Caner H, Can A, Atalay B, Erdogan B, Albayrak A H, Kilinc K, Bavbek M, Altinors N
Department of Neurosurgery, Baskent University Faculty of Medicine, Ankara, Turkey.
Acta Neurochir (Wien). 2004 Jun;146(6):611-21; discussion 621. doi: 10.1007/s00701-003-0209-9. Epub 2004 Mar 25.
The aims were to investigate the early effects of graded, closed, mild head injury on neurofilament protein (NF160) and microtubule-associated protein-2 (MAP2) and to examine the levels of lipid peroxidation and the impact of mexilitine, inhibitor of lipid peroxidation, pretreatment on tissue damage.
One hundred and twenty-six rats were divided into groups as follows: Group 1 (n = 14) were controls; group 2 (n = 56) sustained trauma alone; and group 3 (n = 56) were pretreated with mexilitine (50 mg/kg). Groups 2 and 3 were subdivided into subgroups (n = 14 each), which were subjected to 100 g/cm2, 125 g/cm2, 150 g/cm2, and 175 g/cm2 trauma forces, respectively. Two hours after trauma, the frontal lobes from all groups were removed and processed for lipid peroxidation H&E staining, immunofluorescent labelling of neurofilaments and microtubules with anti-NF160 and anti-MAP2 antibodies.
Compared to control findings, all the trauma-only animals showed increased lipid peroxidation levels and the elevations paralleled the amount of force applied. Administration of mexilitine significantly reduced the level of lipid peroxidation. In NF160 stainings, in group 2, the degree of impairment in axonal organization paralleled the different levels of force that were applied. Groups 3C and 3D (mexilitine pretreated) showed well-preserved axons and intact perikarya. In MAP2 stainings group 2 animals showed remarkably less MAP2 staining throughout the sections. There were no significant differences in MAP2 staining intensity or pattern among the group 2 subgroups. In contrast, in the sections from the group 3 animals, the level of MAP2 positivity was markedly preserved.
In conclusion, our results show that the cytoskeletal proteins we investigated have different capacities for resisting injury, and that MAP2 is more vulnerable to injury than NF160. One of the reason for this cytoskeletal disruption may be increased lipid peroxidation. Inhibition of lipid peroxidation by pre-treatment with 50-mg/kg mexilitine significantly reduces the level of lipid peroxidation and may protect MAP2 and NF160 integrity in closed mild head injury. This protection is inversely proportional to the magnitude of the applied force.
研究分级、闭合性轻度颅脑损伤对神经丝蛋白(NF160)和微管相关蛋白2(MAP2)的早期影响,并检测脂质过氧化水平以及美西律(脂质过氧化抑制剂)预处理对组织损伤的影响。
126只大鼠分为以下几组:第1组(n = 14)为对照组;第2组(n = 56)仅遭受创伤;第3组(n = 56)用美西律(50 mg/kg)预处理。第2组和第3组再细分为亚组(每组n = 14),分别施加100 g/cm²、125 g/cm²、150 g/cm²和175 g/cm²的创伤力。创伤后2小时,取出所有组的额叶,进行脂质过氧化检测、苏木精-伊红(H&E)染色、用抗NF160和抗MAP2抗体对神经丝和微管进行免疫荧光标记。
与对照组结果相比,所有仅受创伤的动物脂质过氧化水平均升高,且升高程度与施加的力大小平行。美西律给药显著降低了脂质过氧化水平。在NF160染色中,第2组轴突组织的损伤程度与施加的不同力水平平行。第3组C和D(美西律预处理)显示轴突保存良好,核周体完整。在MAP2染色中,第2组动物在整个切片中MAP2染色明显减少。第2组亚组之间MAP2染色强度或模式无显著差异。相反,在第3组动物的切片中,MAP2阳性水平明显保留。
总之,我们的结果表明,我们研究的细胞骨架蛋白具有不同的抗损伤能力,且MAP2比NF160更容易受到损伤。这种细胞骨架破坏的原因之一可能是脂质过氧化增加。用50 mg/kg美西律预处理抑制脂质过氧化可显著降低脂质过氧化水平,并可能保护闭合性轻度颅脑损伤中MAP2和NF160的完整性。这种保护作用与施加力的大小成反比。