Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/15449
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dc.contributor.authorDeachapunya C.
dc.contributor.authorThongsaard W.
dc.date.accessioned2021-04-05T04:34:12Z-
dc.date.available2021-04-05T04:34:12Z-
dc.date.issued2009
dc.identifier.issn1252208
dc.identifier.other2-s2.0-77957307242
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/15449-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-77957307242&partnerID=40&md5=15d6a48533c598627191f6b326516395
dc.description.abstractINTRODUCTION: Barakol, an active constituent extracted from Cassia siamea, has been shown to have anxiolytic effects similar to diazepam when treated intraperitoneally. OBJECTIVE: Acute and chronic oral administrations of barakol on anxiolytic, locomotor and exploratory behaviors were examined in rats using an elevated plus maze followed by a holeboard apparatus in comparison with the anxiolytic diazepam. MATERIAL AND METHOD: Male Wistar rats were divided into the acute and chronic treatment groups. The acutely-treated rats were given orally with vehicle control (distilled water, p.o.), diazepam (5 mg/kg, p.o.) and barakol (10, 30 and 100 mg/kg, p.o.) while the chronically-treated rats received the same treatment for 30 consecutive days. The anxiolytic behavior was tested on the elevated plus maze for 5 min and immediately followed by the holeboard to test for the directed exploratory behavior for 10 min. RESULTS: Acute and chronic oral administration of barakol (10, 30 and 100 mg/kg, p.o.) produced no significant changes in anxiolytic parameters tested on the elevated plus maze compared to diazepam which significantly increased the percentage of the open/total time and the time spent on the open arms. On the other hand, all parameters tested using the holeboard were not affected by barakol or diazepam when given acutely. When given chronically, all doses of barakol significantly decreased the number of head-dips and the total time spent head-dipping with no changes in the number of grooms or rears per minute. CONCLUSION: Acute and chronic oral administration of barakol had no anxiolytic and locomotor effects. However, it exerted a sedative effect as shown by a reduction in the directed exploratory behaviors.
dc.subjectanxiolytic agent
dc.subjectbarakol
dc.subjectbenzopyran derivative
dc.subjectdiazepam
dc.subjectphenalene derivative
dc.subjectplant extract
dc.subjectacute disease
dc.subjectanimal
dc.subjectanimal behavior
dc.subjectanxiety
dc.subjectarticle
dc.subjectchronic disease
dc.subjectdrug effect
dc.subjecthuman
dc.subjectoral drug administration
dc.subjectphytotherapy
dc.subjectrat
dc.subjectSenna
dc.subjectWistar rat
dc.subjectAcute Disease
dc.subjectAdministration, Oral
dc.subjectAnimals
dc.subjectAnti-Anxiety Agents
dc.subjectAnxiety
dc.subjectBehavior, Animal
dc.subjectBenzopyrans
dc.subjectChronic Disease
dc.subjectDiazepam
dc.subjectHumans
dc.subjectPhenalenes
dc.subjectPhytotherapy
dc.subjectPlant Extracts
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectSenna Plant
dc.titleBehavioral effects of acute and chronic oral administration of barakol in rats.
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationJournal of the Medical Association of Thailand = Chotmaihet thangphaet. Vol 92 Suppl 3, No. (2009), p.S29-37
Appears in Collections:Scopus 1983-2021

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