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金合欢心材提取物中的植物化学物质可降低黄嘌呤氧化酶诱导的小鼠血清尿酸水平:它们可能作为黄嘌呤氧化酶抑制剂的用途。

Phytochemicals from Acacia confusa heartwood extracts reduce serum uric acid levels in oxonate-induced mice: their potential use as xanthine oxidase inhibitors.

机构信息

School of Forestry and Resource Conservation, National Taiwan University, Taipei 106, Taiwan.

出版信息

J Agric Food Chem. 2010 Sep 22;58(18):9936-41. doi: 10.1021/jf102689k.

DOI:10.1021/jf102689k
PMID:20806936
Abstract

In this study, the antihyperuricemic effect of Acacia confusa heartwood extracts and their phytochemicals on potassium oxonate (PO)-induced acute hyperuricemia was investigated for the first time. All treatments at the same dosage (100 mmol/kg) were administered to the abdominal cavity of PO-induced hyperuricemic mice, and serum uric acid level was measured at 3 h after administration. In experimental mice, serum uric acid level was significantly suppressed by the administration of A. confusa heartwood extracts and their major phytochemicals, (-)-2,3-cis-3,4-cis-3,3',4,4',7,8-hexahydroxyflavan, (-)-2,3-cis-3,4-cis-4'-methoxy-3,3',4,7,8-pentahydroxyflavan, melanoxetin, transilitin, and okanin, relative to the PO group. The direct inhibitory effect of these five compounds on xanthine oxidase (XOD) activity was examined using isothermal titration calorimetry (ITC). Among them, melanoxetin showed a more remarkable inhibitory effect on XOD activity than allopurinol, a clinical drug used for XOD inhibitor. To further understand the stereochemistry between XOD and melanoxetin (or allopurinol), structure-based molecular modeling was performed. Melanoxetin undergoes extended interactions in the hydrophobic region via the 3',4'-dihydroxyphenyl moiety, thus accounting for its higher binding affinity to XOD than allopurinol. These results indicate that A. confusa heartwood extracts and their major phytochemicals exhibit strong XOD inhibitory effects, which reduce serum uric acid levels while inhibiting uric acid generation in purine metabolism.

摘要

在这项研究中,首次研究了金合欢心材提取物及其植物化学物质对氧嗪酸钾(PO)诱导的急性高尿酸血症的抗高尿酸血症作用。将相同剂量(100mmol/kg)的所有治疗药物腹腔注射到 PO 诱导的高尿酸血症小鼠中,并在给药后 3 小时测量血清尿酸水平。在实验小鼠中,金合欢心材提取物及其主要植物化学物质((-)-2,3-cis-3,4-cis-3,3',4,4',7,8-六羟基黄酮、(-)-2,3-cis-3,4-cis-4'-甲氧基-3,3',4,7,8-五羟基黄酮、melanoxetin、transilitin 和 okanin 显著抑制了血清尿酸水平,与 PO 组相比。使用等温滴定量热法(ITC)检查了这五种化合物对黄嘌呤氧化酶(XOD)活性的直接抑制作用。其中,melanoxetin 对 XOD 活性的抑制作用比用于 XOD 抑制剂的临床药物别嘌醇更为显著。为了进一步了解 XOD 与 melanoxetin(或别嘌醇)之间的立体化学,进行了基于结构的分子建模。Melanoxetin 通过 3',4'-二羟基苯基部分在疏水区中发生扩展相互作用,从而解释了其与 XOD 的结合亲和力高于别嘌醇。这些结果表明,金合欢心材提取物及其主要植物化学物质具有很强的 XOD 抑制作用,可降低血清尿酸水平,同时抑制嘌呤代谢中尿酸的生成。

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