Salvia miltiorrhiza Extract Prevents the Occurrence of Early Atherosclerosis in Apoe -/- Mice via TLR4/ NF-kB Pathway.

Q2 Medicine
Ruoyu Wu, Linqi Zhang, Hongjun Xu, Hongxu Chen, Wei Zhao, Yongjie Zhou, Luyang Zhou, Jiangli Wu, Shengjun An
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引用次数: 1

Abstract

Objective: Salvia miltiorrhiza (SM) contains four major aqueous active ingredients, which have been isolated, purified and identified as danshensu (DSS), salvianolic acid A (Sal-A), salvianolic acid B (Sal-B) and protocatechuic aldehyde (PAL), A mixture of these four ingredients is called SABP. Although aqueous extract from Salvia miltiorrhiza has been traditionally used to treat cardiovascular diseases, the efficacy and function of the optimal ratio of SABP in preventing and treating cardiovascular diseases remain unknown. This study aims to explore the antiinflammatory mechanisms underlying the attenuation of atherosclerosis development by aqueous extract from Salvia miltiorrhiza.

Methods: Male ApoE-/- mice (6 weeks) were randomly allocated into three groups: the model group (Model), the SABP group (SABP), and the rosuvastatin calcium group (RC). Male C57BL/6 mice (6 weeks) were used as a control group. All mice were fed with an ordinary diet. After 8 weeks of treatment, the lipid profiles in serum and the lactate dehydrogenase (LDH) and creatine kinase (CK) in heart tissue were measured using an automatic biochemical analyzer. Alterations of the thoracic aorta and the heart were assessed using Hematoxylin and eosin staining. The protein expression of Toll-like receptor 4 (TLR4), TGF beta-activated kinase 1 (TAK1), nuclear factor kappa-B (NF-κB), interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α) in the heart tissue were determined though immunohistochemistry and western blotting analysis.

Results: The serum low-density lipoprotein cholesterol (LDL-C), triglyceride (TG), and total cholesterol (TC) levels were increased, and the high-density lipoprotein cholesterol (HDL-C) level was decreased in ApoE-/- mice. SABP significantly decreased serum lipid levels and improved histopathology in the thoracic aorta. In addition. SABP treatment inhibited the expression of TLR4, TAK1, NF-κB, IL-6 and TNF-α in the heart in ApoE-/- mice. The LDH and CK in the heart did not differ significantly among different groups, and the heart did not have obvious pathological changes.

Conclusion: These findings indicated that SABP may exert an anti-atherosclerotic effect by lowering blood lipids and inhibiting inflammatory response via TLR4/ NF-κB signaling pathway.

Abstract Image

Abstract Image

Abstract Image

丹参提取物通过TLR4/ NF-kB途径预防Apoe -/-小鼠早期动脉粥样硬化的发生
目的:丹参(SM)中含有四种主要的水相活性成分,经分离纯化鉴定为丹参素(DSS)、丹酚酸A (Sal-A)、丹酚酸B (Sal-B)和原儿茶醛(PAL),这四种成分的混合物称为SABP。虽然丹参水提物传统上用于治疗心血管疾病,但SABP的最佳配比在预防和治疗心血管疾病中的功效和功能尚不清楚。本研究旨在探讨丹参水提物抑制动脉粥样硬化发展的抗炎机制。方法:雄性ApoE-/-小鼠(6周)随机分为3组:模型组(model)、SABP组(SABP)和瑞舒伐他汀钙组(RC)。以雄性C57BL/6小鼠(6周)为对照组。所有的老鼠都吃普通的食物。治疗8周后,采用全自动生化分析仪测定血清脂质及心脏组织乳酸脱氢酶(LDH)和肌酸激酶(CK)水平。采用苏木精和伊红染色评估胸主动脉和心脏的变化。采用免疫组化和western blotting检测心肌组织中toll样受体4 (TLR4)、TGF β活化激酶1 (TAK1)、核因子κ b (NF-κB)、白细胞介素6 (IL-6)、肿瘤坏死因子α (TNF-α)的蛋白表达。结果:ApoE-/-小鼠血清低密度脂蛋白胆固醇(LDL-C)、甘油三酯(TG)、总胆固醇(TC)水平升高,高密度脂蛋白胆固醇(HDL-C)水平降低。SABP显著降低血清脂质水平,改善胸主动脉组织病理学。此外。SABP可抑制ApoE-/-小鼠心脏组织中TLR4、TAK1、NF-κ b、IL-6、TNF-α的表达。各组心脏LDH、CK无明显差异,心脏无明显病理改变。结论:SABP可能通过TLR4/ NF-κB信号通路降低血脂,抑制炎症反应,从而发挥抗动脉粥样硬化作用。
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来源期刊
Cardiovascular and Hematological Agents in Medicinal Chemistry
Cardiovascular and Hematological Agents in Medicinal Chemistry Medicine-Cardiology and Cardiovascular Medicine
CiteScore
2.70
自引率
0.00%
发文量
34
期刊介绍: Cardiovascular & Hematological Agents in Medicinal Chemistry aims to cover all the latest and outstanding developments in medicinal chemistry and rational drug design for the discovery of new Cardiovascular & Hematological Agents. Each issue contains a series of timely in-depth reviews written by leaders in the field covering a range of current topics in Cardiovascular & Hematological medicinal chemistry. Cardiovascular & Hematological Agents in Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments in cardiovascular & hematological drug discovery.
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