首页|期刊导航|食品工业科技|桂花乙醇提取物对高脂血症小鼠血脂异常与肠道菌群紊乱的改善作用

桂花乙醇提取物对高脂血症小鼠血脂异常与肠道菌群紊乱的改善作用OA

Ameliorative Effects of Osmanthus fragrans Ethanol Extract on Dyslipidemia and Gut Microbiota Dysbiosis in Hyperlipidemic Mice

中文摘要英文摘要

目的:探讨桂花乙醇提取物(Osmanthus fragrans ethanol extract,OFE)调节高脂血症小鼠肠道菌群紊乱、促进胆固醇逆向转运改善血脂异常的作用机制.方法:高脂饲料喂养 6周建立高脂血症小鼠模型,分为正常组、模型组、OFE低剂量组、OFE高剂量组、辛伐他汀组,灌胃给药 5周,测定小鼠体重、空腹血糖、肝脏指数,检测血清脂质与氧化应激水平,胆固醇逆向转运途径关键蛋白水平,HE染色法观察肝脏组织的病理形态变化,并通过 16S rRNA高通量测序分析小鼠粪便肠道菌群多样性与组成变化.结果:桂花乙醇提取物能够降低模型小鼠的肝脏指数、血糖水平(P<0.01);降低血清中甘油三酯(triglyceride,TG)、总胆固醇(total cholesterol,TC)和低密度脂蛋白胆固醇(low-density lipoprotein cholesterol,LDL-C)水平(P<0.05或P<0.01或P<0.001),提高高密度脂蛋白胆固醇(high-density lipoprotein cholesterol,HDL-C)水平(P<0.01);降低丙二醛(malondialdehyde,MDA)水平(P<0.01),提高总超氧化物歧化酶(superoxide dismutase,SOD)、过氧化氢酶(catalase,CAT)、总抗氧化能力(total antioxidant capacity,T-AOC)水平(P<0.05或P<0.01或P<0.001);改善肝脏脂肪变性,抑制炎症,减轻细胞损伤;提高血清中ATP结合盒转运蛋白A1(ATP binding cassette transporter A1,ABCA1)和载脂蛋白A1(apolipoprotein A1,ApoA-Ⅰ)水平(P<0.001);调节肠道菌群多样性,降低厚壁菌门/拟杆菌门(Firmicutes to Bacteroidota,F/B)比率(P<0.05).结论:OFE具有降低高脂血症小鼠脂质积累与氧化应激水平,改善血脂异常作用,可能与其促进胆固醇逆向转运、纠正肠道菌群紊乱有关.

Objective:To investigate the mechanism of Osmanthus fragrans ethanol extract(OFE)in ameliorating dyslipidemia via modulation of gut microbiota dysbiosis and enhancement of reverse cholesterol transport(RCT)in hyperlipidemic mice.Methods:Hyperlipidemic mice models were established by feeding a high-fat diet for 6 weeks,they were divided into five groups:normal control,model,OFE low-dose,OFE high-dose,and simvastatin groups.After 5 weeks of oral administration,body weight,fasting blood glucose,and liver index were measured.Serum lipid and oxidative stress levels,key proteins levels in the RCT pathway were measured.Hepatic histopathological changes were observed by HE staining,and gut microbiota diversity and compositional changes in feces were analyzed using 16S rRNA high-throughput sequencing.Results:OFE could reduce liver index and blood glucose levels in model mice(P<0.01);decrease serum levels of triglyceride(TG),total cholesterol(TC),and low-density lipoprotein cholesterol(LDL-C)levels(P<0.05 or P<0.01 or P<0.001),while elevating high-density lipoprotein cholesterol(HDL-C)levels(P<0.01);reduce malondialdehyde(MDA)levels(P<0.01)and enhance superoxide dismutase(SOD),catalase(CAT),and total antioxidant capacity(T-AOC)levels(P<0.05,P<0.01,or P<0.001).Additionally,OFE ameliorated hepatic steatosis,suppressed inflammation,and mitigated cellular damage.It upregulated serum levels of ATP-binding cassette transporter A1(ABCA1)and apolipoprotein A1(ApoA-Ⅰ)(P<0.001)and modulated gut microbiota diversity while reducing the Firmicutes to Bacteroidota(F/B)ratio(P<0.05).Conclusion:OFE exhibited potential therapeutic effects in hyperlipidemic mice by attenuating lipid accumulation and oxidative stress levels,as well as improving dyslipidemia,which might be associated with its ability to enhance cholesterol reverse transport(RCT)and ameliorate gut microbiota dysbiosis.

胡月;黄飞翔;樊炳;黄文静;张彪;韩雪;谢兴亮;盛艳梅

成都医学院药学院,结构特异性小分子药物研究四川省高等学校重点实验室,四川 成都 610500成都医学院药学院,结构特异性小分子药物研究四川省高等学校重点实验室,四川 成都 610500成都医学院药学院,结构特异性小分子药物研究四川省高等学校重点实验室,四川 成都 610500成都医学院药学院,结构特异性小分子药物研究四川省高等学校重点实验室,四川 成都 610500成都医学院药学院,结构特异性小分子药物研究四川省高等学校重点实验室,四川 成都 610500成都医学院药学院,结构特异性小分子药物研究四川省高等学校重点实验室,四川 成都 610500成都医学院药学院,结构特异性小分子药物研究四川省高等学校重点实验室,四川 成都 610500成都医学院药学院,结构特异性小分子药物研究四川省高等学校重点实验室,四川 成都 610500

医药卫生

桂花高脂血症胆固醇逆向转运肠道菌群作用机制

Osmanthus fragranshyperlipidemiareverse cholesterol transportgut microbiotamechanism of action

《食品工业科技》 2026 (3)

403-411,9

四川省中医药管理局项目(2024MS538).

10.13386/j.issn1002-0306.2025010223

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