Haynes L E, Griffiths M R, Hyde R E, Barber D J, Mitchell I J
School of Psychology, University of Birmingham, B15 2TT, Birmingham, UK.
Neuroscience. 2001;104(1):57-69. doi: 10.1016/s0306-4522(01)00070-7.
It has been shown previously that the synthetic corticosteroid dexamethasone induces apoptosis of granule cells in the dentate gyrus and striatopallidal neurons in the dorsomedial caudate-putamen. We investigated whether or not dexamethasone can induce damage to other neuronal populations. This issue was addressed using OX42 immunohistochemistry to visualise activated microglia and thereby gauge the extent of dexamethasone-induced neuronal death. A single dose of dexamethasone (20mg/kg, i.p.) administered to young male Sprague-Dawley rats induced a strong microglial reaction which was restricted to the striatum, the dentate gyrus and all of the CA subfields of the hippocampus. Some OX42-immunoreactive cells were also seen in the lateral septal nucleus. Subsequent quantitative analysis of silver/methenamine-stained sections confirmed that acute administration of dexamethasone induced apoptosis in the striatum and all regions of the hippocampus at doses as low as 0.7mg/kg. In contrast, dexamethasone failed to induce apoptosis in the lateral septal nucleus at doses up to 20mg/kg. The levels of dexamethasone-induced striatal and hippocampal apoptosis were attenuated by pretreatment with the corticosteroid receptor antagonist RU38486 (Mifepristone), which implies that the cell death was mediated by a corticosteroid receptor-dependent process. We further determined whether dexamethasone induced sublethal damage to neurons by quantifying reductions in the number of microtubule-associated protein-2-immunoreactive striatal and hippocampal cells following injection of the corticosteroid. Dexamethasone induced dramatic decreases in the striatum, with the dorsomedial caudate-putamen being particularly affected. Similar damage was seen in the hippocampus, with the dentate gyrus and CA1 and CA3 subfields being particularly vulnerable.Equivalent corticosteroid-induced neuronal damage may occur in mood disorders, where the levels of endogenous corticosteroids are often raised. Corticosteroid-induced damage of striatal and hippocampal neurons may also account for some of the cognitive deficits seen following administration of the drugs to healthy volunteers.
先前的研究表明,合成皮质类固醇地塞米松可诱导齿状回颗粒细胞和背内侧尾状核 - 壳核中的纹状体苍白球神经元凋亡。我们研究了地塞米松是否会对其他神经元群体造成损伤。通过OX42免疫组织化学来可视化活化的小胶质细胞,从而评估地塞米松诱导的神经元死亡程度,以此解决该问题。给年轻雄性Sprague-Dawley大鼠腹腔注射单剂量地塞米松(20mg/kg)会引发强烈的小胶质细胞反应,该反应局限于纹状体、齿状回以及海马体的所有CA亚区。在外侧隔核中也可见到一些OX42免疫反应性细胞。随后对银/六胺染色切片进行的定量分析证实,急性给予地塞米松,低至0.7mg/kg的剂量即可诱导纹状体和海马体所有区域的细胞凋亡。相比之下,高达20mg/kg的地塞米松剂量未能诱导外侧隔核细胞凋亡。皮质类固醇受体拮抗剂RU38486(米非司酮)预处理可减轻地塞米松诱导的纹状体和海马体凋亡水平,这表明细胞死亡是由皮质类固醇受体依赖性过程介导的。我们进一步通过量化注射皮质类固醇后微管相关蛋白 - 2免疫反应性纹状体和海马体细胞数量的减少,来确定地塞米松是否会对神经元造成亚致死性损伤。地塞米松可使纹状体显著减少,背内侧尾状核 - 壳核受影响尤为明显。海马体也出现类似损伤,齿状回以及CA1和CA3亚区特别易受影响。在情绪障碍中,内源性皮质类固醇水平通常会升高,可能会发生同等程度的皮质类固醇诱导的神经元损伤。皮质类固醇诱导的纹状体和海马体神经元损伤也可能是健康志愿者服用这些药物后出现一些认知缺陷的部分原因。