Biomedical Research and Innovation Platform, South African Medical Research Council, Tygerberg, South Africa.
Division of Medical Physiology, Faculty of Health Sciences, Stellenbosch University, Tygerberg, South Africa.
PLoS One. 2019 May 2;14(5):e0216172. doi: 10.1371/journal.pone.0216172. eCollection 2019.
Aspalathin is a rooibos flavonoid with established blood glucose lowering properties, however, its efficacy to moderate complications associated with hepatic insulin resistance is unknown. To study such effects, C3A liver cells exposed to palmitate were used as a model of hepatic insulin resistance. These hepatocytes displayed impaired substrate metabolism, including reduced glucose transport and free fatty acid uptake. These defects included impaired insulin signaling, evident through reduced phosphatidylinositol-4,5-bisphosphate 3-kinase/ protein kinase B (PI3K/AKT) protein expression, and mitochondrial dysfunction, depicted by a lower mitochondrial respiration rate. Aspalathin was able to ameliorate these defects by correcting altered substrate metabolism, improving insulin signaling and mitochondrial bioenergetics. Activation of 5'-adenosine monophosphate-activated protein kinase (AMPK) may be a plausible mechanism by which aspalathin increases hepatic energy expenditure. Overall, these results encourage further studies assessing the potential use of aspalathin as a nutraceutical to improve hepatocellular energy expenditure, and reverse metabolic disease-associated complications.
Aspalathin 是一种源自南非路易波士茶的类黄酮,具有降低血糖的作用,但它对改善与肝胰岛素抵抗相关的并发症的疗效尚不清楚。为了研究这种效果,我们使用棕榈酸处理的 C3A 肝细胞作为肝胰岛素抵抗的模型。这些肝细胞表现出受损的底物代谢,包括葡萄糖转运和游离脂肪酸摄取减少。这些缺陷包括胰岛素信号受损,表现为磷脂酰肌醇-4,5-二磷酸 3-激酶/蛋白激酶 B(PI3K/AKT)蛋白表达减少和线粒体功能障碍,表现为线粒体呼吸率降低。Aspalathin 能够通过纠正改变的底物代谢、改善胰岛素信号和线粒体生物能来改善这些缺陷。激活 5'-单磷酸腺苷激活的蛋白激酶(AMPK)可能是 aspalathin 增加肝能量消耗的合理机制。总的来说,这些结果鼓励进一步研究评估 aspalathin 作为一种营养保健品的潜在用途,以改善肝细胞能量消耗,并逆转与代谢疾病相关的并发症。