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首页> 外文期刊>Journal of Alzheimer's disease: JAD >Beneficial Effect of a CNTF Tetrapeptide on Adult Hippocampal Neurogenesis, Neuronal Plasticity, and Spatial Memory in Mice.
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Beneficial Effect of a CNTF Tetrapeptide on Adult Hippocampal Neurogenesis, Neuronal Plasticity, and Spatial Memory in Mice.

机译:CNTF四肽对成年海马神经发生,神经元可塑性和小鼠空间记忆的有益作用。

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A therapeutic strategy against cognitive disorders like Alzheimer's disease is to take advantage of the regenerative ability of the brain and the properties of neurotrophic factors to shift the balance from neurodegeneration to neurogenesis and neuronal plasticity. Although the ciliary neurotrophic factor (CNTF) has some of the required neuroprotective characteristics, its clinical use, due to its side effects, i.e., anorexia, skeletal muscle loss, hyperalgesia, cramps, and muscle pain, has not materialized. In the present study, we report that Peptide 6c (GDDL) that corresponds to CNTF amino acid residues 147-150, enhances the dentate gyrus neurogenesis and neuronal plasticity, and improves cognition without weight loss or any other apparent side effects in mice. Normal adult C57Bl6 mice received subcutaneous implants of extended release depot pellets containing vehicle or Peptide 6c for 30 days of continuous dosing. Dentate gyrus neurogenesis was assessed by stereological analysis of cells expressing neuronal markers, doublecortin and NeuN, and BrdU uptake. We found that Peptide 6c significantly increased early neuronal commitment, differentiation, and survival of newborn progenitor cells. These newborn neurons were functionally integrated into the hippocampal network, since basal expression of c-fos was enhanced and neuronal plasticity was increased, as reflected by higher expression of MAP2a,b and synaptophysin. Consequently, Peptide 6c treatment improved encoding of hippocampal-dependent information in a spatial reference memory task in mice. Overall, these findings demonstrated the therapeutic potential of Peptide 6c for regeneration of the brain and improvement of cognition.
机译:针对诸如阿尔茨海默氏病等认知障碍的治疗策略是利用大脑的再生能力和神经营养因子的特性,将平衡从神经退行性转变为神经发生和神经元可塑性。尽管睫状神经营养因子(CNTF)具有某些必需的神经保护特性,但由于其副作用,即厌食,骨骼肌丢失,痛觉过敏,痉挛和肌肉疼痛,其临床应用尚未实现。在本研究中,我们报道了对应于CNTF氨基酸残基147-150的6c肽(GDDL),增强了齿状回神经发生和神经元可塑性,并改善了认知,而没有体重减轻或小鼠其他任何明显的副作用。正常成年C57B16小鼠皮下植入了含有媒介物或6c肽的缓释长效药丸,进行了3​​0天的连续给药。通过对表达神经元标记,双皮质素和NeuN以及BrdU摄取的细胞进行立体分析,评估了齿状回的神经发生。我们发现肽6c显着增加了新生儿祖细胞的早期神经元定向,分化和存活。这些新生神经元在功能上已整合到海马网络中,因为c-fos的基础表达增强,神经元可塑性增强,这由MAP2a,b和突触素的更高表达所反映。因此,肽6c处理改善了小鼠在空间参考记忆任务中海马依赖性信息的编码。总体而言,这些发现证明了6c肽对于大脑再生和认知能力的治疗潜力。

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