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类黄酮前体作为降血糖和降血脂药物的核心结构:大鼠体内研究

Core structure of flavonoids precursor as an antihyperglycemic and antihyperlipidemic agent: an in vivo study in rats.

作者信息

Najafian Mahmoud, Ebrahim-Habibi Azadeh, Yaghmaei Parichehreh, Parivar Kazem, Larijani Bagher

机构信息

Islamic Azad University, Tehran, Iran.

出版信息

Acta Biochim Pol. 2010;57(4):553-60. Epub 2010 Nov 9.

Abstract

trans-Chalcone is the core structure of naringenin chalcone, located halfway in the biosynthesis pathway of flavonoids. Flavonoids have been reported as mammalian alpha-amylase inhibitors, a property which could be useful in the management of postprandial hyperglycemia in diabetes and related disorders. As a mammalian alpha-amylase inhibitor in vitro, the putative beneficial effect of trans-chalcone on diabetes was tested in a streptozotocin-induced rat model of diabetes type 1, and the results analyzed with commonly used statistical methods. Significant reduction of blood glucose levels and beneficial effect on dyslipidemia were observed in diabetic rats, as well as reduction of disturbing consequences of diabetes such as high urine volume and water intake. trans-chalcone was observed to have a weight loss-inductive effect, alongside with a reduction in food intake, which is suggestive of a therapeutic potential of this compound in overweight and obese patients.

摘要

反式查尔酮是柚皮素查尔酮的核心结构,位于类黄酮生物合成途径的中间位置。据报道,类黄酮是哺乳动物α-淀粉酶抑制剂,这一特性可能有助于治疗糖尿病及相关疾病的餐后高血糖。作为一种体外哺乳动物α-淀粉酶抑制剂,在链脲佐菌素诱导的1型糖尿病大鼠模型中测试了反式查尔酮对糖尿病的假定有益作用,并采用常用统计方法对结果进行分析。在糖尿病大鼠中观察到血糖水平显著降低,对血脂异常有有益作用,同时减少了糖尿病的不良后果,如高尿量和高饮水量。观察到反式查尔酮具有诱导体重减轻的作用,同时食物摄入量减少,这表明该化合物对超重和肥胖患者具有治疗潜力。

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