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南京医科大学学报(自然科学版) 第45卷第8期
·1092 · Journal of Nanjing Medical University(Natural Sciences) 2025年8月
·基础研究·
三七总皂苷下调CD36信号通路对高脂饲料喂养小鼠血小板高
反应性的抑制作用
张春梅 ,胡锦秋 ,毕晓艳 ,马军羽 ,李梦瑶 ,李 荣 ,牙甫礼 2*
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大理大学公共卫生学院实验教学中心,营养与食品卫生学教研室,云南 大理 671000
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[摘 要] 目的:探讨膳食补充三七总皂苷(total saponins of Panax notoginseng,PNS)对高脂血症模型小鼠血小板高反应性的
影响及其可能的分子机制。方法:将8周龄健康雄性C57BL/6J小鼠随机分为4组,即低脂饲料(low⁃fat diet,LFD)喂饲组(LFD
组)、LFD+PNS 组(LFD中添加PNS 200 mg/kg饲料)、高脂饲料(high⁃fat diet,HFD)喂饲组(HFD组)、HFD+PNS 组(HFD中添加
PNS 200 mg/kg饲料),实验干预12 周后处死小鼠,分离血浆和提取纯化血小板,使用试剂盒检测血脂水平,血小板聚集仪测定
血小板最大聚集率,流式细胞术和酶联免疫吸附法检测血小板活化指标,实时定量PCR技术检测血小板CD36 mRNA表达水
平,Western blot免疫印迹实验检测血小板CD36蛋白表达、Src和p47 phox 的磷酸化水平。结果:与LFD组相比,HFD组小鼠血浆
总胆固醇、甘油三酯和低密度脂蛋白胆固醇显著升高,膳食补充PNS可显著降低小鼠的血脂水平。在激动剂凝血酶的刺激下,
膳食补充PNS显著降低由HFD诱导的小鼠血小板聚集和活化,如抑制血小板表面CD62P的表达和血小板因子4(platelet factor 4,
PF4)及趋化因子配体5(chemokine ligand 5,CCL5)的释放,提示PNS可降低HFD诱导的小鼠血小板高反应性。机制上,膳食补
充PNS显著降低由HFD诱导的小鼠血小板CD36 mRNA 和蛋白表达,并且显著抑制由HFD诱导血小板CD36下游信号通路的
活化,包括下调Src和p47 phox 的磷酸化水平。此外,膳食补充 PNS 可显著抑制由HFD组小鼠血浆诱导的血小板表面CD62P的
表达,在CD36 分子的中和性抗体FA6⁃152的作用下,PNS的抑制作用被消除。结论:膳食补充PNS对高脂饲料喂养小鼠的血
小板高反应性具有抑制作用,其作用机制可能是下调CD36信号通路,本研究为PNS改善高脂血症及其相关慢性代谢性疾病中
血栓形成提供参考价值。
[关键词] 三七总皂苷;血小板高反应性;CD36 信号通路;高脂血症
[中图分类号] R282.71 [文献标志码] A [文章编号] 1007⁃4368(2025)08⁃1092⁃09
doi:10.7655/NYDXBNSN241340
Total saponins of Panax notoginseng attenuate platelet hyperreactivity through down ⁃
regulating CD36 signalling pathway in mice fed a high⁃fat diet
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ZHANG Chunmei ,HU Jinqiu ,BI Xiaoyan ,MA Junyu ,LI Mengyao ,LI Rong ,YA Fuli 2*
Department of Laboratory Teaching Center,Department of Nutrition,School of Public Health,Dali University,Dali
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671000,China
[Abstract] Objective:The current study aims to assess the efficacy of total saponins of Panax notoginseng(PNS)supplementation
on platelet hyperreactivity in hyperlipidemic mice as well as to clarify the underlying mechanisms in vivo. Methods:Healthy male
C57BL/6J mice(aged 8 weeks)were randomly divided into four groups and fed either a low⁃fat diet(LFD group),a LFD supplemented
with PNS(200 mg/kg diet,LFD+PNS group),a high⁃fat diet(HFD group),or a HFD supplemented with PNS(200 mg/kg diet,HFD+
PNS group)for 12 weeks. After that all mice were killed,and the plasma and purified platelets were prepared,followed by
measurement levels of plasma lipid profile using commercial assay kits. A platelet aggregometer was used to measure maximal
aggregation ratio. Platelet activation was determined by flow cytometry and enzyme⁃linked immunosorbent assays. Real⁃time PCR
technique was used to detect CD36 mRNA expression,and Western blot was used to measure protein expression levels of CD36 and
phox
phosphorylation of Src and p47 . Results:When compared with those in LFD group,the plasma levels of total cholesterol,triglyceride
[基金项目] 国家自然科学基金(82260638);云南省基础研究专项面上项目(202401AT070081)
通信作者(Corresponding author),E⁃mail:yafuli@yeah.net(ORCID:0000⁃0002⁃7810⁃4403)
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