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神经性疼痛的蛋白质组学:大鼠模型中受影响的蛋白质和信号通路

Proteomics of neuropathic pain: proteins and signaling pathways affected in a rat model.

作者信息

Sui Ping, Watanabe Hiroyuki, Ossipov Michael H, Bakalkin Georgy, Artemenko Konstantin, Bergquist Jonas

机构信息

Analytical Chemistry, Department of Chemistry - BMC and SciLifeLab and ‡Molecular Neuropsychopharmacology, Department of Pharmaceutical Biosciences, Uppsala University , P.O. Box 599, Husargatan 3, 75124 Uppsala, Sweden.

出版信息

J Proteome Res. 2014 Sep 5;13(9):3957-65. doi: 10.1021/pr500241q. Epub 2014 Jul 28.

Abstract

The myriad proteins may be involved in the mechanisms underlying the development and maintenance of neuropathic pain, an extremely disabling condition that originates from pathology of the nervous system. To address the mechanisms, we here analyzed proteins and cellular networks in the dorsal spinal cord mediating pain processing in a well-established rat model of neuropathic pain induced by spinal nerve ligation (SNL). Labeling-based proteomic methods together with high-resolution mass spectrometry for proteome analysis were applied. 38 proteins including synapsin 1 and microtubule-associated protein 2 were identified as differently expressed in the SNL group. Pathway analysis suggests that maladaptive changes in the levels of these proteins may contribute to abnormal synaptic transmission and neuronal intracellular signaling underlying the onset and development of neuropathic pain.

摘要

众多蛋白质可能参与了神经性疼痛发生和维持的潜在机制,神经性疼痛是一种极其致残的病症,源于神经系统的病变。为了探究其机制,我们在此分析了脊髓背角中介导疼痛处理的蛋白质和细胞网络,该研究采用了一种成熟的大鼠脊髓神经结扎(SNL)诱导的神经性疼痛模型。我们应用了基于标记的蛋白质组学方法以及用于蛋白质组分析的高分辨率质谱法。包括突触素1和微管相关蛋白2在内的38种蛋白质被鉴定为在SNL组中差异表达。通路分析表明,这些蛋白质水平的适应性改变可能导致神经性疼痛发作和发展过程中异常的突触传递和神经元细胞内信号传导。

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