Sievenpiper John L, Arnason John T, Leiter Lawrence A, Vuksan Vladimir
Department of Nutritional Sciences, Faculty of Medicine, University of Toronto, Clinical Nutrition and Risk Factor Modification Centre, St. Michael's Hospital, #6 138-61 Queen Street East, Toronto, Ontario M5C 2T2, CANADA.
J Am Coll Nutr. 2003 Dec;22(6):524-32. doi: 10.1080/07315724.2003.10719331.
We have repeatedly reported that a batch of American ginseng with a specific ginsenoside (glycosidal saponin) profile decreases acute postprandial glycemia. We investigated whether Asian ginseng is able to replicate this glycemia-lowering efficacy in two separate acute dose escalation studies.
Each study was conducted in a separate sample of 11 healthy subjects (gender: 8M:3F and 6M:5F, age: 29 +/- 2y and 27 +/- 3y, BMI: 28.5 +/- 2.1 kg/m(2) and 26.9 +/- 1.4 kg/m(2)) using a randomized, single-blind, placebo-controlled, multiple-crossover design. Treatments consisted of 0 (placebo), 1, 2, and 3 g of Asian ginseng for the first study and 0 (placebo), 3, 6, and 9 g Asian ginseng for the second study administered 40 minutes before a 75g-OGTT protocol with blood drawn at -40, 0, 15, 30, 45, 60, 90, and 120 minutes. Ginsenosides were analyzed by HPLC-UV.
Neither the main effect of pooled-treatment, nor dose, nor either factors interaction with time was significant for incremental plasma glucose and insulin. But the diagnostically and therapeutically relevant two-hour plasma glucose (2h-PG) value was significantly higher for pooled Asian ginseng treatment than placebo (5.46 +/- 0.31 versus 4.99 +/- 0.30 mmol/L, p = 0.050). Ginsenoside analyses showed that the Asian ginseng contained up to 96% lower and sevenfold higher quantities of various ginsenosides and their ratios than our previous efficacious batch of American ginseng.
Asian ginseng showed both null and opposing effects on indices of acute postprandial plasma glucose and insulin. This is in contrast to our findings with American ginseng. One explanation may be the marked ginsenoside differences. Practitioners and consumers should be aware of ginseng's variable effects.
我们曾多次报告,一批具有特定人参皂苷(糖苷类皂苷)谱的西洋参可降低餐后急性血糖。我们在两项独立的急性剂量递增研究中调查了亚洲人参是否能够复制这种降血糖功效。
每项研究均在11名健康受试者(性别:第一项研究为8男3女,第二项研究为6男5女;年龄:第一项研究为29±2岁,第二项研究为27±3岁;体重指数:第一项研究为28.5±2.1kg/m²,第二项研究为26.9±1.4kg/m²)的不同样本中进行,采用随机、单盲、安慰剂对照、多次交叉设计。第一项研究的治疗包括0(安慰剂)、1、2和3克亚洲人参,第二项研究的治疗包括0(安慰剂)、3、6和9克亚洲人参,在75克口服葡萄糖耐量试验(OGTT)前40分钟给药,在-40、0、15、30、45、60、90和120分钟采血。通过高效液相色谱-紫外检测法分析人参皂苷。
合并治疗的主效应、剂量以及这两个因素与时间的交互作用对血浆葡萄糖和胰岛素增量均无显著影响。但合并亚洲人参治疗的诊断和治疗相关的两小时血浆葡萄糖(2h-PG)值显著高于安慰剂(5.46±0.3)。