Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/34685
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 18269/20496 (89%)
Visitors : 10519090      Online Users : 755
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://ir.cnu.edu.tw/handle/310902800/34685


    题名: In Vitro and In Vivo Nephroprotective Effects of Nelumbo nucifera Seedpod Extract against Cisplatin-Induced Renal Injury
    作者: Chen, Jui-Yi
    Tsai, Chia-Lin
    Tseng, Chiao-Yun
    Yu, Pei-Rong
    Chang, Yu-Hsuan
    Wong, Yue-Ching
    Lin, Hui-Hsuan
    Chen, Jing-Hsien
    贡献者: Chi Mei Hospital
    Department of Health and Nutrition, Chia Nan University of Pharmacy & Science
    Chung Shan Medical University
    Chung Shan Medical University Hospital
    关键词: dna-damage response
    induced nephrotoxicity
    oxidative stress
    cytochrome-c
    apoptosis
    platinum
    mechanisms
    quercetin
    cells
    inhibition
    日期: 2022
    上传时间: 2023-12-11 14:05:05 (UTC+8)
    出版者: MDPI
    摘要: Cisplatin has been considered a chemotherapeutic drug for treating human tumors, and one of the noteworthy side effects of cisplatin is nephrotoxicity. Amelioration of cisplatin-induced nephrotoxicity is necessary. Lotus seedpod extract (LSE) mainly composed of quercetin-3-glucuronide has been revealed for antioxidant and anti-tumor effects. However, the effects of LSE on cisplatin-induced nephrotoxicity are still unknown. This study aims to explore the in vitro and in vivo protective effect and possible mechanism of LSE on cisplatin-induced nephrotoxicity. Results showed that co-treatment of LSE with cisplatin raised the viability of rat renal tubular epithelial NRK-52E cells and decreased oxidative stress and cell apoptosis when compared to the cells treated with cisplatin alone. The molecular mechanisms analyzed found that LSE could reduce the expressions of apoptotic factors, including Bax, Bad, t-Bid, and caspases. In the in vivo study, LSE improved the cisplatin-induced levels of serum markers of kidney function, glomerular atrophy, and the degree of apoptosis in the kidneys. This is the first study to display that LSE prevents cisplatin-induced nephrotoxicity by reducing oxidative stress and apoptosis. Thus, LSE could be a novel and natural chemoprotective agent for cisplatin chemotherapy in the future.
    關聯: PLANTS-BASEL, v.11, n.23, pp.3357
    显示于类别:[Dept. of Health and Nutrition (including master's program)] Periodical Articles

    文件中的档案:

    档案 描述 大小格式浏览次数
    index.html0KbHTML353检视/开启
    plants11233357.pdf4682KbAdobe PDF116检视/开启


    在CNU IR中所有的数据项都受到原著作权保护.

    TAIR相关文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