Evidence map›Paper›PMID 40781882›Full record

ArticlePhysiological reports2025

Effects of pyruvate administration on mRNA expression of inflammatory cytokines in adipose tissue and whole-body glucose metabolism in male mice.

Taichi Ando, Reo Takeda, Ryotaro Kano, Tatsuya Kusano, Yudai Nonaka, Yutaka Kano, Daisuke Hoshino

Abstract read
In one paragraph

Article in Physiological reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Taichi AndoBioscience and Technology Program, Department of Engineering Science, The University of Electro-Communications, Tokyo, Japan.
Reo TakedaCellular and Molecular Biotechnology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Ibaraki, Japan.
Ryotaro KanoBioscience and Technology Program, Department of Engineering Science, The University of Electro-Communications, Tokyo, Japan.
Tatsuya KusanoBioscience and Technology Program, Department of Engineering Science, The University of Electro-Communications, Tokyo, Japan.
Yudai NonakaInstitute of Liberal Arts and Science, Kakuma-Machi, Kanazawa University, Kanazawa, Japan.
Yutaka KanoBioscience and Technology Program, Department of Engineering Science, The University of Electro-Communications, Tokyo, Japan.
Daisuke HoshinoBioscience and Technology Program, Department of Engineering Science, The University of Electro-Communications, Tokyo, Japan.ORCID 0000-0003-0065-8470

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) 20H04071MEXT | Japan Society for the Promotion of Science (JSPS) 24K02812
6 · The paper itself

Abstract

Pyruvate administration leads to the accumulation of intracellular lactate in adipocytes and affects inflammatory cytokine production and whole-body glucose metabolism. Therefore, the purpose of this study was to determine whether pyruvate administration improves the dysfunction of glucose metabolism induced by high-fat diet (HFD) intake. In an acute experiment, intraperitoneal injection of male mice with sodium pyruvate (1 g/kg body weight) increased pyruvate and lactate concentrations in blood and epididymal white adipose tissue (eWAT). In a chronic experiment, male mice were divided into three groups: normal diet, HFD with saline administration (HFD + SAL), and HFD with sodium pyruvate administration (HFD + PYR); the HFD + PYR group was injected with pyruvate five times a week for 8 weeks. Insulin concentrations in the basal state and during an oral glucose tolerance test were significantly lower in the HFD + PYR group than in the HFD + SAL group. The mRNA expression of inflammatory cytokines (tumor necrosis factor-alpha and interleukin 6) and a M2 macrophage polarity marker in eWAT was significantly higher in the HFD + PYR group than in the other groups. These results suggest that chronic pyruvate administration partially improves whole-body glucose metabolic dysfunction in HFD-fed mice, accompanied by increased mRNA expression of inflammatory cytokines and a M2 macrophage marker in the eWAT.

Indexed as

Adipose TissueAdipose Tissue, WhiteCytokinesGlucosePyruvic AcidAnimalsDiet, High-FatInterleukin-6MaleMiceMice, Inbred C57BLRNA, MessengerTumor Necrosis Factor-alphaCytokinesGlucoseInterleukin-6Pyruvic AcidRNA, MessengerTumor Necrosis Factor-alphaIL‐6lactateobesitywhite adipose tissue

Identifiers

PMID40781882
PMCPMC12334852

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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.