首页> 外文期刊>Journal of Surgical Research: Clinical and Laboratory Investigation >Phosphoinositide 3-kinase/Akt pathway is involved in mediating the anti-inflammation effects of magnesium sulfate
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Phosphoinositide 3-kinase/Akt pathway is involved in mediating the anti-inflammation effects of magnesium sulfate

机译:磷酸肌醇3-激酶/ Akt途径参与介导硫酸镁的抗炎作用

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Background: We sought to elucidate whether enhancing phosphoinositide 3-kinase (PI3K)/Akt activity is a crucial mechanism underlying the anti-inflammation effects of magnesium sulfate (MgSO4). Materials and methods: Murinemacrophages (RAW264.7 cells)were stimulatedwith endotoxin, endotoxin plus MgSO4, or endotoxin plusMgSO4 plus PI3K inhibitor (LY294002 orwortmannin). Control groups were run simultaneously. After harvesting, we assayed the expression of inflammatory mediators, transcriptional factor nuclear factor kB (NF-κB), and Akt. Results: MgSO4 significantly attenuated endotoxin-induced upregulation of inflammatory mediators and NF-κB, as macrophages treated with endotoxin plus MgSO4 had significantly lower tumor necrosis factor a (P =0.022), macrophage inflammatory protein 2 (P =0.040), phosphorylated (p)-NF-κB p65 (P =0.003) and p-inhibitor-κB (P 0.001) concentrations as well as lower NF-κB DNA binding (P =0.001) than macrophages treated with endotoxin alone. Moreover, macrophages treated with endotoxin plus MgSO4 plus LY294002 or wortmannin had significantly higher tumor necrosis factor a (P =0.013 and P 0.001), macrophage inflammatory protein 2 (P =0.023 and P =0.003), p-NF-κB p65 (P =0.006 and P 0.001), and p-inhibitor-κB (P =0.001 and P 0.001) concentrations, as well as higher NFκB DNA binding (P =0.038 and P =0.009), than macrophages treated with endotoxin plus MgSO4, suggesting that PI3K inhibitors reversed these effects of MgSO4. In contrast, macrophages treated with endotoxin plus MgSO4 had significantly higher p-Akt concentration than macrophages treated with endotoxin alone (P =0.004). Moreover, macrophages treated with endotoxin plus MgSO 4 also had significantly higher p-Akt concentration than macrophages treated with endotoxin plus MgSO4 plus LY294002 or wortmannin (P =0.004 and P 0.001). Conclusions: Enhancing PI3K/Akt activity is a crucial mechanism underlying the antiinflammation effects of MgSO4.
机译:背景:我们试图阐明增强磷酸肌醇3激酶(PI3K)/ Akt活性是否是潜在的硫酸镁(MgSO4)抗炎作用的关键机制。材料和方法:用内毒素,内毒素加MgSO4或内毒素加MgSO4加PI3K抑制剂(LY294002或渥曼青霉素)刺激鼠巨噬细胞(RAW264.7细胞)。对照组同时进行。收获后,我们分析了炎症介质,转录因子核因子kB(NF-κB)和Akt的表达。结果:MgSO4显着减弱了内毒素诱导的炎症介质和NF-κB的上调,因为内毒素加MgSO4处理的巨噬细胞具有显着降低的肿瘤坏死因子a(P = 0.022),巨噬细胞炎性蛋白2(P = 0.040),磷酸化(p )-NF-κBp65(P = 0.003)和p-抑制剂-κB(P <0.001)的浓度以及较低的NF-κBDNA结合(P = 0.001)比仅用内毒素治疗的巨噬细胞低。此外,用内毒素加MgSO4加LY294002或渥曼青霉素处理的巨噬细胞具有明显更高的肿瘤坏死因子a(P = 0.013和P <0.001),巨噬细胞炎性蛋白2(P = 0.023和P = 0.003),p-NF-κBp65( P = 0.006和P <0.001)和p-抑制剂-κB(P = 0.001和P <0.001)浓度以及更高的NFκBDNA结合率(P = 0.038和P = 0.009),高于用内毒素加MgSO4处理的巨噬细胞,表明PI3K抑制剂逆转了MgSO4的这些作用。相反,用内毒素加MgSO4处理的巨噬细胞的p-Akt浓度明显高于仅用内毒素处理的巨噬细胞(P = 0.004)。此外,内毒素加MgSO 4处理的巨噬细胞也比内毒素加MgSO 4加上LY294002或渥曼青霉素处理的巨噬细胞具有更高的p-Akt浓度(P = 0.004,P <0.001)。结论:增强PI3K / Akt活性是MgSO4抗炎作用的关键机制。

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