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Icariin modulates FLNB/ACTB/CCND1 signaling pathway to mitigate OGD/R injury in H9C2 cardiomyocytes
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Ce CAO, Jian-shu SONG, Li-li YANG, Zi-xin LIU, Qing-mei ZHOU, Lei LI, Jian-hua FU*, Jian-xun LIU*
Acta Pharmaceutica Sinica | 2026, 61(4) : 1258 - 1266
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Acta Pharmaceutica Sinica | 2026, 61(4): 1258-1266
• Original Articles •
Icariin modulates FLNB/ACTB/CCND1 signaling pathway to mitigate OGD/R injury in H9C2 cardiomyocytes
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Ce CAO, Jian-shu SONG, Li-li YANG, Zi-xin LIU, Qing-mei ZHOU, Lei LI, Jian-hua FU*, Jian-xun LIU*
Affiliations
  • Institute of Basic Medical Sciences of Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing Key Laboratory of Chinese Materia Pharmacology, National Clinical Research Center of Traditional Chinese Medicine for Cardiovascular Diseases, Beijing 100091, China
Published: 2026-04-12 doi: 10.16438/j.0513-4870.2025-1324
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To investigate the regulatory effects of icariin (ICA) on the proliferation of H9C2 cardiomyocytes injured by oxygen and glucose deprivation/reperfusion (OGD/R) and on filamin B (FLNB)/β-actin (ACTB)/cyclin D1 (CCND1) signaling pathway, H9C2 cardiomyocytes were used as the research model. Cell viability was determined using the cell counting kit-8 assay. The cells were divided into three groups, normal control group, OGD/R group, and ICA group. The normal control group was cultured under normal conditions, while the other two groups were subjected to 4 hours of OGD followed by 2 hours of reperfusion. Enzyme-linked immunosorbent assay was employed to measure the levels of aspartate transaminase (AST), lactate dehydrogenase (LDH), and creatine kinase (CK). Transcriptome sequencing was performed to identify the target genes of ICA in H9C2 cells; differentially expressed genes (DEGs) were analyzed via gene ontology (GO) functional annotation and Kyoto encyclopedia of genes and genomes (KEGG) pathway enrichment. Molecular docking and molecular dynamics simulation were used to evaluate the binding affinity between ICA and core targets. Compared with the OGD/R group, ICA groups at concentrations of 1-10 μmol·L-1 exerted a significant protective effect, and the levels of AST, LDH, and CK were notably decreased. Transcriptome sequencing results revealed that ICA significantly regulated 436 common DEGs in H9C2 cells after OGD/R, primarily affecting biological functions such as anatomical structure morphogenesis, protein binding, and intracellular anatomical structure, as well as signaling pathways including focal adhesion and pathways in cancer. STRING database analysis identified core targets including FLNB, ACTB, and CCND1. ICA significantly reversed the OGD/R-induced upregulation of FLNB, ACTB, and CCND1 expression. Molecular docking demonstrated strong binding between ICA and the core differential proteins, and molecular dynamics simulation confirmed that ICA significantly maintained the stability of FLNB protein. In conclusion, ICA can alleviate OGD/R-induced injury in H9C2, reduce the levels of AST, LDH, and CK, and downregulate the expression of FLNB, ACTB, and CCND1. This protective effect may be closely associated with ICA's binding to FLNB directly and subsequent mediation of the ACTB/CCND1 signaling pathway.

icariin  /  cardiomyocyte  /  proliferation  /  FLNB/ACTB/CCND1  /  oxygen and glucose deprivation/reperfusion
曹策, 宋鉴书, 杨丽丽, 刘子馨, 周青梅, 李磊, 付建华, 刘建勋. 淫羊藿苷调节FLNB/ACTB/CCND1信号通路减轻H9C2心肌细胞OGD/R损伤. 药学学报, 2026 , 61 (4) : 1258 -1266 . DOI: 10.16438/j.0513-4870.2025-1324
Ce CAO, Jian-shu SONG, Li-li YANG, Zi-xin LIU, Qing-mei ZHOU, Lei LI, Jian-hua FU, Jian-xun LIU. Icariin modulates FLNB/ACTB/CCND1 signaling pathway to mitigate OGD/R injury in H9C2 cardiomyocytes[J]. Acta Pharmaceutica Sinica, 2026 , 61 (4) : 1258 -1266 . DOI: 10.16438/j.0513-4870.2025-1324
Year 2026 volume 61 Issue 4
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Article Info
doi: 10.16438/j.0513-4870.2025-1324
  • Receive Date:2025-11-07
  • Online Date:2026-09-21
  • Published:2026-04-12
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  • Received:2025-11-07
  • Revised:2025-12-24
Affiliations
    Institute of Basic Medical Sciences of Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing Key Laboratory of Chinese Materia Pharmacology, National Clinical Research Center of Traditional Chinese Medicine for Cardiovascular Diseases, Beijing 100091, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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