Inhibitory Effects of Loranthus Parasiticus Extract on Carbohydrate Digestive Enzymes and Postprandial Hyperglycemia

Min-jung Park, Jae-Eun Park, Ji-Sook Han
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Abstract

This study was designed to investigate whether Loranthus parasiticus extract (LPE) could inhibit the activities of carbohydrate digestive enzymes and alleviate postprandial hyperglycemia in diabetic mice. Lyophilized L. parasiticus was extracted with 80% ethanol and concentrated. The inhibitory effects of LPE on carbohydrate digestive enzymes were evaluated by examining α-glucosidase and αamylase, and it was seen to inhibit the activities of both enzymes in a dose-dependent manner. More specifically, the IC50 values of LPE against α-glucosidase and α-amylase were 0.121±0.007 and 0.157± 0.004 mg/ml, respectively, significantly lower than those of acarbose, showing that LPE has stronger inhibitory effects than the positive control. These results suggest that LPE strongly inhibits the activities of these digestive enzymes. Blood glucose levels in the control group of diabetic mice increased to 490.00±28.52 mg/dl and 474.60±25.30 mg/dl at 60 and 120 min after a meal, respectively. However, when LPE was added to starch, postprandial blood glucose levels were significantly reduced (463.0±23.73 and 418.5±24.50 mg/dl at 60 and 120 min, respectively; p<0.05). The area under the curve also significantly decreased following administration of LPE, with no cytotoxicity. These results therefore indicate that LPE could be used as an α-glucosidase and α-amylase inhibitor and delay carbohydrate digestion and, thus, glucose absorption after a meal.
寄生蜂提取物对碳水化合物消化酶和餐后高血糖的抑制作用
本实验旨在探讨寄生萝兰提取物(LPE)是否能抑制糖尿病小鼠碳水化合物消化酶活性,缓解餐后高血糖。用80%乙醇提取冻干的寄生乳杆菌,并进行浓缩。通过α-葡萄糖苷酶和α淀粉酶的检测,研究了LPE对碳水化合物消化酶的抑制作用,发现LPE对α-葡萄糖苷酶和α淀粉酶的抑制作用呈剂量依赖性。具体而言,LPE对α-葡萄糖苷酶和α-淀粉酶的IC50值分别为0.121±0.007和0.157±0.004 mg/ml,显著低于阿卡波糖,表明LPE对α-葡萄糖苷酶和α-淀粉酶的抑制作用强于阳性对照。这些结果表明,LPE对这些消化酶的活性有较强的抑制作用。对照组糖尿病小鼠的血糖水平在餐后60min和120min分别升高至490.00±28.52 mg/dl和474.60±25.30 mg/dl。而在淀粉中添加LPE后,60 min和120 min餐后血糖水平分别显著降低(463.0±23.73和418.5±24.50 mg/dl);p < 0.05)。在给予LPE后,曲线下的面积也显著减少,无细胞毒性。因此,LPE可以作为α-葡萄糖苷酶和α-淀粉酶抑制剂,延缓碳水化合物的消化,从而延缓餐后葡萄糖的吸收。
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