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投稿时间:2024-04-18
投稿时间:2024-04-18
中文摘要: 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。
Abstract: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 αglucosidase 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 exhibited 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,respectively,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),remarkedly increased glucose tolerance. Besides,alloxan-induced body weight loss was ameliorated,and total cholesterol 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.
文章编号:202502003 中图分类号: 文献标志码:
基金项目:四川省科技计划项目(2022YFS0435);广东省重点领域研发计划项目(2022B1111050003);成都市科技项目(2022-YF05-00447-SN)
作者 | 单位 |
方京梅1,姚倩2,黄亚萱2,魏玉娇1,姚才梅2,刘平3,郭晓强2 * | 1.成都大学 食品与生物工程学院,四川 成都 610106;2.成都大学 药学院,四川 成都 610106;3.成都大学附属医院,四川 成都 610081 |
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