首页> 美国卫生研究院文献>Frontiers in Molecular Neuroscience >Can We Use 235-Triphenyltetrazolium Chloride-Stained Brain Slices for Other Purposes? The Application of Western Blotting
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Can We Use 235-Triphenyltetrazolium Chloride-Stained Brain Slices for Other Purposes? The Application of Western Blotting

机译:我们可以将235-三苯基四唑氯化物染色的脑片用于其他目的吗?蛋白质印迹法的应用

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摘要

2,3,5-Triphenyltetrazolium chloride (TTC) staining is a commonly used method to determine the volume of the cerebral infarction in experimental stroke models. The TTC staining protocol is considered to interfere with downstream analyses, and it is unclear whether TTC-stained brain samples can be used for biochemistry analyses. However, there is evidence indicating that, with proper optimization and handling, TTC-stained brains may remain viable for protein analyses. In the present study, we aimed to rigorously assess whether TTC can reliably be used for western blotting of various markers. In this study, brain samples obtained from C57BL/6 male mice were treated with TTC (TTC+) or left untreated (TTC−) at 1 week after photothrombotic occlusion or sham surgery. Brain regions were dissected into infarct, thalamus, and hippocampus, and proteins were extracted by using radioimmunoprecipitation assay buffer. Protein levels of apoptosis, autophagy, neuronal, glial, vascular, and neurodegenerative-related markers were analyzed by western blotting. Our results showed that TTC+ brains display similar relative changes in most of the markers compared with TTC− brains. In addition, we validated that these analyses can be performed in the infarct as well as other brain regions such as the thalamus and hippocampus. Our findings demonstrate that TTC+ brains are reliable for protein analyses using western blotting. Widespread adoption of this approach will be key to lowering the number of animals used while maximizing data.
机译:2,3,5-三苯四唑氯化物(TTC)染色是确定实验性卒中模型中脑梗死体积的常用方法。 TTC染色方案被认为会干扰下游分析,目前尚不清楚是否可将TTC染色的脑样本用于生物化学分析。但是,有证据表明,通过适当的优化和处理,TTC染色的大脑可能仍然可以进行蛋白质分析。在本研究中,我们旨在严格评估TTC是否可以可靠地用于各种标记的蛋白质印迹。在这项研究中,从C57BL / 6雄性小鼠获得的脑样本在光栓形成或假手术后1周用TTC(TTC +)处理或未经治疗(TTC-)。将脑区域分为梗塞区,丘脑区和海马区,并使用放射免疫沉淀测定缓冲液提取蛋白质。通过蛋白质印迹分析细胞凋亡,自噬,神经元,神经胶质,血管和神经退行性相关标志物的蛋白质水平。我们的结果表明,与TTC-大脑相比,TTC +大脑在大多数标记中显示出相似的相对变化。此外,我们验证了可以在梗死区域以及其他大脑区域(如丘脑和海马体)中执行这些分析。我们的发现表明TTC +大脑对于使用蛋白质印迹的蛋白质分析是可靠的。这种方法的广泛采用将是在最大化数据的同时减少所用动物数量的关键。

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