Thakuri Laxmi Sen, Park Chul Min, Park Jin Woo, Rhyu Dong Young
Department of Nutraceutical Resources, Mokpo National University, Jeonnam, 58554, Republic of Korea.
Department of Biomedicine, Health & Life Convergence Sciences, BK21 FOUR, Mokpo National University, Jeonnam, 58554, Republic of Korea.
J Tradit Complement Med. 2023 Jul 18;14(1):82-90. doi: 10.1016/j.jtcme.2023.07.006. eCollection 2024 Jan.
Insulin resistance (IR) is a pathological condition in which cells fail to respond normally to insulin. Loss of insulin sensitivity disrupts glucose homeostasis and elevates the risk of developing the metabolic syndrome that includes Type 2 diabetes. This study assesses the effect on subcritical-water extract of (GC) at 210 °C (GCSW210) in IR induction models of high glucose (HG)-induced zebrafish larvae and dexamethasone (DEX)-induced L6 myotubes.
The dose of HG and DEX for IR induction in zebrafish larvae and L6 myotubes was 130 mM or 0.5 μM. The capacity of glucose uptake was quantified by fluorescence staining or intensity. In addition, the activation of protein and mRNA expressions for insulin signaling (insulin-dependent or independent pathways) was measured.
Exposure of zebrafish larvae to HG significantly reduced the intracellular glucose uptake with dose-dependnet manner compared to control. However, the group treated with GCSW210 significantly averted HG levels like the insulin-treated group, and significantly up- or down-regulated the mRNA expressions related to insulin production () and insulin signaling pathways. Moreover, the treatment with GCSW210 effectively regulated the protein expression of PI3K/AKT, AMPK, and GLUT4 involved in the action of insulin in IR models of L6 myotubes compared to DEX-treated control. Our data indicate that GCSW210 stimulates activation of PI3K/AKT and AMPK pathways to attenuate the development of IR induced by HG in zebrafish and DEX in L6 myotubes. In conclusion, GCSW210 is a potential agent for alleviating various diseases associated with the insulin resistance.
胰岛素抵抗(IR)是一种细胞无法对胰岛素正常作出反应的病理状态。胰岛素敏感性的丧失会破坏葡萄糖稳态,并增加患包括2型糖尿病在内的代谢综合征的风险。本研究评估了210°C下的绞股蓝(GC)亚临界水提取物(GCSW210)对高糖(HG)诱导的斑马鱼幼体和地塞米松(DEX)诱导的L6肌管胰岛素抵抗诱导模型的影响。
用于诱导斑马鱼幼体和L6肌管胰岛素抵抗的HG和DEX剂量分别为130 mM或0.5 μM。通过荧光染色或强度对葡萄糖摄取能力进行定量。此外,还测量了胰岛素信号传导(胰岛素依赖性或非依赖性途径)的蛋白质和mRNA表达的激活情况。
与对照组相比,将斑马鱼幼体暴露于HG会以剂量依赖性方式显著降低细胞内葡萄糖摄取。然而,GCSW210处理组与胰岛素处理组一样,显著避免了HG水平升高,并显著上调或下调了与胰岛素产生()和胰岛素信号通路相关的mRNA表达。此外,与DEX处理的对照组相比,在L6肌管胰岛素抵抗模型中,GCSW210处理有效地调节了参与胰岛素作用的PI3K/AKT、AMPK和GLUT4的蛋白质表达。我们的数据表明,GCSW210刺激PI3K/AKT和AMPK途径的激活,以减轻斑马鱼中HG和L6肌管中DEX诱导的胰岛素抵抗的发展。总之,GCSW210是一种缓解与胰岛素抵抗相关的各种疾病的潜在药物。