Department of Pharmacology, School of Pharmacy, Fourth Military Medical University, Xi'an, China; Key Laboratory of Gastrointestinal Pharmacology of Chinese Materia Medica of the State Administration of Traditional Chinese Medicine, Xi'an, China.
Department of Natural Medicine & Institute of Materia Medica, School of Pharmacy, Fourth Military Medical University, Xi'an, China.
Toxicol Appl Pharmacol. 2018 Feb 15;341:56-63. doi: 10.1016/j.taap.2018.01.007. Epub 2018 Feb 2.
Atherosclerosis is characterized by chronic inflammation in vascular wall. Previous studies suggest that Kuwanon G (KWG) exerts anti-inflammatory activities. However, the effect of KWG on atherosclerosis remains unexplored.
To explore whether KWG affects macrophage foam cell formation in vitro and atherogenesis in vivo.
RAW 264.7 macrophages were stimulated with ox-LDL for 24h to induce foam cell formation and treated with KWG. Foam cell formation was determined by ORO staining and enzymatic analysis. Pro-inflammatory cytokines mRNA levels were tested by Real-time PCR method. Further molecular mechanism was investigated using Western blot. In vivo, ApoE mice were fed with high-fat diet and intraperitoneally injected with KWG. Atherosclerotic lesion was accessed by H&E and ORO staining. Plaque composition was evaluated by immunohistochemistry and Sirius Red staining. Serum lipid profile and inflammatory cytokines were evaluated by enzymatic method and ELISA.
KWG significantly decreased intracellular lipid accumulation and inflammatory cytokines mRNA levels in macrophages through enhancing LXRα-ABCA1/ABCG1 pathway and inhibiting NFκB activation. Administrated with KWG remarkably reduced the atherosclerotic lesion areas and macrophage content in the plaque of high-fat diet fed ApoE mice. KWG also reduced hyperlipidemia and serum inflammatory cytokines in vivo.
Taken together, these data highlight that KWG can attenuate atherosclerosis through inhibiting foam cell formation and inflammatory response.
动脉粥样硬化的特征是血管壁的慢性炎症。先前的研究表明,桑酮 G(KWG)具有抗炎活性。然而,KWG 对动脉粥样硬化的影响尚未得到探索。
探讨 KWG 是否影响体外巨噬细胞泡沫细胞形成和体内动脉粥样硬化形成。
用 ox-LDL 刺激 RAW 264.7 巨噬细胞 24 小时诱导泡沫细胞形成,并用 KWG 处理。通过 ORO 染色和酶分析测定泡沫细胞形成。通过实时 PCR 方法检测促炎细胞因子 mRNA 水平。进一步通过 Western blot 研究其分子机制。在体内,用高脂肪饮食喂养 ApoE 小鼠,并腹腔内注射 KWG。通过 H&E 和 ORO 染色评估动脉粥样硬化病变。通过免疫组织化学和 Sirius Red 染色评估斑块组成。通过酶法和 ELISA 评估血清脂质谱和炎症细胞因子。
KWG 通过增强 LXRα-ABCA1/ABCG1 通路和抑制 NFκB 激活,显著减少巨噬细胞内的脂质积累和炎症细胞因子 mRNA 水平。给予 KWG 可显著减少高脂饮食喂养的 ApoE 小鼠的动脉粥样硬化病变面积和斑块中的巨噬细胞含量。KWG 还降低了体内的高脂血症和血清炎症细胞因子。
综上所述,这些数据表明 KWG 通过抑制泡沫细胞形成和炎症反应来减轻动脉粥样硬化。