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Isopropyl 3-(3,4-Dihydroxyphenyl)-2-hydroxypropanoate Alleviates Palmitic Acid-Induced Vascular Aging in HUVEC Cells
Xin He1,2,3, Xiaohui Zheng4, Weidong Xie1
1State Key Laboratory of Chemical Oncogenomics, Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.
Isopropyl 3-(3,4-dihydroxyphenyl)-2-hydroxypropanoate (IDHP) delays vascular aging and protects against hyperlipidemia-induced injury by reducing oxidative stress and ferroptosis. This antioxidant agent offers new therapeutic potential for cardiovascular disease.
Area of Science:
- Cardiovascular Science
- Cellular Biology
- Biochemistry
Background:
- Vascular aging contributes to cardiovascular diseases like hypertension and atherosclerosis.
- Hyperlipidemia and vascular wall fat accumulation are implicated in vascular aging.
- Isopropyl 3-(3,4-dihydroxyphenyl)-2-hydroxypropanoate (IDHP) shows cardiovascular protective effects potentially linked to ferroptosis.
Purpose of the Study:
- To investigate the protective effect of IDHP on hyperlipidemia-induced vascular aging.
- To elucidate the mechanism of IDHP involving senescence and ferroptosis in human umbilical vein endothelial cells (HUVECs).
Main Methods:
- Palmitic acid induction of HUVECs to model vascular aging and lipotoxicity.
- Assessment of IDHP's effects on cellular senescence markers.
- Measurement of ferrous ion accumulation, lipid peroxidation, and reactive oxygen species (ROS).
- Analysis of ferroptosis signaling pathways.
Main Results:
- IDHP treatment delayed vascular aging in HUVECs.
- IDHP reduced ferrous ion accumulation and lipid peroxidation.
- IDHP attenuated excessive ROS production and ferroptosis signaling.
- IDHP protected vascular endothelial cells from palmitic acid-induced injury.
Conclusions:
- IDHP exhibits antioxidant properties that slow lipotoxicity-induced vascular senescence.
- The protective mechanism involves regulating the ROS/ferroptosis pathway.
- IDHP demonstrates potential as a therapeutic agent for delaying vascular aging in dyslipidemia.
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