Biological activities of phenolic compounds and triterpenoids from the Galls of Terminalia chebula

Nine phenolic compounds, including two phenolic carboxylic acids, 1 and 2, seven hydrolyzable tannins, 3-9, eight triterpenoids, including four oleanane-type triterpene acids, 10-13, and four of their glucosides, 14-17, isolated from a MeOH extract of the gall of Terminalia chebula Retz. (myrobalan...

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Main Authors: Aranya Manosroi, Pensak Jantrawut, Eri Ogihara, Ayako Yamamoto, Makoto Fukatsu, Ken Yasukawa, Harukuni Tokuda, Nobutaka Suzuki, Jiradej Manosroi, Toshihiro Akihisa
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Published: 2018
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spelling th-cmuir.6653943832-523012018-09-04T09:24:59Z Biological activities of phenolic compounds and triterpenoids from the Galls of Terminalia chebula Aranya Manosroi Pensak Jantrawut Eri Ogihara Ayako Yamamoto Makoto Fukatsu Ken Yasukawa Harukuni Tokuda Nobutaka Suzuki Jiradej Manosroi Toshihiro Akihisa Biochemistry, Genetics and Molecular Biology Chemical Engineering Chemistry Nine phenolic compounds, including two phenolic carboxylic acids, 1 and 2, seven hydrolyzable tannins, 3-9, eight triterpenoids, including four oleanane-type triterpene acids, 10-13, and four of their glucosides, 14-17, isolated from a MeOH extract of the gall of Terminalia chebula Retz. (myrobalan tree; Combretaceae), were evaluated for their inhibitory activities against melanogenesis in B16 melanoma cells induced by α-melanocyte-stimulating hormone (α-MSH), against the EpsteinBarr virus early antigen (EBV-EA) activation induced by 12-O-tetradecanoylphorbol 13-acetate (TPA) in Raji cells, and against TPA-induced inflammation in mice. Their 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical-scavenging activities and cytotoxic activities against four human cancer cell lines were also evaluated. Compounds 6-9 and 12 exhibited potent inhibitory activities against melanogenesis (39.3-66.3% melanin content) with low toxicity to the cells (74.5-105.9% cell viability) at a concentration of 10 μM. Western-blot analysis revealed that isoterchebulin (8) reduced the protein levels of MITF (=microphtalmia-associated transcription factor), tyrosinase, and TRP-1 (=tyrosine-related protein 1), mostly in a concentration-dependent manner. Eight triterpenoids, 10-17, showed potent inhibitory effects on EBV-EA induction with the IC50values in the range of 269-363 mol ratio/32 pmol TPA, while these compounds exhibited no DPPH scavenging activities (IC50>100 μM). On the other hand, the nine phenolic compounds, 1-9, exhibited potent radical-scavenging activities (IC501.4-10.9 μM) with weak inhibitory effects on EBV-EA induction (IC50460-518 mol ratio/32 pmol TPA). The tannin 6 and seven triterpenoids, 10-16, have been shown to inhibit TPA-induced inflammation (1 μg/ear) in mice with the ID50values in the range of 0.06-0.33 μmol/ear. Arjungenin (10) exhibited inhibitory effect on skin-tumor promotion in an in vivo two-stage mouse-skin carcinogenesis test based on 7,12-dimethylbenz[a]anthracene (DMBA) as initiator and with TPA as promoter. Compounds 1, 2, 4, 5, 7-9, 12, and 13, against HL60 cell line, compounds 1 and 4, against AZ521 cell line, and compounds 1, 11, and 12, against SK-BR-3 cell line, showed moderate cytotoxic activities (IC5013.9-73.2 μM). Copyright © 2013 Verlag Helvetica Chimica Acta AG, Zürich. 2018-09-04T09:23:17Z 2018-09-04T09:23:17Z 2013-01-01 Journal 16121880 16121872 2-s2.0-84882309818 10.1002/cbdv.201300149 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84882309818&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/52301
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Biochemistry, Genetics and Molecular Biology
Chemical Engineering
Chemistry
