Antinociceptive and anti-inflammatory activities of ethanol-soluble acidic component from Ganoderma atrum by suppressing mannose receptor

The current study aimed to investigate antinociceptive and anti-inflammatory activities of ethanol-soluble acidic component from Ganoderma atrum (ESAC) and possible mechanisms involved. Our results showed that ESAC had significant abilities to relieve pain caused by thermal stimulation in mice. In the writhing response, ESAC could reduce the number of writhing responses induced by acetic acid in mice. Moreover, naloxone antagonized analgesic effects of ESAC and morphine, indicating that their analgesic effects might be achieved through opioid receptors. Subsequently, ESAC were found to control aberrant inflammation by reducing phagocytosis, nitric oxide (NO) and IL-1 beta in Lipopolysaccharides (LPS)-stimulated macrophages. Meanwhile, ESAC up-regulated antiinflammatory parameters IL-10 and mannose receptor (MR). Furthermore, a combination of MR inhibitor and ESAC significantly blocked these anti-inflammatory activities compare with ESAC alone. Collectively, ESAC was demonstrated to perform antinociceptive and anti-inflammatory capacities, indicating that MR played a key role in ESAC-mediated anti-inflammatory activities.

Automated summary

This study aimed to investigate the antinociceptive and anti-inflammatory activities of an ethanol-soluble acidic component from Ganoderma atrum and the possible mechanisms involved. The results showed that this component could relieve thermal pain in mice and reduce acetic acid-induced writhing responses. It was also found to control inflammation by reducing phagocytosis, nitric oxide, and IL-1 beta, while up-regulating IL-10 and mannose receptor. The study demonstrated the antinociceptive and anti-inflammatory capacities of this component, with a key role played by the mannose receptor.