Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14235
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dc.contributor.authorNusuetrong P.
dc.contributor.authorSotanaphun U.
dc.contributor.authorTep-Areenan P.
dc.date.accessioned2021-04-05T03:33:42Z-
dc.date.available2021-04-05T03:33:42Z-
dc.date.issued2012
dc.identifier.issn1252208
dc.identifier.other2-s2.0-84876900461
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14235-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84876900461&partnerID=40&md5=c7096cb25f8a0bce0bfd8e5550767525
dc.description.abstractThe aim of the present study is to investigate the effect of standardized Phikud Navakot extract (NVKE) on aortic rings from male Sprague Dawley rats. Changes in tension were measured using an isometric force transducer and recorded on the PowerLab recording system. Vasorelaxant effect of NVKE was examined in the presence of indomethacin (10 microM), NG-nitro L-arginine methyl ester (L-NAME, 300 microM), methoxamine (0.1-300 microM), carbachol (1 nanoM-30 microM), or sodium nitroprusside (0.1 nanoM-10 microM). The results showed that NVKE (1-300 microg/mL) caused vasorelaxation in a concentration-dependent manner with a pEC50 value of 4.27 + 0.24 and R max of 67.7 + 13.9%. Pretreatment with indomethacin or L-NAME did not affect NVKE-induced vasorelaxation. However, co-incubation of indomethacin and L-NAME significantly reduced (p < 0.05) vasorelaxation to NVKE (100 microg/mL). Pre-treatment with NVKE significantly decreased (p < 0.05) endothelium-dependent relaxations to carbachol (Rmax = 52.90 + 14.3%), but not to sodium nitroprusside. Moreover, contractions to methoxamine were unaffected after pretreatment with NVKE. The present study suggested that NVKE decreased vasorelaxation to carbachol in the rat aorta, which may exert at least against muscarinic receptors. These findings support the use of Phikud Navakot, a major ingredient of Yahom Navakot, against dizziness and fainting.
dc.subjectcarbachol
dc.subjectindometacin
dc.subjectmethoxamine
dc.subjectnitric oxide synthase
dc.subjectnitroprusside sodium
dc.subjectPhikud Navakot extract
dc.subjectplant extract
dc.subjectprostaglandin synthase inhibitor
dc.subjectunclassified drug
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectarticle
dc.subjectconcentration response
dc.subjectcontrolled study
dc.subjectherbal medicine
dc.subjectmale
dc.subjectnonhuman
dc.subjectrat
dc.subjectthoracic aorta
dc.subjectvascular ring
dc.subjectvasodilatation
dc.subjectAnalysis of Variance
dc.subjectAnimals
dc.subjectAorta, Thoracic
dc.subjectCarbachol
dc.subjectDrug Combinations
dc.subjectEndothelium, Vascular
dc.subjectIndomethacin
dc.subjectMale
dc.subjectMethoxamine
dc.subjectNG-Nitroarginine Methyl Ester
dc.subjectNitroprusside
dc.subjectPlant Extracts
dc.subjectRats
dc.subjectRats, Sprague-Dawley
dc.subjectTransducers
dc.subjectVasodilation
dc.subjectVasodilator Agents
dc.titleEffects of Phikud Navakot extract on vascular reactivity in the isolated rat aorta
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationJournal of the Medical Association of Thailand. Vol 95, No.SUPPL.12 (2012), p.S1-S7
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