4.7 Article

Ginsenosides regulation of lysophosphatidylcholine profiles underlies the mechanism of Shengmai Yin in attenuating atherosclerosis

Journal

JOURNAL OF ETHNOPHARMACOLOGY
Volume 277, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2021.114223

Keywords

Shengmai Yin; Ginsenosides; Atherosclerosis; Metabolomics; Lipidomics; Lysophosphatidylcholine

Funding

  1. National Natural Science Foundation of China [81720108032, 81930109, 81973559, 81773986]
  2. Project for Major New Drug Innovation and Development [2018ZX09711001-002-003, 2018ZX09711002-001-004]
  3. Overseas Expertise Introduction Project for Discipline Innovation [G20582017001]
  4. 'DoubleFirst Class' Initiative Project [CPU2018GF09]
  5. anming Project of Medicine in Shenzhen [SZSM201801060]

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The traditional Chinese medicine preparation Shengmai Yin and its components, especially red ginseng saponin extracts, showed significant effects in reducing serum cholesterol levels and aortic root plaque areas in mouse models of hypercholesteremia and atherosclerosis. The ginsenosides from Shengmai Yin were found to exert therapeutic effects by maintaining lipid homeostasis, particularly cholesterol and lysophosphatidylcholines.
Ethnopharmacological relevance: The traditional Chinese medicine (TCM) preparation, Shengmai Yin (SMY), is widely applied in cardiovascular disease treatments. However, the pharmacological mechanism of its therapeutic effects has not been fully clarified. Aim of this study: This study aimed to clearly define the efficacy and underlying mechanism of SMY and its active components in protecting against atherosclerosis. Materials and methods: The pharmacological effects of SMY and its components were evaluated upon a mouse hypercholesteremia model induced by a high cholesterol diet (HCD) for 12 weeks and Apoe- /- mice, a mouse atherosclerosis model. Pathological indicators including serum cholesterol levels, cytokines and histological changes in aortic root plaques were assessed. Untargeted metabolomic, untargeted lipidomic and targeted lipidomic changing profiles were investigated to clarify pharmacological mechanisms. Results: SMY and red ginseng crude extracts (GE) significantly decreased the serum cholesterol levels in hypercholesteremia mice and reduced the aortic root plaque areas and exerted antiatherogenic efficacy in Apoe- / - mice. Moreover, total red ginseng saponin extracts (TGS) showed the most apparent improvement on maintaining lipid homeostasis, representing the effects of red ginseng in SMY on atherosclerosis treatment. Mechanically, TGS inhibited serum secreted phospholipase A2 (sPLA2) activity and lowered the serum levels of lysophosphatidylcholine (lysoPC), which is a risk factor for atherosclerosis. Conclusions: Our findings revealed that ginsenosides from SMY exerted therapeutic effects on atherosclerosis by maintaining lipid homeostasis including cholesterol and lysoPCs.

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