Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/34685
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    CNU IR > Offices > 123 >  Item 310902800/34685
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/34685


    Title: In Vitro and In Vivo Nephroprotective Effects of Nelumbo nucifera Seedpod Extract against Cisplatin-Induced Renal Injury
    Authors: Chen, Jui-Yi
    Tsai, Chia-Lin
    Tseng, Chiao-Yun
    Yu, Pei-Rong
    Chang, Yu-Hsuan
    Wong, Yue-Ching
    Lin, Hui-Hsuan
    Chen, Jing-Hsien
    Contributors: Chi Mei Hospital
    Chia Nan University of Pharmacy & Science
    Chung Shan Medical University
    Chung Shan Medical University
    Chung Shan Medical University
    Chung Shan Medical University Hospital
    Keywords: dna-damage response
    induced nephrotoxicity
    oxidative stress
    cytochrome-c
    apoptosis
    platinum
    mechanisms
    quercetin
    cells
    inhibition
    Date: 2022
    Issue Date: 2023-12-11 14:05:05 (UTC+8)
    Publisher: MDPI
    Abstract: 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.
    Relation: PLANTS-BASEL, v.11, n.CB2, pp.CC2, pp.-,
    Appears in Collections:[Offices] 123

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