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作 者:何荣[1] 冯国华[1] 张富东[1] 熊凡[1] 李玲[1] 高丽辉[1]
机构地区:[1]昆明医科大学生物医学工程研究中心,昆明650500
出 处:《中药药理与临床》2013年第3期54-57,共4页Pharmacology and Clinics of Chinese Materia Medica
基 金:国家自然科学基金资助项目(30760306);云南省应用基础研究计划重点项目(2006C009Z)
摘 要:目的:研究芒果苷(Mangiferin,MF)对α-葡萄糖苷酶的抑制作用。方法:通过建立体外α-葡萄糖苷酶抑制剂微孔筛选模型,对芒果苷进行α-葡萄糖苷酶抑制活性研究,并采用林贝氏作图法判断抑制作用类型;研究芒果苷对正常小鼠可溶性淀粉、蔗糖和葡萄糖耐量的影响。结果:芒果苷(IC50=164.16 mg/L)体外α-葡萄糖苷酶抑制活性高于阳性药阿卡波糖(Acarbose,IC50=1095.65 mg/L),且抑制率随浓度增加而增加,为竞争性抑制剂;体内研究表明灌胃给予芒果苷(50mg/kg和100mg/kg)能明显抑制正常动物对淀粉、蔗糖等多糖的吸收,但对葡萄糖的吸收并无影响。结论:芒果苷有α-葡萄糖苷酶抑制活性。He Rong,Feng Guohua,Zhang Fudong,Xiong Fan,Li Ling,Gao Lihui(Biomedical Engineering Reaserach Center,Kunming Medical University,Kunming 650500) Objective:Mangiferin,a xanthone glucoside,is an active phytochemical exist in various plants.In the present study,the inhibitory action of mangiferin on the activity of alpha-glucosidase is investigated.Methods: An optimized microplate-based method was developed to characterize the mangiferin on the activity of α-glucosidase inhibition.The related inhibition type of mangiferin was identified from Lineweaver-Burk plots.The inhibitory effects of mangiferin on polysaccharide absorption were investigated in normal mice.Results: In vitro,mangiferin significantly inhibited the activity of α-glucosidase,in a concentration-dependent manner,with a IC50 value of 164.16 mg/L,which was more potent than that of acarbose(IC50 = 1095.65 mg/L).The inhibition type of mangiferin was competitive.In vivo,mangiferin,given by intragastrically 50 mg/kg and 100 mg/kg,markedly reduced the absorption of starch and sucrose in normal mice,but has no effect on the absorption of glucose.Conclusion: Mangiferin has obvious inhibitory activity on α-glucosidase in vitro and in vivo.
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