# PCSK9 Inhibitor Alirocumab Improves Diabetic Cardiomyopathy Through the ERK/p38 MAPK Signaling Pathway

**Authors:** Shan Lin, Bangwei Wu, Shengjia Sun, Tao Sun

PMC · DOI: 10.3390/ijms27052341 · 2026-03-02

## TL;DR

Alirocumab, a PCSK9 inhibitor, protects against diabetic heart disease by improving heart function and reducing damage through a specific signaling pathway.

## Contribution

This study demonstrates that alirocumab improves diabetic cardiomyopathy via the ERK/p38 MAPK pathway, offering new therapeutic insights.

## Key findings

- Alirocumab enhances cell viability and reduces oxidative stress in high-glucose H9c2 cells.
- Alirocumab reduces myocardial hypertrophy and improves cardiac function in diabetic cardiomyopathy mice.
- Alirocumab activates the ERK/p38 MAPK pathway to exert protective effects on diabetic hearts.

## Abstract

PCSK9 is a gene associated with familial hypercholesterolemia and is involved in other biological processes such as apoptosis, autophagy, and inflammatory responses. This study aims to further validate whether PCSK9 inhibitors can improve diabetic cardiomyopathy and elucidate their mechanisms of action. This study utilized H9c2 cells and C57BL/6J mice to validate the efficacy of the PCSK9 inhibitor alirocumab through in vivo and in vitro experiments. In vitro, alirocumab was shown to enhance cell viability and reduce oxidative stress in H9c2 cells under high glucose stress. It can also decrease the expression levels of inflammatory reaction and mitochondrial apoptosis-related proteins. Through in vivo experiments, we demonstrated that alirocumab can reduce myocardial hypertrophy and improve cardiac function in diabetic cardiomyopathy mice. Meanwhile, alirocumab treatment increased mitochondrial size and quantity in the hearts of diabetic cardiomyopathy mice, promoted mitochondrial fusion, and reduced the number of damaged mitochondria. Alirocumab could also reduce the percentage of myocardial fibrosis and oxidative stress in mice. Finally, we found that alirocumab can improve cardiac function in diabetic cardiomyopathy through the ERK/p38 MAPK pathway. Our data demonstrate that the PCSK9 inhibitor alirocumab provides protective effects against diabetic cardiomyopathy, offering fundamental experimental support for its clinical application in this condition.

## Linked entities

- **Genes:** PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738], EPHB2 (EPH receptor B2) [NCBI Gene 2048], P38mapk (p38 map kinase) [NCBI Gene 692545]
- **Chemicals:** alirocumab (PubChem CID 88214187)

## Full-text entities

- **Genes:** Mapk1 (mitogen-activated protein kinase 1) [NCBI Gene 26413] {aka 9030612K14Rik, ERK, Erk2, MAPK2, PRKM2, Prkm1}, Mapk14 (mitogen-activated protein kinase 14) [NCBI Gene 26416] {aka CSBP2, Crk1, Csbp1, Mxi2, PRKM14, PRKM15}, Pcsk9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 100102] {aka FH3, HCHOLA3, Narc1, PC9}
- **Diseases:** inflammatory (MESH:D007249), familial hypercholesterolemia (MESH:D006938), myocardial hypertrophy (MESH:D006984), Diabetic Cardiomyopathy (MESH:D058065), myocardial fibrosis (MESH:D005355)
- **Chemicals:** glucose (MESH:D005947), Alirocumab (MESH:C571059)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

13 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12985983/full.md

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Source: https://tomesphere.com/paper/PMC12985983