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.
Yang LiJing LiuXu LiuCun-Jin SuQi-Lin ZhangZhi-Hong WangLei-Fang CaoXue-Yan GuoYa HuangWeifeng LuoTong LiuPublished in: Neuroscience bulletin (2019)
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.
Keyphrases
- prefrontal cortex
- high fat diet induced
- binding protein
- signaling pathway
- poor prognosis
- cell proliferation
- insulin resistance
- wild type
- metabolic syndrome
- cerebral ischemia
- physical activity
- oxidative stress
- cognitive impairment
- stem cells
- skeletal muscle
- major depressive disorder
- sleep quality
- bipolar disorder
- adipose tissue
- mesenchymal stem cells
- soft tissue
- climate change
- brain injury
- endothelial cells
- replacement therapy