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针对神经退行性疾病的神经保护作用:新型混合神经保护肽Colivelin的研发。

Neuroprotection against neurodegenerative diseases: development of a novel hybrid neuroprotective peptide Colivelin.

作者信息

Chiba Tomohiro, Nishimoto Ikuo, Aiso Sadakazu, Matsuoka Masaaki

机构信息

Department of Anatomy and Pharmacology, KEIO University School of Medicine, Shinjuku-ku, Tokyo, Japan.

出版信息

Mol Neurobiol. 2007 Feb;35(1):55-84.

Abstract

Neuronal death is directly implicated in the pathogenesis of neurodegenerative diseases (NDDs). NDDs cannot be cured because the mechanisms underlying neuronal death are too complicated to be therapeutically suppressed. Neuroprotective factors, such as neurotrophins, certain growth factors, neurotrophic cytokines, and short neuroprotective peptides, support neuronal survival in both physiological and pathological conditions, suggesting that these factors may be good drug candidates for NDDs. We recently generated a novel neuroprotective peptide named Colivelin by attaching activity-dependent neurotrophic factor (ADNF) to the N-terminus of a potent Humanin derivative, AGA-(C8R)HNG17. HN was originally identified from an Alzheimer's disease (AD) brain as an endogenous neuroprotective peptide that suppresses ADrelevant toxicity. Colivelin protects neurons from death relevant to NDDs by activating two independent prosurvival signals: an ADNF-mediated Ca2+/calmodulin-dependent protein kinase IV pathway and an HN-mediated STAT3 pathway. The neuroprotective effect of Colivelin provides novel insights into therapy for NDDs.

摘要

神经元死亡直接参与神经退行性疾病(NDDs)的发病机制。由于神经元死亡的潜在机制过于复杂而难以通过治疗手段抑制,NDDs无法治愈。神经保护因子,如神经营养因子、某些生长因子、神经营养细胞因子和短神经保护肽,在生理和病理条件下均能支持神经元存活,这表明这些因子可能是治疗NDDs的良好候选药物。我们最近通过将活性依赖的神经营养因子(ADNF)连接到一种有效的人源in衍生肽AGA-(C8R)HNG17的N端,生成了一种名为Colivelin的新型神经保护肽。人源in最初是从阿尔茨海默病(AD)大脑中鉴定出来的一种内源性神经保护肽,可抑制与AD相关的毒性。Colivelin通过激活两个独立的促存活信号来保护神经元免受与NDDs相关的死亡:一个是ADNF介导的Ca2+/钙调蛋白依赖性蛋白激酶IV途径,另一个是HN介导的STAT3途径。Colivelin的神经保护作用为NDDs的治疗提供了新的见解。

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