diamondAbstract read
In one paragraph

Article in Experimental animals, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

16 citing papers in PubMed, 35 citations in OpenAlex.

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  10. Acute oral toxicity assessment and anti-hyperuricemic activity ofSaudi journal of biological sciences · 2022
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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

6 authors at 2 institutions in 1 country.

Dong-Hong TangMedical Primate Research Center of China, Institute of Medical Biology, Chinese Academy of Medical Sciences/Peking Union Medical College, No. 935, Jiaoling Road, Kunming, Yunnan 650118, P.R. China.
You-Song YeMedical Primate Research Center of China, Institute of Medical Biology, Chinese Academy of Medical Sciences/Peking Union Medical College, No. 935, Jiaoling Road, Kunming, Yunnan 650118, P.R. China.
Chen-Yun WangMedical Primate Research Center of China, Institute of Medical Biology, Chinese Academy of Medical Sciences/Peking Union Medical College, No. 935, Jiaoling Road, Kunming, Yunnan 650118, P.R. China.
Zhe-Li LiMedical Primate Research Center of China, Institute of Medical Biology, Chinese Academy of Medical Sciences/Peking Union Medical College, No. 935, Jiaoling Road, Kunming, Yunnan 650118, P.R. China.
Hong ZhengKunming Medical University, 1168 West Chunrong Road, Yuhua Avenue, Chenggong District, Kunming, Yunnan 650504, P.R. China.
Kai-Li MaMedical Primate Research Center of China, Institute of Medical Biology, Chinese Academy of Medical Sciences/Peking Union Medical College, No. 935, Jiaoling Road, Kunming, Yunnan 650118, P.R. China.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNKunming Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Potassium oxonate, a selectively competitive uricase inhibitor, produced hyperuricemia (HUA) in rodents in a previous study. In this study, we employed the tree shrew as an animal model to study potassium oxonate-induced HUA. The effect of allopurinol (ALLO), a uric acid reducer, was also examined in this model. Potassium oxonate at doses of 5, 20, 40, 60, 80, 100, and 1,000 mg/kg was given intraperitoneally to tree shrews. The results showed that potassium oxonate can effectively increase the levels of uric acid in tree shrews at doses ranging from 40 to 100 mg/kg. Semiquantitative RT-PCR showed that the xanthine dehydrogenase/oxidase (XDH/XO) mRNA expression level was significantly higher in the liver tissue of tree shrews with high levels of uric acid. There were no changes in serum urea nitrogen, or serum creatinine values. ALLO can significantly decrease serum uric acid levels (P<0.01) and raise XDH/XO mRNA expression levels in the liver tissue of tree shrews with HUA. XDH/XO mRNA expression levels did not change in untreated tree shrews. Studies on acute toxicity in the tree shrew did not show any significantly abnormal signs. There were no adverse effects at the macroscopic level up to doses ≤100 mg/kg. Potassium oxonate induced acute HUA in tree shrews at lower doses compared with other animal models. Potassium oxonate-treated tree shrews may be a potential animal model for studying pathogenic mechanism and evaluating a new therapeutic agent for treatment of HUA in humans.

Indexed as

Disease Models, AnimalTupaiaAcute DiseaseAllopurinolAnimalsDose-Response Relationship, DrugEnzyme InhibitorsGene ExpressionHumansHyperuricemiaInjections, IntraperitonealLiverOxonic AcidRNA, MessengerUrate OxidaseUric AcidAllopurinolEnzyme InhibitorsOxonic Acidpotassium oxonateRNA, MessengerUrate OxidaseUric AcidXanthine Dehydrogenaseallopurinolhyperuricemiapotassium oxonatetree shrewxanthine dehydrogenase/oxidase (XDH/XO)

Identifiers

PMID28302963
PMCPMC5543241
OpenAlexW2605970491

What OpenQuestion 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 OpenQuestion graph.