PANCREATIC LIPASE AND α-AMYLASE INHIBITORY POTENTIAL OF MANGOSTEEN (GARCINIA MANGOSTANA LINN.) PERICARP EXTRACT

I. Adnyana, Alkilany Salem Abuzaid, Elin Yulinah Iskandar, N. Kurniati
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引用次数: 32

Abstract

Background: Obesity is a disorder of lipid metabolism and the enzyme involved in this process could be selectively targeted to develop anti obesity drugs. Inhibition of digestive enzymes is one of the most widely studies mechanisms used to determine the hypolipidemic and hypoglycemic agent of natural products for anti-obesity agent screening. Aims: To evaluate the inhibitory potential of G. mangostana extract, xanthone and α-mangosteen compound toward pancreatic lipase and α-amylase enzyme as once of anti-obesity mechanism. Material and Methods: The IC50 value of the mangosteen pericarp extract, xanthone, and α-mangosteen toward pancreatic lipase and α-amylase were determined in vitro compared to orlistat and acarbose as standard drugs. Results: Mangosteen pericarp extract contains phenol, terpenoid, saponin, flavonoid and tannin. Mangosteen pericarp extract is a more active compound in inhibiting the PPL activity compared to α-mangosteen, and xanthone. Mangosteen pericarp extract shows the higher activity compared to xanthone but still lower activity compared to α-mangosteen. However, its activity is still lower than standard drugs. Conclusions: Our in vitro, confirmed that the mangosteen pericarp extract has the phytochemical bioactive content that possesses anti-obesity potential through pancreatic lipase and α-amylase inhibitory activity.
山竹对胰脂肪酶和α-淀粉酶的抑制作用果皮中提取
背景:肥胖是一种脂质代谢紊乱,参与这一过程的酶可以选择性地靶向开发抗肥胖药物。消化酶的抑制作用是研究最广泛的机制之一,用于确定降血脂和降血糖的天然产物,用于抗肥胖药物的筛选。目的:探讨山竹提取物、山酮和α-山竹复合物对胰脂肪酶和α-淀粉酶的抑制作用及其抗肥胖机制。材料与方法:以山竹果皮提取物、山酮、α-山竹提取物为对照品,体外测定其对胰脂肪酶和α-淀粉酶的IC50值。结果:山竹果皮提取物含有酚、萜类、皂苷、黄酮类和单宁。山竹果皮提取物对PPL活性的抑制作用比α-山竹果皮提取物和山酮更有效。山竹果皮提取物的活性高于山蒽酮,但低于α-山竹果皮提取物的活性。然而,其活性仍低于标准药物。结论:体外实验证实山竹果皮提取物具有抑制胰脂肪酶和α-淀粉酶抑制肥胖的植物化学生物活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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