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DC Field | Value | Language |
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dc.contributor.author | Saiyudthong S. | |
dc.contributor.author | Marsden C.A. | |
dc.date.accessioned | 2021-04-05T03:35:20Z | - |
dc.date.available | 2021-04-05T03:35:20Z | - |
dc.date.issued | 2011 | |
dc.identifier.issn | 0951418X | |
dc.identifier.other | 2-s2.0-79957809174 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/14520 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-79957809174&doi=10.1002%2fptr.3325&partnerID=40&md5=4ca76b2ebc4fee092817500cb7eb7290 | |
dc.description.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. | |
dc.subject | 4 aminobutyric acid | |
dc.subject | 4 aminobutyric acid A receptor | |
dc.subject | bergamot oil | |
dc.subject | corticosterone | |
dc.subject | diazepam | |
dc.subject | acute stress | |
dc.subject | animal experiment | |
dc.subject | animal model | |
dc.subject | anxiety | |
dc.subject | anxiety disorder | |
dc.subject | aromatherapy | |
dc.subject | article | |
dc.subject | controlled study | |
dc.subject | corticosterone blood level | |
dc.subject | emotion | |
dc.subject | GABAergic system | |
dc.subject | hypothalamic paraventricular nucleus | |
dc.subject | locomotion | |
dc.subject | male | |
dc.subject | maze test | |
dc.subject | neurotransmission | |
dc.subject | nonhuman | |
dc.subject | rat | |
dc.subject | task performance | |
dc.subject | tranquilizing activity | |
dc.subject | Administration, Inhalation | |
dc.subject | Animals | |
dc.subject | Anti-Anxiety Agents | |
dc.subject | Anxiety Disorders | |
dc.subject | Corticosterone | |
dc.subject | Diazepam | |
dc.subject | Male | |
dc.subject | Maze Learning | |
dc.subject | Oils, Volatile | |
dc.subject | Plant Extracts | |
dc.subject | Plant Oils | |
dc.subject | Rats | |
dc.subject | Rats, Wistar | |
dc.subject | Citrus aurantium | |
dc.subject | Rattus | |
dc.subject | Rutaceae | |
dc.title | Acute effects of bergamot oil on anxiety-related behaviour and corticosterone level in rats | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Phytotherapy Research. Vol 25, No.6 (2011), p.858-862 | |
dc.identifier.doi | 10.1002/ptr.3325 | |
Appears in Collections: | Scopus 1983-2021 |
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