Ildan F, Polat S, Göcer A I, Oner A, Isbir T, Mete U O, Kaya M, Karadayi A
Department of Neurosurgery, Cukurova University, School of Medicine, Balcali, Adana, Turkiye.
Acta Neurochir (Wien). 1996;138(3):338-45. doi: 10.1007/BF01411746.
The sodium-potassium activated and magnesium dependent adenosine-5'-triphosphatase (Na(+)-K(+)/Mg(+2) ATPase EC.3.6.1.3.) activity and lipid peroxidation and early ultrastructural findings were determined in rat brain at the acute stage of ischaemia produced by permanent unilateral occlusion of the middle cerebral artery (MCA). The effects of the pretreatment with intravenous high-dose methylprednisolone (MP) on these biochemical indices and ultrastructural findings were also evaluated in the same model. The rats were divided into four groups. In group I, 10 rats were used to determine Na(+)-K(+)/Mg(+2) ATPase activity and the extent of lipid peroxidation by measuring the malondialdehyde (MDA) content and normal ultrastructural findings. In group II on 20 rats, only subtemporal craniectomy was done in order to determine the effects of the surgical procedure on these indices and findings. This group was treated intravenously with saline solution before occlusion. In group III with MCA occlusion, saline solution was administered intravenously to 20 rats in the same amount of methylprednisolone used in group IV, ten minutes before the occlusion. In Group IV, a single high-dose (30 mg/kg) of methylprednisolone was administered intravenously, ten minutes before occlusion in 20 rats. After occlusion of the middle cerebral artery, Na(+)-K(+)/Mg(+2) ATPase activity was decreased promptly in the first ten minutes in the ischaemic hemisphere and remained at a lower level than the contralateral hemispheres in the same group and the normal levels in group I, during 120 minutes of ischaemia. A single dose methylprednisolone pretreatment prohibited the inactivation of Na(+)-K(+)/Mg(+2) ATPase. On the other hand, there was significant difference in malondialdehyde content between group I and group III. Malondialdehyde levels were significantly increased following ischaemia and a non-significant increase was observed in the contralateral hemisphere. Methylprednisolone treatment significantly decreased malondialdehyde content on the side of the ischaemic hemisphere. We conclude that there is a positive relationship between membrane-bound enzyme Na(+)-K(+)/Mg(+2) ATPase activity, malondialdehyde content and early ultrastructural changes in the treated group with MP. These data suggest that the pretreatment injection of high doses (30 mg/kg) methylprednisolone contribute to the protection of the brain from ischaemia with stabilization of the cell membrane by effecting the lipid peroxidation and the activation of Na(+)-K(+)/Mg(+2) ATPase.
通过永久性单侧大脑中动脉(MCA)闭塞诱导大鼠急性缺血,测定了钠钾激活且依赖镁的腺苷 - 5'-三磷酸酶(Na(+)-K(+)/Mg(+2) ATPase EC.3.6.1.3.)活性、脂质过氧化以及早期超微结构变化。在同一模型中,还评估了静脉注射高剂量甲泼尼龙(MP)预处理对这些生化指标和超微结构变化的影响。将大鼠分为四组。在第一组中,10只大鼠用于通过测量丙二醛(MDA)含量来测定Na(+)-K(+)/Mg(+2) ATPase活性和脂质过氧化程度以及正常超微结构变化。在第二组的20只大鼠中,仅进行颞下颅骨切除术,以确定手术操作对这些指标和变化的影响。该组在闭塞前静脉注射生理盐水。在第三组MCA闭塞组中,20只大鼠在闭塞前10分钟静脉注射与第四组相同剂量的甲泼尼龙的生理盐水。在第四组中,20只大鼠在闭塞前10分钟静脉注射单次高剂量(30 mg/kg)甲泼尼龙。大脑中动脉闭塞后,缺血半球在最初10分钟内Na(+)-K(+)/Mg(+2) ATPase活性迅速下降,并在120分钟缺血期间维持在低于同组对侧半球以及第一组正常水平的状态。单次剂量甲泼尼龙预处理可阻止Na(+)-K(+)/Mg(+2) ATPase的失活。另一方面,第一组和第三组之间丙二醛含量存在显著差异。缺血后丙二醛水平显著升高,对侧半球观察到非显著性升高。甲泼尼龙治疗显著降低了缺血半球一侧的丙二醛含量。我们得出结论,在MP治疗组中,膜结合酶Na(+)-K(+)/Mg(+2) ATPase活性、丙二醛含量与早期超微结构变化之间存在正相关关系。这些数据表明,高剂量(30 mg/kg)甲泼尼龙预处理通过影响脂质过氧化和激活Na(+)-K(+)/Mg(+2) ATPase,有助于稳定细胞膜,从而保护大脑免受缺血损伤。