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首页> 外文期刊>Neural regeneration research >Diffusion-weighted magnetic resonance imaging reflects activation of signal transducer and activator of transcription 3 during focal cerebral ischemia/reperfusion
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Diffusion-weighted magnetic resonance imaging reflects activation of signal transducer and activator of transcription 3 during focal cerebral ischemia/reperfusion

机译:弥散加权磁共振成像反映了局灶性脑缺血/再灌注过程中信号转导子和转录激活子3的激活

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Signal transducer and activator of transcription (STAT) is a unique protein family that binds to DNA, coupled with tyrosine phosphorylation signaling pathways, acting as a transcriptional regulator to mediate a variety of biological effects. Cerebral ischemia and reperfusion can activate STATs signaling pathway, but no studies have confirmed whether STAT activation can be verified by diffusion-weighted magnetic resonance imaging (DWI) in rats after cerebral ischemia/reperfusion. Here, we established a rat model of focal cerebral ischemia injury using the modified Longa method. DWI revealed hyperintensity in parts of the left hemisphere before reperfusion and a low apparent diffusion coefficient. STAT3 protein expression showed no significant change after reperfusion, but phosphorylated STAT3 expression began to increase after 30 minutes of reperfusion and peaked at 24 hours. Pearson correlation analysis showed that STAT3 activation was correlated positively with the relative apparent diffusion coefficient and negatively with the DWI abnormal signal area. These results indicate that DWI is a reliable representation of the infarct area and reflects STAT phosphorylation in rat brain following focal cerebral ischemia/reperfusion.
机译:信号转导子和转录激活子(STAT)是与DNA结合的独特蛋白质家族,与酪氨酸磷酸化信号通路耦合,可作为转录调节因子来介导多种生物学作用。脑缺血和再灌注可以激活STATs信号通路,但尚无研究证实是否可以通过脑缺血/再灌注后大鼠的扩散加权磁共振成像(DWI)验证STAT的激活。在这里,我们使用改良的Longa方法建立了局灶性脑缺血损伤的大鼠模型。 DWI显示再灌注前左半球部分出现高强度,表观扩散系数低。再灌注后STAT3蛋白表达无明显变化,但再灌注30分钟后磷酸化STAT3表达开始增加,并在24小时达到高峰。 Pearson相关分析表明,STAT3激活与相对表观扩散系数呈正相关,与DWI异常信号区域呈负相关。这些结果表明,DWI是梗塞区域的可靠代表,并反映了局灶性脑缺血/再灌注后大鼠脑中的STAT磷酸化。

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