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Hydroxysafflor Yellow A Attenuates Hydrogen Peroxide-Induced Oxidative Damage on Human Umbilical Vein Endothelial
Yuefeng Xie1, Yan Guo1,2, ShiDong Cao1
1College of Life Science, Zhejiang Chinese Medical University, Hangzhou, Zhejiang 310053, China.
Insights
Hydroxysafflor yellow A (HSYA) repairs oxidative damage in human umbilical vein endothelial cells (HUVECs). This traditional Chinese medicine component protects against hydrogen peroxide (H2O2)-induced injury by modulating key proteins and pathways.
Area of Science:
- Cardiovascular Research
- Cell Biology
- Traditional Chinese Medicine
Background:
- Endothelial cell oxidative stress is a primary driver of cardiovascular diseases.
- Hydroxysafflor yellow A (HSYA), derived from safflower, is a traditional Chinese medicine used for ischemic cardiovascular conditions.
Purpose of the Study:
- To investigate HSYA's protective effects against oxidative damage in human umbilical vein endothelial cells (HUVECs) induced by hydrogen peroxide (H2O2).
- To elucidate the underlying molecular mechanisms of HSYA's action for potential clinical applications in cardiovascular disease treatment.
Main Methods:
- Established an H2O2-induced oxidative injury model in HUVECs.
- Assessed cell viability (MTT assay) and proliferation (EdU staining).
- Measured intracellular glutathione (GSH/GSSG ratio), superoxide dismutase (SOD) activity, and reactive oxygen species (ROS) levels.
- Evaluated protein expression of BAX, Bcl-2, PTEN, and AKT via Western blotting.
Main Results:
- HSYA significantly reduced H2O2-induced HUVEC damage.
- HSYA increased intracellular GSH/GSSG ratio and SOD activity while decreasing ROS levels.
- HSYA upregulated AKT and Bcl-2 protein expression and downregulated BAX and PTEN protein expression.
Conclusions:
- HSYA demonstrates significant repair effects on H2O2-induced oxidative damage in HUVECs.
- HSYA's protective mechanisms involve modulating the BAX/Bcl-2 expression ratio and the AKT/PTEN signaling pathway.
Abstract:
Oxidative stress of endothelial cells is thought to be a principal cause that induces many cardiovascular diseases. Hydroxysafflor yellow A (HSYA) is a major active component in traditional Chinese medicine safflower and has been used to cure ischemic cardiovascular diseases in China for many years. This study aims to investigate whether HSYA has a repairing effect on oxidative damage of human umbilical vein endothelial cells (HUVECs) induced by H2O2 and to provide a theoretical basis for the clinical treatment of cardiovascular diseases related to traditional Chinese medicine. Based on the establishment of an H2O2-induced HUVEC oxidative injury model, the cell viability and proliferation rate were measured by the MTT assay and EdU staining. The intracellular GSH/GSSG ratio and SOD activity were determined by kits. The ROS level was detected by flow cytometry. And the BAX, Bcl-2, PTEN, and AKT expressions were evaluated with western blotting methods. The results showed that HSYA treatment significantly attenuated the H2O2-induced HUVEC cell damage, increased the intracellular GSH/GSSG ratio and unit SOD activity also, and decreased the intracellular ROS levels. Furthermore, HSYA increased the expressions of AKT and Bcl-2 proteins and inhibited the expressions of BAX and PTEN proteins. These suggest that HSYA exerts repair effects on H2O2-induced oxidative damage in HUVECs, and the mechanisms may be related to the influence of BAX/Bcl-2 expression and AKT/PTEN signal pathway expression.
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