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White Ginseng Ameliorates Depressive Behavior and Increases Hippocampal 5-HT Level in the Stressed Ovariectomized Rats.
- Source :
-
BioMed research international [Biomed Res Int] 2019 Feb 11; Vol. 2019, pp. 5705232. Date of Electronic Publication: 2019 Feb 11 (Print Publication: 2019). - Publication Year :
- 2019
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Abstract
- Postmenopausal depression is closely associated with depletion of estrogen which modulates transmission of 5-HT, a key neurotransmitter that regulates stress-managing circuits in the brain. In this study, antidepressive efficacy of white ginseng ( Panax gingseng Meyer, WG) was evaluated in stressed ovariectomized rats. Female Sprague Dawley rats were ovariectomized and repeatedly restraint stressed for 2 weeks (2h/day). Thirty minutes before restraint stress, rats were administered saline (control), WG 200 mg/kg (p.o.), WG 400 mg/kg (p.o.), or fluoxetine (PC, 10 mg/kg, i.p.). Tail suspension test (TST) and forced swimming test (FST) were performed to assess antidepressant effect of WG. After behavioral tests, levels of serum corticosterone (CORT) and hippocampal 5-HT were measured. Significant decrease of immobility time in TST and FST was shown in rats administered with PC or WG 400 compared to the control. WG200-treated rats showed remarkable reduction in immobility time of TST. PC, WG 200, or WG 400-administred group exhibited significant reduction of CORT compared to the control. PC or WG-treated rats exhibited remarkable increase in hippocampal 5-HT concentration compared to the control. Hippocampal 5-HT levels in WG groups were higher than those in the PC group. The present study demonstrated that WG had antidepressant efficacy in an animal model of menopausal depression. Treatment with WG enhanced hippocampal 5-HT level while suppressing depressive symptom and serum CORT level. These results provide evidence that WG plays an important role in activating serotonergic neurons in stressful situation, suggesting that WG might be a reliable natural alternative of antidepressant drugs to treat menopausal depression.<br />Competing Interests: The authors have no conflicts of interest to declare.<br /> (Copyright © 2019 Daehyuk Jang et al.)
- Subjects :
- Animals
Antidepressive Agents chemistry
Antidepressive Agents pharmacology
Brain drug effects
Brain physiopathology
Depression genetics
Depression physiopathology
Depressive Disorder genetics
Depressive Disorder physiopathology
Disease Models, Animal
Hindlimb Suspension methods
Hippocampus drug effects
Hippocampus metabolism
Humans
Rats
Stress, Psychological drug therapy
Stress, Psychological genetics
Stress, Psychological physiopathology
Swimming
Depression drug therapy
Depressive Disorder drug therapy
Panax chemistry
Serotonin metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2314-6141
- Volume :
- 2019
- Database :
- MEDLINE
- Journal :
- BioMed research international
- Publication Type :
- Academic Journal
- Accession number :
- 31612144
- Full Text :
- https://doi.org/10.1155/2019/5705232