Slusarczyk Wojciech, Olakowska Edyta, Larysz-Brysz Magdalena, Woszczycka-Korczyńska Izabella, de Carrillo Daria Gendosz, Węglarz Władysław P, Lewin-Kowalik Joanna, Marcol Wiesław
Department of Physiology, Medical University of Silesia, Katowice, Poland.
Institute of Nuclear Physics, Polish Academy of Sciences, Krakow, Poland.
Neural Regen Res. 2019 Jul;14(7):1255-1261. doi: 10.4103/1673-5374.251334.
Spinal cord injury (SCI) causes disturbances of motor skills. Free radicals have been shown to be essential for the development of spinal cord trauma. Despite some progress, until now no effective pharmacological therapies against SCI have been verified. The purpose of our experiment was to investigate the neuroprotective effects of ebselen on experimental SCI. Twenty-two rats subjected to SCI were randomly subjected to SCI with no further treatment (n = 10) or intragastric administration of ebselen (10 mg/kg) immediately and 24 hours after SCI. Behavioral changes were assessed using the Basso, Beattie, and Bresnahan locomotor scale and footprint test during 12 weeks after SCI. Histopathological and immunohistochemical analyses of spinal cords and brains were performed at 12 weeks after SCI. Magnetic resonance imaging analysis of spinal cords was also performed at 12 weeks after SCI. Rats treated with ebselen presented only limited neurobehavioral progress as well as reduced spinal cord injuries compared with the control group, namely length of lesions (cysts/scars) visualized histopathologically in the spinal cord sections was less but cavity area was very similar. The same pattern was found in T2-weighted magnetic resonance images (cavities) and diffusion-weighted images (scars). The number of FluoroGold retrogradely labeled neurons in brain stem and motor cortex was several-fold higher in ebselen-treated rats than in the control group. The findings suggest that ebselen has only limited neuroprotective effects on injured spinal cord. All exprimental procedures were approved by the Local Animal Ethics Committee for Experiments on Animals in Katowice (Katowice, Poland) (approval No. 19/2009).
脊髓损伤(SCI)会导致运动技能障碍。自由基已被证明在脊髓创伤的发展中起着至关重要的作用。尽管取得了一些进展,但迄今为止,尚未证实有针对SCI的有效药物治疗方法。我们实验的目的是研究依布硒啉对实验性SCI的神经保护作用。22只遭受SCI的大鼠被随机分为两组,一组在SCI后不做进一步处理(n = 10),另一组在SCI后立即及24小时后经胃内给予依布硒啉(10 mg/kg)。在SCI后的12周内,使用Basso、Beattie和Bresnahan运动量表以及足迹试验评估行为变化。在SCI后12周对脊髓和脑进行组织病理学和免疫组织化学分析。在SCI后12周还对脊髓进行磁共振成像分析。与对照组相比,接受依布硒啉治疗的大鼠仅表现出有限的神经行为改善以及脊髓损伤减轻,即组织病理学观察到的脊髓切片中病变(囊肿/瘢痕)长度较短,但空洞面积非常相似。在T2加权磁共振图像(空洞)和扩散加权图像(瘢痕)中也发现了相同的模式。与对照组相比,依布硒啉治疗的大鼠脑干和运动皮层中逆行性荧光金标记神经元的数量高出几倍。这些发现表明依布硒啉对受损脊髓仅具有有限的神经保护作用。所有实验程序均获得了卡托维兹当地动物实验伦理委员会(波兰卡托维兹)的批准(批准号19/2009)。