芡实亚临界水提取物可改善高糖诱导的斑马鱼胰岛素抵抗和地塞米松诱导的 L6 肌管胰岛素抵抗

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Laxmi Sen Thakuri , Chul Min Park , Jin Woo Park , Dong Young Rhyu
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引用次数: 0

摘要

背景和目的胰岛素抵抗(IR)是细胞不能对胰岛素做出正常反应的一种病理状态。胰岛素敏感性的丧失会破坏葡萄糖稳态,并增加患代谢综合征(包括 2 型糖尿病)的风险。本研究评估了210 °C下雏菊亚临界水提取物(GCSW210)对高葡萄糖(HG)诱导的斑马鱼幼体和地塞米松(DEX)诱导的L6肌细胞管IR诱导模型的影响。葡萄糖摄取能力通过荧光染色或强度进行量化。结果和结论与对照组相比,暴露于 HG 的斑马鱼幼体以剂量依赖网络的方式显著降低了细胞内葡萄糖摄取量。然而,用 GCSW210 处理的斑马鱼组与胰岛素处理的斑马鱼组一样,能显著避免 HG 水平,并能显著上调或下调与胰岛素分泌(insα)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,GCSW210能有效调节IR模型L6肌管中参与胰岛素作用的PI3K/AKT、AMPK和GLUT4的蛋白表达。我们的数据表明,GCSW210能刺激PI3K/AKT和AMPK通路的活化,从而减轻HG诱导的斑马鱼IR和DEX诱导的L6肌管IR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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Gracilaria chorda subcritical-water extracts as ameliorant of insulin resistance induced by high-glucose in zebrafish and dexamethasone in L6 myotubes

Gracilaria chorda subcritical-water extracts as ameliorant of insulin resistance induced by high-glucose in zebrafish and dexamethasone in L6 myotubes

Background and aim

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 Gracilaria chorda (GC) at 210 °C (GCSW210) in IR induction models of high glucose (HG)-induced zebrafish larvae and dexamethasone (DEX)-induced L6 myotubes.

Experimental procedure

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.

Results and conclusion

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 (insα) 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.

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CiteScore
7.20
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