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首页> 外文期刊>Journal of neuroendocrinology >Action of glucocorticoids on survival of nerve cells: promoting neurodegeneration or neuroprotection?
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Action of glucocorticoids on survival of nerve cells: promoting neurodegeneration or neuroprotection?

机译:糖皮质激素对神经细胞存活的作用:促进神经变性或神经保护作用?

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Extensive studies during the past decades provided compelling evidence that glucocorticoids (GCs) have the potential to affect the development, survival and death of neurones. These observations, however, reflect paradoxical features of GCs, as they may be critically involved in both neurodegenerative and neuroprotective processes. Hence, we first address different aspects of the complex role of GCs in neurodegeneration and neuroprotection, such as concentration dependent actions of GCs on neuronal viability, anatomical diversity of GC-mediated mechanisms in the brain and species and strain differences in GC-induced neurodegeneration. Second, the modulatory action of GCs during development and ageing of the central nervous system, as well as the contribution of altered GC balance to the pathogenesis of neurodegenerative disorders is considered. In addition, we survey recent data as to the possible mechanisms underlying the neurodegenerative and neuroprotective actions of GCs. As such, two major aspects will be discerned: (i) GC-dependent offensive events, such as GC-induced inhibition of glucose uptake, increased extracellular glutamate concentration and concomitant elevation of intracellular Ca(2+), decrease in GABAergic signalling and regulation of local GC concentrations by 11 beta-hydroxysteroid dehydrogenases; and (ii) GC-related cellular defence mechanisms, such as decrease in after-hyperpolarization, increased synthesis and release of neurotrophic factors and lipocortin-1, feedback regulation of Ca(2+) currents and induction of antioxidant enzymes. The particular relevance of these mechanisms to the neurodegenerative and neuroprotective effects of GCs in the brain is discussed.
机译:在过去的几十年中,广泛的研究提供了令人信服的证据,即糖皮质激素(GCs)有可能影响神经元的发育,存活和死亡。但是,这些观察结果反映了GC的自相矛盾的特征,因为它们可能与神经变性和神经保护过程都至关重要。因此,我们首先讨论GC在神经变性和神经保护中复杂作用的不同方面,例如GC对神经元生存力的浓度依赖性作用,GC介导的大脑和物种的机制的解剖多样性以及GC诱导的神经变性的菌株差异。第二,考虑了中枢神经系统发育和衰老过程中GC的调节作用,以及GC平衡改变对神经退行性疾病发病机理的贡献。此外,我们调查了有关GC的神经退行性和神经保护作用的潜在机制的最新数据。因此,将识别两个主要方面:(i)依赖GC的进攻性事件,例如GC诱导的葡萄糖摄取抑制,细胞外谷氨酸浓度增加和细胞内Ca(2+)随之升高,GABA能信号传导和调节降低11种β-羟类固醇脱氢酶对局部GC浓度的影响; (ii)与GC相关的细胞防御机制,例如减少超极化后,神经营养因子和lipocortin-1的合成和释放增加,Ca(2+)电流的反馈调节和抗氧化剂的诱导。讨论了这些机制与大脑中GC的神经变性和神经保护作用的特殊相关性。

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