Open AccessThe Role of Ophiopogonin D in Atherosclerosis: Impact on Lipid Metabolism and Gut Microbiota
Author(s) -
Yaxin Zhang,
Shanshan Qu,
Lihua Zhang,
Yin Gu,
Yi-Hao Chen,
Zhiyong Huang,
Menghua Liu,
Wei Zou,
Jing Jiang,
Junqi Chen,
Yujue Wang,
Fenghua Zhou
Publication year - 2021
Publication title -
the american journal of chinese medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.025
H-Index - 63
eISSN - 1793-6853
pISSN - 0192-415X
DOI - 10.1142/s0192415x21500683
Subject(s) - lipid metabolism , gut flora , steatosis , simvastatin , insulin resistance , hyperlipidemia , endocrinology , medicine , apolipoprotein e , metabolic syndrome , cholesterol , apolipoprotein b , biology , immunology , disease , diabetes mellitus
Gut microbiota has been proven to play an important role in many metabolic diseases and cardiovascular disease, particularly atherosclerosis. Ophiopogonin D (OPD), one of the effective compounds in Ophiopogon japonicus, is considered beneficial to metabolic syndrome and cardiovascular diseases. In this study, we have illuminated the effect of OPD in ApoE knockout (ApoE[Formula: see text] mice on the development of atherosclerosis and gut microbiota. To investigate the potential ability of OPD to alleviate atherosclerosis, 24 eight-week-old male ApoE[Formula: see text] mice (C57BL/6 background) were fed a high-fat diet (HFD) for 12 weeks, and 8 male C57BL/6 mice were fed a normal diet, serving as the control group. ApoE[Formula: see text] mice were randomly divided into the model group, OPD group, and simvastatin group ([Formula: see text]= 8). After treatment for 12 consecutive weeks, the results showed that OPD treatment significantly decreased the plaque formation and levels of serum lipid compared with those in the model group. In addition, OPD improved oral glucose tolerance and insulin resistance as well as reducing hepatocyte steatosis. Further analysis revealed that OPD might attenuate atherosclerosis through inhibiting mTOR phosphorylation and the consequent lipid metabolism signaling pathways mediated by SREBP1 and SCD1 in vivo and in vitro. Furthermore, OPD treatment led to significant structural changes in gut microbiota and fecal metabolites in HFD-fed mice and reduced the relative abundance of Erysipelotrichaceae genera associated with cholesterol metabolism. Collectively, these findings illustrate that OPD could significantly protect against atherosclerosis, which might be associated with the moderation of lipid metabolism and alterations in gut microbiota composition and fecal metabolites.