Cytoprotective Potential of Rutin and Quercetin in Swiss Mice Exposed to Gamma Radiation

S. Patil, T. Ghodke, Shilpa Patil, K. Swaroop, H. Somashekarappa
{"title":"Cytoprotective Potential of Rutin and Quercetin in Swiss Mice Exposed to Gamma Radiation","authors":"S. Patil, T. Ghodke, Shilpa Patil, K. Swaroop, H. Somashekarappa","doi":"10.21276/ijlssr.2017.3.5.10","DOIUrl":null,"url":null,"abstract":"Radioprotective mechanisms of Rutin (RUT) and Quercetin (QRT) against gamma radiation was studied by investigating recovery of histopathology of intestinal mucosa and bone marrow in Swiss albino mice. These mice were treated with RUT (10mg/kg.b.wt.) and QRT (20mg/kg.b.wt.) once daily for five consecutive days and exposed to 7.5 Gy of gamma radiation after the last administration. RUT and QRT treatment before exposure to 7.5 Gy of gamma radiation. To assess the intestinal and bone marrow protective potential of RUT and QRT, histological analysis was carried out by observing the villus height, crypt survival, number of goblet cells/villus section and dead cells/villus section in the mouse jejunum and bone marrow cellularity at 24 hours post-irradiation. Mice exposed gamma radiation caused a significant decline in the villus height and crypt number with an increase in goblet and dead cell number with a significant decrease in bone marrow nucleated cells. The potent antioxidant nature of RUT and QRT mitigate the oxidative stress induced by gamma radiation and thus protect the mice from gastrointestinal damage. Key-wordsRutin, Quercetin, Cytoprotective, Irradiation INTRODUCTION Radiation therapy has been successfully used to treat malignant tumours of different histological origin and stages, (individually or in combination with chemotherapy and surgery, or both) for several decades. The response of mammalian cells to ionizing radiations at the cellular and molecular level is complex and is an active irreversible process that is dependent on both the radiation dose and the tissue-weighting factor . Most of the tissue damage caused by ionizing radiation is mediated by the reactive oxygen species (ROS) generated from the interaction between radiation and water molecules in cells . These ROS react with biological molecules including proteins, lipids, lipoproteins and DNA . Many synthetic compounds have been studied for their ability to protect against adverse effects of radiation ever since the original observation of radioprotection by Patt and co-workers . Access this article online Quick Response Code Website:","PeriodicalId":22509,"journal":{"name":"The International Journal of Life-Sciences Scientific Research","volume":"20 1","pages":"1322-1328"},"PeriodicalIF":0.0000,"publicationDate":"2017-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The International Journal of Life-Sciences Scientific Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21276/ijlssr.2017.3.5.10","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Radioprotective mechanisms of Rutin (RUT) and Quercetin (QRT) against gamma radiation was studied by investigating recovery of histopathology of intestinal mucosa and bone marrow in Swiss albino mice. These mice were treated with RUT (10mg/kg.b.wt.) and QRT (20mg/kg.b.wt.) once daily for five consecutive days and exposed to 7.5 Gy of gamma radiation after the last administration. RUT and QRT treatment before exposure to 7.5 Gy of gamma radiation. To assess the intestinal and bone marrow protective potential of RUT and QRT, histological analysis was carried out by observing the villus height, crypt survival, number of goblet cells/villus section and dead cells/villus section in the mouse jejunum and bone marrow cellularity at 24 hours post-irradiation. Mice exposed gamma radiation caused a significant decline in the villus height and crypt number with an increase in goblet and dead cell number with a significant decrease in bone marrow nucleated cells. The potent antioxidant nature of RUT and QRT mitigate the oxidative stress induced by gamma radiation and thus protect the mice from gastrointestinal damage. Key-wordsRutin, Quercetin, Cytoprotective, Irradiation INTRODUCTION Radiation therapy has been successfully used to treat malignant tumours of different histological origin and stages, (individually or in combination with chemotherapy and surgery, or both) for several decades. The response of mammalian cells to ionizing radiations at the cellular and molecular level is complex and is an active irreversible process that is dependent on both the radiation dose and the tissue-weighting factor . Most of the tissue damage caused by ionizing radiation is mediated by the reactive oxygen species (ROS) generated from the interaction between radiation and water molecules in cells . These ROS react with biological molecules including proteins, lipids, lipoproteins and DNA . Many synthetic compounds have been studied for their ability to protect against adverse effects of radiation ever since the original observation of radioprotection by Patt and co-workers . Access this article online Quick Response Code Website:
芦丁和槲皮素对γ辐射下瑞士小鼠的细胞保护作用
研究芦丁(RUT)和槲皮素(QRT)对γ射线辐射的保护作用机制,探讨芦丁(RUT)和槲皮素(QRT)对γ射线辐射的保护作用机制。这些小鼠每天一次接受RUT (10mg/kg.b.wt)和QRT (20mg/kg.b.wt)治疗,连续5天,最后一次给药后接受7.5 Gy的伽马辐射。接受7.5 Gy γ辐射前的RUT和QRT治疗。通过观察小鼠空肠绒毛高度、隐窝存活率、杯状细胞/绒毛切片数量、死细胞/绒毛切片数量及辐照后24 h小鼠骨髓细胞数量,对RUT和QRT对小鼠肠道和骨髓的保护作用进行组织学分析。暴露于γ辐射的小鼠绒毛高度和隐窝数量明显下降,杯状细胞和死细胞数量增加,骨髓有核细胞明显减少。RUT和QRT有效的抗氧化特性减轻了γ辐射引起的氧化应激,从而保护小鼠免受胃肠道损伤。几十年来,放射治疗已经成功地用于治疗不同组织学来源和分期的恶性肿瘤(单独或联合化疗和手术,或两者)。哺乳动物细胞在细胞和分子水平上对电离辐射的反应是一个复杂的、主动的、不可逆的过程,它既依赖于辐射剂量,也依赖于组织加权因子。电离辐射引起的组织损伤大多是由辐射与细胞内水分子相互作用产生的活性氧(ROS)介导的。这些活性氧与生物分子发生反应,包括蛋白质、脂质、脂蛋白和DNA。自从帕特和他的同事最初观察到辐射防护以来,许多合成化合物都被研究了它们抵御辐射不利影响的能力。在线阅读本文快速响应代码网站:
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信