Zhang Shucha, Myracle Angela, Xiao Ke, Yan Ping, Ye Tao, Janle Elsa, Raftery Daniel
Department of Neurosurgery, Brigham and Women's Hospital, 221 Longwood Ave, Boston, MA 02115, USA.
Food Science and Human Nutrition, University of Maine, 5735 Hitchner Hall, Orono, ME 04469, USA.
J Nutr Food Sci. 2013;3(6). doi: 10.4172/2155-9600.1000239. Epub 2013 Nov 11.
This study has investigated the metabolic effects of catechin-rich green tea (GT) and its formulation with ascorbic acid (AA) on the Zucker rat model of type 2 diabetes. AA is used to protect the GT catechins during digestion and increase bioavailability. Thirty two Zucker diabetic fatty (ZDF) rats were randomly divided into four groups (n=8 in each group) and treated with water, GT, AA and GT+AA respectively for five weeks. Urinary metabolic profiles were determined using H NMR spectroscopy. Fourteen metabolites were identified and their 24-hr excretions were quantified. Changes in the 14 metabolites demonstrated differential treatment effects on the metabolism of ZDF rats. GT and AA were found to be able to independently reduce urinary excretions of most metabolites that were over-excreted in the control diabetic rats, such as oxidative stress marker metabolites and TCA cycle metabolites. GT showed a great potential in controlling metabolic acidosis by suppressing the excretion of lactic acid and acetic acid from diabetic rats and GT+AA showed a remarkably stronger suppression than GT while AA was unable to suppress these two acids. Further investigation is needed to better understand the role of GT and/or formulated GT in altering the metabolic pathways in the diabetic animal model as well as in humans.
本研究调查了富含儿茶素的绿茶(GT)及其与抗坏血酸(AA)的配方对2型糖尿病Zucker大鼠模型的代谢影响。AA用于在消化过程中保护GT儿茶素并提高生物利用度。将32只Zucker糖尿病肥胖(ZDF)大鼠随机分为四组(每组n = 8),分别用水、GT、AA和GT + AA处理五周。使用核磁共振氢谱(1H NMR)光谱法测定尿液代谢谱。鉴定出14种代谢物并对其24小时排泄量进行定量。这14种代谢物的变化表明对ZDF大鼠的代谢有不同的治疗效果。发现GT和AA能够独立降低对照糖尿病大鼠中排泄过多的大多数代谢物的尿液排泄量,如氧化应激标志物代谢物和三羧酸循环代谢物。GT在通过抑制糖尿病大鼠乳酸和乙酸的排泄来控制代谢性酸中毒方面具有很大潜力,并且GT + AA显示出比GT更强的抑制作用,而AA无法抑制这两种酸。需要进一步研究以更好地了解GT和/或配方GT在改变糖尿病动物模型以及人类代谢途径中的作用。