4.7 Article

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

期刊

FREE RADICAL BIOLOGY AND MEDICINE
卷 89, 期 -, 页码 1057-1066

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2015.08.013

关键词

Neurodegeneration; Zebrafish; Rat organotypic cerebellar cultures; MPP+

资金

  1. Science and Technology Development Fund of Macao SAR [078/2011/A3, 134/2014/A3]
  2. Overseas
  3. Hong Kong
  4. Natural National Science Foundation of China [81328025]
  5. Research Committee-University of Macau [MYRG2015-00214-ICMS-QRCM]
  6. Research Fund of State Key Laboratory of Chinese Medicine and Molecular Pharmacology (Incubation)
  7. Shenzhen
  8. National Science Foundation of China [21173156]
  9. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

向作者/读者索取更多资源

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.

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