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Antidiabetic Property of Symplocos cochinchinensis Is Mediated by Inhibition of Alpha Glucosidase and Enhanced Insulin Sensitivity

机译:抑制α糖苷酶和增强胰岛素敏感性介导Symplocos cochinchinensis的抗糖尿病作用

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摘要

The study is designed to find out the biochemical basis of antidiabetic property of Symplocos cochinchinensis (SC), the main ingredient of ‘Nisakathakadi’ an Ayurvedic decoction for diabetes. Since diabetes is a multifactorial disease, ethanolic extract of the bark (SCE) and its fractions (hexane, dichloromethane, ethyl acetate and 90% ethanol) were evaluated by in vitro methods against multiple targets relevant to diabetes such as the alpha glucosidase inhibition, glucose uptake, adipogenic potential, oxidative stress, pancreatic beta cell proliferation, inhibition of protein glycation, protein tyrosine phosphatase-1B (PTP-1B) and dipeptidyl peptidase-IV (DPP-IV). Among the extracts, SCE exhibited comparatively better activity like alpha glucosidase inhibition (IC50 value-82.07±2.10 µg/mL), insulin dependent glucose uptake (3 fold increase) in L6 myotubes, pancreatic beta cell regeneration in RIN-m5F (3.5 fold increase) and reduced triglyceride accumulation (22% decrease) in 3T3L1 cells, protection from hyperglycemia induced generation of reactive oxygen species in HepG2 cells (59.57% decrease) with moderate antiglycation and PTP-1B inhibition. Chemical characterization by HPLC revealed the superiority of SCE over other extracts due to presence and quantity of bioactives (beta-sitosterol, phloretin 2′glucoside, oleanolic acid) in addition to minerals like magnesium, calcium, potassium, sodium, zinc and manganese. So SCE has been subjected to oral sucrose tolerance test to evaluate its antihyperglycemic property in mild diabetic and diabetic animal models. SCE showed significant antihyperglycemic activity in in vivo diabetic models. We conclude that SC mediates the antidiabetic activity mainly via alpha glucosidase inhibition, improved insulin sensitivity, with moderate antiglycation and antioxidant activity.
机译:这项研究旨在找出Symplocos cochinchinensis(SC)的抗糖尿病特性的生化基础,Symplocos cochinchinensis(SC)是“阿育吠陀”糖尿病药“ Nisakathakadi”的主要成分。由于糖尿病是一种多因素疾病,因此通过体外方法针对与糖尿病相关的多个目标(例如,α葡萄糖苷酶抑制作用,葡萄糖)对树皮的乙醇提取物(SCE)及其馏分(己烷,二氯甲烷,乙酸乙酯和90%乙醇)进行了评估。摄取,成脂潜能,氧化应激,胰岛β细胞增殖,蛋白质糖基化抑制,蛋白质酪氨酸磷酸酶1B(PTP-1B)和二肽基肽酶IV(DPP-IV)。在这些提取物中,SCE表现出相对更好的活性,如α葡糖苷酶抑制(IC50值-82.07±2.10 µg / mL),L6肌管中胰岛素依赖性葡萄糖摄取(增加3倍),RIN-m5F中胰腺β细胞再生(增加3.5倍)。 )并减少了3T3L1细胞中甘油三酸酯的积累(减少了22%),免受高血糖的影响,诱导了HepG2细胞中活性氧的生成(减少了59.57%),同时具有适度的抗糖化和PTP-1B抑制作用。通过HPLC进行的化学表征显示,除了镁,钙,钾,钠,锌和锰等矿物质外,由于生物活性物质(β-谷甾醇,促绿素2'葡萄糖苷,齐墩果酸)的存在和数量,SCE优于其他提取物。因此,SCE已接受口服蔗糖耐受性测试,以评估其在轻度糖尿病和糖尿病动物模型中的降血糖性能。 SCE在体内糖尿病模型中显示出显着的降血糖活性。我们得出的结论是,SC主要通过α葡萄糖苷酶抑制,改善的胰岛素敏感性,中等的抗糖化作用和抗氧化活性来介导抗糖尿病活性。

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