# Hyperuricemia in ob/ob mice relates to hepatocellular pyruvate metabolism/ xanthine oxidase axis

**Authors:** Shan Zhang, Shasha Hu, Haibo Tan, Ertao Jia

PMC · DOI: 10.1371/journal.pone.0328794 · PLOS One · 2025-08-06

## TL;DR

This study shows that high uric acid in obese mice is linked to liver pyruvate metabolism and xanthine oxidase activity.

## Contribution

The study identifies a novel link between hyperuricemia in obesity and the hepatocellular pyruvate metabolism/xanthine oxidase pathway.

## Key findings

- Ob/ob mice show elevated serum uric acid and xanthine oxidase activity.
- Hepatocellular xanthine oxidase activity in hyperlipidemia is associated with pyruvate metabolism.
- Pyruvate dehydrogenase levels are reduced in hyperlipidemic hepatocytes.

## Abstract

The study aimed to examine the association between obesity and hyperuricemia in ob/ob mice.

An animal model of obesity was developed using male ob/ob mice. Biochemical parameter test kits were used to measure serum uric acid (UA), hepatic xanthine oxidase (XOD) activity, serum creatinine (Scr), serum lipid profiles, and blood urea nitrogen (BUN). Then, liver tissues were collected for hematoxylin and eosin (H&E) staining, flow cytometry, and western blot (WB) analysis. Furthermore, Huh-7 cells were co-cultured with THP-1 macrophages for 24 hours, with or without LPS + IFN-γ or PA, and subsequently analyzed for XOD activity. In addition, the Huh-7 cells stimulated with PA were analyzed by metabolomics and validated by WB and RT-qPCR.

Levels of Serum lipid profiles, UA, and XOD activity are elevated in ob/ob mice. In ob/ob mice, liver M1 macrophage polarization is markedly enhanced. In vitro studies show that elevated XOD activity in hepatocytes during hyperlipidemia does not correlate with M1 macrophage polarization. Metabolomics showed that the XOD activity of hepatocytes in hyperlipidemia may be related to pyruvate metabolism. Moreover, the protein and mRNA levels of pyruvate dehydrogenase (PDH), an enzyme that limits pyruvate accumulation, were significantly down-regulated in Huh-7 cells with PA stimulation.

Hyperuricemia in ob/ob mice relates to hepatocellular pyruvate metabolism/ xanthine oxidase axis.

## Linked entities

- **Diseases:** obesity (MONDO:0011122), hyperuricemia (MONDO:0002144)

## Full-text entities

- **Genes:** Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, Lep (leptin) [NCBI Gene 16846] {aka ob, obese}, Xdh (xanthine dehydrogenase) [NCBI Gene 22436] {aka XO, Xor, Xox-1, Xox1}
- **Diseases:** hyperlipidemia (MESH:D006949), obesity (MESH:D009765), Hyperuricemia (MESH:D033461)
- **Chemicals:** PA (MESH:D011478), LPS (MESH:D008070), lipid (MESH:D008055), eosin (MESH:D004801), pyruvate (MESH:D019289), creatinine (MESH:D003404), H&amp;E (-), UA (MESH:D014527), hematoxylin (MESH:D006416)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** THP-1 — Homo sapiens (Human), Childhood acute monocytic leukemia, Cancer cell line (CVCL_0006), ob — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_S603), Huh-7 — Homo sapiens (Human), Adult hepatocellular carcinoma, Cancer cell line (CVCL_0336)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12327685/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12327685/full.md

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Source: https://tomesphere.com/paper/PMC12327685