Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/17312
Title: Protective effect of purple corn silk extract against ultraviolet-B-induced cell damage in human keratinocyte cells
Authors: Poorahong W.
Innalak S.
Ungsurungsie M.
Watanapokasin R.
Keywords: caspase
histone H2AX
nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase 1
plant extract
protein Bak
protein Bax
protein bcl 2
protein bcl xl
purple corn silk
radioprotective agent
reactive oxygen metabolite
unclassified drug
apoptosis
Article
cell damage
cell protection
cell survival
cell viability
comparative study
controlled study
cytotoxicity
DNA damage
drug effect
HaCat cell line
human
human cell
immunofluorescence
maize
mitochondrial membrane potential
MTT assay
polyacrylamide gel electrophoresis
priority journal
protein expression
protein localization
radiation exposure
radiation protection
stigma
ultraviolet B radiation
Western blotting
Issue Date: 2021
Abstract: Ultraviolet-B (UVB) could lead to inflammation and cell death induction. Purple corn silk (PCS), part of female flower of corn has multiple pharmacological properties. This investigation focused on determining the preventive effects of PCS extract on human keratinocyte HaCaT cell damage induced by UVB irradiation. Cells were irradiated with 25 mJ/cm2UVB after pre-treated with PCS extract for 1 h. Then, the cells were then placed in culture medium followed by subsequent experiments. Cell survival was determined by MTT assay. The immunofluorescence, DCFH-DA, JC-1, and Hoeshst33342 staining assays were used to determine γ-H2AX, intracellular reactive oxygen species (ROS), membrane potential of mitochondria, and nuclear condensation, respectively. Western blot analysis was used to investigate the proteins expression. The statistically significant comparison was calculated by analysis of variance at P < 0.05. The fluorescence and protein band intensity were quantified by Image J densitometer. The results indicated cell survival was increased upon PCS extract pretreatment followed by UVB exposure. PCS extract decreased γ-H2AX expression, intracellular ROS overproduction, and nuclear condensation in cells induced by UVB. Furthermore, The PCS extract pretreatment attenuated apoptosis response through stabilized mitochondrial membrane potential, decreased apoptosis mediator proteins including Bax, Bak, cleaved-caspases, and cleaved-PARP, and increased Bcl-2 and Bcl-xL expression comparing to the UVB-treated control. This finding demonstrated that the PCS extract can reduce the deleterious effects from UVB exposure through decreased intracellular ROS, DNA damage, and apoptosis induction on HaCaT cells. © 2021 Wolters Kluwer Medknow Publications. All rights reserved.
URI: https://ir.swu.ac.th/jspui/handle/123456789/17312
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85105407118&doi=10.4103%2fjaptr.JAPTR_238_20&partnerID=40&md5=49d60616bfbf5fe3990f7e502466434f
ISSN: 1105558
Appears in Collections:Scopus 1983-2021

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