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c-FOS PROTEIN AND NADPH-DIAPHORASE DETECTION IN RAT MIDBRAEV AND SPINAL CORD AFTER CONTUSION INJURY

机译:C-FOS蛋白和NADPH-透明酶在挫伤后大鼠中脑和脊髓的检测

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Spinal cord injury appears to involve neuroplastic remodeling or cell death that is the result of intense neuronal cells response to lesion. The damage may occur near the site of lesion, as well as in proximal brain areas. Thus, neurons located in brain centers and functionally connected to the damaged areas may present constitutive changes after spinal cord damage. Experimental studies and clinical observations show that spinal cord trauma may be amplified by secondary neuronal damage. However, little is known about the molecular mechanism that initiates and maintains this neuronal reaction. We have started an investigation of neural changes induced by acute spinal cord injury. We assessed the degree of functional neurologic impairment that follows spinal cord injury by behavioral tests and histological methods. In lesioned areas and throughout the central nervous system expression of the transcription factor protein c-Fos was investigated by immunocytochemistry. The localization of c-Fos may indicate, in addition to neuronal activation, spatial and temporal patterns related to the type of stimulus and to the long-term variation in neuronal physiology. In parallel, to identify spinal neurons that synthesize Nitric Oxide, cells and fibers histochemically stained for NADPH diaphorase (a nitric oxide synthase), were studied. Fos expression was detected in NADPH-diaphorase positive cells at intermedio lateral column, central canal, dorsal horn, including nucleus trigeminalis caudalis, two hours after contusion by weight drop. It was found that NADPH-diaphorase is induced in spinal motoneurons, neurons that are normally NADPH-diaphorase negative; however, no Fos protein expression was detected in these cells. The results suggest that central nervous system areas close or proximal to the lesion site, are activated after contusion by weight drop. In addition they show that Fos protein expression and changes on NADPH-diaphorase activity after spinal cord contusion are not necessarily dependent on each other.
机译:脊髓损伤似乎涉及神经塑性重塑或细胞死亡,这是强烈神经元细胞对病变的反应的结果。病变部位以及近端脑区域附近可能发生损坏。因此,位于脑中中心并且在功能上连接到受损区域的神经元可以在脊髓损伤后存在本构剖视图。实验研究和临床观察表明,脊髓创伤可以通过次要神经元损伤扩增。然而,关于引发并保持这种神经元反应的分子机制很少。我们已经开始调查急性脊髓损伤诱导的神经变化。我们评估了行为试验和组织学方法遵循脊髓损伤的功能性神经系统损伤程度。通过免疫细胞化学研究了在损伤的区域和整个中枢神经系统的表达中,研究了转录因子蛋白C-FOS的表达。除了与刺激类型相关的神经元激活,空间和时间模式以及神经元生理学的长期变化之外,C-FOS的定位也可以表明。并行地鉴定合成一氧化氮,细胞和纤维的脊髓神经元,研究了用于NADPH透镜酶(一氧化氮合酶)的细胞和纤维。在中间侧柱,中央运河,背角,包括核心三角形的核心阳性细胞中检测到FOS表达,在挫伤后2小时后,核心下降两小时。发现NADPH-透典酶在脊柱运动神经元,神经元通常是NADPH-透明酶阴性的神经元;然而,在这些细胞中没有检测到FOS蛋白表达。结果表明,在挫伤后,封闭或近端的中枢神经系统区域闭合或近端,在挫折后被激活。此外,它们表明FOS蛋白表达和脊髓挫伤后NADPH-透明酶活性的变化不一定依赖于彼此。

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