| Literature DB >> 25463525 |
W Wang1, Y Lu2, Z Xue2, C Li2, C Wang3, X Zhao2, J Zhang2, X Wei2, X Chen2, W Cui2, Q Wang4, W Zhou2.
Abstract
The possible involvement of the PI3K/AKT/BDNF/VGF signaling in rapid-acting antidepressant-like effects of antidepressants has been explored progressively by more studies. However, whether this signaling participates in the antidepressant-like effects of acetyl-l-carnitine (ALC) has not been examined. Herein, we assessed the antidepressant-like effects of ALC using the forced swimming test (FST). Our results demonstrated the dose-effect relationship of acute administration of ALC (5, 25, 50 and 100mg/kg, i.p.) and showed that it dose-dependently decreased the immobility time on FST of mice. In addition, ALC (100 mg/kg, i.p.) also reversed depressive-like behavior and the down-regulation of phosphorylated AKT (pAKT), brain-derived neurotrophic factor (BDNF) and neuropeptide VGF in the hippocampus and prefrontal cortex of mice induced by chronic unpredictable mild stress (CUMS) paradigm. Further, intra-cerebroventricular (i.c.v.) infusions of LY294002 (10 nmol/side), a specific phosphatidylinositol 3-kinase (PI3K) inhibitor, significantly prevented the antidepressant-like effect of ALC (100mg/kg, i.p.). In conclusion, our results demonstrated that ALC exerts rapid-acting antidepressant-like effects that might be mediated by the PI3K/AKT/BDNF/VGF signaling pathway.Entities:
Keywords: acetyl-l-carnitine; brain-derived neurotrophic factor; depression; neuropeptide VGF; phosphatidylinositol 3-kinase
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Year: 2014 PMID: 25463525 DOI: 10.1016/j.neuroscience.2014.11.025
Source DB: PubMed Journal: Neuroscience ISSN: 0306-4522 Impact factor: 3.590