Citation

Han XM, Huang F, Jiao ML, Liu HR, Zhao ZH, Zhan HQ, Guo SY. Biol. Pharm. Bull. 2020; 43(10): 1490-1500.

Copyright

(Copyright © 2020, Pharmaceutical Society of Japan)

DOI

10.1248/bpb.b20-00093

PMID

32788507

Abstract

Depression is the most significant risk factor for suicide, yet the causes are complex and disease mechanism remains unclear. The incidence and disability rate of depression are very high and the efficacy of some traditional antidepressants is not completely satisfactory. Recently, some studies have found that benzofurans have anti-oxidation and anti-monoamine oxidase properties, which are related to depression. Euparin is a monomer compound of benzofuran, previous work by our team found that it improves the behavior of depressed mice. However, additional antidepressant effects and mechanisms of Euparin have not been reported. In this study, the Chronic Unpredictable Mild Stress (CUMS) model of mice was used to further investigate the effect and mechanism of Euparin on depression.

RESULTS showed that Euparin (8, 16 and 32 mg/kg) reduced depression-like behavior in mice compared with the model group. Meanwhile, all doses of Euparin were found to increase the contents of monoamine neurotransmitter and decrease monoamine oxidase and reactive oxygen species (ROS) levels in brain of depression mice. Additionally, Euparin restored CUMS-induced decrease of Spermidine/Spermine N1-Acetyltransferase 1 (SAT1), N-methyl-D-aspartate receptor subtype 2B (NMDAR2B) and brain derived neurotrophic factor (BDNF) expression. These findings demonstrate that Euparin has antidepressant properties, and its mechanism involves the SAT1/NMDAR2B/BDNF signaling pathway.

Language: en

Keywords

Acetyltransferases; Animals; Behavior Observation Techniques; Behavior, Animal; Benzofurans; brain derived neurotrophic factor; Brain-Derived Neurotrophic Factor; depression; Depression; Disease Models, Animal; Dopamine; Dose-Response Relationship, Drug; Drug Evaluation, Preclinical; Euparin; Frontal Lobe; Hippocampus; Humans; Male; Mice; monoaminergic neurotransmitter; Neurotransmitter Agents; Norepinephrine; oxidative stress; Receptors, N-Methyl-D-Aspartate; Serotonin; signal pathway; Signal Transduction; Specific Pathogen-Free Organisms; Stress, Psychological