Smith-Swintosky V L, Pettigrew L C, Sapolsky R M, Phares C, Craddock S D, Brooke S M, Mattson M P
Sanders-Brown Research Center on Aging, University of Kentucky, Lexington 40536-0230, USA.
J Cereb Blood Flow Metab. 1996 Jul;16(4):585-98. doi: 10.1097/00004647-199607000-00008.
Increasing evidence indicates that glucocorticoids (GCs), produced in response to physical/emotional stressors, can exacerbate brain damage resulting from cerebral ischemia and severe seizure activity. However, much of the supporting evidence has come from studies employing nonphysiological paradigms in which adrenalectomized rats were compared with those exposed to constant GC concentrations in the upper physiological range. Cerebral ischemia and seizures can induce considerable GC secretion. We now present data from experiments using metyrapone (an 11-beta-hydroxylase inhibitor of GC production), which demonstrate that the GC stress-response worsens subsequent brain damage induced by ischemia and seizures in rats. Three different paradigms of brain injury were employed: middle cerebral artery occlusion (MCAO) model of focal cerebral ischemia; four-vessel occlusion (4VO) model of transient global forebrain ischemia; and kainic acid (KA)-induced (seizure-mediated) excitotoxic damage to hippocampal CA3 and CA1 neurons. Metyrapone (200 mg/kg body wt) was administered systemically in a single i.p. bolus 30 min prior to each insult. In the MCAO model, metyrapone treatment significantly reduced infarct volume and also preserved cells within the infarct. In the 4VO model, neuronal loss in region CA1 of the hippocampus was significantly reduced in rats administered metyrapone. Seizure-induced damage to hippocampal pyramidal neurons (assessed by cell counts and immunochemical analyses of cytoskeletal alterations) was significantly reduced in rats administered metyrapone. Measurement of plasma levels of corticosterone (the species-typical GC of rats) after each insult showed that metyrapone significantly suppressed the injury-induced rise in levels of circulating corticosterone. These findings indicate that endogenous corticosterone contributes to the basal level of brain injury resulting from cerebral ischemia and excitotoxic seizure activity and suggest that drugs that suppress glucocorticoid production may be effective in reducing brain damage in stroke and epilepsy patients.
越来越多的证据表明,机体在应对生理/情绪应激源时产生的糖皮质激素(GCs)会加重脑缺血和严重癫痫活动所导致的脑损伤。然而,许多支持性证据来自采用非生理模式的研究,这些研究将肾上腺切除的大鼠与暴露于生理范围上限恒定GC浓度的大鼠进行比较。脑缺血和癫痫可诱导大量GC分泌。我们现在展示使用美替拉酮(一种GC产生的11-β-羟化酶抑制剂)进行实验的数据,这些数据表明GC应激反应会使大鼠后续由缺血和癫痫诱导的脑损伤恶化。采用了三种不同的脑损伤模式:大脑中动脉闭塞(MCAO)局灶性脑缺血模型;四血管闭塞(4VO)短暂性全脑缺血模型;以及 kainic acid(KA)诱导的(癫痫介导的)对海马CA3和CA1神经元的兴奋性毒性损伤。在每次损伤前30分钟,以单次腹腔注射大剂量(200 mg/kg体重)的方式全身给予美替拉酮。在MCAO模型中,美替拉酮治疗显著减小了梗死体积,并且还保护了梗死区内的细胞。在4VO模型中,给予美替拉酮的大鼠海马CA1区的神经元损失显著减少。给予美替拉酮的大鼠中,癫痫诱导的对海马锥体神经元的损伤(通过细胞计数和细胞骨架改变的免疫化学分析评估)显著减少。每次损伤后对血浆皮质酮(大鼠典型的GC)水平的测量表明,美替拉酮显著抑制了损伤诱导的循环皮质酮水平升高。这些发现表明内源性皮质酮促成了脑缺血和兴奋性毒性癫痫活动导致的基础脑损伤水平,并提示抑制糖皮质激素产生的药物可能对减少中风和癫痫患者的脑损伤有效。