Biological activities of salvianolic acid B from Salvia miltiorrhiza on type 2 diabetes induced by high-fat diet and streptozotocin

Biological activities of salvianolic acid B from Salvia miltiorrhiza on type 2 diabetes induced by high-fat diet and streptozotocin
复制标题

丹参丹酚酸B对高脂饮食和链脲佐菌素诱导的2型糖尿病的生物活性

DOI:
10.3109/13880209.2014.959611
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发表时间:
2015-01-01
影响因子:
3.8
通讯作者:
Lu, Jinjian
Lu, Jinjian
中科院分区:
医学3区
文献类型:
--
作者:
Huang, Mingqing;Wang, Peijian;Lu, Jinjian

文献摘要

被引文献

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摘要背景:丹参Bge。(Labibiridine)已被广泛用于治疗糖尿病几个世纪。丹参酸B(SalB)是丹参中的主要活性成分,但其抗糖尿病活性及其可能机制尚不清楚。目的:目的:探讨SalB对2型糖尿病大鼠糖代谢、脂代谢、胰岛素抵抗、氧化应激及糖原合成的影响。材料与方法:将高脂饮食(HFD)和链脲佐菌素(STZ)诱导的糖尿病大鼠随机分为模型组、SalB组(50、100、200 mg/kg)和罗格列酮组。结果如下:与模型组相比,SalB(100和200 mg/kg)组血糖和胰岛素水平分别降低23.8和21.7%(p < 0.05和p < 0.01)和31.3和26.6%(p < 0.05),胰岛素敏感性指数分别升高10.9和9.3%(p < 0.05)。他们还显着降低总胆固醇(分别为24.9%和27.9%; p < 0.01),低密度脂蛋白胆固醇(56.2%和64.6%; p < 0.01),非酯化脂肪酸(分别为32.1%和37.9%; p < 0.01),肝糖原(分别为41.3%和60.5%; p < 0.01),肌糖原(分别增加33.2和38.6%; p < 0.05),并增加高密度脂蛋白胆固醇(分别增加50.0和61.4%; p < 0.05和p < 0.01),这些都是最初被HFD和链脲佐菌素改变的。此外,SalB(200 mg/kg)显著降低甘油三酯和丙二醛(分别为31.5%和29.0%; p < 0.05和p < 0.01),并增加超氧化物歧化酶(分别为56.6%; p < 0.01),而这些变化最初是由HFD和链脲佐菌素引起的。讨论与结论:结果表明,SalB能抑制糖尿病大鼠的症状,其作用可能部分与其胰岛素敏感性、糖原合成和抗氧化活性有关。
Abstract Context: Salvia miltiorrhiza Bge. (Labiatae) has been widely used for treating diabetes for centuries. Salvianolic acid B (SalB) is the main bioactive component in Salvia miltiorrhiza; however, its antidiabetic activity and possible mechanism are not yet clear. Objective: To investigate the effects of SalB on glycometabolism, lipid metabolism, insulin resistance, oxidative stress, and glycogen synthesis in type 2 diabetic rat model. Materials and methods: High-fat diet (HFD) and streptozotocin-induced diabetic rats were randomly divided into model group, SalB subgroups (50, 100, and 200 mg/kg), and rosiglitazone group. Results: Compared with the model group, SalB (100 and 200 mg/kg) significantly decreased blood glucose (by 23.8 and 21.7%; p < 0.05 and p < 0.01) and insulin (by 31.3 and 26.6%; p < 0.05), and increased insulin sensitivity index (by 10.9 and 9.3%; p < 0.05). They also significantly decreased total cholesterol (by 24.9 and 27.9%; p < 0.01), low-density lipoprotein cholesterol (by 56.2 and 64.6%; p < 0.01), non-esterified fatty acids (by 32.1 and 37.9%; p < 0.01), hepatic glycogen (by 41.3 and 60.5%; p < 0.01), and muscle glycogen (by 33.2 and 38.6%; p < 0.05), and increased high-density lipoprotein cholesterol (by 50.0 and 61.4%; p < 0.05 and p < 0.01), which were originally altered by HFD and streptozotocin. In addition, SalB (200 mg/kg) markedly decreased triglyceride and malondialdehyde (by 31.5 and 29.0%; p < 0.05 and p < 0.01), and increased superoxide dismutase (by 56.6%; p < 0.01), which were originally altered by HFD and streptozotocin. Discussion and conclusion: The results indicate that SalB can inhibit symptoms of diabetes mellitus in rats and these effects may partially be correlated with its insulin sensitivity, glycogen synthesis and antioxidant activities.