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土茯苓醇提物及其主成分落新妇苷的体内外降糖活性

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为比较土茯苓醇提物及其主成分落新妇苷的体内外降糖活性,测定土茯苓醇提物与落新妇苷对α-葡萄糖苷酶和胰脂肪酶的抑制作用,并考察样品对酶的荧光淬灭速率;采用四氧嘧啶法建立糖尿病小鼠模型,研究落新妇苷及醇提物的体内降糖活性。结果表明,土茯苓醇提物对α-葡萄糖苷酶和胰脂肪酶的抑制作用显著高于落新妇苷;对酶的荧光淬灭速率常数分别是落新妇苷的 3。32 倍和 5。89 倍,表明土茯苓醇提物对酶有更强的亲和力。与糖尿病模型组相比,土茯苓醇提物和落新妇苷均能显著降低糖尿病小鼠的空腹血糖(P<0。01),改善四氧嘧啶引起的小鼠体质量下降,显著提高糖耐量,降低血清总胆固醇和甘油三酯水平,并对高糖引起的肝肾损伤具有保护作用,能显著降低肝肾指数(P<0。05)。与落新妇苷相比,土茯苓醇提物具有更好的生理活性。
In vivo and in vitro Hypoglycemic Activity of Alcoholic Extract from Smilax glabra Roxb and Its Principal Component Astilbin
In vivo and in vitro hypoglycemic activities of Smilax glabra Roxb's(E-RSG)alcoholic extract and its main component astilbin were compared in this study.Inhibitory activity of E-RSG and astilbin against α-glucosidase and pancreatic lipase were determined,respectively.Fluorescence quenching rates of the samples on the enzymes were examined.A diabetic mouse model was established by the alloxan method to investigate the in vivo hypoglycemic activity of astilbin and E-RSG.Results showed that,compared to astilbin,E-RSG ex-hibited a significantly higher inhibitory effect against α-glucosidase and pancreatic lipase.The fluorescence quenching rate constant of the extract toward the enzymes was 3.32 and 5.89 times that of astilbin,respec-tively,indicating that E-RSG's affinity with the enzymes was stronger.Compared with the diabetic model group,both E-RSG and astilbin significantly reduced fasting blood glucose of diabetic mice(P<0.01),remark-edly increased glucose tolerance.Besides,alloxan-induced body weight loss was ameliorated,and total choles-terol and triglyceride levels were decreased.In addition,hepatic and renal indexes were significantly decreased(P<0.05),exerting a protective effect against hyperglycemia-induced hepatic and renal injuries.Compared to astilbin,E-RSG presented better physiological activity.

Smilax glabra Roxbastilbinhypoglycemicα-glucosidasepancreatic lipase

方京梅、姚倩、黄亚萱、魏玉娇、姚才梅、刘平、郭晓强

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成都大学食品与生物工程学院,四川成都 610106

成都大学药学院,四川成都 610106

成都大学附属医院,四川成都 610081

土茯苓 落新妇苷 降血糖 α-葡萄糖苷酶 胰脂肪酶

2025

食品研究与开发
天津市食品研究所,天津市食品工业生产力促进中心

食品研究与开发

影响因子:0.561
ISSN:1005-6521
年,卷(期):2025.46(2)