2018
DOI: 10.1016/j.jphotobiol.2017.11.002
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The extended production of UV-induced reactive oxygen species in L929 fibroblasts is attenuated by posttreatment with Arrabidaea chica through scavenging mechanisms

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Cited by 24 publications
(18 citation statements)
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“…The purpose of fibroblast study was to investigate release behavior of PPADT nanoparticles in an environment with biologically relevant concentrations of ROS. Several methods have been used to challenge skin cells to produce increased levels of ROS, such as UV light, low pH, addition of serum amyloid A (5–15 μg/mL), IR irradiation, and addition of ROS species. Silverberg and co-workers used different concentrations of H 2 O 2 to produce increased levels of ROS in fibroblasts, which was initially attempted here . Surprisingly, we found that changing the tonicity of the growth medium also challenged the cells to produce increased levels of ROS.…”
Section: Discussionmentioning
confidence: 99%
“…The purpose of fibroblast study was to investigate release behavior of PPADT nanoparticles in an environment with biologically relevant concentrations of ROS. Several methods have been used to challenge skin cells to produce increased levels of ROS, such as UV light, low pH, addition of serum amyloid A (5–15 μg/mL), IR irradiation, and addition of ROS species. Silverberg and co-workers used different concentrations of H 2 O 2 to produce increased levels of ROS in fibroblasts, which was initially attempted here . Surprisingly, we found that changing the tonicity of the growth medium also challenged the cells to produce increased levels of ROS.…”
Section: Discussionmentioning
confidence: 99%
“…Hydrogen peroxide (H 2 O 2 ) was used to establish an intracellular oxidative stress model [ 35 ]. ROS were analyzed using a CM-H 2 DCFDA molecular probe (Invitrogen, C.A., U.S.A.), which was measured on the basis of fluorescence because of the conversion of fluorescent DCF in the presence of ROS as nonfluorescent H 2 DCFDA dye readily penetrated in the cells [ 36 ], which is a commonly used system for directly evaluating cellular redox states, and is a typical indicator of oxidative stress [ 37 , 38 ]. The L-929 cells were seeded on the GO, GO/RGD, GO/AST, and GO/RGD/AST films.…”
Section: Methodsmentioning
confidence: 99%
“…The use of several methodologies to evaluate the effects of F. chica extracts for the control of oxidative stress allowed for a more complete view of this mechanism. Other authors, such as Torres et al in 2018 [ 138 ] and Teixeira et al in 2017 [ 171 ], have included other free radical neutralization assays, such as ABTS (2,2’-Azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) and FRAP (ferric reducing antioxidant power), thus reaffirming the biological effects of F. chica [ 138 , 169 , 170 , 171 ].…”
Section: Pharmacological Propertiesmentioning
confidence: 99%
“…Martins et al, in 2016 [ 169 ] and Ribeiro et al, working in 2018 [ 170 ], demonstrated the antioxidant capacity of a hydroethanolic extract of Fridericia chica in the presence of both the free radical DPPH and the oxidative damage induced by ultraviolet radiation. The use of several methodologies to evaluate the effects of F. chica extracts for the control of oxidative stress allowed for a more complete view of this mechanism.…”
Section: Pharmacological Propertiesmentioning
confidence: 99%