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中国精品科技期刊2020
马娜娜,韩丽娟,杨永晶,等. 黄刺多糖对STZ诱导的Ⅰ型糖尿病大鼠糖脂代谢的调节作用[J]. 食品工业科技,2024,45(16):348−357. doi: 10.13386/j.issn1002-0306.2023090056.
引用本文: 马娜娜,韩丽娟,杨永晶,等. 黄刺多糖对STZ诱导的Ⅰ型糖尿病大鼠糖脂代谢的调节作用[J]. 食品工业科技,2024,45(16):348−357. doi: 10.13386/j.issn1002-0306.2023090056.
MA Nana, HAN Lijuan, YANG Yongjing, et al. Effect of Berberis dasystachya Polysaccharide on Glucose and Lipid Metabolisms in STZ-induced Type I Diabetic Rats[J]. Science and Technology of Food Industry, 2024, 45(16): 348−357. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023090056.
Citation: MA Nana, HAN Lijuan, YANG Yongjing, et al. Effect of Berberis dasystachya Polysaccharide on Glucose and Lipid Metabolisms in STZ-induced Type I Diabetic Rats[J]. Science and Technology of Food Industry, 2024, 45(16): 348−357. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023090056.

黄刺多糖对STZ诱导的Ⅰ型糖尿病大鼠糖脂代谢的调节作用

Effect of Berberis dasystachya Polysaccharide on Glucose and Lipid Metabolisms in STZ-induced Type I Diabetic Rats

  • 摘要: 为探究黄刺多糖(Berberis dasystachya Maxim. Polysaccharide,BDP)对链脲佐菌素(STZ)诱导的I型糖尿病大鼠的糖脂代谢的调节作用,本文采用STZ诱导I型糖尿病大鼠模型,糖尿病模型大鼠随机分为模型对照组、多糖低剂量组(BDP-L,100 mg/kg)、中剂量组(BDP-M,200 mg/kg)、高剂量组(BDP-H,400 mg/kg)。灌胃28 d后,监测大鼠体重及血糖变化,测定血脂水平、脂代谢酶活性及体内抗氧化酶活等指标。结果表明:黄刺多糖给药第28 d,与模型组相比BDP给药组的血糖、血脂水平均显著降低(P<0.05),其中高剂量组血糖下降39.16%(P<0.01)。BDP给药组的血清胰岛素水平、肝糖原(HG)水平有所增加(P<0.05或P<0.01),其中高剂量组的大鼠血清胰岛素水平增加1.28倍(P<0.01),HG水平增加89.79%(P<0.01)。相比较模型组大鼠,经BDP给药后大鼠/血清和胰腺中的过氧化氢酶(CAT),超氧化物歧化酶(SOD)和还原型谷胱甘肽(CSH-Px)以剂量依赖性方式显著增加(P<0.05或P<0.01),丙二醛(MDA)含量显著减少(P<0.05)。综上,黄刺多糖通过改善Ⅰ型糖尿病大鼠氧化应激从而保护胰岛β细胞的损伤,进而改善糖尿病大鼠的糖脂代谢。

     

    Abstract: In order to provide theoretical support for diabetes prevention and therapy, this study investigated the regulatory effect of Berberis dasystachya Maxim. Polysaccharide (BDP) on glucose and lipid metabolism in streptozotocin (STZ)-induced diabetic rats. Diabetic model rats were randomly assigned to the model control group, low-dose polysaccharide group (BDP-L, 10 mg/kg), mid-dose polysaccharide group (BDP-M, 200 mg/kg), and high-dose group (BDP-H, 400 mg/kg). Blood lipid levels, lipid metabolic enzyme activity, and antioxidant enzyme activity served as evaluation markers. Results showed that after 28 days of administering yellow thorn polysaccharide, the BDP-treated groups exhibited significantly (P<0.05) lower blood glucose and lipid levels compared to the model group, with a remarkable 39.16% reduction in blood glucose in the high-dose group (P<0.01). In contrast, serum insulin levels and hepatic glycogen (HG) levels increased in the BDP-treated groups (P<0.05 or P<0.01), with a 1.28-fold increase in serum insulin (P<0.01) and an 89.79% increase in HG (P<0.01) in the high-dose group. Furthermore, compared to the model group, serum and pancreatic levels of catalase (CAT), superoxide dismutase (SOD), and reduced glutathione (GSH-Px) were significantly elevated (P<0.05 or P<0.01), while malondialdehyde (MDA) levels were considerably reduced (P<0.05) in a dose-dependent manner following BDP treatment. In conclusion, BDP effectively improved glucolipid metabolism in diabetic rats by alleviating oxidative stress, ultimately safeguarding pancreatic β-cell integrity in type I diabetes.

     

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