首页> 美国卫生研究院文献>Iranian Journal of Pharmaceutical Research : IJPR >Efficacy of Alpha Glucosidase Inhibitor from Marine Actinobacterium in the Control of Postprandial Hyperglycaemia in Streptozotocin (STZ) Induced Diabetic Male Albino Wister Rats
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Efficacy of Alpha Glucosidase Inhibitor from Marine Actinobacterium in the Control of Postprandial Hyperglycaemia in Streptozotocin (STZ) Induced Diabetic Male Albino Wister Rats

机译:海洋放线杆菌的α-葡萄糖苷酶抑制剂在控制链脲佐菌素(STZ)诱导的糖尿病雄性白化病大鼠餐后高血糖中的功效

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摘要

The current study was carried out to evaluate the in-vitro and in-vivo efficiency of alpha glucosidase inhibitor of marine actinobacteria in the control of postprandial hyperglycaemia. Soil samples were collected from salterns, coastal area in Kothapatnam, Ongole, Andhra Pradesh, India. Among the actinobacterial isolates tested for yeastα-glucosidase inhibitory activity, only three isolates showed prominent inhibition. The patient isolate was selected and identified as Streptomyces coelicoflavus SRBVIT13 using 16S r-RNA gene sequencing. In in-vitro studies, the chloroform extract of Streptomyces coelicoflavus SRBVIT13 showed significant enzyme inhibitory activity against yeast and mammalian α-glucosidaseenzymes. In animal studies, the oral ingestion of chloroform extract (600 mg/kg) of S. coelicoflavus SRBVIT13 in maltose and sucrose loaded diabetic rats, showed significant regulation of postprandial blood glucose by 82.25% and a 77.25% reduction, respectively. The lead compound from S. coelicoflavusSRBVIT13 was isolated, purified, characterized, and identified by stranded analytical techniques as 2-t-butyl-5-chloromethyl-3-methyl-4-oxoimidazolidine-1-carboxylic acid, t-butyl ester. The results obtained in the present study are promising and the bioactive compound from S. coelicoflavusSRBVIT13 may be considered as a potential agent in regulating the postprandial hyperglycaemia.
机译:目前的研究旨在评估海洋放线菌中α-葡萄糖苷酶抑制剂在餐后高血糖控制中的体外和体内效率。土壤样本是从印度安得拉邦昂戈尔科萨帕特南沿海地区的盐厂收集的。在对酵母α-葡萄糖苷酶抑制活性进行测试的放线菌分离株中,只有三个分离株表现出显着的抑制作用。使用16S r-RNA基因测序选择患者分离株并将其鉴定为拟链霉菌黄褐菌SRBVIT13。在体外研究中,链霉菌Strofomyces coelicoflavus SRBVIT13的氯仿提取物对酵母和哺乳动物α-葡萄糖苷敏感酶具有明显的酶抑制活性。在动物研究中,口服麦芽糖和蔗糖的糖尿病大鼠口服氯仿提取物(600 mg / kg)天牛链球菌SRBVIT13的饮食对餐后血糖的调节作用分别为82.25%和77.25%,分别降低。分离,纯化,表征和鉴定了来自co.coelicoflavusSRBVIT13的先导化合物,将其鉴定为2-叔丁基-5-氯甲基-3-甲基-4-氧代咪唑烷-1-羧酸叔丁酯。在本研究中获得的结果是有希望的,并且可认为来自S. coelicoflavusSRBVIT13的生物活性化合物可能是调节餐后高血糖的潜在药物。

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