Departamento de Neuroquímica, Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suarez S.S.A., Mexico; Maestría en Ciencias Farmacéuticas, Universidad Autónoma Metropolitana, Unidad Xochimilco, Mexico.
Neurosci Lett. 2012 Apr 11;514(1):102-5. doi: 10.1016/j.neulet.2012.02.068. Epub 2012 Mar 3.
After spinal cord injury (SCI), a complex cascade of pathophysiological processes rapidly damages the nervous tissue. The initial damage spreads to the surrounding tissue by different mechanisms, including oxidative stress. We have recently reported that the induction of metallothionein (MT) protein is an endogenous rapid-response mechanism after SCI. Since the participation of MT in neuroprotective processes after SCI is still unknown, the aim of the present study was to evaluate the possible neuroprotective effect of exogenously administered MT-II during the acute phase after SCI in rats. Female Wistar rats weighing 200-250g were submitted to spinal cord contusion by means of a computer-controlled device (NYU impactor). Rats received several doses of MT-II (3.2, 10 and 100μg) at 2 and 8h after SCI. Results of the BBB scale were statistically analysed using an ANOVA of repeated-measures, followed by Tukey's test. Among the three doses tested, only 10 and 100μg were able to significantly increase (p<0.05) BBB scale scores eight weeks after SCI from a mean of 7.88 in the control group, to means of 12.63 and 10.88 for the 10 and 100μg doses of MT-II, respectively. The amount of spared tissue was also higher in the groups treated with 10 and 100μg, as compared to the control group values. Results from the present study demonstrate a significant neuroprotective effect of exogenously administered MT-II. Further studies are needed in order to characterize the mechanisms involved in this neuroprotective action.
脊髓损伤(SCI)后,一系列复杂的病理生理过程迅速损害神经组织。初始损伤通过不同的机制扩散到周围组织,包括氧化应激。我们最近报道,金属硫蛋白(MT)蛋白的诱导是 SCI 后的一种内源性快速反应机制。由于 MT 参与 SCI 后神经保护过程的情况尚不清楚,本研究的目的是评估外源性 MT-II 在 SCI 后急性期对大鼠的可能神经保护作用。体重为 200-250g 的雌性 Wistar 大鼠通过计算机控制装置(NYU 冲击器)进行脊髓挫伤。大鼠在 SCI 后 2 小时和 8 小时接受多次 MT-II(3.2、10 和 100μg)剂量。BBB 量表的结果使用重复测量方差分析进行统计学分析,然后进行 Tukey 检验。在所测试的三个剂量中,只有 10 和 100μg 能够在 SCI 后 8 周显著增加(p<0.05)BBB 量表评分,从对照组的平均 7.88 增加到 10 和 100μg MT-II 剂量组的平均 12.63 和 10.88。与对照组相比,用 10 和 100μg 处理的组中保留的组织量也更高。本研究的结果表明,外源性 MT-II 具有显著的神经保护作用。需要进一步的研究来阐明这种神经保护作用涉及的机制。