首页> 外文期刊>结合医学学报:英文版 >Antihyperglycaemic activity of ethylacetate extract of Chlorophytum alismifolium in type 2 diabetes:The involvement of peroxisome proliferator-activated receptor-γand dipeptidyl peptidase-4
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Antihyperglycaemic activity of ethylacetate extract of Chlorophytum alismifolium in type 2 diabetes:The involvement of peroxisome proliferator-activated receptor-γand dipeptidyl peptidase-4

机译:2型糖尿病叶绿素乙酸乙酯提取物的抗血糖药物:过氧化物体增殖物激活受体-γ和二肽基肽酶-4的累积

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摘要

Objective:This research is to investigate the antihyperglycaemic activity and the underlying mechanisms of action of the ethylacetate extract of Chlorophytum alismifolium(EACA)tubers in a type 2 diabetes model.Methods:The tubers were processed and sequentially extracted in hexane followed by ethylacetate,using a Soxhlet apparatus,and subjected to gas chromatography-mass spectrometry(GC–MS).The acute toxicity of EACA was investigated in albino Wistar rats.An antihyperglycaemic study was carried out using high-fat diet(pelletized diet and margarine in the ratio of 10:1 and 20%fructose solution)and streptozotocin-induced hyperglycaemic Wistar rats.The effects of the extract(150,300 and 600 mg/kg)on blood glucose level,insulin,peroxisome proliferator-activated receptor-c(PPAR-c)and dipeptidyl peptidase-4(DPP-4)were evaluated using enzyme-linked immunosorbent assay.Results:The oral median lethal dose in Wistar rats was estimated to be>5000 mg/kg.Treatment with EACA at all doses significantly reduced the fasting blood glucose levels,compared to the hyperglycaemic control,and over time.Administration of EACA increased the serum insulin and PPAR-c levels while decreasing DPP-4 levels.GC–MS analysis revealed the presence of 13 compounds,with isothiazole and isoxazolidine covering total area of 24.6%and 22.69%,respectively.Conclusion:The findings from this study showed that EACA has important compounds with beneficial effect in type 2 diabetes and acts by increasing insulin secretion and PPAR-c level and decreasing DPP-4 activity.
机译:目的:本研究旨在调查抗血糖活性和氯化乙酸乙酯溶液(EACA)在2型糖尿病模型中的乙酰乙酸乙酯提取物的潜在机制。方法:用己烷加工并依次萃取块茎,然后用乙酸乙酯索氏素仪,并进行气相色谱 - 质谱(GC-MS)。在白化病原大鼠中研究了EACA的急性毒性。使用高脂饮食(造粒饮食和人造黄油以比例的比例进行抗血糖研究10:1和20%的果糖溶液)和链脲佐菌素诱导的高血糖Wistar大鼠。提取物(150,300和600 mg / kg)对血糖水平,胰岛素,过氧化物体增殖物激活受体-c(PPAR-C)的影响使用酶联免疫吸附试验评估二肽基肽酶-4(DPP-4)。结果:Wistar大鼠中的口腔中值致命剂量估计为> 5000mg / kg.Treatment,所有剂量都有显着性y减少了血液血糖水平,与高血糖控制相比,随着时间的推移。EACA的发行量增加了血清胰岛素和PPAR-C水平,同时降低了DPP-4水平。GC-MS分析显示出13种化合物的存在,用异噻唑伊索唑烷覆盖总面积为24.6%和22.69%。结论:本研究的结果表明,EACA在2型糖尿病中具有重要的化合物,通过增加胰岛素分泌和PPAR-C水平和降低DPP-4来作用。活动。

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  • 来源
    《结合医学学报:英文版》 |2021年第001期|P.78-84|共7页
  • 作者单位

    Department of Pharmacology and Therapeutics Ahmadu Bello University Zaria PMB-1044 Nigeria Department of Pharmacology and Therapeutics Bayero University Kano PMB-3011 Nigeria Department of Human Physiology Ahmadu Bello University Zaria PMB-1044 Nigeria Department of Pharmacognosy and Drug Development Ahmadu Bello University Zaria PMB-1044 Nigeria;

    Department of Pharmacology and Therapeutics Ahmadu Bello University Zaria PMB-1044 Nigeria Department of Pharmacology and Therapeutics Bayero University Kano PMB-3011 Nigeria Department of Human Physiology Ahmadu Bello University Zaria PMB-1044 Nigeria Department of Pharmacognosy and Drug Development Ahmadu Bello University Zaria PMB-1044 Nigeria;

    Department of Pharmacology and Therapeutics Ahmadu Bello University Zaria PMB-1044 Nigeria Department of Pharmacology and Therapeutics Bayero University Kano PMB-3011 Nigeria Department of Human Physiology Ahmadu Bello University Zaria PMB-1044 Nigeria Department of Pharmacognosy and Drug Development Ahmadu Bello University Zaria PMB-1044 Nigeria;

    Department of Pharmacology and Therapeutics Ahmadu Bello University Zaria PMB-1044 Nigeria Department of Pharmacology and Therapeutics Bayero University Kano PMB-3011 Nigeria Department of Human Physiology Ahmadu Bello University Zaria PMB-1044 Nigeria Department of Pharmacognosy and Drug Development Ahmadu Bello University Zaria PMB-1044 Nigeria;

    Department of Pharmacology and Therapeutics Ahmadu Bello University Zaria PMB-1044 Nigeria Department of Pharmacology and Therapeutics Bayero University Kano PMB-3011 Nigeria Department of Human Physiology Ahmadu Bello University Zaria PMB-1044 Nigeria Department of Pharmacognosy and Drug Development Ahmadu Bello University Zaria PMB-1044 Nigeria;

    Department of Pharmacology and Therapeutics Ahmadu Bello University Zaria PMB-1044 Nigeria Department of Pharmacology and Therapeutics Bayero University Kano PMB-3011 Nigeria Department of Human Physiology Ahmadu Bello University Zaria PMB-1044 Nigeria Department of Pharmacognosy and Drug Development Ahmadu Bello University Zaria PMB-1044 Nigeria;

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  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类 晶体结构;
  • 关键词

    Chlorophytum alismifolium; Diabetes mellitus; Gas chromatography-mass spectrometry; Insulin; Peroxisome proliferator-activated receptor-c; Dipeptidyl-peptidase 4;

    机译:叶绿素肌性纤维素;糖尿病;气相色谱 - 质谱;胰岛素;过氧化物体增殖剂活化受体-c;二肽基肽酶4;
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