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Valeriana officinalis root extract suppresses physical stress by electric shock and psychological stress by nociceptive stimulation-evoked responses by decreasing the ratio of monoamine neurotransmitters to their metabolites

Cited 12 time in Web of Science Cited 14 time in Scopus
Authors

Jung, Hyo Young; Yoo, Dae Young; Kim, Woosuk; Nam, Sung Min; Kim, Jong Whi; Choi, Jung Hoon; Kwak, Youn-Gil; Yoon, Yeo Sung; Hwang, In Koo

Issue Date
2014-12-11
Publisher
BioMed Central
Citation
BMC Complementary and Alternative Medicine, 14(1):476
Keywords
Valeriana officinalisPhysical stressPsychological stressSerotoninNorepinephrineHippocampusAmygdala
Description
This is an Open Access article distributed under the terms of the Creative
Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and
reproduction in any medium, provided the original work is properly credited.
Abstract
Abstract

Background
In this study, we investigate the effects of valerian root extracts (VE) on physical and psychological stress responses by utilizing a communication box.


Methods
Eight-week-old ICR mice received oral administration of VE (100mg/kg/0.5ml) or equal volume of distilled water in every day for 3weeks prior to being subjected to physical or psychological stress for 3days, which are induced by communication box developed for physical electric shock and psychological stress by nociceptive stimulation-evoked responses. The stress condition was assessed by forced swimming test and serum corticosterone levels. In addition, norepinephrine (NE), serotonin (5-HT), and their metabolites such as 3-methoxy-4-hydroxyphenylethyleneglycol sulfate (MHPG-SO4) and 5-hydroxyindoleacetic acid (5-HIAA) were measured in the hippocampus and amygdala at 1h after final stress condition, respectively.


Results
Immobility time and corticosterone levels were significantly increased in both the physical and psychological stress groups compared to the control group. The administration of VE significantly reduced these parameters in both the physical and psychological stress groups. In addition, compared to the control group, physical and psychological stress groups showed significantly increased levels of MHPG-SO4 and 5-HIAA in the hippocampus and amygdala, respectively. The administration of VE significantly suppressed the increase of MHPG-SO4 and 5-HIAA in the two stress groups.


Conclusion
These results suggest that VE can suppress physical and psychological stress responses by modulating the changes in 5-HT and NE turnover in the hippocampus and amygdala.
Language
English
URI
https://hdl.handle.net/10371/100439
DOI
https://doi.org/10.1186/1472-6882-14-476
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