Lipid regulation of protocatechualdehyde and hydroxysafflor yellow A via AMPK/SREBP2/PCSK9/LDLR signaling pathway in hyperlipidemic zebrafish

被引:2
|
作者
Lin, Bingying
Wan, Haofang [2 ]
Yang, Jiehong [1 ]
Yu, Li [1 ,3 ,5 ]
Zhou, Huifen [2 ,4 ,6 ]
Wan, Haitong [1 ,3 ,4 ,5 ,6 ]
机构
[1] Zhejiang Chinese Med Univ, Sch Basic Med Sci, Hangzhou, Peoples R China
[2] Zhejiang Chinese Med Univ, Acad Chinese Med Sci, Hangzhou, Peoples R China
[3] Zhejiang Chinese Med Univ, Inst Cardiocerebrovasc Dis, Hangzhou, Peoples R China
[4] Zhejiang Chinese Med Univ, Affiliated Hosp 1, Hangzhou, Peoples R China
[5] Key Lab TCM Encephalopathy Zhejiang Prov Grant 202, Hangzhou, Peoples R China
[6] Zhejiang Chinese Med Univ, 548 Binwen Rd, Hangzhou 310053, Peoples R China
基金
中国国家自然科学基金;
关键词
Protocatechualdehyde; Hydroxysafflor yellow A; Hyperlipidemia; TRANSCRIPTION FACTOR; MUTANT; RATS;
D O I
10.1016/j.heliyon.2024.e24908
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The consumption of a high-cholesterol diet is known to cause hyperlipidemia, which is one of the main risk factors for cardiovascular disease. Protocatechualdehyde (PCA) and hydroxysafflor yellow A (HSYA) are the active components of Salvia miltiorrhiza and safflower, respectively. However, their exact mechanism is still unclear. The aim of this study is to investigate its effects on lipid deposition and liver damage in hyperlipidemic zebrafish and its mechanism of antihyperlipidemia. The results showed that the use of PCA and HSYA alone and in combination can improve lipid deposition, slow behavior, abnormal blood flow and liver tissue damage, and the combined use is more effective. Further RT-qPCR results showed that PCA + HSYA can regulate the mRNA levels of PPAR-gamma, SREBP2, SREBP1, HMGCR, PCSK9, mTOR, C/EBP alpha, LDLR, AMPK, HNF-1 alpha and FoxO3a. The PCA + HSYA significantly improves lipid deposition and abnormal liver function in hyperlipidemic zebrafish larvae, which may be related to the AMPK/ SREBP2/PCSK9/LDLR signaling pathway.
引用
收藏
页数:14
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