Department of Aging Control Medicine, Juntendo University Graduate School of Medicine, Bunkyo-Ku, Tokyo 113-0033, Japan.
Institute for Bee Products & Health Science, Yamada Bee Company, Inc., 194 Ichiba, Kagamino-cho, Okayama 708-0393, Japan.
Evid Based Complement Alternat Med. 2013;2013:589169. doi: 10.1155/2013/589169. Epub 2013 Dec 17.
Melinjo (Gnetum gnemon L.) seed extract (MSE) containing trans-resveratrol (3,5,4'-trihydroxy-trans-stilbene) and other derivatives exerts various beneficial effects. However, its mechanism of action in humans remains unknown. In this study, we aimed to investigate beneficial effects of MSE in healthy adult males. In this double-blind, randomized controlled study, 30 males aged 35-70 years with ≤10% flow-mediated dilatation received placebo or 750 mg MSE powder for 8 weeks, and twenty-nine males (45.1 ± 8.8 years old) completed the trial. There was a significant difference in the melinjo and placebo groups. Compared with the placebo control, MSE significantly reduced serum uric acid at 4 weeks and 8 weeks (n = 14 and 15, resp.). HDL cholesterol was significantly increased in the melinjo group. To clarify the mechanism of MSE for reducing uric acid, we investigated xanthine oxidase inhibitory activity, angiotensin II type 1 (AT1) receptor binding inhibition rate, and agonistic activities for PPAR α and PPAR γ . MSE, trans-resveratrol, and a resveratrol dimer, gnetin C (GC), significantly inhibit AT1 receptor binding and exhibit mild agonistic activities for PPAR α and PPAR γ . In conclusion, MSE may decrease serum uric acid regardless of insulin resistance and may improve lipid metabolism by increasing HDL cholesterol.
美林乔(Gnetum gnemon L.)种子提取物(MSE)含有反式白藜芦醇(3,5,4'-三羟基反式芪)和其他衍生物,具有多种有益作用。然而,其在人体中的作用机制尚不清楚。在这项研究中,我们旨在研究 MSE 对健康成年男性的有益作用。在这项双盲、随机对照研究中,30 名年龄在 35-70 岁、血流介导扩张率≤10%的男性接受安慰剂或 750mg MSE 粉末治疗 8 周,29 名男性(45.1±8.8 岁)完成了试验。Melinjo 组和安慰剂组之间存在显著差异。与安慰剂对照组相比,MSE 可显著降低 4 周和 8 周时的血清尿酸(n=14 和 15)。Melinjo 组的高密度脂蛋白胆固醇显著增加。为了阐明 MSE 降低尿酸的机制,我们研究了黄嘌呤氧化酶抑制活性、血管紧张素 II 型 1(AT1)受体结合抑制率以及对 PPARα和 PPARγ的激动活性。MSE、反式白藜芦醇和白藜芦醇二聚体 Gnetin C(GC)均能显著抑制 AT1 受体结合,并对 PPARα和 PPARγ具有温和的激动活性。总之,MSE 可能降低血清尿酸,而与胰岛素抵抗无关,并通过增加高密度脂蛋白胆固醇改善脂质代谢。