Saatman K E, Bareyre F M, Grady M S, McIntosh T K
Department of Neurosurgery, School of Medicine, University of Pennsylvania, Philadelphia 19104, USA.
J Neuropathol Exp Neurol. 2001 Feb;60(2):183-94. doi: 10.1093/jnen/60.2.183.
Traumatic brain injury results in a profound decline in intracellular magnesium ion levels that may jeopardize critical cellular functions. We examined the consequences of preinjury magnesium deficiency and post-traumatic magnesium treatment on injury-induced cytoskeletal damage and cell death at 24 h after injury. Adult male rats were fed either a normal (n = 24) or magnesium-deficient diet (n = 16) for 2 wk prior to anesthesia and lateral fluid percussion brain injury (n = 31) or sham injury (n = 9). Normally fed animals were then randomized to receive magnesium chloride (125 micromol, i.v., n = 10) or vehicle solution (n = 11) at 10 min postinjury. Magnesium treatment reduced cortical cell loss (p < 0.05), cortical alterations in microtubule-associated protein-2 (MAP-2) (p < 0.05), and both cortical and hippocampal calpain-mediated spectrin breakdown (p < 0.05 for each region) when compared to vehicle treatment. Conversely, magnesium deficiency prior to brain injury led to a greater area of cortical cell loss (p < 0.05 compared to vehicle treatment). Moreover, brain injury to magnesium-deficient rats resulted in cytoskeletal alterations within the cortex and hippocampus that were not observed in vehicle- or magnesium-treated animals. These data suggest that cortical cell death and cytoskeletal disruptions in cortical and hippocampal neurons may be sensitive to magnesium status after experimental brain injury, and may be mediated in part through modulation of calpains.
创伤性脑损伤会导致细胞内镁离子水平大幅下降,这可能会危及关键的细胞功能。我们研究了伤前镁缺乏和创伤后镁治疗对损伤后24小时损伤诱导的细胞骨架损伤和细胞死亡的影响。成年雄性大鼠在麻醉和侧方流体冲击性脑损伤(n = 31)或假手术损伤(n = 9)前2周,分别喂食正常饮食(n = 24)或缺镁饮食(n = 16)。然后将正常喂食的动物在伤后10分钟随机分为接受氯化镁(125微摩尔,静脉注射,n = 10)或溶媒溶液(n = 11)。与溶媒治疗相比,镁治疗减少了皮质细胞损失(p < 0.05)、微管相关蛋白-2(MAP-2)的皮质改变(p < 0.05)以及皮质和海马钙蛋白酶介导的血影蛋白分解(每个区域p < 0.05)。相反,脑损伤前的镁缺乏导致更大面积的皮质细胞损失(与溶媒治疗相比p < 0.05)。此外,缺镁大鼠的脑损伤导致皮质和海马内的细胞骨架改变,而在接受溶媒或镁治疗的动物中未观察到这种改变。这些数据表明,实验性脑损伤后,皮质细胞死亡以及皮质和海马神经元中的细胞骨架破坏可能对镁状态敏感,并且可能部分通过钙蛋白酶的调节介导。