无花果(Ficus carica L.)酚类化合物抗高脂血症活性的实验研究

Muh. Shofi
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引用次数: 0

摘要

无花果(Ficus carica L.)属桑科植物,含有大量的酚类化合物,具有降血脂的作用。然而,无花果中的酚类化合物尚未得到深入研究。本研究的目的是确定无花果中酚类化合物的抗高脂血症活性,抑制HMG-CoA还原酶的工作。本研究采用了一种实验技术与硅片法。通过比较无花果和普伐他汀中的酚类化合物与HMG-CoA还原酶受体,采用计算机方法预测了普伐他汀的理化、药代动力学、毒性和分子对接特性。与补骨脂素、8-甲氧基补骨脂素、当归素、加甲藤素和普伐他汀对照化合物相比,芦黄素、Pimpinellin和Seselin具有最高的亲和力值,满足理化、药代动力学和毒性参数。该结合酶的存在能够抑制HMG-CoA还原酶的工作活性,其氨基酸残基为Cys526、Gln814、Ile536、Leu811、Ile762、Pro813、Ala763、Ala556、Val538、Pro535、Tyr533、Met534、Gly765、Tyr517、Val522、Cys527。这些结果表明,无花果中的酚类化合物芦黄素、品皮草素和Seselin可能通过抑制HMG-CoA还原酶的作用而具有抗高血脂作用。
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Activity of Phenolic Compounds in Figs (Ficus carica L.) as Antihyperlipidemic through in Silico Study
Figs (Ficus carica L.) belongs to family Moraceae which contains a lot of phenolic compounds that have an antihyperlipidemic effect. However, the phenolic compounds of figs have not been intensively studied. The purpose of this study was to determine the activity of phenolic compounds in figs as antihyperlipidemic in inhibiting the work of the HMG-CoA reductase enzyme. This research uses an experimental technique with the in silico method. The in-silico method was performed to predict the physicochemical, pharmacokinetic, toxicity, and molecular docking properties by comparing the phenolic compounds in figs and Pravastatin with the HMG-CoA reductase receptor. Rutaretin, Pimpinellin dan Seselin has the highest affinity values, met the physicochemical, pharmacokinetic, and toxicity parameters compared to Psoralen, 8-Methoxypsoralen, Angelicin, Bergapten and Pravastatin control compounds. The presence of this binding enzyme was able to inhibit the work activity of HMG-CoA reductase with amino acid residues Cys526, Gln814, Ile536, Leu811, Ile762, Pro813, Ala763, Ala556, Val538, Pro535, Tyr533, Met534, Gly765, Tyr517, Val522, Cys527. These results suggest that phenolic compounds Rutaretin, Pimpinellin, and Seselin in figs could be an antihyperlipidemic on inhibiting the action of HMG-CoA reductase enzyme.
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