San-wei-tan-xiang capsule attenuates atherosclerosis by increasing lysosomal activity in adipose tissue macrophages

J Ethnopharmacol. 2023 Aug 10:312:116444. doi: 10.1016/j.jep.2023.116444. Epub 2023 Apr 13.

Abstract

Ethnopharmacological relevance: Dyslipidemia is the leading risk factor of atherosclerosis (AS). Adipose tissue macrophages (ATMs) can regulate postprandial cholesterol levels via uptake and hydrolyzation of lipids and regulation of macrophage cholesterol efflux (MCE). San-wei-tan-xiang (SWTX) capsule, a Traditional Chinese medicine, exerts clinical benefits in patients with atherosclerotic cardiovascular diseases.

Aim of the study: This work is aimed to evaluate the chemical ingredients and mechanisms of SWTX in anti-AS.

Materials and methods: The chemical ingredients of SWTX identified by liquid chromatography coupled with tandem mass spectrometry were used for network pharmacological analysis. The atheroprotective function of SWTX was evaluated in ApoE-/- mice fed a cholesterol-enriched diet.

Results: The chemical ingredients identified in SWTX were predicated to be important for lipid metabolism and AS. Animals studies suggested that SWTX effectively attenuated the atherosclerotic plaque growth, elevated postprandial HDL cholesterol levels, elevated the proportion of Tim4 and CD36-expressed ATMs, and upregulated the uptake of lipid and lysosomal activity in ATMs. SWTX-induced elevation of postprandial HDL cholesterol levels was dependent on increased lysosomal activity, since chloroquine, an inhibitor of lysosomal function, blocked the effect of SWTX. Lastly, some predicated bioactive compounds in SWTX can elevate lysosomal activity in vitro.

Conclusion: SWTX could attenuate atherosclerotic plaque formation by elevating lysosomal activity and enhancing MCE in ATMs.

Keywords: Adipose tissue macrophage; Atherosclerosis; Lysosomal activity; Postprandial cholesterol level; San-wei-tan-xiang capsule.

MeSH terms

  • Animals
  • Apolipoproteins E
  • Atherosclerosis* / drug therapy
  • Atherosclerosis* / etiology
  • Atherosclerosis* / prevention & control
  • Cholesterol / metabolism
  • Cholesterol, HDL
  • Lysosomes / metabolism
  • Macrophages
  • Mice
  • Plaque, Atherosclerotic* / metabolism

Substances

  • Cholesterol, HDL
  • Cholesterol
  • Apolipoproteins E