首页> 外文期刊>Brain research >Effect of a graded single constriction of the rat sciatic nerve on pain behavior and expression of immunoreactive NPY and NPY Y1 receptor in DRG neurons and spinal cord.
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Effect of a graded single constriction of the rat sciatic nerve on pain behavior and expression of immunoreactive NPY and NPY Y1 receptor in DRG neurons and spinal cord.

机译:大鼠坐骨神经单次分级收缩对DRG神经元和脊髓中疼痛行为和免疫反应性NPY和NPY Y1受体表达的影响。

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摘要

In the present study, the rat sciatic nerve was constricted to varying degrees using only one ligature with a very thin polyethylene sheath placed between nerve and ligature thread. Complete nerve transection was studied for comparison. With a 40-80% constriction of the nerve we observed allodynia to a similar extent as in the so-called Bennett model based on four loose ligatures. We also monitored changes in the expression of neuropeptide Y (NPY) and the NPY Y1 receptor (Y1R) in the lumbar 4-5 dorsal root ganglia (DRG) and dorsal horn and found upregulation of NPY and downregulation of the Y1R in DRG neurons after injury. These results indicate that similar peptide and receptor changes occur in this model as after axotomy and in other nerve injury models, although the immunohistochemical and behavioral changes seem to be dependent on the degree of constriction of the nerve. Thus, it seems relevant to monitor the degree of constriction when evaluating pain and other post-injury events. The possibility that some of the changes in NPY-ergic neurotransmission are related to the generation of allodynia is discussed; as well as the possibility to use this mononeuropathic model based on a single ligature nerve constriction (SLNC) as a complementary approach to other widely used pain models.
机译:在本研究中,仅使用一根绑带将大鼠坐骨神经收缩至不同程度,在神经和绑扎线之间放置非常薄的聚乙烯鞘。为了比较,研究了完整的神经横切术。在神经收缩40-80%的情况下,我们观察到异常性疼痛的程度与基于四个松散结扎的所谓Bennett模型相似。我们还监测了腰4-5背根神经节(DRG)和背角中神经肽Y(NPY)和NPY Y1受体(Y1R)的表达变化,发现DRG神经元后NPY上调和Y1R的下调受伤。这些结果表明,尽管免疫组化和行为改变似乎取决于神经的收缩程度,但在该模型中与在轴索切开术之后和在其他神经损伤模型中发生相似的肽和受体改变。因此,评估疼痛和其他损伤后事件时监测收缩程度似乎很重要。讨论了NPY能神经传递的某些变化与异常性疼痛的发生有关的可能性。以及使用基于单个结扎神经收缩(SLNC)的单神经病模型作为其他广泛使用的疼痛模型的补充方法的可能性。

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