Beijing Key Laboratory of Gene Resource and Molecular Development, College of Life Sciences, Beijing Normal University, Beijing, China.
State key laboratory of environmental chemistry and ecotoxicology Research Center for Eco-Environmental Science Chinese Academy of Science, Beijing, China.
J Am Heart Assoc. 2017 Oct 2;6(10):e006297. doi: 10.1161/JAHA.117.006297.
DBZ (Danshensu Bingpian Zhi), a synthetic derivative of a natural compound found in traditional Chinese medicine, has been reported to suppress lipopolysaccharide-induced macrophage activation and lipid accumulation in vitro. The aim of this study was to assess whether DBZ could attenuate atherosclerosis at early and advanced stages.
The effects of DBZ on the development of atherosclerosis were studied using apolipoprotein E-deficient (apoE) mice. For early treatment, 5-week-old apoE mice were fed a Western diet and treated daily by oral gavage with or without DBZ or atorvastatin for 10 weeks. For advanced treatment, 5-week-old apoE mice were fed a Western diet for 10 weeks to induce atherosclerosis, and then they were randomly divided into 4 groups and subjected to the treatment of vehicle, 20 mg/kg per day DBZ, 40 mg/kg per day DBZ, or 10 mg/kg per day atorvastatin for the subsequent 10 weeks. We showed that early treatment of apoE mice with DBZ markedly reduced atherosclerotic lesion formation by inhibiting inflammation and decreasing macrophage infiltration into the vessel wall. Treatment with DBZ also attenuated the progression of preestablished diet-induced atherosclerotic plaques in apoE mice. In addition, we showed that DBZ may affect LXR (liver X receptor) function and that treatment of macrophages with DBZ suppressed lipopolysaccharide-stimulated cell migration and oxidized low-density lipoprotein-induced foam cell formation.
DBZ potentially has antiatherosclerotic effects that involve the inhibition of inflammation, macrophage migration, leukocyte adhesion, and foam cell formation. These results suggest that DBZ may be used as a therapeutic agent for the prevention and treatment of atherosclerosis.
DBZ(丹参素冰片酯)是一种从传统中药中发现的天然化合物的合成衍生物,据报道它能抑制脂多糖诱导的体外巨噬细胞激活和脂质堆积。本研究旨在评估 DBZ 是否能减轻动脉粥样硬化的早期和晚期病变。
采用载脂蛋白 E 缺乏(apoE)小鼠研究 DBZ 对动脉粥样硬化发展的影响。早期治疗组,5 周龄 apoE 小鼠给予西方饮食,同时每日口服 DBZ 或阿托伐他汀治疗 10 周。晚期治疗组,5 周龄 apoE 小鼠给予西方饮食 10 周诱导动脉粥样硬化,然后随机分为 4 组,分别给予 vehicle、20mg/kg/天 DBZ、40mg/kg/天 DBZ 或 10mg/kg/天阿托伐他汀治疗 10 周。结果表明,早期 DBZ 治疗能显著抑制炎症反应,减少巨噬细胞向血管壁浸润,从而减少 apoE 小鼠的动脉粥样硬化病变形成。DBZ 还能减轻 apoE 小鼠预先形成的饮食诱导的动脉粥样硬化斑块的进展。此外,我们发现 DBZ 可能影响 LXR(肝 X 受体)功能,DBZ 处理的巨噬细胞抑制脂多糖刺激的细胞迁移和氧化型低密度脂蛋白诱导的泡沫细胞形成。
DBZ 具有抗动脉粥样硬化作用,涉及抑制炎症、巨噬细胞迁移、白细胞黏附和泡沫细胞形成。这些结果提示 DBZ 可能作为预防和治疗动脉粥样硬化的治疗剂。