Please use this identifier to cite or link to this item:
https://ir.swu.ac.th/jspui/handle/123456789/13644
ชื่อเรื่อง: | Effect of Inhaling bergamot oil on depression-related behaviors in chronic stressed rats |
ผู้แต่ง: | Saiyudthong S. Mekseepralard C. |
Keywords: | bergamot oil brain derived neurotrophic factor corticosterone corticotropin fluoxetine bergamot oil brain derived neurotrophic factor corticosterone essential oil vegetable oil animal experiment animal model animal tissue Article chronic stress controlled study depression enzyme immunoassay forced swim test hypothalamus hypophysis adrenal system immobilization stress male nonhuman rat animal blood depression Depressive Disorder drug effects hippocampus hypophysis adrenal system hypothalamus hypophysis system mental stress metabolism Wistar rat Animals Brain-Derived Neurotrophic Factor Corticosterone Depression Depressive Disorder Hippocampus Hypothalamo-Hypophyseal System Male Oils, Volatile Pituitary-Adrenal System Plant Oils Rats Rats, Wistar Stress, Psychological |
วันที่เผยแพร่: | 2015 |
บทคัดย่อ: | Background: 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. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/13644 https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957609830&partnerID=40&md5=79c104783a5d3e2ecbb4b7e2cf8e4c56 |
ISSN: | 1252208 |
Appears in Collections: | Scopus 1983-2021 |
Files in This Item:
There are no files associated with this item.
Items in SWU repository are protected by copyright, with all rights reserved, unless otherwise indicated.