摘要
目的:探讨桑叶总黄酮对2型糖尿病(T2DM)大鼠肝脏的保护作用。方法:选用雄性wistar大鼠,高脂饲料喂养且用链脲佐菌素诱导,复制T2DM模型,模型成功后随即分成模型组、二甲双胍组、桑叶总黄酮高、中、低(200、100、50 mg·kg^(-1)·bw^(-1))剂量组,各药干预4周后,比较各组大鼠的体重和空腹血糖值;称重肝脏,计算肝脏指数;测定血清中甘油三酯(TG)、总胆固醇(TC)和丙氨酸氨基转移酶(ALT)水平;测定肝脏中肝糖原水平,葡萄糖激酶(GK)活性;对肝脏进行HE染色,做病理组织学检查。结果:与模型组相比,桑叶总黄酮高剂量组能降低T2DM大鼠的体重,为(390.79±77.27)g;降低TC、TG和ALT水平,分别为(2.25±0.58)mmol·L^(-1)、(0.92±0.36)mmol·L^(-1)和(69.36±5.58)U·L^(-1);增加肝糖原含量,为(12.22±1.50)mg·g^(-1);提高GK活性,为(10.33±1.30)m IU·min^(-1)·mg protein^(-1);减轻肝脏脂肪变性,改善肝脏病理。结论:桑叶总黄酮在预防和改善T2DM肝损伤方面具有一定的应用开发潜力。
Objective:To observe the effect of total flavonoids of mulberry leaves on liver in type 2 diabetic rats.Methods:The male wistar rats were fed with high fat diet and streptozotocin to induce the type 2 diabetic model and the model rats were divided into five groups randomly:model group,metformin group,total flavonoids of mulberry leaves dose groups(200,100,50 mg·kg^(-1)·bw^(-1)i.g). After 4 weeks,levels of weight,blood glucose,organ coefficient,total cholesterol(TC),triglyceride(TG) and alanine aminotransferase(ALT) in serum were observed;hepatic glycogen,hepatic GK activity,and liver samples were observed pathologically with HE staining. Results:Compared with the model group,total flavonoids of mulberry leaves high dose group could reduce the levels of weight(390.79±77.27) g,TC(2.25±0.58) mmol·L^(-1),TG(0.92±0.36) mmol·L^(-1) and ALT(69.36±5.58) U·L^(-1),increase the content of hepatic glycogen(12.22±1.50) mg·g^(-1),improve the activity of GK( 10. 33 ± 1. 30) m IU·min^(-1)·mg protein^(-1), obviously alleviate the histopathologic changes including fatty degeneration. Conclusion:It showed that total flavonoids of mulberry leaves had potential to be developed in the aspect of preventing and improving liver damage in type 2 diabetic.
出处
《食品工业科技》
CAS
CSCD
北大核心
2016年第8期340-343,共4页
Science and Technology of Food Industry
基金
四川省省级大学生创新创业训练计划项目(201313705013)
成都医学院校级大学生创新实验项目(CXJS201419)
成都医学院实验室开放项目(Kf201406)
关键词
2型糖尿病
桑叶总黄酮
肝糖原
葡萄糖激酶
丙氨酸氨基转移酶
type 2 diabetes mellitus
total flavonoids of mulberry leaves
hepatic glycogen
glucokinase
alanine aminotransferase