Polysaccharide CM1 from Cordyceps militaris hinders adipocyte differentiation and alleviates hyperlipidemia in LDLR(+/-) hamsters

Lipids Health Dis. 2021 Dec 13;20(1):178. doi: 10.1186/s12944-021-01606-6.

Abstract

Background: Cordyceps militaris is cultured widely as an edible mushroom and accumulating evidence in mice have demonstrated that the polysaccharides of Cordyceps species have lipid-lowering effects. However, lipid metabolism in mice is significantly different from that in humans, making a full understanding of the mechanisms at play critical.

Methods: After 5 months, the hamsters were weighed and sampled under anesthesia after overnight fasting. The lipid-lowering effect and mechanisms of the polysaccharide CM1 was investigated by cellular and molecular technologies. Furthermore, the effect of the polysaccharide CM1 (100 μg/mL) on inhibiting adipocyte differentiation was investigated in vitro.

Results: CM1, a polysaccharide from C. militaris, significantly decreased plasma total cholesterol, triglyceride and epididymal fat index in LDLR(+/-) hamsters, which have a human-like lipid profile. After 5 months' administration, CM1 decreased the plasma level of apolipoprotein B48, modulated the expression of key genes and proteins in liver, small intestine, and epididymal fat. CM1 also inhibited preadipocyte differentiation in 3T3-L1 cells by downregulating the key genes involved in lipid droplet formation.

Conclusions: The polysaccharide CM1 lowers lipid and adipocyte differentiation by several pathways, and it has potential applications for hyperlipidemia prevention.

Keywords: Adipocyte; Hyperlipidemia; Lipid homeostasis; NPC1L1; Polysaccharide.

MeSH terms

  • Adipocytes / drug effects*
  • Animals
  • Cell Differentiation / drug effects*
  • Cordyceps / chemistry*
  • Cricetinae
  • Fungal Polysaccharides / pharmacology*
  • Fungal Polysaccharides / therapeutic use
  • Hyperlipidemias / drug therapy*
  • Immunoblotting
  • Male
  • Real-Time Polymerase Chain Reaction
  • Receptors, LDL / metabolism*

Substances

  • Fungal Polysaccharides
  • Receptors, LDL