Neuroscience bulletin · 2019
Antidepressant-Like Action of Single Facial Injection of Botulinum Neurotoxin A is Associated with Augmented 5-HT Levels and BDNF/ERK/CREB Pathways in Mouse Brain.
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Li Yang, Liu Jing, Liu Xu, Su Cun-Jin, Zhang Qi-Lin, Wang Zhi-Hong, Cao Lei-Fang, Guo Xue-Yan, Huang Ya, Luo Weifeng, Liu Tong
Аннотация
The present study was designed to examine the therapeutic effects of Botulinum neurotoxin A (BoNT/A) on depression-like behaviors in mice and to explore the potential mechanisms. These results revealed that a single facial injection of BoNT/A induced a rapid and prolonged improvement of depression-like behaviors in naïve and space-restriction-stressed (SRS) mice, reflected by a decreased duration of immobility in behavioral despair tests. BoNT/A significantly increased the 5-hydroxytryptamine (5-HT) levels in several brain regions, including the hippocampus and hypothalamus, in SRS mice. BoNT/A increased the expression of the N-methyl-D-aspartate receptor subunits NR1 and NR2B in the hippocampus, which were significantly decreased in SRS mice. Furthermore, BoNT/A significantly increased the expression of brain-derived neurotrophic factor (BDNF) in the hippocampus, hypothalamus, prefrontal cortex, and amygdala, which were decreased in SRS mice. Finally, BoNT/A transiently increased the levels of phosphorylated extracellular signal-regulated kinase (p-ERK) and cAMP-response element binding protein (p-CREB), which were suppressed in the hippocampus of SRS mice. Collectively, these results demonstrated that BoNT/A treatment has anti-depressant-like activity in mice, and this is associated with increased 5-HT levels and the activation of BDNF/ERK/CREB pathways in the hippocampus, supporting further investigation of BoNT/A therapy in depression.
Предметные рубрики MeSH
AmygdalaAnimalsAntidepressive AgentsBehavior, AnimalBotulinum Toxins, Type ABrainBrain-Derived Neurotrophic FactorCyclic AMP Response Element-Binding ProteinDepressionHippocampusHypothalamusMAP Kinase Signaling SystemMaleMiceMice, Inbred ICRModels, AnimalPrefrontal CortexReceptors, N-Methyl-D-AspartateSerotoninSignal Transduction