Amelioration of obesity, glucose intolerance, and oxidative stress in high-fat diet and low-dose streptozotocin-induced diabetic rats by combination consisting of "curcumin with piperine and quercetin".

ISRN Pharmacology Pub Date : 2012-01-01 Epub Date: 2012-03-08 DOI:10.5402/2012/957283
Ginpreet Kaur, Meena C
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引用次数: 52

Abstract

Curcumin is an important nutraceutical that has enormous potential for a variety of diseases, but the medicinal properties of curcumin cannot be utilized due to its low in vivo bioavailability. Therefore, in view of the foregoing, there is an extensive need for combinatorial extract "curcumin with piperine and quercetin" which may enhance bioavailability of oral curcumin by inhibiting the enzymes responsible for the metabolism of curcumin. Thus, the present study investigated the effect of combinatorial extract of curcumin on obesity, glucose intolerance, and oxidative stress in high fat diet and low-dose streptozotocin-induced rats. Oral administration of combinatorial extract for 28 days significantly (P < 0.05) reduced PGL (64.84%), PTG (88.94%), LDL (26.38%) and PTC (50.23%) levels, respectively and improved glucose tolerance (P < 0.05) significantly to exogenously administered glucose (2 g/kg) at 60, 90, and 120 min interval on OGTT. The results for antioxidant potential indicate that at 100 mg/kg dose of combinatorial extract of curcumin significantly prevented the high-fat diet and low-dose streptozotocin-induced changes in the oxidative stress parameters (P < 0.01) which supports popular medicinal uses of this combinatorial extract as antihyperglycemic and hypolipidemic and is likely to bring this promising natural product to the forefront of therapeutic agents in the in the treatment of "metabolic syndrome".

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姜黄素与胡椒碱、槲皮素复合改善高脂肪饮食和低剂量链脲佐菌素诱导的糖尿病大鼠肥胖、葡萄糖耐受不良和氧化应激
姜黄素是一种重要的营养保健品,对多种疾病具有巨大的治疗潜力,但由于其体内生物利用度较低,无法充分发挥其药用价值。因此,鉴于上述情况,广泛需要“姜黄素与胡椒碱和槲皮素”的组合提取物,该提取物可以通过抑制姜黄素代谢的酶来提高口服姜黄素的生物利用度。因此,本研究探讨了姜黄素组合提取物对高脂肪饮食和低剂量链脲佐菌素诱导的大鼠肥胖、葡萄糖耐受不良和氧化应激的影响。口服组合提取物28 d可显著(P < 0.05)降低PGL(64.84%)、PTG(88.94%)、LDL(26.38%)和PTC(50.23%)水平,并可显著提高OGTT间歇60、90和120 min对外源性葡萄糖(2 g/kg)的糖耐量(P < 0.05)。结果表明,姜黄素组合提取物在100 mg/kg剂量下显著阻止高脂肪饮食和低剂量链脲佐菌素引起的氧化应激参数变化(P < 0.01),支持了姜黄素组合提取物作为抗高血糖和降血脂药物的广泛应用,并有可能使这一有前途的天然产物成为治疗“代谢综合征”的药物的前沿。
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