# Imeglimin Inhibits Macrophage Foam Cell Formation and Atherosclerosis in Streptozotocin-Induced Diabetic ApoE-Deficient Mice

**Authors:** Ji Yeon Lee, Yup Kang, Ja Young Jeon, Seung Jin Han

PMC · DOI: 10.3390/cells14070472 · Cells · 2025-03-21

## TL;DR

Imeglimin, a diabetes drug, reduces foam cell formation and atherosclerosis in diabetic mice by improving cholesterol transport and lowering glucose and LDL levels.

## Contribution

This study reveals imeglimin's novel role in preventing atherosclerosis in diabetes through AMPK-mediated regulation of cholesterol transporters.

## Key findings

- Imeglimin inhibits foam cell formation by upregulating ABCA1 and ABCG1 and downregulating CD36.
- In diabetic ApoE−/− mice, imeglimin reduces atherosclerotic plaque area and lowers glucose and LDL cholesterol.
- The effects of imeglimin are mediated through AMPK activation.

## Abstract

Atherosclerotic cardiovascular disease is a major complication of diabetes, whose progression is significantly accelerated by hyperglycemia. Imeglimin, a novel oral antidiabetic agent, has demonstrated efficacy in glucose control; however, its role in diabetes-related cardiovascular complications has not yet been fully explored. This study aimed to investigate the effects of imeglimin on foam cell formation and atherosclerosis in the context of diabetes. THP-1 macrophages were treated with oxidized low-density lipoprotein (LDL) and high glucose to induce foam cell formation in vitro. Additionally, ApoE−/− mice with streptozotocin-induced diabetes were used to determine the effects of imeglimin in vivo by analyzing metabolic parameters and atherosclerotic plaque formation. Imeglimin inhibited macrophage-derived foam cell formation by promoting the expression of ATP-binding cassette transporters (ABC) A1 and ABCG1 and downregulating the expression of CD36. The effects of imeglimin on ABCG1 and CD36 expression regulation was mediated by AMPK. In diabetic ApoE−/− mice, imeglimin reduced the atherosclerotic plaque area, decreased fasting glucose and LDL cholesterol levels, and upregulated ABCG1 expression in the liver and aorta. These findings suggest that imeglimin may have a preventive effect on foam cell formation and a therapeutic role in atherosclerosis progression in diabetic conditions.

## Linked entities

- **Genes:** ABCA1 (ATP binding cassette subfamily A member 1) [NCBI Gene 19], ABCG1 (ATP binding cassette subfamily G member 1) [NCBI Gene 9619], CD36 (CD36 molecule (CD36 blood group)) [NCBI Gene 948], PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562]
- **Chemicals:** Imeglimin (PubChem CID 24812808)
- **Diseases:** diabetes (MONDO:0005015), atherosclerotic cardiovascular disease (MONDO:1060134)

## Full-text entities

- **Genes:** Abcg1 (ATP binding cassette subfamily G member 1) [NCBI Gene 11307] {aka Abc8, White}
- **Diseases:** Atherosclerosis (MESH:D050197), cardiovascular complications (MESH:D002318), Diabetic (MESH:D003920), hyperglycemia (MESH:D006943)
- **Chemicals:** Imeglimin (MESH:C575881), Streptozotocin (MESH:D013311), glucose (MESH:D005947)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** THP-1 — Homo sapiens (Human), Childhood acute monocytic leukemia, Cancer cell line (CVCL_0006)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11988081/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC11988081/full.md

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Source: https://tomesphere.com/paper/PMC11988081