Evidence map›Paper›PMID 41555772›Full record

ArticleAnimal models and experimental medicine2026

Establishment of a novel cynomolgus monkey model of hyperuricemia.

Ji-Wei Wang, Le Zhang, Can Yang, Guan-Cong Luo, Rui-Chang Liu, Yan-Jun Xu, Sheng Cheng, Wen-Yu Jiang, Richard Ward, Yang Yang and 3 more

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Article in Animal models and experimental medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

13 authors.

Ji-Wei WangDepartment of Pharmaceutical Engineering, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China.ORCID 0000-0001-9469-8881
Le ZhangDepartment of Pharmaceutical Engineering, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China.
Can YangDepartment of Pharmaceutical Engineering, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China.
Guan-Cong LuoDepartment of Pharmaceutical Engineering, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China.
Rui-Chang LiuDepartment of Pharmaceutical Engineering, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China.
Yan-Jun XuDepartment of Pharmaceutical Engineering, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China.
Sheng ChengDepartment of Pharmaceutical Engineering, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China.
Wen-Yu JiangDepartment of Pharmaceutical Engineering, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China.
Richard WardCentre for Translational Pharmacology, Institute of Molecular Cell and Systems Biology, College of Medicine, University of Glasgow, Glasgow, UK.
Yang YangDepartment of Pharmaceutical Engineering, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China.
Cheng XiangDepartment of Pharmaceutical Engineering, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China.
Shu AnDepartment of Pharmaceutical Engineering, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China.
Tian-Rui XuDepartment of Pharmaceutical Engineering, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China.

Funding

Major Science and Technology Project of Yunnan Province (Grant No. 202202AG050008)National Natural Science Foundation of China 32 160 157National Natural Science Foundation of China 82 160 564The Yunnan "Xingdian Talent Program" Yunling Scholar Project, (Grant No. CA24129L025A)
6 · The paper itself

Abstract

backgroundChronic hyperuricemia is associated with complications such as gout and uric acid nephropathy, but uric acid also exhibits biological activities (e.g., antioxidant effects, potential neuroprotective properties against neurodegenerative diseases). Nonhuman primates are ideal models for studying neurodegenerative diseases; however, existing nonhuman primate hyperuricemia models cannot sustain long-term elevated serum uric acid levels, nor recapitulate the impaired uric acid excretion observed in clinical hyperuricemic patients.

methodsFirst, we detected uricase expression in cynomolgus monkeys and compared it with that in mice. Then, we established a cynomolgus monkey hyperuricemia model by administering a mixture of potassium oxonate, hydrochlorothiazide, and adenine via fruits and vegetables. We further analyzed the regulatory effects of this model on uric acid metabolism (synthesis, degradation, and excretion) and the expression of uric acid transporter genes in the intestine and kidney.

resultsCynomolgus monkeys express functional uricase, but at a lower level than mice. The established model maintained stable, long-term hyperuricemia by three mechanisms: increasing intestinal and renal uric acid excretion load, inhibiting hepatic uric acid degradation, and promoting uric acid synthesis. Additionally, the model downregulated the expression of intestinal/renal uric acid-secreting transporter genes, while upregulating uric acid-reabsorbing transporter genes.

conclusionsThis novel cynomolgus monkey hyperuricemia model provides a new tool for investigating the association between hyperuricemia and neurodegenerative diseases, and will help clarify the mechanism by which serum uric acid influences cognitive function.

Indexed as

Disease Models, AnimalHyperuricemiaMacaca fascicularisAdenineAnimalsHydrochlorothiazideKidneyMaleMiceOxonic AcidUrate OxidaseUric AcidAdenineHydrochlorothiazideOxonic Acidpotassium oxonateUrate OxidaseUric Aciddisease modelhyperuricemianonhuman primateuricase

Identifiers

PMID41555772
PMCPMC13042960

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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.