Composition for alleviating ultraviolet radiation-induced damage
A composition, ultraviolet technology, applied in the fields of drug combination, food science, drug delivery, etc., can solve problems such as skin damage
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Embodiment 1
[0061] UV damage reducing effect of methionine
[0062] method
[0063] cell culture
[0064] As the cells, commercially available human neonatal dermal fibroblasts (Cryo NHDF-Neo, Sanko Pure Chemical Industries, Ltd.) were used. The cells were 2 x 10 5Cells / mL were inoculated into a commercially available 35mm diameter petri dish (BD FALCON 353001, Becton Dickinson, Japan), and a commercially available cell culture medium (D-MEM (1 g / L glucose), Wako Pure culture medium (hereinafter referred to as "normal medium") supplemented with 10% fetal bovine serum. The cells can be cultured in the normal medium supplemented with 1% antibiotic (15240-062, GIBCO). The cells were incubated at 37°C, 5% CO 2 and incubated under saturated water vapor conditions for about 24 hours.
[0065] After that, the medium used for culturing the cells was replaced with the addition of 1×10 -3 % BSO (L-buthionine-(S,R)-sulfoximine, Wako Pure Chemical Industries), which is a biosynthesis inhibitor...
Embodiment 2
[0086] UV damage reducing effect of serine
[0087] method
[0088] Cell culture, amino acid addition before ultraviolet irradiation, ultraviolet irradiation, amino acid addition after ultraviolet irradiation, and quantification of cell damage were performed in the same manner as in Example 1. at 7.5 or 9J / cm 2 Irradiate ultraviolet (UV-A). When studying the effect of adding serine before ultraviolet irradiation (hereinafter referred to as "addition of serine before irradiation".) and adding serine after irradiation with ultraviolet light (hereinafter referred to as "addition of serine after irradiation".), 0.0001 to 100 μM of L-serine (197 -00403, Wako Pure Chemical Industries Ltd.) and D-serine (197-08823, Wako Pure Chemical Industries Ltd.). The effect of adding serine after irradiation was evaluated by irradiating cells with 7.5 J / cm 2 After 21 hours of UV-A, the cells were returned to the normal medium and cultured for 21 hours, and D-serine was added to the cultured ...
Embodiment 3
[0099] UV damage reducing effect of D-cycloserine
[0100] method
[0101] Cell culture, amino acid addition before ultraviolet irradiation, ultraviolet irradiation, amino acid addition after ultraviolet irradiation, and quantification of cell damage were performed in the same manner as in Example 1. at 9J / cm 2 Irradiate ultraviolet (UV-A). D-cycloserine (C6880, Sigma) at 0.0001 to 100 μM was used to study the effect of adding D-cycloserine (hereinafter referred to as “addition of D-cycloserine before irradiation”) before ultraviolet irradiation.
[0102] Result of adding D-cycloserine before irradiation
[0103] Figure 7 Shown to investigate the effect of adding D-cycloserine before irradiation on irradiation by UV-A 9J / cm 2 Experimental results of UV-induced damage to fibroblasts. The error bar of each experimental condition represents the standard deviation of the measured value of the experimental result repeated 3 to 4 times under the same condition. In addition, ...
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