Effects of lithium and valproic acid on BDNF protein and gene expression in an in vitro human neuron-like model of degeneration

被引:16
作者
Croce, Nicoletta [1 ,2 ]
Mathe, Aleksander A. [3 ]
Gelfo, Francesca [1 ,4 ]
Caltagirone, Carlo [1 ,4 ]
Bernardini, Sergio [2 ]
Angelucci, Francesco [1 ]
机构
[1] IRCCS Santa Lucia Fdn, Rome, Italy
[2] Univ Roma Tor Vergata, Dept Internal Med, Rome, Italy
[3] Karolinska Inst, Dept Clin Neurosci, Stockholm, Sweden
[4] Univ Roma Tor Vergata, Dept Syst Med, Rome, Italy
关键词
Lithium; valproic acid; BDNF; SH-SY5Y; L-glutamate; excitotoxicity; neuronal survival; MOOD STABILIZERS LITHIUM; NEUROTROPHIC FACTOR BDNF; NERVE GROWTH-FACTOR; HISTONE DEACETYLASE INHIBITORS; CELLULAR PLASTICITY CASCADES; RESONANCE-IMAGING FINDINGS; ALZHEIMERS-DISEASE; BIPOLAR DISORDER; SYNAPTIC PLASTICITY; SIGNALING PATHWAY;
D O I
10.1177/0269881114529379
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
One of the common effects of lithium (Li) and valproic acid (VPA) is their ability to protect against excitotoxic insults. Neurodegenerative and neuropsychiatric diseases may be also associated with altered trophic support of brain-derived neurotrophic factor (BDNF), the most widely distributed neurotrophin in the central nervous system. However, despite these evidences, the effect of Li-VPA combination on BDNF after excitoxic insult has been inadequately investigated. We address this issue by exposing a human neuroblastoma cell line (SH-SY5Y) to neurotoxic concentration of L-glutamate and exploring whether the neuroprotective action of Li-VPA on these cells is associated with changes in BDNF protein and mRNA levels. The results showed that pre-incubation of Li-VPA abolished the toxic effect of glutamate on SH-SY5Y cell survival and this neuroprotective effect was associated with increased synthesis and mRNA expression of BDNF after 24 and 48 h of incubation. In conclusion, this study demonstrates that the neuroprotective effects of Li-VPA against glutamate-induced neurotoxicity in SH-SY5Y neuroblastoma cells is associated with increased synthesis and mRNA expression of BDNF. These data further support the idea that these two drugs can be used for prevention and/or treatment of glutamate-related neurodegenerative disorders.
引用
收藏
页码:964 / 972
页数:9
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