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Anti-Melanogenesis Activity of Supercritical Carbon Dioxide Extract from Perilla frutescens Seeds 被引量:1
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作者 Satoshi Suzuki Hitomi Fujisawa +1 位作者 Junpei Abe Ken-ichi Kimura 《Advances in Biological Chemistry》 CAS 2023年第1期42-55,共14页
Perilla frutescens seed (PFS) oil is reported to inhibit skin photoaging;however, its effect on melanogenesis has not yet been investigated. Herein, we tested the anti-melanogenesis activity of an oil-based extract fr... Perilla frutescens seed (PFS) oil is reported to inhibit skin photoaging;however, its effect on melanogenesis has not yet been investigated. Herein, we tested the anti-melanogenesis activity of an oil-based extract from PFS with supercritical carbon dioxide (scCO<sub>2</sub>). In a cell culture system, B16 mouse melanoma cells were treated with the PFS scCO<sub>2</sub> extract and other samples. The PFS scCO<sub>2</sub> extract decreased melanin production by approximately 90% in B16 mouse melanoma cells without cytotoxicity at 100 μg/mL. This effect was greater than that of the well-known melanogenesis inhibitor, kojic acid. Although a hexane-extracted PFS oil and a squeezed PFS oil also decreased melanin production in the B16 cells, the inhibitory effect of the PFS scCO<sub>2</sub> extract was higher than both of these. Chemical analysis of the PFS scCO<sub>2</sub> extract and squeezed PFS oil showed that almost 90% of the components of both oils were α-linolenic acid, linoleic acid, and oleic acid. Furthermore, the ratio of those three fatty acids across both samples was almost the same. When the three fatty acids were mixed in the same ratio as in the PFS scCO<sub>2</sub> extract, the IC<sub>50</sub> of the mixture for melanin production in B16 melanoma cells was identical to that of the PFS scCO<sub>2</sub> extract. However, the IC<sub>50</sub> of the squeezed PFS oil was approximately 6.6 times higher than that of the mixture. Although those fatty acids are the main inhibitory ingredients against melanin production in all of the extracts, some factor(s) in the squeezed PFS reduce their affinity with the cells. These results indicated that the PFS scCO<sub>2</sub> extract could be a superior melanogenesis inhibitor. Although its main ingredients are probably the same as those of the squeezed PFS oil, it is necessary to extract with scCO<sub>2</sub> for stronger anti-melanogenesis activity. 展开更多
关键词 Perilla frutescens MELANOGENESIS Supercritical Carbon Dioxide b16 mouse melanoma cells
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青蒿素类药联合紫杉醇对小鼠黑色素瘤B16细胞的增殖抑制作用 被引量:3
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作者 薛林路 李国铭 +3 位作者 邓长生 王琪 徐勤 宋健平 《中药新药与临床药理》 CAS CSCD 北大核心 2016年第1期49-53,共5页
目的观察青蒿琥酯(ATS)、双氢青蒿素(DHA)和紫杉醇(Taxol)及ATS联合Taxol对小鼠黑色素瘤B16细胞的增殖抑制作用,评价各组药物对小鼠黑色素瘤B16细胞的杀伤作用,初步探讨ATS与Taxol联合给药对小鼠黑色素瘤B16细胞是否有协同增效作用。方... 目的观察青蒿琥酯(ATS)、双氢青蒿素(DHA)和紫杉醇(Taxol)及ATS联合Taxol对小鼠黑色素瘤B16细胞的增殖抑制作用,评价各组药物对小鼠黑色素瘤B16细胞的杀伤作用,初步探讨ATS与Taxol联合给药对小鼠黑色素瘤B16细胞是否有协同增效作用。方法采用CCK-8法检测ATS、DHA和Taxol单药对小鼠黑色素瘤B16细胞作用24 h和48 h的抑制作用,并计算半数抑制浓度(IC_(50))值;检测ATS联合Taxol不同配比AT(1∶1)、AT(3∶2)和AT(7∶3)对小鼠黑色素瘤B16细胞作用48 h的抑制作用。运用质量作用中效定理和药物合并指数定理分析两药联合是否具有协同增效作用。结果 ATS、DHA和Taxol单药作用于小鼠黑色素瘤B16细胞的IC_(50)值,在24 h时,分别为126.56,86.09,3.27μmol·L^(-1);在48 h时,分别为1.36,15.11,0.97μmol·L^(-1)。ATS联合Taxol 3个浓度组AT(1∶1)、AT(3∶2)和AT(7∶3)对小鼠黑色素瘤B16细胞作用48 h,联合用药合并指数(CI)均小于1。结论 ATS、DHA和Taxol单药对小鼠黑色素瘤B16细胞的增殖抑制作用随着药物浓度和时间的增加而明显增加,呈剂量和时间依赖性。青蒿琥酯联合紫杉醇抑制小鼠黑色素瘤B16细胞增殖,有良好的协同增效作用。 展开更多
关键词 青蒿琥酯 紫杉醇 小鼠黑色素瘤b16细胞
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