Li Na, Wang Xiao-yan, Liu Chun-chang, Zhang Qin-li, Niu Qiao
School of Public Health, Shanxi Medical University, Taiyuan 030001, China.
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2011 May;29(5):343-8.
To investigate the effects of caspase-3 siRNA on the neurobehavior of mice exposed to aluminum.
Male KunMing mice (3 months old) were randomly divided into 4 groups by weight:blank control group (4 microl normal saline), Al group (4 microl 0.5% AlCl3), Al plus empty vector group(3 microl 0.5% AlCl3 plus control siRNA expression vector)and Al plus RNAi group (3 microl 0.5% AlCl3 plus targeted siRNA expression vector). All groups were treated by lateral cerebral ventricle micro-injection for 5 days. The neurobehavior was tested by the Morris water maze test, Open-field and Step-down tests for all treated mice. Pathological changes in hippocampus was observed by electron microscopy, the caspase-3 gene expression levels were detected using RT-PCR.
The results of Step-down test indicated that as compared with control group, the latent time [LT, (44.67 +/- 10.60) s] in A1 group decreased significantly, the error number (3.63 +/- 0.52) in Al group increased significantly and the LT [(68.00 +/- 14.70) s] in Al plus empty vector group decreased significantly (P<0.05). the LT [(239.50 +/- 19.36) s] in Al plus RNAi group increased significantly and the error number in Al plus RNAi group decreased significantly, as compared with Al group (P<0.05). The results of Morris water maze test showed that as compared with control group, the LT in Al group increased significantly, and residence time in the former platform quadrant decreased significantly and the LT in Al plus empty vector group increased significantly (P<0.05). The LT in Al plus RNAi group was significantly longer than that in Al group (P<0.05). The results of open-field test demonstrated that as compared with control group, the time in the central grid in Al group and Al plus empty vector group increased significantly, the rearing number and the modification number in Al group and Al plus empty vector group decreased significantly (P< 0.05). As compared with Al group, the time in the central grid in Al plus RNAi group decreased, the inter-cell number, the rearing number and the modification number increased significantly (P<0.05). The results of electron microscopic examination exhibited that a slight change of hippocampal cells appeared in control group, the obvious pathological changes of hippocampal cells appeared in Al group and Al plus empty vector group, but the pathological changes of hippocampal cells in Al plus RNAi group significantly reduced as compared with Al group. The results of thionin staining indicated that the layers of neural cells of hippocampal CA3 were more clear and there was not obvious denatured injury of neural cells of hippocampal CA3 in control group. The number and Nissl body color of neural cells of hippocampal CA3 in Al group and Al plus empty vector group decreased significantly. After RNA interference, the number and Nissl body color of neural cells of hippocampal CA3 increased obviously. The expression levels of caspase-3 gene in Al group and Al plus empty vector group were 2.24 +/- 0.57 and 2.28 +/- 0.33, respectively, which were significantly higher than that (1.00 +/- 0.00) in control group (P<0.05). The expression level of caspase-3 gene in Al plus RNAi group was 0.44 +/- 0.08, which was significantly lower than those in Al group and control group (P<0.05).
Aluminum can decrease the learning and memorizing ability, and inhibited the activity or exploration function of mice. It is suggested that Caspase-3 siRNA may reduce the neurotoxicity induced by aluminum to a certain extent.
探讨半胱天冬酶 -3小干扰RNA(caspase-3 siRNA)对铝暴露小鼠神经行为的影响。
将3月龄雄性昆明小鼠按体重随机分为4组:空白对照组(4 μl生理盐水)、铝组(4 μl 0.5%氯化铝)、铝加空载体组(3 μl 0.5%氯化铝加对照小干扰RNA表达载体)和铝加RNA干扰组(3 μl 0.5%氯化铝加靶向小干扰RNA表达载体)。所有组均通过侧脑室微量注射给药5天。采用莫里斯水迷宫试验、旷场试验和跳台试验对所有处理后的小鼠进行神经行为测试。通过电子显微镜观察海马体的病理变化,采用逆转录聚合酶链反应(RT-PCR)检测半胱天冬酶-3基因表达水平。
跳台试验结果表明,与对照组相比,铝组的潜伏期[LT,(44.67±10.60)秒]显著缩短,错误次数(3.63±0.52)显著增加,铝加空载体组的LT[(68.00±14.70)秒]显著缩短(P<0.05)。与铝组相比,铝加RNA干扰组的LT[(239.50±19.36)秒]显著延长,错误次数显著减少(P<0.05)。莫里斯水迷宫试验结果显示,与对照组相比,铝组的LT显著延长,在前平台象限的停留时间显著减少,铝加空载体组的LT显著延长(P<0.05)。铝加RNA干扰组的LT显著长于铝组(P<0.05)。旷场试验结果表明,与对照组相比,铝组和铝加空载体组在中央格的停留时间显著增加,铝组和铝加空载体组的直立次数和修饰次数显著减少(P<0.05)。与铝组相比,铝加RNA干扰组在中央格的停留时间减少,细胞间次数、直立次数和修饰次数显著增加(P<0.05)。电子显微镜检查结果显示,对照组海马细胞有轻微变化,铝组和铝加空载体组海马细胞出现明显病理变化,但与铝组相比,铝加RNA干扰组海马细胞的病理变化明显减轻。硫堇染色结果表明,对照组海马CA3区神经细胞层较清晰,海马CA3区神经细胞无明显变性损伤。铝组和铝加空载体组海马CA3区神经细胞数量和尼氏体颜色显著减少。RNA干扰后,海马CA3区神经细胞数量和尼氏体颜色明显增加。铝组和铝加空载体组半胱天冬酶-3基因表达水平分别为2.24±0.57和2.28±0.33,显著高于对照组(1.00±0.00)(P<0.05)。铝加RNA干扰组半胱天冬酶-3基因表达水平为0.44±0.08,显著低于铝组和对照组(P<0.05)。
铝可降低小鼠的学习记忆能力,抑制小鼠的活动或探索功能。提示半胱天冬酶-3 siRNA可能在一定程度上减轻铝诱导的神经毒性。