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...
Saved in:
Main Authors: | , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
2014
|
Online Access: | http://www.scopus.com/inward/record.url?eid=2-s2.0-84882309818&partnerID=40&md5=bc33cde62b52ee7485eb88f8d3b9e85b http://cmuir.cmu.ac.th/handle/6653943832/4707 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Chiang Mai University |
Language: | English |
id |
th-cmuir.6653943832-4707 |
---|---|
record_format |
dspace |
spelling |
th-cmuir.6653943832-47072014-08-30T02:42:45Z Biological activities of phenolic compounds and triterpenoids from the Galls of Terminalia chebula Manosroi A. Jantrawut P. Ogihara E. Yamamoto A. Fukatsu M. Yasukawa K. Tokuda H. Suzuki N. Manosroi J. Akihisa T. 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 IC50 values 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 (IC50 1.4-10.9 μM) with weak inhibitory effects on EBV-EA induction (IC50 460-518 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 ID50 values 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 (IC50 13.9-73.2 μM). Copyright © 2013 Verlag Helvetica Chimica Acta AG, Zürich. 2014-08-30T02:42:45Z 2014-08-30T02:42:45Z 2013 Article 16121872 10.1002/cbdv.201300149 CBHIA http://www.scopus.com/inward/record.url?eid=2-s2.0-84882309818&partnerID=40&md5=bc33cde62b52ee7485eb88f8d3b9e85b http://cmuir.cmu.ac.th/handle/6653943832/4707 English |
institution |
Chiang Mai University |
building |
Chiang Mai University Library |
country |
Thailand |
collection |
CMU Intellectual Repository |
language |
English |
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 IC50 values 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 (IC50 1.4-10.9 μM) with weak inhibitory effects on EBV-EA induction (IC50 460-518 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 ID50 values 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 (IC50 13.9-73.2 μM). Copyright © 2013 Verlag Helvetica Chimica Acta AG, Zürich. |
format |
Article |
author |
Manosroi A. Jantrawut P. Ogihara E. Yamamoto A. Fukatsu M. Yasukawa K. Tokuda H. Suzuki N. Manosroi J. Akihisa T. |
spellingShingle |
Manosroi A. Jantrawut P. Ogihara E. Yamamoto A. Fukatsu M. Yasukawa K. Tokuda H. Suzuki N. Manosroi J. Akihisa T. Biological activities of phenolic compounds and triterpenoids from the Galls of Terminalia chebula |
author_facet |
Manosroi A. Jantrawut P. Ogihara E. Yamamoto A. Fukatsu M. Yasukawa K. Tokuda H. Suzuki N. Manosroi J. Akihisa T. |
author_sort |
Manosroi A. |
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 |
2014 |
url |
http://www.scopus.com/inward/record.url?eid=2-s2.0-84882309818&partnerID=40&md5=bc33cde62b52ee7485eb88f8d3b9e85b http://cmuir.cmu.ac.th/handle/6653943832/4707 |
_version_ |
1681420287859490816 |