Cornflower Extract and Its Active Components Alleviate Dexamethasone-Induced Muscle Wasting by Targeting Cannabinoid Receptors and Modulating Gut Microbiota

Nutrients. 2024 Apr 11;16(8):1130. doi: 10.3390/nu16081130.

Abstract

Sarcopenia, a decline in muscle mass and strength, can be triggered by aging or medications like glucocorticoids. This study investigated cornflower (Centaurea cyanus) water extract (CC) as a potential protective agent against DEX-induced muscle wasting in vitro and in vivo. CC and its isolated compounds mitigated oxidative stress, promoted myofiber growth, and boosted ATP production in C2C12 myotubes. Mechanistically, CC reduced protein degradation markers, increased mitochondrial content, and activated protein synthesis signaling. Docking analysis suggested cannabinoid receptors (CB) 1 and 2 as potential targets of CC compounds. Specifically, graveobioside A from CC inhibited CB1 and upregulated CB2, subsequently stimulating protein synthesis and suppressing degradation. In vivo, CC treatment attenuated DEX-induced muscle wasting, as evidenced by enhanced grip strength, exercise performance, and modulation of muscle gene expression related to differentiation, protein turnover, and exercise performance. Moreover, CC enriched gut microbial diversity, and the abundance of Clostridium sensu stricto 1 positively correlated with muscle mass. These findings suggest a multifaceted mode of action for CC: (1) direct modulation of the muscle cannabinoid receptor system favoring anabolic processes and (2) indirect modulation of muscle health through the gut microbiome. Overall, CC presents a promising therapeutic strategy for preventing and treating muscle atrophy.

Keywords: Centaurea cyanus; cannabinoid receptors; dexamethasone; gut microbiota; muscle atrophy.

MeSH terms

  • Animals
  • Cell Line
  • Dexamethasone* / adverse effects
  • Dexamethasone* / pharmacology
  • Gastrointestinal Microbiome* / drug effects
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Muscle Fibers, Skeletal / drug effects
  • Muscle Fibers, Skeletal / metabolism
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / metabolism
  • Muscular Atrophy* / chemically induced
  • Muscular Atrophy* / drug therapy
  • Oxidative Stress / drug effects
  • Plant Extracts* / pharmacology
  • Receptor, Cannabinoid, CB1 / metabolism
  • Receptors, Cannabinoid / metabolism
  • Sarcopenia / drug therapy

Substances

  • Plant Extracts
  • Dexamethasone
  • Receptors, Cannabinoid
  • Receptor, Cannabinoid, CB1