{"title":"辣木叶提取物的抗氧化和细胞保护作用","authors":"S. Xuan, A. Kim, Y. Jeong, N. Lee, S. Park","doi":"10.15230/SCSK.2016.42.3.217","DOIUrl":null,"url":null,"abstract":": In this study, we investigated the antioxidative and cellular protective effects on HaCaT cells and erythrocytes of Moringa oleifera ( M. oleifera ) leaves extract and its fractions. All experiments were performed with 50% ethanol extract, ethyl acetate fraction and aglycone fraction of M. oleifera leaves. The free radical scavenging activity (FSC 50 ) of the extract and fractions of M. oleifera leaves were in the following order: 50% ethanol extract (77.10 µ g/mL) < ethyl acetate fraction (20.63 µ g/mL) < aglycone fraction (17.00 µ g/mL) by using the 1, 1-diphenyl-2-picrylhydrazyl. In Fe 3+ -EDTA/H 2 O 2 system using the luminol, reactive oxygen species (ROS) scavenging activities (total antioxidant capacity, OSC 50 ) of aglycone fraction (OSC 50 = 0.63 µ g/mL) was the strongest among all extracts, which was much higher than L-ascorbic acid (1.50 µ g/mL). In the 1 O 2 -induced cellular damage of erythrocytes, the cellular protective effects of 50% ethanol extract ( τ 50 = 46.9 min) and aglycone fraction ( τ 50 = 122.1 min) were higher than (+)- α -tocopherol ( τ 50 = 37.7 min), known as a lipophilic antioxidant at 10 µ g/mL. After cell damage induced by 400 mJ/cm 2 UVB irradiation, the cellular protective effects of ethyl acetate and aglycone fraction of M. oleifera leaves extract were showed on the concentration from 0.20 to 1.56 µ g/mL. These results suggest that M. oleifera leaves extract and its fractions can function as a natural antioxidant agent in cosmetics on skin exposed to UV radiation by protecting cellular mem-brane against ROS.","PeriodicalId":17401,"journal":{"name":"Journal of the Society of Cosmetic Scientists of Korea","volume":"1 1","pages":"217-226"},"PeriodicalIF":0.0000,"publicationDate":"2016-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Antioxidant and Cellular Protective Effects of Moringa oleifera Leaves Extract\",\"authors\":\"S. Xuan, A. Kim, Y. Jeong, N. Lee, S. Park\",\"doi\":\"10.15230/SCSK.2016.42.3.217\",\"DOIUrl\":null,\"url\":null,\"abstract\":\": In this study, we investigated the antioxidative and cellular protective effects on HaCaT cells and erythrocytes of Moringa oleifera ( M. oleifera ) leaves extract and its fractions. All experiments were performed with 50% ethanol extract, ethyl acetate fraction and aglycone fraction of M. oleifera leaves. The free radical scavenging activity (FSC 50 ) of the extract and fractions of M. oleifera leaves were in the following order: 50% ethanol extract (77.10 µ g/mL) < ethyl acetate fraction (20.63 µ g/mL) < aglycone fraction (17.00 µ g/mL) by using the 1, 1-diphenyl-2-picrylhydrazyl. In Fe 3+ -EDTA/H 2 O 2 system using the luminol, reactive oxygen species (ROS) scavenging activities (total antioxidant capacity, OSC 50 ) of aglycone fraction (OSC 50 = 0.63 µ g/mL) was the strongest among all extracts, which was much higher than L-ascorbic acid (1.50 µ g/mL). In the 1 O 2 -induced cellular damage of erythrocytes, the cellular protective effects of 50% ethanol extract ( τ 50 = 46.9 min) and aglycone fraction ( τ 50 = 122.1 min) were higher than (+)- α -tocopherol ( τ 50 = 37.7 min), known as a lipophilic antioxidant at 10 µ g/mL. After cell damage induced by 400 mJ/cm 2 UVB irradiation, the cellular protective effects of ethyl acetate and aglycone fraction of M. oleifera leaves extract were showed on the concentration from 0.20 to 1.56 µ g/mL. These results suggest that M. oleifera leaves extract and its fractions can function as a natural antioxidant agent in cosmetics on skin exposed to UV radiation by protecting cellular mem-brane against ROS.\",\"PeriodicalId\":17401,\"journal\":{\"name\":\"Journal of the Society of Cosmetic Scientists of Korea\",\"volume\":\"1 1\",\"pages\":\"217-226\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the Society of Cosmetic Scientists of Korea\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15230/SCSK.2016.42.3.217\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Society of Cosmetic Scientists of Korea","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15230/SCSK.2016.42.3.217","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Antioxidant and Cellular Protective Effects of Moringa oleifera Leaves Extract
: In this study, we investigated the antioxidative and cellular protective effects on HaCaT cells and erythrocytes of Moringa oleifera ( M. oleifera ) leaves extract and its fractions. All experiments were performed with 50% ethanol extract, ethyl acetate fraction and aglycone fraction of M. oleifera leaves. The free radical scavenging activity (FSC 50 ) of the extract and fractions of M. oleifera leaves were in the following order: 50% ethanol extract (77.10 µ g/mL) < ethyl acetate fraction (20.63 µ g/mL) < aglycone fraction (17.00 µ g/mL) by using the 1, 1-diphenyl-2-picrylhydrazyl. In Fe 3+ -EDTA/H 2 O 2 system using the luminol, reactive oxygen species (ROS) scavenging activities (total antioxidant capacity, OSC 50 ) of aglycone fraction (OSC 50 = 0.63 µ g/mL) was the strongest among all extracts, which was much higher than L-ascorbic acid (1.50 µ g/mL). In the 1 O 2 -induced cellular damage of erythrocytes, the cellular protective effects of 50% ethanol extract ( τ 50 = 46.9 min) and aglycone fraction ( τ 50 = 122.1 min) were higher than (+)- α -tocopherol ( τ 50 = 37.7 min), known as a lipophilic antioxidant at 10 µ g/mL. After cell damage induced by 400 mJ/cm 2 UVB irradiation, the cellular protective effects of ethyl acetate and aglycone fraction of M. oleifera leaves extract were showed on the concentration from 0.20 to 1.56 µ g/mL. These results suggest that M. oleifera leaves extract and its fractions can function as a natural antioxidant agent in cosmetics on skin exposed to UV radiation by protecting cellular mem-brane against ROS.