Publication:
Antimicrobial and antioxidative activities of bioactive constituents from Hydnophytum formicarum Jack.

dc.contributor.authorPrachayasittikul S.
dc.contributor.authorBuraparuangsang P.
dc.contributor.authorWorachartcheewan A.
dc.contributor.authorIsarankura-Na-Ayudhya C.
dc.contributor.authorRuchirawat S.
dc.contributor.authorPrachayasittikul V.
dc.date.accessioned2021-04-05T04:32:01Z
dc.date.available2021-04-05T04:32:01Z
dc.date.issued2008
dc.date.issuedBE2551
dc.description.abstractHydnophytum formicarum Jack. (Rubiaceae) is a medicinal plant whose tubers possesses cardiovascular, anti-inflammatory and antiparasitic effects and have been used for the treatment of hepatitis, rheumatism and diarrhea. Herein we report the isolation of its active constituents and the testing of their antimicrobial activity against 27 strains of microorganisms using an agar dilution method and of their antioxidative activity using the DPPH and SOD assays. The results show that the crude hexane, dichloromethane, ethyl acetate and methanol extracts exert such activities. Particularly, the crude ethyl acetate extract exhibits antigrowth activity against many Gram-positive and Gram-negative bacteria with MIC 256 μg/mL. Shewanella putrefaciens ATCC 8671 is completely inhibited at a lower MIC (128 μg/mL). Interestingly, Corynebacterium diphtheriae NCTC 10356 is inhibited by all the tested extracts. Significantly, the ethyl acetate extract is also the most potent antioxidant, showing 83.31% radical scavenging activity with IC50 8.40 μg/mL in the DPPH assay. The other extracts display weak to moderate antioxidative activities, ranging from 28.60-56.80% radical scavenging. The SOD assay shows that methanol extract exhibits the highest activity (74.19% inhibition of superoxide radical). The dichloromethane and ethyl acetate extracts display comparable SOD activity. The promising bioactivities of the crude ethyl acetate extract guided the first isolation of bioactive flavonoid and phenolic compounds: isoliquiritigenin (2), protocatechualdehyde (3), butin (4) and butein (5) from this species. Their structures have been fully established by 1D and 2D NMR. In addition, stigmasterol was isolated from the crude hexane and dichloromethane extracts. The antimicrobial and cytotoxic activities of compounds 3-5 were evaluated. The tested compounds were inactive against HuCCA-1 and KB cell lines, showing ED50> 10 μg/mL. Protocatechualdehyde (3) completely inhibits the growth of Plesiomonas shigelloides with MIC ≤60 μg/mL. As a result, we propose that Hydnophytum formicarum Jack. can serve as a new source enriched with potent antioxidative and antimicrobial agents. © 2008 by MDPI.
dc.format.mimetypeapplication/pdf
dc.identifier.citationMolecules. Vol 13, No.4 (2008), p.904-921
dc.identifier.doi10.3390/molecules13040904
dc.identifier.issn14203049
dc.identifier.other2-s2.0-43049113152
dc.identifier.urihttps://hdl.handle.net/20.500.14740/4084
dc.rights.holderScopus
dc.subject.otherAntiinfective agent
dc.subject.otherAntioxidant
dc.subject.otherCell extract
dc.subject.otherPlant extract
dc.subject.otherScavenger
dc.subject.otherSuperoxide dismutase
dc.subject.otherAnimal
dc.subject.otherArticle
dc.subject.otherBacterium
dc.subject.otherCell death
dc.subject.otherChemistry
dc.subject.otherDrug effect
dc.subject.otherIsolation and purification
dc.subject.otherMetabolism
dc.subject.otherMicrobiological examination
dc.subject.otherRubiaceae
dc.subject.otherTumor cell line
dc.subject.otherAnimals
dc.subject.otherAnti-Infective Agents
dc.subject.otherAntioxidants
dc.subject.otherBacteria
dc.subject.otherCell Death
dc.subject.otherCell Extracts
dc.subject.otherCell Line, Tumor
dc.subject.otherFree Radical Scavengers
dc.subject.otherMicrobial Sensitivity Tests
dc.subject.otherPlant Extracts
dc.subject.otherRubiaceae
dc.subject.otherSuperoxide Dismutase
dc.titleAntimicrobial and antioxidative activities of bioactive constituents from Hydnophytum formicarum Jack.
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-43049113152&doi=10.3390%2fmolecules13040904&partnerID=40&md5=525988bba733a353d4f1484c1392bf16

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