中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Polyvinylpyrrolidone-Polydatin nanoparticles protect against oxaliplatin induced intestinal toxicity in vitro and in vivo

文献类型:期刊论文

作者Zhou, Shilin3; Sun, Yuxuan3; Wang, Kaidi3; Gao, Xintao3; Dong, Kehong3; Wang, Jing2; Wu, Xiaochen3; Guo, Chuanlong1,3
刊名FOOD AND CHEMICAL TOXICOLOGY
出版日期2024-02-01
卷号184页码:11
关键词Oxaliplatin Intestinal toxicity Polydatin DNA damage cGAS-STING
ISSN号0278-6915
DOI10.1016/j.fct.2023.114427
通讯作者Wu, Xiaochen(wxcguest@126.com) ; Guo, Chuanlong(guochuanlong@qust.edu.cn)
英文摘要Oxaliplatin (OXL) is a first-line drug for the treatment of colon cancer, with excellent efficacy. Intestinal toxicity is a common side effect of OXL, with unclear pathogenesis and a lack of effective treatment strategies. Polydatin (PD) has anti-inflammatory and antioxidant activities and is a potential drug for treating intestinal diseases, but its poor water solubility limits its application. In this study, polyvinylpyrrolidone (PVP) was used as a carrier to prepare nanoparticles loaded with PD (PVP-PD), with a particle size of 92.42 nm and exhibiting sustained release properties. In vitro results showed that PVP-PD protected NCM460 cells from OXL induced injury, mitochondrial membrane potential (MMP) disruption, and accumulation of reactive oxygen species (ROS). The in vivo results demonstrated the protective effect of PVP-PD on intestinal toxicity induced by OXL, such as alleviating weight loss and colon length reduction induced by OXL. Both in vivo and in vitro mechanisms indicated that OXL induced DNA damage and activated the cGAS-STING pathway, further inducing the expression of inflammatory factors such as IL-1 beta and TNF-alpha. PVP-PD alleviated the aforementioned changes induced by OXL by inhibiting the DNA damage-cGAS-STING pathway. In summary, our study demonstrated that the DNA damage-cGAS-STING pathway was involved in OXL induced intestinal toxicity, and PVP-PD provided a potential strategy for treating OXL induced intestinal toxicity.
WOS关键词CHEMOTHERAPY-INDUCED NAUSEA ; OXIDATIVE STRESS ; STING PATHWAY ; CGAS ; DNA ; CANCER ; INJURY ; 2ND-MESSENGER ; SENESCENCE ; MANAGEMENT
资助项目National Natural Science Foundation of China[22307060] ; Shandong Provincial Natural Science Foundation[ZR2020QH359] ; Open Fund of CAS ; Shandong Province Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences[KF2022NO06] ; Program for Young Talents of Science and Technology in Universities of Inner Mongolia[NJYT-18-B29] ; Doctoral Scientific Research Foundation of Inner Mongolia[BTTCRCQD2018001]
WOS研究方向Food Science & Technology ; Toxicology
语种英语
WOS记录号WOS:001298946100001
出版者PERGAMON-ELSEVIER SCIENCE LTD
源URL[http://ir.qdio.ac.cn/handle/337002/198167]  
专题海洋研究所_实验海洋生物学重点实验室
通讯作者Wu, Xiaochen; Guo, Chuanlong
作者单位1.Chinese Acad Sci, Key Lab Expt Marine Biol, Inst Oceanol, Qingdao 266071, Peoples R China
2.Baotou Teachers Coll, Dept Biol Sci & Technol, Baotou 014030, Peoples R China
3.Qingdao Univ Sci & Technol, Coll Chem Engn, Dept Pharm, Qingdao 266042, Peoples R China
推荐引用方式
GB/T 7714
Zhou, Shilin,Sun, Yuxuan,Wang, Kaidi,et al. Polyvinylpyrrolidone-Polydatin nanoparticles protect against oxaliplatin induced intestinal toxicity in vitro and in vivo[J]. FOOD AND CHEMICAL TOXICOLOGY,2024,184:11.
APA Zhou, Shilin.,Sun, Yuxuan.,Wang, Kaidi.,Gao, Xintao.,Dong, Kehong.,...&Guo, Chuanlong.(2024).Polyvinylpyrrolidone-Polydatin nanoparticles protect against oxaliplatin induced intestinal toxicity in vitro and in vivo.FOOD AND CHEMICAL TOXICOLOGY,184,11.
MLA Zhou, Shilin,et al."Polyvinylpyrrolidone-Polydatin nanoparticles protect against oxaliplatin induced intestinal toxicity in vitro and in vivo".FOOD AND CHEMICAL TOXICOLOGY 184(2024):11.

入库方式: OAI收割

来源:海洋研究所

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