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Title: | Acute effects of bergamot oil on anxiety-related behaviour and corticosterone level in rats |
Authors: | Saiyudthong S. Marsden C.A. |
Keywords: | 4 aminobutyric acid 4 aminobutyric acid A receptor bergamot oil corticosterone diazepam acute stress animal experiment animal model anxiety anxiety disorder aromatherapy article controlled study corticosterone blood level emotion GABAergic system hypothalamic paraventricular nucleus locomotion male maze test neurotransmission nonhuman rat task performance tranquilizing activity Administration, Inhalation Animals Anti-Anxiety Agents Anxiety Disorders Corticosterone Diazepam Male Maze Learning Oils, Volatile Plant Extracts Plant Oils Rats Rats, Wistar Citrus aurantium Rattus Rutaceae |
Issue Date: | 2011 |
Abstract: | Bergamot essential oil (BEO), Citrus aurantium subsp. bergamia (Risso) Wright & Arn. (Rutaceae), is used widely in aromatherapy to reduce stress and anxiety despite limited scientific evidence. A previous study showed that BEO significantly increased gamma-aminobutyric acid levels in rat hippocampus, suggesting potential anxiolytic properties. The aim of this study was to investigate the effect of BEO (1.0%, 2.5% and 5.0% w/w) administered to rats on both anxiety-related behaviours (the elevated plus-maze (EPM) and hole-board tests) and stress-induced levels of plasma corticosterone in comparison with the effects of diazepam. Inhalation of BEO (1% and 2.5%) and injection of diazepam (1 mg/kg, i.p.) significantly increased the percentage of open arm entries on the EPM. The percentage time spent in the open arms was also significantly enhanced following administration of either BEO (2.5% and 5%) or diazepam. Total arm entries were significantly increased with the highest dose (5%), suggesting an increase in locomotor activity. In the hole-board test, 2.5% BEO and diazepam significantly increased the number of head dips. 2.5% BEO and diazepam attenuated the corticosterone response to acute stress caused by exposure to the EPM. In conclusion, both BEO and diazepam exhibited anxiolytic-like behaviours and attenuated HPA axis activity by reducing the corticosterone response to stress. Copyright © 2010 John Wiley & Sons, Ltd. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/14520 https://www.scopus.com/inward/record.uri?eid=2-s2.0-79957809174&doi=10.1002%2fptr.3325&partnerID=40&md5=4ca76b2ebc4fee092817500cb7eb7290 |
ISSN: | 0951418X |
Appears in Collections: | Scopus 1983-2021 |
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