The PTEN inhibitor bpV(pic) promotes neuroprotection against amyloid β-peptide (25-35)-induced oxidative stress and neurotoxicity

作者：Liu, Xiao-Ying; Zhang, Li-Jing; Chen, Zhou^*; Liu, Li-Bin^*

来源：Neurological Research, 2017, 39(8): 758-765.

DOI：10.1080/01616412.2017.1317916

• A beta(25-35)
• bpV(pic)
• oxidative stress
• neurodegeneration
• neuroprotection

Objectives: The aim of this study was to elucidate the mechanism underlying the neuroprotective effects of the phosphatase and tensin homolog (PTEN) inhibitor, bisperoxovanadium-pic [bpV(pic)]. @@@ Methods: We determined the effects of bpV(pic) on amyloid-beta-peptide-(25-35)-induced neurotoxicity, particularly intracellular reactive oxygen species (ROS) production and mitochondria-mediated apoptotic signaling, in a human neuroblastoma (SH-SY5Y) cell model. @@@ Results: We found that exposure of SH-SY5Y cells to amyloid beta peptides (A beta(25-35)) resulted in a significant reduction in cell viability accompanied by increased lactate dehydrogenase (LDH) release, elevated levels of intracellular ROS, and decreased superoxide dismutase (SOD) activities, all of which were reversed by co-treatment with bpV(pic). Moreover, bpV(pic) induced significant protection against A beta(25-35)-induced apoptosis, and effectively suppressed mitochondria-dependent apoptotic signaling triggered by A beta(25-35). @@@ Discussion: A beta peptides are thought to cause neurodegeneration in Alzheimer's disease (AD), via the induction of free radical oxidative stress. Our results indicate that bpV(pic) provides protection against A beta(25-35)-induced oxidative stress and neurotoxicity, suggesting that bpV(pic) could be a potential therapeutic candidate in the treatment of neurodegenerative diseases such as AD.

• 出版日期2017
• 单位福建医科大学