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首页> 外文期刊>Molecules >Electro-Acupuncture at Neiguan Pretreatment Alters Genome-Wide Gene Expressions and Protects Rat Myocardium against Ischemia-Reperfusion
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Electro-Acupuncture at Neiguan Pretreatment Alters Genome-Wide Gene Expressions and Protects Rat Myocardium against Ischemia-Reperfusion

机译:内关预处理电针可改变基因组全基因表达并保护大鼠心肌免于缺血再灌注

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摘要

This study investigated genome-wide gene expressions and the cardioprotective effects of electro-acupuncture pretreatment at the PC6 Neiguan acupoint on myocardial ischemia reperfusion (I/R) injury. Male SD rats were randomly divided into four groups: sham operation (SO), I/R, electro-acupuncture at the PC6 Neiguan acupoint pretreatment (EA) and electro-acupuncture at non-acupoint pretreatment (NA). Compared with the I/R group, the survival rate of the EA group was significantly increased, the arrhythmia score, infarction area, serum concentrations of CK, LDH and CK-Mb and plasma level of cTnT were significantly decreased. RNA-seq results showed that 725 genes were up-regulated and 861 genes were down-regulated under I/R conditions compared to the SO group; both EA and NA reversed some of these gene expression levels (592 in EA and 238 in NA group). KEGG pathway analysis indicated that these genes were involved in multiple pathways, including ECM, MAPK signaling, apoptosis, cytokine and leukocyte pathways. In addition, some pathways were uniquely regulated by EA, but not NA pretreatment, such as oxidative stress, cardiac muscle contraction, gap junction, vascular smooth muscle contraction, hypertrophic, NOD-like receptor, and P53 and B-cell receptor pathways. This study was first to reveal the gene expression signatures of acute myocardial I/R injury and electro-acupuncture pretreatment in rats.
机译:这项研究调查了全基因组基因表达以及在PC6内关穴上电针预处理对心肌缺血再灌注(I / R)损伤的心脏保护作用。将雄性SD大鼠随机分为四组:假手术(SO),I / R,PC6内关穴预处理(EA)电针和非穴预处理(NA)电针。与I / R组相比,EA组的生存率明显提高,心律失常评分,梗死面积,血清CK,LDH和CK-Mb浓度以及血浆cTnT水平明显降低。 RNA-seq结果显示,与SO组相比,在I / R条件下725个基因被上调,而861个基因被下调。 EA和NA均逆转了其中一些基因表达水平(EA中为592,NA组中为238)。 KEGG途径分析表明,这些基因参与了多种途径,包括ECM,MAPK信号传导,凋亡,细胞因子和白细胞途径。此外,某些途径是由EA唯一调控的,而NA预处理则没有,例如氧化应激,心肌收缩,间隙连接,血管平滑肌收缩,肥大,NOD样受体以及P53和B细胞受体途径。这项研究首次揭示了大鼠急性心肌I / R损伤和电针预处理的基因表达特征。

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