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Mechanism of astaxanthin relieving lipopolysaccharide (LPS)-induced acute liver injury in mice
被引:0
|作者:
He, Min
[1
]
Deng, Xin-Yi
[1
]
Zhu, Yan-Bin
[1
]
Hao, Jie
[1
]
Kay, Matthew
[2
]
Zhang, Hua
[2
,3
]
Chen, Jin Jun
[1
]
Chen, Zhi-Bao
[1
,4
]
机构:
[1] Guangdong Ocean Univ, Dept Coll Coastal Agr, Zhanjiang, Guangdong, Peoples R China
[2] Yancheng Teachers Univ, Sch Pharm, Yancheng, Jiangsu, Peoples R China
[3] Jiangsu Prov Engn Res Ctr Tumor Targeted Nano Diag, Yancheng, Jiangsu, Peoples R China
[4] Natl Saline Alkali Tolerant Rice Technol Innovat C, South China Branch, Zhanjiang, Guangdong, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
Astaxanthin;
Acute liver injury;
LPS;
NF-xB;
Nrf2;
D O I:
10.1590/0103-8478cr20230102
中图分类号:
S3 [农学(农艺学)];
学科分类号:
0901 ;
摘要:
Acute liver injury (ALI) is an important medical problem that requires effective therapy. Astaxanthin (AST) is a carotenoid, and the beneficial effects of astaxanthin, including anti-oxidative, anti-inflammatory and anti-tumour activities, have been identified. The present study was designed to elucidate the protective effects of astaxanthin against ALI and their underlying mechanisms. RAW264.7 macrophages were treated with dimethyl sulfoxide combined with different doses of astaxanthin for 12 h. Mice were fed with or without astaxanthin for up to 7 days. LPS was administered to induce inflammation. We assessed histopathology, oxidative stress, inflammation and apoptosis .The results indicated that astaxanthin attenuated LPS-induced oxidative stress, inflammation and cell apoptosis both in vivo and in vitro. In vivo and in vitro experiments showed that astaxanthin down regulated the nuclear factor-kappa beta (NF-xB), nuclear factor erythroid 2-related factor 2 (Nrf2) and NLR family pyrin domain containing 3 (NLRP3) signalling pathways, inhibiting the LPS-induced inflammatory response, oxidative stress and cell apoptosis, and alleviating LPS-induced ALI in mice.
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