Synergistic Effects of Guan-Xin-Er-Hao and Hydroxysafflor Yellow A on Atherosclerosis in ApoE-/- Mice: Unveiling Antioxidant and Anti-Inflammatory Mechanisms

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Abstract
Pharmacognosy Research,2025,17,2,665-678.
Published:April 2025
Type:Original Article
Authors:
Author(s) affiliations:

Wenya Huang1, Le Zhang1, Li Zhou1, Zhifang Cai1, Kaige Wu2, Yu Wang2, Runze Zhou1, Min Xu1, Jia Li1, Yunke Huang1, 3, Ping Ren1, Xi Huang1,*

1Institute of Depression and Comorbidity, Nanjing University of Chinese Medicine, Nanjing, CHINA.

2Xiangya Hospital of Central South University, Changsha, CHINA.

3Women’s Hospital School of Medicine, Zhejiang University, Hangzhou, CHINA.

Abstract:

Background: The Guan-Xin-Er-Hao (GXII) decoction, a traditional Chinese medicine, contains hydroxysafflor yellow A (HSYA) as its main active compound for treating coronary heart disease. Objectives: This study aimed to assess the therapeutic efficacy of HSYA compared to GXII and elucidate its molecular mechanisms in combating atherosclerosis. Materials and Methods: Guan-Xin-Er-Hao (GXII) was analyzed using HPLC-MS, which identified three main absorbable components: Hydroxysafflor Yellow A (HSYA), Ferulic Acid and Tanshinol. Among them, HSYA demonstrated the most pronounced effects in the in vitro experiments, leading to its selection for subsequent in vivo studies due to its high content and superior bioavailability within GXII. ApoE−/− mice were fed a high-fat diet for eight weeks and treated orally with GXII or HSYA. Atherosclerotic plaque areas and plasma lipid levels served as indicators of anti-atherosclerotic activity. Oxidative stress markers (malondialdehyde, superoxide dismutase, glutathione peroxidase, catalase) and inflammatory mediators (tumor necrosis factor-α, vascular cell adhesion molecule-1, interleukin-1β) were evaluated using enzyme-linked immunosorbent assays, western blotting and reverse transcription-polymerase chain reaction. Results: The Contribution Rate (CR) analysis indicated that HSYA significantly influenced serum lipid levels, oxidative stress markers and inflammatory protein/mRNA levels, with HSYA demonstrating a CR exceeding 90% relative to GXII. These findings underscore HSYA's predominant role within GXII in exerting anti-atherosclerotic effects through mitigation of oxidative stress and inflammation. Conclusion: The synergistic actions of GXII and HSYA reveal a promising therapeutic approach for atherosclerosis, offering valuable insights into their antioxidant and anti-inflammatory mechanisms in ApoE−/− mice.

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Mechanism of action of Guan-Xin-Er-Hao (GXII) and hydroxysafflor yellow A (HSYA) in ameliorating atherosclerosis in ApoE−/− mice involves antioxidant and anti-inflammatory effects. The figure illustrates the antioxidant and anti-inflammatory mechanisms of Guan-Xin-Er-Hao and Hydroxysafflor Yellow A. By balancing antioxidant enzymes and MDA production; they reduce Reactive Oxygen Species (ROS); thereby alleviating endothelial dysfunction and oxidative stress. ROS-induced inflammation increases VCAM-1 expression; promoting immune cell adhesion and migration; leading to foam cell formation and the secretion of inflammatory cytokines like TNF-α and IL-1β; which exacerbate atherosclerosis progression and vascular inflammation.

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