Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13644
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dc.contributor.authorSaiyudthong S.
dc.contributor.authorMekseepralard C.
dc.date.accessioned2021-04-05T03:25:19Z-
dc.date.available2021-04-05T03:25:19Z-
dc.date.issued2015
dc.identifier.issn1252208
dc.identifier.other2-s2.0-84957609830
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13644-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84957609830&partnerID=40&md5=79c104783a5d3e2ecbb4b7e2cf8e4c56
dc.description.abstractBackground: Bergamot essential oil (BEO) possesses sedation and anxiolytic properties similar to diazepam. After long period of exposure to stressors, including restrained stress, depressive-like behavior can be produced. BEO has been suggested to reduce depression. However, there is no scientific evidence supporting this property. Objective: To investigate the effect of BEO in chronic stressed rats on: 1) behavior related depressive disorder, 2) hypothalamic pituitary adrenal (HPA) axis response, and iii) brain-derived neurotrophic factor (BDNF) protein levels in hippocampus. Material and Method: Male Wistar rats, weighing 200 to 250 g, were induced chronic restrained stress 15 minutes daily for two weeks. For the next two weeks, these rats were divided into four groups, control-i.p., fluoxetine-i.p., control-inhale, and BEO-inhale. Fluoxetine (10 mg/kg i.p.) or saline was intraperitoneally administered daily while 2.5% BEO or saline was inhaled daily. At the end of the treatment, rats were assessed for depressive-like behavior using the forced swimming test (FST). After the behavioral test, the animals were immediately decapitated and trunk blood samples were collected for the measurement of corticosterone and adrenocorticotropic hormone (ACTH) levels and hippocampus was dissected and stored in a freezer at -80 °C until assay for BDNF protein. Results: BEO and fluoxetine significantly decreased the immobility time in the FST (p<0.05). Fluoxetine tended to decrease serum corticosterone and significantly (p<0.05) decreased serum ACTH while BEO had no effect on these two stress hormones. For BDNF protein determination, neither BEO nor fluoxetine had any effect on BDNF protein levels in hippocampus compared to their controls. Conclusion: The inhalation of BEO decrease behavior related depressive disorder similar to fluoxetine but has no effect on HPA axis response and BDNF protein levels in chronic restrained stress. © 2015, Medical Association of Thailand. All rights reserved.
dc.subjectbergamot oil
dc.subjectbrain derived neurotrophic factor
dc.subjectcorticosterone
dc.subjectcorticotropin
dc.subjectfluoxetine
dc.subjectbergamot oil
dc.subjectbrain derived neurotrophic factor
dc.subjectcorticosterone
dc.subjectessential oil
dc.subjectvegetable oil
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectchronic stress
dc.subjectcontrolled study
dc.subjectdepression
dc.subjectenzyme immunoassay
dc.subjectforced swim test
dc.subjecthypothalamus hypophysis adrenal system
dc.subjectimmobilization stress
dc.subjectmale
dc.subjectnonhuman
dc.subjectrat
dc.subjectanimal
dc.subjectblood
dc.subjectdepression
dc.subjectDepressive Disorder
dc.subjectdrug effects
dc.subjecthippocampus
dc.subjecthypophysis adrenal system
dc.subjecthypothalamus hypophysis system
dc.subjectmental stress
dc.subjectmetabolism
dc.subjectWistar rat
dc.subjectAnimals
dc.subjectBrain-Derived Neurotrophic Factor
dc.subjectCorticosterone
dc.subjectDepression
dc.subjectDepressive Disorder
dc.subjectHippocampus
dc.subjectHypothalamo-Hypophyseal System
dc.subjectMale
dc.subjectOils, Volatile
dc.subjectPituitary-Adrenal System
dc.subjectPlant Oils
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectStress, Psychological
dc.titleEffect of Inhaling bergamot oil on depression-related behaviors in chronic stressed rats
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationJournal of the Medical Association of Thailand. Vol 98, (2015), p.S152-S159
Appears in Collections:Scopus 1983-2021

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