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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四肽对小鼠成年海马神经发生,神经元塑性和空间记忆的有益作用。

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摘要

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:反对阿尔茨海默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素的性质,以将神经变性与神经发生和神经元可塑性的平衡转移。虽然纤毛神经营养因子(CNTF)具有一些所需的神经保护特性,但其临床用途,由于其副作用,即厌食症,骨骼肌丧失,痛觉过敏,痉挛和肌肉疼痛,尚未实现。在本研究中,我们报告说,对应于CNTF氨基酸残基的肽6C(GDDL)增强了牙齿的陀螺神经发生和神经元塑性,并改善了对小鼠的重量损失或任何其他表观副作用的认知。正常成人C57BL6小鼠接受了含有载体或肽6c的延长释放贮剂颗粒的皮下植入物,持续30天连续给药。通过表达神经元标志物,双峰素和Neun和Brdu摄取的细胞的立体学分析来评估牙齿牙齿发生的神经发生。我们发现肽6C显着提高了新生儿祖细胞的早期神经元预防,分化和存活。这些新生儿神经元在功能上集成到海马网络中,因为C-FOS的基础表达增强,并且由于MAP2A,B和Sypaptophysin的较高表达而增加了神经元可塑性。因此,肽6C处理在小鼠中的空间参考记忆任务中改进了海马依赖信息的编码。总体而言,这些研究结果证明了肽6C的治疗潜力,用于再生的大脑再生和认知的改善。

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