The Natural Compound Dansameum Reduces foam Cell Formation by Downregulating CD36 and Peroxisome Proliferator‑activated Receptor‑gamma; Expression

Background: Atherosclerosis‑induced vascular disorders are major causes of death in most western countries. During the development of atherosclerotic lesions, foam cell formation is essential and formed through the expression of CD36 and the peroxisome proliferator‑activated receptor gamma (PPAR‑γ). Objective: To investigate whether dansameum extract (DSE) could show anti‑atherosclerotic effect through down‑regulating cellular redox state including CD36 and PARP‑γ expression in oxidative low‑density lipoprotein (oxLDL)‑treated RAW264.7 cells and on differentiated foam cells in ApoE Knockout (ApoE‑/‑) mice. Materials and Methods: The Korean polyherbal medicine DSE was prepared from three plants in the following proportions: 40 g of Salvia miltiorrhiza root, 4 g of Amomumxanthioides fruit, and 4 g of Santalum album lignum. The immunohistochemistry and reverse transcription‑polymerase chain reaction was used for analysis of protein and mRNA involved in foam cell formation. Results: We first showed that effects of DSE on foam cell formation in both oxLDL‑induced RAW264.7 cells and in blood vessels from apolipoprotein E deficientApoE‑/‑ mice with high fat diet‑fed. DSE treatment significantly reduced the expression of CD36 and PPAR‑γ in oxLDL‑stimulated RAW264.7 cells and ApoE‑/‑mice, in the latter case by regulating heme oxygenase‑1. Furthermore, DSE treatment also reduced cellular lipid content in vitro and in vivo experiments. Conclusion: Our data suggest that DSE may have anti‑atherosclerotic properties through regulating foam cell formation.