Kudolo George B, Wang Wen, Javors Martin, Blodgett Janet
Department of Clinical Laboratory Sciences, MSC 6246, University of Texas HSC at San Antonio, 7703 Floyd Curl Drive, 78229-3900, USA.
Clin Nutr. 2006 Aug;25(4):606-16. doi: 10.1016/j.clnu.2005.12.012. Epub 2006 May 15.
BACKGROUND & AIMS: Ginkgo biloba extract (EGb 761) has been shown to ameliorate some defects associated with the insulin resistance syndrome and so patients with Type 2 diabetes mellitus (T2DM) may be inclined to co-ingest the herb with their medications, such as metformin. This study was designed to determine if the co-ingestion of EGb 761 and metformin would alter the pharmacokinetic properties of metformin in T2DM patients and persons without diabetes, who may ingest it for other purposes.
Normal glucose tolerance (NGT) subjects (n=10; age, 39.2+/-14.0 years; fasting plasma glucose (FPG), 90+/-7 mg/dl; body mass index (BMI), 24.1+/-3.7 kg/m(2)) and 10 T2DM patients (n=10; age, 51.7+/-8.9 years; FPG, 150+/-7 mg/dl; BMI, 33.7+/-5.7 kg/m(2)) completed a randomized, double-blind, placebo-controlled crossover study. They ingested either EGb 761 (12 0mg/day as a single dose) or a vegetable-based placebo during each arm for 3 months. At the end of each arm, the NGT subject ingested a single 500 mg dose of metformin (non-diabetics) and the T2DM subject took his/her prescribed metformin dose (250-850 mg) with 120 mg EGb 761. Blood and urine samples were collected over an 8-h period, and in the case of T2DM subjects, additionally over the first 2h of the subsequent 3 days.
Ingestion of EGb 761 produced no significant changes in diagnostic laboratory tests in either group, except reducing glycosylated hemoglobin A(1c) levels (from 7.7+/-1.2 to 7.2+/-0.9%, P<0.05) in T2DM the subjects. The pharmacokinetic parameters of metformin were all significantly different (P<0.05) between the NGT (500 mg) and 8 out of 10 of the T2DM subjects who were prescribed 500 mg of metformin during the placebo cycles. During the EGb 761 cycles, only the elimination half-life in the T2DM subjects was significantly increased (0.117+/-0.085 to 0.141+/-0.100, P<0.05).
The co-ingestion of 120 mg of EGb 761 and 500 mg of metformin did not significantly affect the pharmacokinetic properties of metformin. Further studies are required to verify this observation for smaller and larger dose of metformin with other doses of EGb 761, since T2DM patients on medication constitute a very heterogeneous group.
银杏叶提取物(EGb 761)已被证明可改善与胰岛素抵抗综合征相关的一些缺陷,因此2型糖尿病(T2DM)患者可能倾向于将这种草药与他们的药物(如二甲双胍)一起服用。本研究旨在确定EGb 761与二甲双胍同时服用是否会改变T2DM患者以及可能因其他目的服用它的非糖尿病患者体内二甲双胍的药代动力学特性。
正常糖耐量(NGT)受试者(n = 10;年龄,39.2±14.0岁;空腹血糖(FPG),90±7mg/dl;体重指数(BMI),24.1±3.7kg/m²)和10名T2DM患者(n = 10;年龄,51.7±8.9岁;FPG,150±7mg/dl;BMI,33.7±5.7kg/m²)完成了一项随机、双盲、安慰剂对照的交叉研究。在每个阶段,他们服用EGb 761(120mg/天,单剂量)或植物性安慰剂,为期3个月。在每个阶段结束时,NGT受试者服用单剂量500mg二甲双胍(非糖尿病患者),T2DM受试者服用其规定剂量的二甲双胍(250 - 850mg)加120mg EGb 761。在8小时内采集血液和尿液样本,对于T2DM受试者,在随后3天的头2小时内还额外采集样本。
服用EGb 761后,两组的诊断实验室检查均无显著变化,但T2DM受试者的糖化血红蛋白A1c水平有所降低(从7.7±1.2%降至7.2±0.9%,P<0.05)。在安慰剂周期中,服用500mg二甲双胍的NGT受试者与10名T2DM受试者中的8名之间,二甲双胍的药代动力学参数均有显著差异(P<0.05)。在EGb 761周期中,仅T2DM受试者的消除半衰期显著延长(从0.117±0.085增至0.141±0.100,P<0.05)。
120mg EGb 与500mg二甲双胍同时服用对二甲双胍的药代动力学特性无显著影响。由于正在服药的T2DM患者构成一个非常异质的群体,因此需要进一步研究以验证对于不同剂量的二甲双胍与其他剂量的EGb 761的这一观察结果。