spellingShingle Biochemistry, Genetics and Molecular Biology
Chemical Engineering
Chemistry
Aranya Manosroi
Pensak Jantrawut
Eri Ogihara
Ayako Yamamoto
Makoto Fukatsu
Ken Yasukawa
Harukuni Tokuda
Nobutaka Suzuki
Jiradej Manosroi
Toshihiro Akihisa
Biological activities of phenolic compounds and triterpenoids from the Galls of Terminalia chebula
description Nine phenolic compounds, including two phenolic carboxylic acids, 1 and 2, seven hydrolyzable tannins, 3-9, eight triterpenoids, including four oleanane-type triterpene acids, 10-13, and four of their glucosides, 14-17, isolated from a MeOH extract of the gall of Terminalia chebula Retz. (myrobalan tree; Combretaceae), were evaluated for their inhibitory activities against melanogenesis in B16 melanoma cells induced by α-melanocyte-stimulating hormone (α-MSH), against the EpsteinBarr virus early antigen (EBV-EA) activation induced by 12-O-tetradecanoylphorbol 13-acetate (TPA) in Raji cells, and against TPA-induced inflammation in mice. Their 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical-scavenging activities and cytotoxic activities against four human cancer cell lines were also evaluated. Compounds 6-9 and 12 exhibited potent inhibitory activities against melanogenesis (39.3-66.3% melanin content) with low toxicity to the cells (74.5-105.9% cell viability) at a concentration of 10 μM. Western-blot analysis revealed that isoterchebulin (8) reduced the protein levels of MITF (=microphtalmia-associated transcription factor), tyrosinase, and TRP-1 (=tyrosine-related protein 1), mostly in a concentration-dependent manner. Eight triterpenoids, 10-17, showed potent inhibitory effects on EBV-EA induction with the IC50values in the range of 269-363 mol ratio/32 pmol TPA, while these compounds exhibited no DPPH scavenging activities (IC50>100 μM). On the other hand, the nine phenolic compounds, 1-9, exhibited potent radical-scavenging activities (IC501.4-10.9 μM) with weak inhibitory effects on EBV-EA induction (IC50460-518 mol ratio/32 pmol TPA). The tannin 6 and seven triterpenoids, 10-16, have been shown to inhibit TPA-induced inflammation (1 μg/ear) in mice with the ID50values in the range of 0.06-0.33 μmol/ear. Arjungenin (10) exhibited inhibitory effect on skin-tumor promotion in an in vivo two-stage mouse-skin carcinogenesis test based on 7,12-dimethylbenz[a]anthracene (DMBA) as initiator and with TPA as promoter. Compounds 1, 2, 4, 5, 7-9, 12, and 13, against HL60 cell line, compounds 1 and 4, against AZ521 cell line, and compounds 1, 11, and 12, against SK-BR-3 cell line, showed moderate cytotoxic activities (IC5013.9-73.2 μM). Copyright © 2013 Verlag Helvetica Chimica Acta AG, Zürich.
format Journal
author Aranya Manosroi
Pensak Jantrawut
Eri Ogihara
Ayako Yamamoto
Makoto Fukatsu
Ken Yasukawa
Harukuni Tokuda
Nobutaka Suzuki
Jiradej Manosroi
Toshihiro Akihisa
author_facet Aranya Manosroi
Pensak Jantrawut
Eri Ogihara
Ayako Yamamoto
Makoto Fukatsu
Ken Yasukawa
Harukuni Tokuda
Nobutaka Suzuki
Jiradej Manosroi
Toshihiro Akihisa
author_sort Aranya Manosroi
title Biological activities of phenolic compounds and triterpenoids from the Galls of Terminalia chebula
title_short Biological activities of phenolic compounds and triterpenoids from the Galls of Terminalia chebula
title_full Biological activities of phenolic compounds and triterpenoids from the Galls of Terminalia chebula
title_fullStr Biological activities of phenolic compounds and triterpenoids from the Galls of Terminalia chebula
title_full_unstemmed Biological activities of phenolic compounds and triterpenoids from the Galls of Terminalia chebula
title_sort biological activities of phenolic compounds and triterpenoids from the galls of terminalia chebula
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84882309818&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/52301
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