Publication: Diarylheptanoid 7-(3,4 dihydroxyphenyl)-5-hydroxy-1-phenyl-(1E)-1-heptene from Curcuma comosa Roxb. protects retinal pigment epithelial cells against oxidative stress-induced cell death
dc.contributor.author | Thunchnok Jitsanong | en_US |
dc.contributor.author | Kornnika Khanobdee | en_US |
dc.contributor.author | Pawinee Piyachaturawat | en_US |
dc.contributor.author | Kanokpan Wongprasert | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.contributor.other | Suranaree University of Technology | en_US |
dc.date.accessioned | 2018-05-03T08:42:45Z | |
dc.date.available | 2018-05-03T08:42:45Z | |
dc.date.issued | 2011-02-01 | en_US |
dc.description.abstract | Chronic exposure to oxidative stress causes damage to retinal pigment epithelial cells which may lead to the development of age-related macular degeneration, the major cause of vision loss in humans. Anti-oxidants provide a natural defense against retinal cell damage. The present study was designed to evaluate the potential anti-oxidant activity and protective effect of two diarylheptanoids isolated from a medicinal herb Curcuma comosa; 7-(3,4 dihydroxyphenyl)-5-hydroxy-1-phenyl-(1E)-1-heptene (compound A), and 1,7-diphenyl-4(E),6(E)-heptadien-3-ol (compound B) against oxidative stress (H 2 O 2 )-induced human retinal pigment epithelial (APRE-19) cell death. The 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay indicated that the anti-oxidant activity (IC 50 ) of compound A was similar to that of vitamin C. Pre-treatment of ARPE-19 cells with 20μM compound A for 4h afforded greater protection against the insult from 500μM H 2 O 2 , compared to a similar protection period for compound B. Compound A lowered H 2 O 2 -induced lipid peroxidation, malondialdehyde formation and intracellular reactive oxygen species. Furthermore, compound A ameliorated the H 2 O 2 -induced decrease in anti-oxidant enzyme activities and subsequent apoptotic cell death in ARPE-19 cells in a dose and time-dependent manner. These results suggest that compound A protects ARPE-19 cells against oxidative stress, in part, by enhancing several anti-oxidant defense mechanisms. Therefore, compound A may have therapeutic potential for diseases associated with oxidative stress, particularly degenerative retinal diseases. © 2010 Elsevier Ltd. | en_US |
dc.identifier.citation | Toxicology in Vitro. Vol.25, No.1 (2011), 167-176 | en_US |
dc.identifier.doi | 10.1016/j.tiv.2010.10.014 | en_US |
dc.identifier.issn | 08872333 | en_US |
dc.identifier.other | 2-s2.0-78650519024 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/12821 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78650519024&origin=inward | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Diarylheptanoid 7-(3,4 dihydroxyphenyl)-5-hydroxy-1-phenyl-(1E)-1-heptene from Curcuma comosa Roxb. protects retinal pigment epithelial cells against oxidative stress-induced cell death | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78650519024&origin=inward | en_US |