靶向JNK信号通路治疗脑卒中和帕金森病。

Chia-Yi Kuan, Robert E Burke
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引用次数: 103

摘要

c-Jun nh2末端激酶(JNK)信号通路经常由细胞应激诱导,并与神经元死亡相关。这种独特的性质使JNK信号成为开发药物干预的有希望的目标。在几种神经系统疾病中,JNK信号尤其与缺血性中风和帕金森病有关。JNK信号通路的抑制剂包括上游激酶抑制剂(例如CEP-1347), JNK的小化学抑制剂(SP600125和AS601245),以及JNK与其底物相互作用的肽抑制剂(D-JNKI和I-JIP)。本文综述了JNK信号诱导细胞凋亡的机制以及这些JNK抑制剂的细胞保护作用的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting the JNK signaling pathway for stroke and Parkinson's diseases therapy.

The c-Jun NH2-terminal Kinase (JNK) signaling pathway is frequently induced by cellular stress and correlated with neuronal death. This unique property makes JNK signaling a promising target for developing pharmacological intervention. Among several neurological disorders, JNK signaling is particularly implicated in ischemic stroke and Parkinson's disease. The inhibitors of the JNK signaling pathway include upstream kinase inhibitors (for example, CEP-1347), small chemical inhibitors of JNK (SP600125 and AS601245), and peptide inhibitors of the interaction between JNK and its substrates (D-JNKI and I-JIP). The mechanisms by which JNK signaling induces apoptosis and evidence of cytoprotective effects of these JNK inhibitors are summarized in the present review.

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