Cargando…

Phenolic constituents of Pulicaria undulata (L.) C.A. Mey. sub sp. undulata (Asteraceae): Antioxidant protective effects and chemosystematic significances

One new naturally isoflavone compound, 5,7,2′,3′,4′ penta hydroxyl isoflavone-4′-O-β-glucopyranoside (1) was isolated from the aqueous methanol extract (AME) of Pulicaria undulata subsp. undulata, together with seven known compounds: kaempferol (2), kaempferol 3-O-β-glucoside (3), quercetin (4), que...

Descripción completa

Detalles Bibliográficos
Autores principales: Hussein, Sameh R., Marzouk, Mona M., Soltan, Maha M., Ahmed, Emad K., Said, Mahmoud M., Hamed, Ahmed R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taiwan Food and Drug Administration 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9332527/
https://www.ncbi.nlm.nih.gov/pubmed/28911675
http://dx.doi.org/10.1016/j.jfda.2016.09.008
_version_ 1784758669615824896
author Hussein, Sameh R.
Marzouk, Mona M.
Soltan, Maha M.
Ahmed, Emad K.
Said, Mahmoud M.
Hamed, Ahmed R.
author_facet Hussein, Sameh R.
Marzouk, Mona M.
Soltan, Maha M.
Ahmed, Emad K.
Said, Mahmoud M.
Hamed, Ahmed R.
author_sort Hussein, Sameh R.
collection PubMed
description One new naturally isoflavone compound, 5,7,2′,3′,4′ penta hydroxyl isoflavone-4′-O-β-glucopyranoside (1) was isolated from the aqueous methanol extract (AME) of Pulicaria undulata subsp. undulata, together with seven known compounds: kaempferol (2), kaempferol 3-O-β-glucoside (3), quercetin (4), quercetin 3-O-β-glucoside (5), quercetin 3-O-β-galactoside (6), quercetin 3,7-di OCH(3) (7), and caffeic acid (8). Their structures were established through chemical (acid hydrolysis) and spectral analysis (UV, NMR, and ESIM). The AME and some isolated compounds were evaluated as protective agents. Free radical scavenging using a microscaled 2,2-diphenyl-1-picrylhydrazyl assay was used to assess the direct antioxidant properties that were evaluated by the ability to protect murine Hepa1c1c7 liver cells against damage induced by the organic peroxide tert-butyl hydroperoxide. The neutral red uptake assay (NRU) was used to record the activity. Results of the 2,2-diphenyl-1-picrylhydrazyl assay recorded differential scavenging properties in ascending order: 5,7,2′,3′,4′ penta hydroxyl isoflavone-4′-O-β-glucopyranoside > quercetin > quercetin 3-O-galactoside > caffeic acid > quercetin 3,7-di-OCH(3) > kaempferol with 50% inhibitory concentrations of 3.9 μM, 7.5 μM, 11.4 μM, 12.2 μM, 78.1 μM, and 252.3 μM, respectively. The antioxidative potential reveals the potency of AME, quercetin, and quercetin 3,7-di-OCH(3). The latter compound showed full protection at 100 μM (33 μg/mL) against the induced toxicant effect where the 50% effective concentration was calculated as 33.6 ± 1.7 μM (11.1 μg/mL). In addition to quercetin, which was extensively shown previously as a cytoprotective agent, AME was less potent; it was capable of protecting 75% at 100 μg/mL with 50% effective concentration of 92.3 ± 4 μg/mL. Moreover, the isolated flavonoids were found to be significantly chemosystematic markers.
format Online
Article
Text
id pubmed-9332527
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Taiwan Food and Drug Administration
record_format MEDLINE/PubMed
spelling pubmed-93325272022-08-09 Phenolic constituents of Pulicaria undulata (L.) C.A. Mey. sub sp. undulata (Asteraceae): Antioxidant protective effects and chemosystematic significances Hussein, Sameh R. Marzouk, Mona M. Soltan, Maha M. Ahmed, Emad K. Said, Mahmoud M. Hamed, Ahmed R. J Food Drug Anal Original Article One new naturally isoflavone compound, 5,7,2′,3′,4′ penta hydroxyl isoflavone-4′-O-β-glucopyranoside (1) was isolated from the aqueous methanol extract (AME) of Pulicaria undulata subsp. undulata, together with seven known compounds: kaempferol (2), kaempferol 3-O-β-glucoside (3), quercetin (4), quercetin 3-O-β-glucoside (5), quercetin 3-O-β-galactoside (6), quercetin 3,7-di OCH(3) (7), and caffeic acid (8). Their structures were established through chemical (acid hydrolysis) and spectral analysis (UV, NMR, and ESIM). The AME and some isolated compounds were evaluated as protective agents. Free radical scavenging using a microscaled 2,2-diphenyl-1-picrylhydrazyl assay was used to assess the direct antioxidant properties that were evaluated by the ability to protect murine Hepa1c1c7 liver cells against damage induced by the organic peroxide tert-butyl hydroperoxide. The neutral red uptake assay (NRU) was used to record the activity. Results of the 2,2-diphenyl-1-picrylhydrazyl assay recorded differential scavenging properties in ascending order: 5,7,2′,3′,4′ penta hydroxyl isoflavone-4′-O-β-glucopyranoside > quercetin > quercetin 3-O-galactoside > caffeic acid > quercetin 3,7-di-OCH(3) > kaempferol with 50% inhibitory concentrations of 3.9 μM, 7.5 μM, 11.4 μM, 12.2 μM, 78.1 μM, and 252.3 μM, respectively. The antioxidative potential reveals the potency of AME, quercetin, and quercetin 3,7-di-OCH(3). The latter compound showed full protection at 100 μM (33 μg/mL) against the induced toxicant effect where the 50% effective concentration was calculated as 33.6 ± 1.7 μM (11.1 μg/mL). In addition to quercetin, which was extensively shown previously as a cytoprotective agent, AME was less potent; it was capable of protecting 75% at 100 μg/mL with 50% effective concentration of 92.3 ± 4 μg/mL. Moreover, the isolated flavonoids were found to be significantly chemosystematic markers. Taiwan Food and Drug Administration 2016-12-22 /pmc/articles/PMC9332527/ /pubmed/28911675 http://dx.doi.org/10.1016/j.jfda.2016.09.008 Text en © 2017 Taiwan Food and Drug Administration https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC-BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Original Article
Hussein, Sameh R.
Marzouk, Mona M.
Soltan, Maha M.
Ahmed, Emad K.
Said, Mahmoud M.
Hamed, Ahmed R.
Phenolic constituents of Pulicaria undulata (L.) C.A. Mey. sub sp. undulata (Asteraceae): Antioxidant protective effects and chemosystematic significances
title Phenolic constituents of Pulicaria undulata (L.) C.A. Mey. sub sp. undulata (Asteraceae): Antioxidant protective effects and chemosystematic significances
title_full Phenolic constituents of Pulicaria undulata (L.) C.A. Mey. sub sp. undulata (Asteraceae): Antioxidant protective effects and chemosystematic significances
title_fullStr Phenolic constituents of Pulicaria undulata (L.) C.A. Mey. sub sp. undulata (Asteraceae): Antioxidant protective effects and chemosystematic significances
title_full_unstemmed Phenolic constituents of Pulicaria undulata (L.) C.A. Mey. sub sp. undulata (Asteraceae): Antioxidant protective effects and chemosystematic significances
title_short Phenolic constituents of Pulicaria undulata (L.) C.A. Mey. sub sp. undulata (Asteraceae): Antioxidant protective effects and chemosystematic significances
title_sort phenolic constituents of pulicaria undulata (l.) c.a. mey. sub sp. undulata (asteraceae): antioxidant protective effects and chemosystematic significances
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9332527/
https://www.ncbi.nlm.nih.gov/pubmed/28911675
http://dx.doi.org/10.1016/j.jfda.2016.09.008
work_keys_str_mv AT husseinsamehr phenolicconstituentsofpulicariaundulatalcameysubspundulataasteraceaeantioxidantprotectiveeffectsandchemosystematicsignificances
AT marzoukmonam phenolicconstituentsofpulicariaundulatalcameysubspundulataasteraceaeantioxidantprotectiveeffectsandchemosystematicsignificances
AT soltanmaham phenolicconstituentsofpulicariaundulatalcameysubspundulataasteraceaeantioxidantprotectiveeffectsandchemosystematicsignificances
AT ahmedemadk phenolicconstituentsofpulicariaundulatalcameysubspundulataasteraceaeantioxidantprotectiveeffectsandchemosystematicsignificances
AT saidmahmoudm phenolicconstituentsofpulicariaundulatalcameysubspundulataasteraceaeantioxidantprotectiveeffectsandchemosystematicsignificances
AT hamedahmedr phenolicconstituentsofpulicariaundulatalcameysubspundulataasteraceaeantioxidantprotectiveeffectsandchemosystematicsignificances