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首页> 外文期刊>Medical science monitor : >Effect of ERK1/2 Signaling Pathway in Electro-Acupuncture Mediated Up-Regulation of Heme Oxygenase-1 in Lungs of Rabbits with Endotoxic Shock
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Effect of ERK1/2 Signaling Pathway in Electro-Acupuncture Mediated Up-Regulation of Heme Oxygenase-1 in Lungs of Rabbits with Endotoxic Shock

机译:ERK1 / 2信号通路在电针介导内毒素休克家兔肺血红素加氧酶-1上调中的作用

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Background The anti-oxidative and anti-inflammatory activities of electro-acupuncture (EA), a traditional clinical method, are widely accepted, but its mechanisms are not yet well defined. In this study, we investigated the role of extracellular signal-regulated kinases1/2 (ERK1/2) pathways on electro-acupuncture – mediated up-regulation of heme oxygenase-1 (HO-1) in rabbit lungs injured by LPS-induced endotoxic shock. Material and Methods Seventy rabbits were randomly divided into 7 groups: group C, group M, group D, group SEAM, group EAM, group EAMPD, and group PD98059. Male New England white rabbits were given EA treatment on both sides once a day on days 1–5, and then received LPS to replicate the experimental model of injured lung induced by endotoxic shock. Then, they were killed by exsanguination at 6 h after LPS administration. The blood samples were collected for serum examination, and the lungs were removed for pathology examination, determination of wet-to-dry weight ratio, MDA content, SOD activity, serum tumor necrosis factor-α, determination of HO-1 protein and mRNA expression, and determination of ERK1/2 protein. Results The results revealed that after EA treatment, expression of HO-1and ERK1/2 was slightly increased compared to those in other groups, accompanied with less severe lung injury as indicated by lower index of lung injury score, lower wet-to-dry weight ratio, MDA content, and serum tumor necrosis factor-α levels, and greater SOD activity (p<0.05 for all). After pretreatment with ERK1/2 inhibitor PD98059, the effect of EA treatment and expression of HO-1 were suppressed (p<0.05 for all). Conclusions After electro-acupuncture stimulation at ST36 and BL13, severe lung injury during endotoxic shock was attenuated. The mechanism may be through up-regulation of HO-1, mediated by the signal transductions of ERK1/2 pathways. Thus, the regulation of ERK1/2 pathways via electro-acupuncture may be a therapeutic strategy for endotoxic shock.
机译:背景技术电针(EA)的抗氧化和抗炎活性是一种传统的临床方法,已被广泛接受,但其机理尚未明确。在这项研究中,我们调查了细胞外信号调节激酶1/2(ERK1 / 2)通路在电针介导的LPS诱导的内毒素损伤的兔肺中血红素加氧酶-1(HO-1)上调的作用休克。材料与方法70只家兔随机分为7组:C组,M组,D组,SEAM组,EAM组,EAMPD组和PD98059组。在第1至5天,每天对雄性新英格兰白兔进行EA双面治疗,然后接受LPS复制内毒素性休克诱导的肺损伤实验模型。然后,它们在LPS给药后6小时被放血杀死。采集血样进行血清检查,取出肺进行病理检查,确定干重比,MDA含量,SOD活性,血清肿瘤坏死因子-α,测定HO-1蛋白和mRNA表达,并测定ERK1 / 2蛋白。结果结果表明,EA治疗后,HO-1和ERK1 / 2的表达较其他组略有增加,并伴有较轻的肺损伤,表现为较低的肺损伤指数,较低的干湿重比率,MDA含量和血清肿瘤坏死因子-α水平,以及更高的SOD活性(所有P均<0.05)。用ERK1 / 2抑制剂PD98059预处理后,EA处理的效果和HO-1的表达均被抑制(所有p均<0.05)。结论在ST36和BL13电针刺激后,内毒素休克期间的严重肺损伤减轻了。该机制可能是通过上调HO-1介导的,而HO-1的上调是由ERK1 / 2途径的信号转导介导的。因此,通过电针调节ERK1 / 2途径可能是内毒素休克的治疗策略。

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