2016
DOI: 10.1016/j.jphotobiol.2016.10.034
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Stereospecificity of ginsenoside Rg2 epimers in the protective response against UV-B radiation-induced oxidative stress in human epidermal keratinocytes

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Cited by 25 publications
(17 citation statements)
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“…These results suggested that BDB has a protective effect on human keratinocytes against UVB radiation. UVB light stimulates the production of ROS to induce oxidative stress [ 21 , 22 ]. In our previous time-course experiment, we found that the maximal ROS levels induced by UVB exposure appeared at 24 h [ 18 ].…”
Section: Resultsmentioning
confidence: 99%
“…These results suggested that BDB has a protective effect on human keratinocytes against UVB radiation. UVB light stimulates the production of ROS to induce oxidative stress [ 21 , 22 ]. In our previous time-course experiment, we found that the maximal ROS levels induced by UVB exposure appeared at 24 h [ 18 ].…”
Section: Resultsmentioning
confidence: 99%
“…Ginsenoside Rg2 could reduce oxidative stress injury and improve myocardial ischemia and hypoxia by regulating the activities of serum creatine kinase (CK), lactate dehydrogenase (LDH), lipid peroxides (LPOs), superoxide dismutase (SOD), and glutathione peroxidase (GPX) in rats [ 51 ]. Ginsenoside Rg2 was also shown to reduce oxidative stress in human epidermal keratinocytes [ 52 ].…”
Section: Application Of Antioxidant Natural Drugs For Cardiovasculmentioning
confidence: 99%
“…It also protected dopaminergic neurons from 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced toxicity and brain damage from sepsis by inhibiting cerebral inflammation and neuron loss in the hippocampus [80][81][82][83]. Ginsenoside Rg 2 had a protective effect against glutamate-induced neuronal injury and the formation of Ab in PC12 cells, protected memory functions against impairment induced by cerebral ischemia-reperfusion and the neuronal apoptosis, and attenuated the UV-B-induced promatrix metalloproteinase-2 gelatinolytic activity and protein level [84][85][86]. Ginsenoside Rh 1 inhibited the infiltration of inflammatory cells into skin lesions and MMP-1 transcriptional activity and decreased the concentrations of IgE and IL-6 in serum, expression and stability of Ap-1 dimer, c-Fos, and c-Jun by inhibiting the activation of JNK and ERK 1/2 in HepG2 cells [87,88].…”
Section: Improved Health Functionality Through Bioconversionmentioning
confidence: 99%