机构:[1]Department of Cell Biology, College of Life Science and Technology, Jinan University, State Key Laboratory of Bioactive Molecules and Druggability Assessment, Jinan University, National Engineering Research Center of Genetic Medicine, Guangdong Provincial Key Laboratory of Bioengineering Medicine, Guangdong Provincial Biotechnology Drug & Engineering Technology Research Center, Jinan University, Guangzhou 510632, China[2]Department of Infectious Disease, The First Affiliated Hospital of Jinan University, Guangzhou 510630, China[3]School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, China[4]Guangzhou University of Traditional Chinese Medicine, Guangzhou 510006, China深圳市中医院深圳医学信息中心
Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease, with a global prevalence of 25%. Patients with NAFLD are more likely to suffer from advanced liver disease, cardiovascular disease, or type II diabetes. However, unfortunately, there is still a shortage of FDA-approved therapeutic agents for NAFLD. Lian-Mei-Yin (LMY) is a traditional Chinese medicine formula used for decades to treat liver disorders. It has recently been applied to type II diabetes which is closely related to insulin resistance. Given that NAFLD is another disease involved in insulin resistance, we hypothesize that LMY might be a promising formula for NAFLD therapy. Herein, we verify that the LMY formula effectively reduces hepatic steatosis in diet-induced zebrafish and NAFLD model mice in a time- and dose-dependent manner. Mechanistically, LMY suppresses Yap1-mediated Foxm1 activation, which is crucial for the occurrence and development of NAFLD. Consequently, lipogenesis is ameliorated by LMY administration. In summary, the LMY formula alleviates diet-induced NAFLD in zebrafish and mice by inhibiting Yap1/Foxm1 signaling-mediated NAFLD pathology.
基金:
This work was supported by the grants from the National Natural
Science Foundation of China (Nos. 81902801 to Y.Z., 8217329 to A.
H., and 82273833 to X.C.), the Operating Fund of Guangdong
Provincial Key Laboratory of Bioengineering Medicine (No.
2014B030301050 to A.H.), Guangdong grant “Key technologies
for the treatment of brain disorders” (No. 2018B030332001 to A.
H.), the China Postdoctoral Foundation (No. 2019M663375 to Y.
Z.), and Special Funds for the Cultivation of Guangdong College
Students’ Scientific and Technological Innovation (No.
pdjh2021a0051 to X.C.).
语种:
外文
PubmedID:
中科院(CAS)分区:
出版当年[2023]版:
大类|2 区生物学
小类|2 区生物物理3 区生化与分子生物学
最新[2025]版:
大类|2 区生物学
小类|2 区生化与分子生物学2 区生物物理
第一作者:
第一作者机构:[1]Department of Cell Biology, College of Life Science and Technology, Jinan University, State Key Laboratory of Bioactive Molecules and Druggability Assessment, Jinan University, National Engineering Research Center of Genetic Medicine, Guangdong Provincial Key Laboratory of Bioengineering Medicine, Guangdong Provincial Biotechnology Drug & Engineering Technology Research Center, Jinan University, Guangzhou 510632, China
共同第一作者:
通讯作者:
推荐引用方式(GB/T 7714):
Zhang Peiguang,Cao Jieqiong,Liang Xujing,et al.Lian-Mei-Yin formula alleviates diet-induced hepatic steatosis by suppressing Yap1/FOXM1 pathway-dependent lipid synthesis[J].Acta Biochimica Et Biophysica Sinica.2024,doi:10.3724/abbs.2024025.
APA:
Zhang Peiguang,Cao Jieqiong,Liang Xujing,Su Zijian,Zhang Bihui...&Zhang Yibo.(2024).Lian-Mei-Yin formula alleviates diet-induced hepatic steatosis by suppressing Yap1/FOXM1 pathway-dependent lipid synthesis.Acta Biochimica Et Biophysica Sinica,,
MLA:
Zhang Peiguang,et al."Lian-Mei-Yin formula alleviates diet-induced hepatic steatosis by suppressing Yap1/FOXM1 pathway-dependent lipid synthesis".Acta Biochimica Et Biophysica Sinica .(2024)