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Mixed micelles loaded with hesperidin protect against acetaminophen induced acute liver injury by inhibiting the mtDNA-cGAS-STING pathway
Dong, Kehong1; Sun, Yuxuan1; Gao, Xintao1; Wang, Jing2; Wu, Xiaochen1; Guo, Chuanlong1,3
2024
发表期刊COLLOIDS AND SURFACES B-BIOINTERFACES
ISSN0927-7765
卷号233页码:12
通讯作者Guo, Chuanlong(guochuanlong@qust.edu.cn)
摘要Excessive acetaminophen (APAP) is the main cause of drug-induced acute liver failure, and the pathogenesis has not been elucidated and there is a lack of effective drugs. Hesperidin (Hes), a rich flavanone in citrus peel with excellent biological activities, is a potential agent for treatment liver injury. Due to poor water solubility of Hes, this study prepared mixed micelles using polyvinyl pyrrolidone (PVP K17) and poloxamer 188, and encapsulated Hes (Hes-MMs). The results showed that Hes-MMs exhibited a uniform spherical shape with a particle size of 66.80 +/- 0.83 nm, and Hes-MMs significantly improved the dispersibility, antioxidant activity, and cellular up -take of Hes. In vitro results showed that Hes-MMs protected the proliferation inhibition of HepG2 cells induced by APAP, inhibited the production of reactive oxygen species (ROS) and the damage of mitochondrial membrane potential (MMP) induced by APAP. Furthermore, Hes-MMs exerted liver protective effects by inhibiting APAP induced mtDNA release and activating the cGAS-STING pathway. In vivo results demonstrated that Hes-MMs showed protective and therapeutic effects on APAP induced liver injury, and their mechanisms were related to the mtDNA-cGAS-STING signaling pathway. In summary, our study demonstrated that the mtDNA-cGAS-STING pathway was involved in APAP induced acute liver injury, and Hes-MMs might be a potential therapeutic agent for treating APAP induced acute liver injury.
关键词Acetaminophen Liver injury Hesperidin MtDNA CGAS-STING
DOI10.1016/j.colsurfb.2023.113656
收录类别SCI
语种英语
资助项目Shandong Provincial Natural Science Foundation[ZR2020QH359] ; Open Fund of CAS ; Open Fund of CAS and 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Biophysics ; Chemistry ; Materials Science
WOS类目Biophysics ; Chemistry, Physical ; Materials Science, Biomaterials
WOS记录号WOS:001119630400001
出版者ELSEVIER
WOS关键词DRUG-DELIVERY ; IN-VIVO ; MITOCHONDRIAL ; HEPATOTOXICITY ; ATTENUATION ; ABSORPTION ; HESPERETIN ; STRESS ; CANCER
引用统计
文献类型期刊论文
条目标识符http://ir.qdio.ac.cn/handle/337002/184132
专题实验海洋生物学重点实验室
通讯作者Guo, Chuanlong
作者单位1.Qingdao Univ Sci & Technol, Coll Chem Engn, Dept Pharm, Qingdao 266042, Peoples R China
2.Baotou Teachers Coll, Dept Biol Sci & Technol, Baotou 014030, Peoples R China
3.Chinese Acad Sci, Inst Oceanol, Key Lab Expt Marine Biol, Qingdao 266071, Peoples R China
通讯作者单位实验海洋生物学重点实验室
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GB/T 7714
Dong, Kehong,Sun, Yuxuan,Gao, Xintao,et al. Mixed micelles loaded with hesperidin protect against acetaminophen induced acute liver injury by inhibiting the mtDNA-cGAS-STING pathway[J]. COLLOIDS AND SURFACES B-BIOINTERFACES,2024,233:12.
APA Dong, Kehong,Sun, Yuxuan,Gao, Xintao,Wang, Jing,Wu, Xiaochen,&Guo, Chuanlong.(2024).Mixed micelles loaded with hesperidin protect against acetaminophen induced acute liver injury by inhibiting the mtDNA-cGAS-STING pathway.COLLOIDS AND SURFACES B-BIOINTERFACES,233,12.
MLA Dong, Kehong,et al."Mixed micelles loaded with hesperidin protect against acetaminophen induced acute liver injury by inhibiting the mtDNA-cGAS-STING pathway".COLLOIDS AND SURFACES B-BIOINTERFACES 233(2024):12.
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