Smit Sybrand Engelbrecht, Johnson Rabia, Van Vuuren Mignon Alberta, Huisamen Barbara
Division of Medical Physiology, Stellenbosch University, Cape Town, South Africa.
Biomedical Research and Innovation Platform, South African Medical Research Council, Cape Town, South Africa.
Planta Med. 2018 Jan;84(2):75-82. doi: 10.1055/s-0043-117415. Epub 2017 Aug 3.
Rooibos, an indigenous South African plant ingested as herbal tea, is well known for its antioxidant effects. This study investigated aspalathin (CHO), a dihydrochalcone unique to rooibos, for hypoglycemic effects in the context of age- and obesity-induced insulin resistance and the mechanisms involved. Male Wistar rats were allocated into three groups: 16 - 30 weeks feeding with either standard rat chow or a high-caloric diet, or 6 - 10 weeks feeding with standard rat chow. Ventricular cardiomyocytes were isolated by collagenase perfusion digestion, and glucose uptake was determined by 2-[H]-deoxyglucose accumulation. Viability was tested by trypan blue exclusion or propidium iodide staining. The high-caloric diet significantly increased body weight gain (508.5 ± 50.0 vs. 417.3 ± 40.0 g), visceral adiposity (42.30 ± 10.1 vs. 21.75 ± 7.0 g), and fasting blood glucose (5.7 ± 0.4 vs. 4.7 ± 0.1 mM). Aspalathin (10 µM for 90 min) induced 2-[H]-deoxyglucose uptake in young cardiomyocytes (37.2 ± 13.9 vs. 25.7 ± 2.5 pmol 2-[H]-deoxyglucose/mg protein) and enhanced insulin-mediated 2-[H]-deoxyglucose uptake in control cells (32.4 ± 6.4 vs. 23.5 ± 10.0 pmol 2-[H]-deoxyglucose/mg protein), but failed to induce 2-[H]-deoxyglucose uptake in high-caloric diet cells. Aspalathin induced glucose uptake in insulin-sensitive cardiomyocytes from young and aged rats, but not in high-caloric diet animals and enhanced the actions of insulin through a PI3K-dependent mechanism, resulting in an additive response.
南非红叶茶是一种原产于南非的植物,人们将其作为花草茶饮用,它以抗氧化作用而闻名。本研究在年龄和肥胖诱导的胰岛素抵抗背景下,研究了南非红叶茶特有的二氢查耳酮阿斯巴甜(CHO)的降血糖作用及其相关机制。雄性Wistar大鼠被分为三组:一组用标准大鼠饲料喂养16 - 30周,一组用高热量饮食喂养,另一组用标准大鼠饲料喂养6 - 10周。通过胶原酶灌注消化分离心室心肌细胞,通过2-[H]-脱氧葡萄糖积累测定葡萄糖摄取。通过台盼蓝排斥或碘化丙啶染色测试细胞活力。高热量饮食显著增加了体重增加(508.5±50.0 vs. 417.3±40.0克)、内脏脂肪(42.30±10.1 vs. 21.75±7.0克)和空腹血糖(5.7±0.4 vs. 4.7±0.1毫摩尔)。阿斯巴甜(10μM,90分钟)诱导年轻心肌细胞摄取2-[H]-脱氧葡萄糖(37.2±13.9 vs. 25.7±2.5皮摩尔2-[H]-脱氧葡萄糖/毫克蛋白质),并增强对照细胞中胰岛素介导的2-[H]-脱氧葡萄糖摄取(32.4±6.4 vs. 23.5±10.0皮摩尔2-[H]-脱氧葡萄糖/毫克蛋白质),但未能诱导高热量饮食细胞摄取2-[H]-脱氧葡萄糖。阿斯巴甜诱导年轻和老年大鼠胰岛素敏感心肌细胞摄取葡萄糖,但在高热量饮食动物中未诱导,且通过PI3K依赖性机制增强胰岛素作用,导致相加反应。