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Scutellariae Radix and Coptidis Rhizoma Improve Glucose and Lipid Metabolism in T2DM Rats via Regulation of the Metabolic Profiling and MAPK/PI3K/Akt Signaling Pathway

机译:通过调节代谢分析和MAPK / PI3K / AKT信号通路,Cocutellariae adrix和Coptidis Rhizoma在T2DM大鼠中改善葡萄糖和脂质代谢

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摘要

Aim Scutellariae Radix (SR) and Coptidis Rhizoma (CR) have often been combined to cure type 2 diabetes mellitus (T2DM) in the clinical practice for over thousands of years, but their compatibility mechanism is not clear. Mitogen-activated protein kinase (MAPK) signaling pathway has been suggested to play a critical role during the process of inflammation, insulin resistance, and T2DM. This study was designed to investigate their compatibility effects on T2DM rats and explore the underlying mechanisms by analyzing the metabolic profiling and MAPK/PI3K/Akt signaling pathway. Methods The compatibility effects of SR and CR were evaluated with T2DM rats induced by a high-fat diet (HFD) along with a low dose of streptozocin (STZ). Ultra performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS) was performed to discover potential biomarkers. The levels of pro-inflammatory cytokines; biochemical indexes in serum, and the activities of key enzymes related to glycometabolism in liver were assessed by ELISA kits. qPCR was applied to examine mRNA levels of key targets in MAPK and insulin signaling pathways. Protein expressions of p65; p-p65; phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K); phosphorylated-PI3K (p-PI3K); protein kinase B (Akt); phosphorylated Akt (p-Akt) and glucose transporter 2 (Glut2) in liver were investigated by Western blot analysis. Results Remarkably, hyperglycaemia, dyslipidemia, inflammation, and insulin resistance in T2DM were ameliorated after oral administration of SR and CR, particularly their combined extracts. The effects of SR, CR, low dose of combined extracts (LSC) and high dose of combined extracts (HSC) on pro-inflammatory cytokine transcription in T2DM rats showed that the MAPK pathway might account for the phenomenon with down-regulation of MAPK (P38 mitogen-activated protein kinases (P38), extracellular regulated protein kinases (ERK), and c-Jun N-terminal kinase (JNK)) mRNA, and protein reduction in p-P65. While mRNA levels of key targets such as insulin receptor substrate 1 (IRS1), PI3K, Akt2, and Glut2 in the insulin signaling pathway were notably up-modulated, phosphorylations of PI3K, Akt, and expression of Glut2 were markedly enhanced. Moreover, the increased activities of phosphoenolpyruvate carboxykinase (PEPCK), fructose-1,6-bisphosphatase (FBPase), glucose 6-phosphatase (G6Pase), and glycogen phosphorylase (GP) were highly reduced and the decreased activities of glucokinase (GK), phosphofructokinase (PFK), pyruvate kinase (PK), and glycogen synthase (GS) in liver were notably increased after treatment. Further investigation indicated that the metabolic profiles of plasma and urine were clearly improved in T2DM rats. Fourteen potential biomarkers (nine in plasma and five in urine) were identified. After intervention, these biomarkers returned to normal level to some extent. Conclusion The results showed that SR, CR, and combined extract groups were normalized. The effects of combined extracts were more remarkable than single herb treatment. Additionally, this study also showed that the metabonomics method is a promising tool to unravel how traditional Chinese medicines work.
机译:目的黄芩(SR)和黄连(CR)往往被结合在临床实践中治愈2型糖尿病(T2DM)已有数千年,但其兼容性的机制尚不清楚。丝裂原活化蛋白激酶(MAPK)信号传导途径已提出炎症,胰岛素抵抗,和T2DM的过程中发挥关键作用。这项研究旨在探讨在2型糖尿病大鼠的兼容性影响,通过分析代谢分析和MAPK / PI3K / Akt信号通路探讨底层机制。方法SR和CR的相容性的效果与链脲霉素的低剂量(STZ)诱导的沿由高脂肪饮食(HFD)T2DM大鼠进行评价。超高效液相色谱 - 四极时间飞行质谱(UPLC-Q-TOF / MS)进行发现潜在的生物标志物。促炎性细胞因子的水平;在血清生化指标,并且在肝脏与糖代谢关键酶的活性通过ELISA试剂盒评估。 qPCR的应用研究在MAPK的主要目标mRNA水平和胰岛素信号通路。 P65的蛋白表达; P-p65的;磷脂酰肌醇-4,5-二磷酸肌醇3-激酶(PI3K);磷酸化PI3K(对PI3K);蛋白激酶B(AKT);磷酸化Akt(P-AKT)和肝脏中葡萄糖转运2(GLUT2)通过Western印迹分析研究。结果值得注意的是,高血糖症,血脂异常,炎症和胰岛素在T2DM性进行SR和CR,特别是它们的合并的萃取物的口服给药后改善。 SR,CR,合并的萃取物(LSC)和促炎症细胞因子的转录合并的萃取液(HSC)在T2DM大鼠高剂量低剂量的效果表明,MAPK途径可能帐户用于与MAPK的下调现象( p38丝裂原活化蛋白激酶(P38),细胞外调节蛋白激酶(ERK),和c-Jun N-末端激酶(JNK))的mRNA,并且在p-P65蛋白的降低。虽然主要目标mRNA水平,如在胰岛素信号转导途径的胰岛素受体底物1(IRS1),PI3K,AKT2,和GLUT2被显着向上调制,PI3K,Akt和GLUT2的表达的磷酸化被显着增强。此外,磷酸烯醇丙酮酸羧增加的活性(PEPCK),果糖-1,6-二磷酸酶(FBP酶),葡萄糖-6-磷酸酶(G6P酶),和糖原磷酸化酶(GP)的高度降低,并且降低的葡糖激酶的活动(GK),在肝脏磷酸果糖激酶(PFK),丙酮酸激酶(PK)和糖原合成酶(GS)治疗后显着增加。进一步的调查表明,血浆和尿中的代谢图谱在2型糖尿病大鼠明显改善。十四潜在生物标志物(九血浆和五个尿液)进行了鉴定。干预后,这些生物标志物恢复到正常水平在一定程度上。结论结果表明,SR,CR,和合并的萃取组分别归一化。合并提取物的效果比单味药治疗更为显着。此外,这项研究还表明,代谢组学方法是一种很有前途的工具解开中国药品如何传统的工作。

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