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Ciliary neurotrophic factor protects hippocampal neurons from excitotoxic damage.

机译:睫状神经营养因子保护海马神经元免受兴奋性毒性损害。

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摘要

The loss of neurons is responsible for many acute neurological disorders as well as chronic neurodegenerative diseases. This cell loss might be prevented by a direct delivery of neurotrophic factors. Therefore, we investigated the capacity of ciliary neurotrophic factor (CNTF) and nerve growth factor (NGF) as well as the combination of both growth factors on the glutamate-induced excitotoxic damage in hippocampal cultures. The exposure of hippocampal neuronal/glial co-cultures to 0.5 mM L-glutamate for 1 h induced pronounced neurotoxicity evaluated 18 h later by trypan blue staining and morphological criteria. The damaged neurons showed both apoptotic and necrotic features. However, CNTF (1-1000 pg/ml) reduced neuronal degeneration when administered 6 and 24 h before induction of injury and remained in contact with the cells until evaluation of neuronal damage. Furthermore, NGF (1 ng/ml) also rescued the hippocampal neurons under the same experimental conditions and with a similar to CNTF potency. However, the co-administration of NGF and CNTF (but not either factor alone) restored the neuronal survival to control levels. Our results support the hypothesis that administering neurotrophic factors could represent an alternative strategy for the treatment of acute and chronic brain disorders.
机译:神经元的丧失导致许多急性神经系统疾病以及慢性神经退行性疾病。通过直接递送神经营养因子可以防止这种细胞丢失。因此,我们研究了睫状神经营养因子(CNTF)和神经生长因子(NGF)的能力,以及这两种生长因子的组合对谷氨酸诱导的海马培养物兴奋性毒性损伤的作用。将海马神经元/神经胶质共培养物暴露于0.5 mM L-谷氨酸盐中1小时,引起明显的神经毒性,用锥虫蓝染色和形态学标准在18 h后评估。受损的神经元同时具有凋亡和坏死特征。然而,CNTF(1-1000 pg / ml)在诱导损伤前6和24 h给药时可减少神经元变性,并保持与细胞接触直至评估神经元损伤。此外,NGF(1 ng / ml)还在相同的实验条件下并以类似于CNTF的功效拯救了海马神经元。但是,NGF和CNTF的共同给药(但不能单独使用任一因子)将神经元存活恢复到控制水平。我们的研究结果支持以下假设:施用神经营养因子可以代表治疗急性和慢性脑部疾病的替代策略。

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