Yuping Li, J. Chang, Cheng-mei Liu, X. Xiong, Y. Gong, Zi-ling Li
{"title":"百合多糖通过减少ROS的产生来防止四氧嘧啶诱导的HIT-T15细胞损伤","authors":"Yuping Li, J. Chang, Cheng-mei Liu, X. Xiong, Y. Gong, Zi-ling Li","doi":"10.1109/ICBEB.2012.264","DOIUrl":null,"url":null,"abstract":"The previous studies of our team and other researchers have shown that two polysaccharides derived from bulbs of lily aqueous extracts (LP-1, LP-2) can decrease fasting blood glucose concentration in diabetic model animal (in vivo). In the present study, we investigated the effects of LP-1 or LP-2 on cultured pancreatic d-cell tumor-derived cell line HIT-T15 that had undergone oxidative damage. The cell viability, insulin secretion, and intracellular reactive oxygen species (ROS) level were investigated in HIT-T15 cells after LP-, alloxan-, or both-treatment, respectively. The metabolic activity of d-cells was determined by MTT assay while the insulin secretion was detected by ELISA technique. Intracellular ROS was detected by fluorescent spectrophotometry using DCFH-DA. The treatment with LP-1 (>; 0.5 mg/ml) or LP-2 (>; 0.1 mg/ml) could significantly elevated the cell viability compared to untreated normal cells (p 1 mg/ml). Importantly, the viability of cells treated with 10 mg/ml LP-2 were almost restored to the levels of alloxan-untreated cells and completely prevented the lowering of glucose-stimulated insulin release. Our investigation suggested that LP-1 or LP-2 reduced the damage of alloxan-induced HIT-T15 cells through scavenging intracellular ROS level. And these data also provide some information when LP-1 or LP-2 is used as a bioactive component for developing a new anti-diabetic agent.","PeriodicalId":6374,"journal":{"name":"2012 International Conference on Biomedical Engineering and Biotechnology","volume":"38 1","pages":"364-367"},"PeriodicalIF":0.0000,"publicationDate":"2012-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Lily Polysaccharide Prevents Alloxan-induced HIT-T15 Cell Damage by Reducing ROS Generation\",\"authors\":\"Yuping Li, J. Chang, Cheng-mei Liu, X. Xiong, Y. Gong, Zi-ling Li\",\"doi\":\"10.1109/ICBEB.2012.264\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The previous studies of our team and other researchers have shown that two polysaccharides derived from bulbs of lily aqueous extracts (LP-1, LP-2) can decrease fasting blood glucose concentration in diabetic model animal (in vivo). In the present study, we investigated the effects of LP-1 or LP-2 on cultured pancreatic d-cell tumor-derived cell line HIT-T15 that had undergone oxidative damage. The cell viability, insulin secretion, and intracellular reactive oxygen species (ROS) level were investigated in HIT-T15 cells after LP-, alloxan-, or both-treatment, respectively. The metabolic activity of d-cells was determined by MTT assay while the insulin secretion was detected by ELISA technique. Intracellular ROS was detected by fluorescent spectrophotometry using DCFH-DA. The treatment with LP-1 (>; 0.5 mg/ml) or LP-2 (>; 0.1 mg/ml) could significantly elevated the cell viability compared to untreated normal cells (p 1 mg/ml). Importantly, the viability of cells treated with 10 mg/ml LP-2 were almost restored to the levels of alloxan-untreated cells and completely prevented the lowering of glucose-stimulated insulin release. Our investigation suggested that LP-1 or LP-2 reduced the damage of alloxan-induced HIT-T15 cells through scavenging intracellular ROS level. And these data also provide some information when LP-1 or LP-2 is used as a bioactive component for developing a new anti-diabetic agent.\",\"PeriodicalId\":6374,\"journal\":{\"name\":\"2012 International Conference on Biomedical Engineering and Biotechnology\",\"volume\":\"38 1\",\"pages\":\"364-367\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-05-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2012 International Conference on Biomedical Engineering and Biotechnology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/ICBEB.2012.264\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2012 International Conference on Biomedical Engineering and Biotechnology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/ICBEB.2012.264","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The previous studies of our team and other researchers have shown that two polysaccharides derived from bulbs of lily aqueous extracts (LP-1, LP-2) can decrease fasting blood glucose concentration in diabetic model animal (in vivo). In the present study, we investigated the effects of LP-1 or LP-2 on cultured pancreatic d-cell tumor-derived cell line HIT-T15 that had undergone oxidative damage. The cell viability, insulin secretion, and intracellular reactive oxygen species (ROS) level were investigated in HIT-T15 cells after LP-, alloxan-, or both-treatment, respectively. The metabolic activity of d-cells was determined by MTT assay while the insulin secretion was detected by ELISA technique. Intracellular ROS was detected by fluorescent spectrophotometry using DCFH-DA. The treatment with LP-1 (>; 0.5 mg/ml) or LP-2 (>; 0.1 mg/ml) could significantly elevated the cell viability compared to untreated normal cells (p 1 mg/ml). Importantly, the viability of cells treated with 10 mg/ml LP-2 were almost restored to the levels of alloxan-untreated cells and completely prevented the lowering of glucose-stimulated insulin release. Our investigation suggested that LP-1 or LP-2 reduced the damage of alloxan-induced HIT-T15 cells through scavenging intracellular ROS level. And these data also provide some information when LP-1 or LP-2 is used as a bioactive component for developing a new anti-diabetic agent.