混合草药提取物对糖尿病前期个体的抗糖化作用

Y. Yonei, R. Miyazaki, Yoko Takahashi, H. Takahashi, K. Nomoto, M. Yagi, H. Kawai, M. Kubo, N. Matsuura
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引用次数: 35

摘要

目的:我们进行了一项双盲、安慰剂对照、平行组研究,以评估混合草药提取物(MHE)对糖尿病前期个体的抗糖基化作用。MHE是用热水萃取法从洋甘菊(Anthemis nobilis)、山楂(Crataegus oxyacantha)、鱼尾草(Houttuynia cordata)和葡萄叶(Vitis vinifera)中提取出来的。我们还评估了MHE是否对一个人的生活质量(QOL)有有利的影响。设计:受试者由26名志愿者组成(男性21名;女:5;年龄:50.5±8.5岁),伴有糖尿病前期(HbA1c: 5.5 - 6.7%)。将患者分为实验组(13例,年龄52.8±8.2岁)和对照组(12例,年龄49.3±7.8岁)。试验组每天给予MHE(固体物质)1200 mg,连续8周。对照组服用安慰剂。结果:采用《抗衰老生活质量问卷》(AAQol)进行组间分析,实验组在“肌肉疼痛/僵硬”、“头痛”、“易发怒”、“不愿与人交谈”、“记忆力减退”、“不能轻易做出判断”等参数得分均有显著提高(p < 0.05)。糖代谢方面,空腹血糖、糖化血红蛋白、糖蛋白、胰岛素均无明显变化。8周后,实验组血液中糖基化中间体3-脱氧葡萄糖酮(3DG)和晚期糖基化终产物Ne-(羧甲基)赖氨酸(CML)和戊苷(AGEs)的含量未见显著变化。然而,在HbA1c等于或高于5.9%的受试者中,亚类组间分析显示,补充MHE显著抑制了试验组CML的升高(p < 0.05),而对照组CML升高。实验组大鼠尿中氧化应激标志物8-羟基-2′-脱氧鸟苷(8-OHdG)和异前列腺素无显著差异。对照组皮肤弹性指数(R2)在4周后开始明显下降(p < 0.05),而试验组皮肤弹性指数有成功维持的趋势。没有与测试产品相关的不良事件。结论:MHE可改善糖代谢异常患者与生活质量相关的症状,并可抑制AGEs之一CML的生成。此外,补充8周MHE被认为是安全的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-Glycation Effect of Mixed Herbal Extract in Individuals with Pre-Diabetes Mellitus
Objective: We conducted a double-blind, placebo-controlled, parallel group study to assess the anti-glycation effect of mixed herbal extract (MHE) in individuals with pre-diabetes mellitus. MHE was produced using hot water extraction from Anthemis nobilis (Roman chamomile), Crataegus oxyacantha (hawthorn berry), Houttuynia cordata (dokudami), and Vitis vinifera (grape leaf). We also assessed whether MHE showed favorable effects on one's quality of life (QOL).Design: The subjects consisted of 26 volunteers (male: 21; female: 5; age: 50.5 ± 8.5 years) with pre- diabetes mellitus (HbA1c: 5.5 - 6.7%). They were divided into two groups, the Test Group (13 subjects, age: 52.8 ± 8.2 years) and the Control Group (12 subjects, age: 49.3 ± 7.8 years). The Test Group was administered 1,200 mg of MHE (solid substance) per day for 8 weeks. The Control Group was administered a placebo.Results: The inter-group analysis using the Anti-Aging QOL Common Questionnaire (AAQol) showed that the score for the parameters, “muscular pain/stiffness”, “headache”, “easily angered”, “reluctance to talk with others”, “memory lapse”, and “inability to readily make judgments” was significantly improved in the Test Group (p ‹ 0.05). In terms of sugar metabolism, no significant variation was observed in fasting blood glucose, HbA1c, glycoalbumin, and insulin. A significant variation was not observed in the Test Group with regard to 3-deoxyglucosone (3DG), an intermediate of glycation, and Ne-(carboxymethyl)lysine (CML) and pentosidine, advanced glycation endproducts (AGEs), in blood after 8 weeks. However, in the subjects with HbA1c of equal to or higher than 5.9%, the subclass inter-group analysis showed that the supplementation of MHE significantly inhibited (p ‹ 0.05) an increase of CML in the Test Group, while CML increased in the Control Group. There was no significant variation in the Test Group regarding the oxidative stress markers, 8-hydroxy-2'-deoxyguanosine (8-OHdG) and isoprostane in urine. The skin elasticity index (R2) obtained by using the cutometer started to decrease significantly in the Control Group after 4 weeks (p ‹ 0.05), while the index showed a tendency that the skin elasticity was successfully maintained in the Test Group. There was no adverse event which was associated with the test product.Conclusion: These results suggest that MHE may improve the symptoms related to QOL as well as inhibit the generation of CML, one of AGEs, in individuals with abnormal sugar metabolism. Furthermore, the 8 weeks supplementation of MHE was considered to be safe.
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