Quantitative analysis and hepatoprotective mechanism of Cistanche deserticola Y. C. Ma against alcohol-induced liver injury in mice

化学 脂肪酸合酶 甘油磷脂 脂质代谢 人参 花生四烯酸 生物化学 脂类学 肝损伤 脂肪肝 亚油酸 药理学 脂肪酸 生物 内科学 磷脂 医学 替代医学 疾病 病理
作者
Jing Wang,Haichao Wang,Huanjun Wang,Yifei Bian,Kai Wang,Xinyuan Zhai,Yuan Li,Ke Wu,Wei Wang,Jie Li,Zhixin Tang,Xiaoming Wang
出处
期刊:Biomedicine & Pharmacotherapy [Elsevier]
卷期号:162: 114719-114719 被引量:4
标识
DOI:10.1016/j.biopha.2023.114719
摘要

Cistanche deserticola Y. C. Ma (CD), known as "desert ginseng", has been found to have hepatoprotective effect. This research aimed to investigate the quality control and its alleviating effect on alcoholic liver injury in mice. In this study, for the first time, a sensitive and efficient ultra-high-performance liquid chromatography with quadrupole ion-trap mass spectrometry (UPLC-Q-TRAP/MS) method was developed to rapidly characterize nine representative phenylethanoid glycosides (PhGs) in the CD extract within 14 min, offering a reference for the quality control standard of this plant. In addition, we found that the CD extract significantly inhibited the weight loss, decreased the liver index, and attenuated excessive lipid deposition, inflammatory and oxidative stress in the mice liver. With the help of the high-throughput lipidomics technique, we discovered that CD markedly reversed 17 lipid metabolites and their involved linoleic acid, arachidonic acid and glycerophospholipid metabolic pathways. As these metabolites are mainly associated with lipid metabolism and liver damage, we further used molecular biological tests to found that CD could regulate the upstream genes and proteins of the lipid metabolism pathway, including adenosine 5'-monophosphate-activated protein kinase (AMPK), sterol regulatory element binding protein-1c (SREBP-1c), fatty acid synthase (FAS), and peroxidase proliferators activate receptors α (PPARα). In conclusion, this study elucidates the modulatory effects of CD on lipid metabolism disorders in alcoholic fatty liver from holistic system and provides a reference for further research and development of CD as a therapeutic agent.
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