Discovery of a novel neuroprotectant, BHDPC, that protects against MPP+/MPTP-induced neuronal death in multiple experimental models

被引:22
作者
Chong, Cheong-Meng [1 ,2 ]
Ma, Dan [3 ,4 ]
Zhao, Chao [3 ,4 ]
Franklin, Robin J. M. [3 ,4 ]
Zhou, Zhong-Yan [1 ,2 ]
Ai, Nana [1 ,2 ]
Li, Chuwen [1 ,2 ]
Yu, Huidong [8 ]
Hou, Tingjun [5 ,6 ,7 ]
Sa, Fei [1 ,2 ]
Lee, Simon Ming-Yuen [1 ,2 ]
机构
[1] Univ Macau, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
[2] Univ Macau, Inst Chinese Med Sci, Macau, Peoples R China
[3] Univ Cambridge, MRC, Cambridge Stem Cell Inst, Wellcome Trust, Cambridge CB2 1TN, England
[4] Univ Cambridge, Dept Clin Neurosci, Cambridge CB2 1TN, England
[5] Zhejiang Univ, Coll Pharmaceut Sci, Hangzhou 310058, Zhejiang, Peoples R China
[6] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Suzhou 215123, Jiangsu, Peoples R China
[7] Soochow Univ, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou 215123, Jiangsu, Peoples R China
[8] Rongene Pharma Co Ltd, Int Business Incubator, Guangzhou Sci Town 510663, Guangdong, Peoples R China
基金
美国国家科学基金会;
关键词
Neurodegeneration; Zebrafish; Rat organotypic cerebellar cultures; MPP+; CELL-DEATH; MITOCHONDRIAL DYSFUNCTION; DOPAMINERGIC-NEURONS; MPTP; APOPTOSIS; MPP+; SUPPORT; DISEASE; 1-METHYL-4-PHENYLPYRIDINIUM; NEUROTOXICITY;
D O I
10.1016/j.freeradbiomed.2015.08.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Progressive degeneration and death of neurons are main causes of neurodegenerative disorders such as Parkinson's disease and Alzheimer's disease. Although some current medicines may temporarily improve their symptoms, no treatments can slow or halt the progression of neuronal death. In this study, a pyrimidine derivative, benzyl 7-(4-hydroxy-3-methoxyphenyl)-5-methyl-4,7-dihydrotetrazolo[1,5-a] pyrimidine-6-carboxylate (BHDPC), was found to attenuate dramatically the MPTP-induced death of dopaminergic neurons and improve behavior movement deficiency in zebrafish, supporting its potential neuroprotective activity in vivo. Further study in rat organotypic cerebellar cultures indicated that BHDPC was able to suppress MPP+-nduced cell death of brain tissue slices ex vivo. The protective effect of BHDPC against MPP+ toxicity was also effective in human neuroblastoma SH-SY5Y cells through restoring abnormal changes in mitochondrial membrane potential and numerous apoptotic regulators. Western blotting analysis indicated that BHDPC was able to activate PIKA/CREB survival signaling and further up-regulate BcI2 expression. However, BHDPC failed to suppress MPP+ -induced cytotoxicity and the increase of caspase 3 activity in the presence of the PIKA inhibitor H89. Taken together, these results suggest that BHDPC is a potential neuroprotectant with prosurvival effects in multiple models of neurodegenerative disease in vitro, ex vivo, and in vivo. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:1057 / 1066
页数:10
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