[火炭解毒通络汤通过调节Nrf2/GPX4通路改善ApoE~(-/-)小鼠动脉粥样硬化病变,抑制铁下沉]。

Q3 Pharmacology, Toxicology and Pharmaceutics
Di Gao, Teng-Hui Tian, Ke-Ying Yu, Xiao Shao, Wen Xue, Zhi-Xuan Zhao, Yue Deng
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引用次数: 0

摘要

本研究旨在阐明活痰解毒通络汤通过调节铁下沉通路对ApoE~(-/-)小鼠动脉粥样硬化(AS)损伤的影响。将75只ApoE~(-/-)小鼠随机分为模型组、活痰解毒通络汤低、中、高剂量组和evolocumab组(n=15),取C57BL/6J小鼠15只作为空白组。空白组小鼠给予正常饮食,其余各组小鼠给予高脂饮食诱导AS。从第9周开始,活血解毒通络汤组小鼠灌胃相应剂量的活血解毒通络汤,空白组和模型组小鼠灌胃等体积蒸馏水。evolocumab组小鼠每2周皮下注射evolocumab 18.2 mg·kg~(-1)。连续干预8周后,采用油红O染色和苏木精-伊红(HE)染色观察主动脉根部脂质沉积和斑块形成情况。马松染色法测定主动脉根部胶原蛋白含量。采用生化试剂盒检测血清总胆固醇(TC)、甘油三酯(TG)、高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇(LDL-C)水平。用比色法测定大鼠主动脉铁~(2+)、超氧化物歧化酶(SOD)、丙二醛(MDA)、谷胱甘肽(GSH)水平。Western blot和RT-qPCR分别检测大鼠主动脉内核因子红系2相关因子2(Nrf2)、谷胱甘肽过氧化物酶4(GPX4)、溶质载体家族7成员11(SLC7A11)、酰基辅酶a合成酶长链家族成员4(ACSL4)蛋白和mRNA水平。免疫荧光法定位Nrf2、GPX4、SLC7A11的表达。结果显示,低、中、高剂量火炭解毒通络汤均能减少AS小鼠主动脉根部斑块形成,增加胶原蛋白含量。同时,活痰解毒通络汤通过降低血清TC、LDL-C、TG水平,提高血清HDL-C水平,改善脂质代谢。火炭解毒通络汤通过提高主动脉GSH、SOD水平,降低MDA水平,抑制主动脉Fe~(2+)的积累,增强大鼠抗氧化能力。此外,活痰解毒通络汤上调Nrf2、GPX4、SLC7A11蛋白和mRNA水平,下调ACSL4蛋白和mRNA水平。综上所述,火炭解毒通络汤可通过激活Nrf2/GPX4通路,减少脂质过氧化,抑制铁下沉,有效缓解ApoE~(-/-)小鼠AS病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Huotan Jiedu Tongluo Decoction inhibits ferroptosis by regulating Nrf2/GPX4 pathway to ameliorate atherosclerotic lesions in ApoE~(-/-) mice].

The purpose of this study was to clarify the effect of Huotan Jiedu Tongluo Decoction on atherosclerosis(AS) injury in ApoE~(-/-) mice by regulating the ferroptosis pathway. Seventy-five ApoE~(-/-) mice were randomly divided into model group, low-, medium-, and high-dose of Huotan Jiedu Tongluo Decoction groups, and evolocumab group(n=15), and 15 C57BL/6J mice were selected as the blank group. Mice in the blank group were fed with a normal diet, and those in the other groups were fed with a high-fat diet to induce AS. From the 9th week, mice in Huotan Jiedu Tongluo Decoction groups were administrated with Huotan Jiedu Tongluo Decoction at corresponding doses by gavage, and those in the blank group and the model group were given an equal volume of distilled water. Mice in the evolocumab group were treated with evolocumab 18.2 mg·kg~(-1 )by subcutaneous injection every 2 weeks. After 8 weeks of continuous intervention, oil red O staining and hematoxylin-eosin(HE) staining were employed to observe the lipid deposition and plaque formation in the aortic root. Masson staining was used to evaluate the collagen content in the aortic root. The serum levels of total cholesterol(TC), triglycerides(TG), high-density lipoprotein cholesterol(HDL-C), and low-density lipoprotein cholesterol(LDL-C) were determined by biochemical kits. The levels of Fe~(2+), superoxide dismutase(SOD), malondialdehyde(MDA), and glutathione(GSH) in the aorta were measured by colorimetry. The protein and mRNA levels of nuclear factor erythroid 2-related factor 2(Nrf2), glutathione peroxidase 4(GPX4), solute carrier family 7 member 11(SLC7A11), and acyl-CoA synthetase long chain family member 4(ACSL4) in the aorta were detected by Western blot and RT-qPCR, respectively. The expression of Nrf2, GPX4, and SLC7A11 was localized by immunofluorescence. The results showed that low-, medium-, and high-dose Huotan Jiedu Tongluo Decoction reduced the plaque formation of aortic root and increased the collagen content in AS mice. At the same time, Huotan Jiedu Tongluo Decoction improved the lipid metabolism by lowering the levels of TC, LDL-C, and TG and elevating the level of HDL-C in the serum. Huotan Jiedu Tongluo Decoction enhanced the antioxidant capacity by elevating the levels of GSH and SOD and lowering the level of MDA in the aorta and inhibiting the accumulation of Fe~(2+) in the aorta. In addition, Huotan Jiedu Tongluo Decoction up-regulated the protein and mRNA levels of Nrf2, GPX4, and SLC7A11, while down-regulating the protein and mRNA levels of ACSL4. In summary, Huotan Jiedu Tongluo Decoction can effectively alleviate AS lesions in ApoE~(-/-) mice by activating the Nrf2/GPX4 pathway, reducing lipid peroxidation, and inhibiting ferroptosis.

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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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