Qu Changsheng, Lu Dunyue, Goussev Anton, Schallert Timothy, Mahmood Asim, Chopp Michael
Department of Neurosurgery, Henry Ford Health Sciences Center, Detroit, USA.
J Neurosurg. 2005 Oct;103(4):695-701. doi: 10.3171/jns.2005.103.4.0695.
Atorvastatin administered after traumatic brain injury (TBI) induced by controlled cortical impact promotes functional improvement in male rats. Note, however, that parallel studies have not been performed in female rats. Therefore, the authors tested the effect of atorvastatin on TBI in female rats.
Atorvastatin (1 mg/kg/day) was orally administered for 7 consecutive days in female Wistar rats starting I day after TBI; control animals received saline. Modified neurological severity scores, the corner turn test, and the Morris water maze test were used to evaluate functional response to treatment. Rats were killed on Day 15 post-TBI, and brain tissue samples were processed for immunohistochemical staining. Atorvastatin administration after brain injury significantly promoted the restoration of spatial memory but did not reduce sensorimotor functional deficits. Treatment of TBI with atorvastatin increased neuronal survival in the CA3 region and the lesion boundary zone and prevented the loss of neuronal processes of damaged neurons in the hippocampal CA3 region but not in the lesion boundary zone on Day 15 after TBI. The protective effect of atorvastatin on the injured neurons perhaps is mediated by increasing the density of vessels in the lesion boundary zone and the hippocampus after TBI.
. These data indicate that atorvastatin is beneficial in the treatment of TBI in female rats, although the effect may differ between sexes.
在控制性皮质撞击诱导的创伤性脑损伤(TBI)后给予阿托伐他汀可促进雄性大鼠的功能改善。然而,请注意,尚未在雌性大鼠中进行平行研究。因此,作者测试了阿托伐他汀对雌性大鼠TBI的影响。
在雌性Wistar大鼠TBI后第1天开始连续7天口服阿托伐他汀(1毫克/千克/天);对照动物接受生理盐水。使用改良的神经严重程度评分、转角试验和莫里斯水迷宫试验来评估对治疗的功能反应。在TBI后第15天处死大鼠,并对脑组织样本进行免疫组织化学染色。脑损伤后给予阿托伐他汀显著促进了空间记忆的恢复,但并未减轻感觉运动功能缺陷。在TBI后第15天,用阿托伐他汀治疗TBI可增加CA3区和损伤边界区的神经元存活,并防止海马CA3区受损神经元的神经突丢失,但在损伤边界区则没有。阿托伐他汀对受损神经元的保护作用可能是通过增加TBI后损伤边界区和海马区的血管密度来介导的。
这些数据表明,阿托伐他汀对雌性大鼠TBI的治疗有益,尽管其效果可能存在性别差异。