Muller Christo J F, Joubert Elizabeth, Pheiffer Carmen, Ghoor Samira, Sanderson Micheline, Chellan Nireshni, Fey Stephen J, Louw Johan
Diabetes Discovery Platform, Medical Research Council (MRC), Tygerberg, South Africa.
Mol Nutr Food Res. 2013 Dec;57(12):2216-22. doi: 10.1002/mnfr.201300294. Epub 2013 Aug 14.
The rare enolic phenylpyruvic acid-2-O-glucoside, (PPAG:Z-2-(β-D-glucopyranosyloxy)-3-phenylpropenoic acid), is one of the major constituents of fermented rooibos infusions. 3-Phenylpyruvic acid (2-oxo-3-phenylpropanoic acid), without the sugar moiety and with a keto form instead of an enolic arrangement, has been shown to enhance insulin release and glucose uptake in muscle cells. The purpose of this study was to assess if PPAG has similar activity on glucose metabolism.
Preliminary in vitro studies confirmed that PPAG, isolated from rooibos, enhanced glucose uptake. A dose-response study in Chang cells showed that PPAG enhanced glucose uptake in the concentration range 1.0-31.6 μM (EC50 = 3.6 μM). In obese insulin-resistant rats, oral administration of PPAG lowered fasting glucose concentrations and improved oral glucose tolerance values; messenger RNA expression of glucokinase, glucose transporter 1 and 2, insulin receptor, peroxisome proliferator-activated receptor alpha, and suppressor of cytokine signaling 3, were increased in the liver. This suggests that the liver is mainly responsible for PPAG bioactivity.
This study describes for the first time that PPAG increases in vitro glucose uptake and improves glucose tolerance in an obese insulin-resistant rat model, suggesting that it has potential as a new class of antidiabetic therapeutics that would contribute to the antidiabetic effect of rooibos.
罕见的烯醇式苯丙酮酸 - 2 - O - 葡萄糖苷,(PPAG:Z - 2 -(β - D - 吡喃葡萄糖氧基)- 3 - 苯基丙烯酸),是发酵的路易波士茶浸液的主要成分之一。3 - 苯丙酮酸(2 - 氧代 - 3 - 苯基丙酸),没有糖部分且为酮式而非烯醇式结构,已被证明可增强肌肉细胞中的胰岛素释放和葡萄糖摄取。本研究的目的是评估PPAG对葡萄糖代谢是否具有类似活性。
初步体外研究证实,从路易波士茶中分离出的PPAG可增强葡萄糖摄取。在Chang细胞中的剂量反应研究表明,PPAG在1.0 - 31.6 μM浓度范围内增强葡萄糖摄取(EC50 = 3.6 μM)。在肥胖胰岛素抵抗大鼠中,口服PPAG可降低空腹血糖浓度并改善口服葡萄糖耐量值;肝脏中葡萄糖激酶、葡萄糖转运蛋白1和2、胰岛素受体、过氧化物酶体增殖物激活受体α以及细胞因子信号转导抑制因子3的信使RNA表达增加。这表明肝脏是PPAG生物活性的主要作用部位。
本研究首次描述了PPAG在体外可增加葡萄糖摄取,并改善肥胖胰岛素抵抗大鼠模型的葡萄糖耐量,表明其有潜力作为一类新型抗糖尿病治疗药物,这可能有助于路易波士茶的抗糖尿病作用。