Alleviation of hypoxia/reoxygenation injury in HL-1 cells by ginsenoside Rg_1 via regulating mitochondrial fusion based on Notch1 signaling pathway.
10.19540/j.cnki.cjcmm.20241219.403
- Author:
Hui-Yu ZHANG
1
;
Xiao-Shan CUI
2
;
Yuan-Yuan CHEN
2
;
Gao-Jie XIN
2
;
Ce CAO
2
;
Zi-Xin LIU
2
;
Shu-Juan XU
2
;
Jia-Ming GAO
2
;
Hao GUO
2
;
Jian-Hua FU
1
Author Information
1. Institute of Basic Medicine, Xiyuan Hospital, China Academy of Chinese Medical Sciences Beijing 100091, China School of Traditional Chinese Medicine, Binzhou Medical College Yantai 264003, China.
2. Institute of Basic Medicine, Xiyuan Hospital, China Academy of Chinese Medical Sciences Beijing 100091, China.
- Publication Type:Journal Article
- Keywords:
Mfn1;
Mfn2;
Notch1;
ginsenoside Rg_1;
mitochondrial fusion;
myocardial ischemia-reperfusion injury(MIRI)
- MeSH:
Ginsenosides/pharmacology*;
Receptor, Notch1/genetics*;
Signal Transduction/drug effects*;
Mice;
Animals;
Mitochondrial Dynamics/drug effects*;
Mitochondria/metabolism*;
Cell Line;
Reactive Oxygen Species/metabolism*;
Oxygen/metabolism*;
Cell Hypoxia/drug effects*;
Cell Survival/drug effects*;
Membrane Potential, Mitochondrial/drug effects*;
Humans
- From:
China Journal of Chinese Materia Medica
2025;50(10):2711-2718
- CountryChina
- Language:Chinese
-
Abstract:
This paper explored the specific mechanism of ginsenoside Rg_1 in regulating mitochondrial fusion through the neurogenic gene Notch homologous protein 1(Notch1) pathway to alleviate hypoxia/reoxygenation(H/R) injury in HL-1 cells. The relative viability of HL-1 cells after six hours of hypoxia and two hours of reoxygenation was detected by cell counting kit-8(CCK-8). The lactate dehydrogenase(LDH) activity in the cell supernatant was detected by the lactate substrate method. The content of adenosine triphosphate(ATP) was detected by the luciferin method. Fluorescence probes were used to detect intracellular reactive oxygen species(Cyto-ROS) levels and mitochondrial membrane potential(ΔΨ_m). Mito-Tracker and Actin were co-imaged to detect the number of mitochondria in cells. Fluorescence quantitative polymerase chain reaction and Western blot were used to detect the mRNA and protein expression levels of Notch1, mitochondrial fusion protein 2(Mfn2), and mitochondrial fusion protein 1(Mfn1). The results showed that compared with that of the control group, the cell activity of the model group decreased, and the LDH released into the cell culture supernatant increased. The level of Cyto-ROS increased, and the content of ATP decreased. Compared with that of the model group, the cell activity of the ginsenoside Rg_1 group increased, and the LDH released into the cell culture supernatant decreased. The level of Cyto-ROS decreased, and the ATP content increased. Ginsenoside Rg_1 elevated ΔΨ_m and increased mitochondrial quantity in HL-1 cells with H/R injury and had good protection for mitochondria. After H/R injury, the mRNA and protein expression levels of Notch1 and Mfn1 decreased, while the mRNA and protein expression levels of Mfn2 increased. Ginsenoside Rg_1 increased the mRNA and protein levels of Notch1 and Mfn1, and decreased the mRNA and protein levels of Mfn2. Silencing Notch1 inhibited the action of ginsenoside Rg_1, decreased the mRNA and protein levels of Notch1 and Mfn1, and increased the mRNA and protein levels of Mfn2. In summary, ginsenoside Rg_1 regulated mitochondrial fusion through the Notch1 pathway to alleviate H/R injury in HL-1 cells.
