2001
DOI: 10.1016/s0887-2333(01)00049-2
|View full text |Cite
|
Sign up to set email alerts
|

Hydrogen peroxide induced stress in human keratinocytes and its effect on bithionol toxicity

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

2
12
0

Year Published

2005
2005
2019
2019

Publication Types

Select...
7
1

Relationship

0
8

Authors

Journals

citations
Cited by 18 publications
(14 citation statements)
references
References 13 publications
2
12
0
Order By: Relevance
“…In the in vivo study (Fig 2), topical application of L-741626 significantly enhanced epidermal hyperplasia induced by barrier disruption. This in vivo effect of L-741626 might be due to elongation of the delay in barrier recovery, as shown in Fig 1. The results of Alamar Blue assay are shown in Fig 7B. The levels of fluorescence indicate the activity of mitochondria, which is considered to be a measure of the viability of the cells (Reid et al, 2001). In this study, the viability closely paralleled the cell number, indicating that the reduction of keratinocyte proliferation by bromocriptine was not due to cytotoxicity of the reagent.…”
Section: Figuresupporting
confidence: 55%
See 1 more Smart Citation
“…In the in vivo study (Fig 2), topical application of L-741626 significantly enhanced epidermal hyperplasia induced by barrier disruption. This in vivo effect of L-741626 might be due to elongation of the delay in barrier recovery, as shown in Fig 1. The results of Alamar Blue assay are shown in Fig 7B. The levels of fluorescence indicate the activity of mitochondria, which is considered to be a measure of the viability of the cells (Reid et al, 2001). In this study, the viability closely paralleled the cell number, indicating that the reduction of keratinocyte proliferation by bromocriptine was not due to cytotoxicity of the reagent.…”
Section: Figuresupporting
confidence: 55%
“…Alamar blue assay To evaluate the cytotoxicity of bromocriptine and L-741626, we carried out Alamar blue assay (Reid et al, 2001). First, we seeded 3x10 4 keratinocytes per well in 12-well plates with 2 mL of KG2 medium (Kurabo) and incubated them for 48 h. Then, the medium was changed and bromocriptine (final concentration 10 nM) or L-741626 (final concentration 10 nM) was applied.…”
Section: Methodsmentioning
confidence: 99%
“…The phenomenon of photo-oxidation might have caused the impairment of metabolic activity in the cells. The Alamar blue assay, which is non-radioactive, has been used in in vitro photocytotoxicity studies of human RPE, cultured ocular lenses (bovine and porcine), mouse neural crest cells, and human keratinocytes [18,36,[38][39][40][41]. Findings from these studies support the use of the Alamar blue as a sensitive assay for monitoring UV-induced changes in intracellular mitochondrial, cytoplasmic and nuclear integrity, all of which are measures of cellular viability [36].…”
Section: Discussionmentioning
confidence: 87%
“…The method employed was similar to that described previously [13,14]. Briefly, a working solution of 2 0 ,7 0 -dichlorofluorescin diacetate (DCFH-DA) in PBS was prepared prior to use and 500 ll well -1 added to each experimental well containing cells grown for 3 days, plus a blank column of wells for reference.…”
Section: Oxidative Stress Assaymentioning
confidence: 99%