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dc.contributor.authorBoonsong Kasempitakpongen_US
dc.contributor.authorWinthana Kusirisinen_US
dc.contributor.authorChurdsak Jaikangen_US
dc.contributor.authorNipon Sermpanichen_US
dc.date.accessioned2018-09-04T10:06:27Z-
dc.date.available2018-09-04T10:06:27Z-
dc.date.issued2015-06-01en_US
dc.identifier.issn22123881en_US
dc.identifier.issn15734013en_US
dc.identifier.other2-s2.0-84930585599en_US
dc.identifier.other10.2174/1573401311666150416231320en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84930585599&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/54003-
dc.description.abstract© 2015 Bentham Science Publishers. Inhibition of acetylcholinesterase (AChE) and prevention of acetylcholine degradation are of the most accepted therapies for Alzheimer’s disease. Aqueous extracts of seventeen Thai medicinal plants were used in traditional Thai medicine for preventing chronic diseases such as diabetes, hypertension and cardiovascular diseases. They were tested for cholinesterase inhibitory properties using the Ellman’s colorimetric method. The extracts were screened for their free radical scavenging properties using 1, 1 diphenyl-2-picrylhydrazyl (DPPH), ferric reducing antioxidant power (FRAP) and metal chelating method. Total phenolic, total flavonoid, total tannin and total alkaloids contented in the extracts were determined. The results found that Cassia siamea (CS) was the most potent inhibitor of AChE activity with IC50value 0.85±0.06 mg/ ml. Lagerstroemia speciasa (LS) had the highest potency to scavenge DPPH radical with 50% scavenging concentration (SC50) value 0.27±0.01 mg/ ml. CS and LS were high in reducing Fe3+to Fe2+with values 1.22±0.06 and 1.49±0.02 mM of Fe2+equivalent, respectively. 1 mg/ml of CS was the highest potency to inhibit AChE activity with 58.83±2.24%. Results showed AChE inhibition ability depended on the amount of total phenolic content. This study highlights CS extract which showed highly potent inhibition of AChE and scavenging of free radicals. Clinical trials and active compounds in CS should be studied for AD therapy in the other models.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectMedicineen_US
dc.subjectNursingen_US
dc.titleAntioxidant and acetylcholinesterase inhibitory potential of thai medicinal plantsen_US
dc.typeJournalen_US
article.title.sourcetitleCurrent Nutrition and Food Scienceen_US
article.volume11en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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