{"title":"玉米叶提取物对过氧化氢诱导鸡胚成纤维细胞凋亡的保护作用","authors":"Balasubramanian Kiruthika , Sudha Devi Manickam , Palghat Raghunathan Padma","doi":"10.1016/j.jopr.2013.06.009","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>It is known that excessive oxidative damage, when unchecked, can result in cell death. Therefore, in the present study, the extent of cell death induced by H<sub>2</sub>O<sub>2</sub>-induced oxidative stress in primary cultured chick embryo fibroblasts and its protection by <em>Zea mays</em> leaf extracts was followed.</p></div><div><h3>Methods</h3><p>Various apoptosis related parameters like cell viability, morphological changes, nuclear changes and apoptotic index were characterized. SRB and MTT assays were used to quantify the extent of cell death in the group exposed to H<sub>2</sub>O<sub>2</sub>, plant extracts and their combination.</p></div><div><h3>Results and discussion</h3><p>The treatment with hydrogen peroxide exhibited cytotoxicity in the primary chick embryo fibroblasts cells. The number of apoptotic cells increased in the oxidant treated groups. When administered along with H<sub>2</sub>O<sub>2</sub>, the leaf extracts resulted in a significantly decreased number of apoptotic cells. The maximum inhibition of H<sub>2</sub>O<sub>2</sub>-induced apoptosis was exhibited by the methanolic extract followed by the aqueous and chloroform extracts.</p></div><div><h3>Conclusion</h3><p>These results indicate that the <em>Zea mays</em> leaves can render protection to chick embryo fibroblasts against H<sub>2</sub>O<sub>2</sub>-induced cell death.</p></div>","PeriodicalId":16787,"journal":{"name":"Journal of Pharmacy Research","volume":"6 6","pages":"Pages 638-646"},"PeriodicalIF":0.0000,"publicationDate":"2013-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jopr.2013.06.009","citationCount":"2","resultStr":"{\"title\":\"Zea mays leaf extracts protects primary chick embryo fibroblast cells from apoptosis induced by hydrogen peroxide in vitro\",\"authors\":\"Balasubramanian Kiruthika , Sudha Devi Manickam , Palghat Raghunathan Padma\",\"doi\":\"10.1016/j.jopr.2013.06.009\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>It is known that excessive oxidative damage, when unchecked, can result in cell death. Therefore, in the present study, the extent of cell death induced by H<sub>2</sub>O<sub>2</sub>-induced oxidative stress in primary cultured chick embryo fibroblasts and its protection by <em>Zea mays</em> leaf extracts was followed.</p></div><div><h3>Methods</h3><p>Various apoptosis related parameters like cell viability, morphological changes, nuclear changes and apoptotic index were characterized. SRB and MTT assays were used to quantify the extent of cell death in the group exposed to H<sub>2</sub>O<sub>2</sub>, plant extracts and their combination.</p></div><div><h3>Results and discussion</h3><p>The treatment with hydrogen peroxide exhibited cytotoxicity in the primary chick embryo fibroblasts cells. The number of apoptotic cells increased in the oxidant treated groups. When administered along with H<sub>2</sub>O<sub>2</sub>, the leaf extracts resulted in a significantly decreased number of apoptotic cells. The maximum inhibition of H<sub>2</sub>O<sub>2</sub>-induced apoptosis was exhibited by the methanolic extract followed by the aqueous and chloroform extracts.</p></div><div><h3>Conclusion</h3><p>These results indicate that the <em>Zea mays</em> leaves can render protection to chick embryo fibroblasts against H<sub>2</sub>O<sub>2</sub>-induced cell death.</p></div>\",\"PeriodicalId\":16787,\"journal\":{\"name\":\"Journal of Pharmacy Research\",\"volume\":\"6 6\",\"pages\":\"Pages 638-646\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2013-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.jopr.2013.06.009\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Pharmacy Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0974694313002466\",\"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 Pharmacy Research","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0974694313002466","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Zea mays leaf extracts protects primary chick embryo fibroblast cells from apoptosis induced by hydrogen peroxide in vitro
Background
It is known that excessive oxidative damage, when unchecked, can result in cell death. Therefore, in the present study, the extent of cell death induced by H2O2-induced oxidative stress in primary cultured chick embryo fibroblasts and its protection by Zea mays leaf extracts was followed.
Methods
Various apoptosis related parameters like cell viability, morphological changes, nuclear changes and apoptotic index were characterized. SRB and MTT assays were used to quantify the extent of cell death in the group exposed to H2O2, plant extracts and their combination.
Results and discussion
The treatment with hydrogen peroxide exhibited cytotoxicity in the primary chick embryo fibroblasts cells. The number of apoptotic cells increased in the oxidant treated groups. When administered along with H2O2, the leaf extracts resulted in a significantly decreased number of apoptotic cells. The maximum inhibition of H2O2-induced apoptosis was exhibited by the methanolic extract followed by the aqueous and chloroform extracts.
Conclusion
These results indicate that the Zea mays leaves can render protection to chick embryo fibroblasts against H2O2-induced cell death.