Silibinin protects against sepsis and septic myocardial injury in an NR1H3-dependent pathway

Free Radic Biol Med. 2022 Jul:187:141-157. doi: 10.1016/j.freeradbiomed.2022.05.018. Epub 2022 May 28.

Abstract

Cardiac dysfunction resulting from sepsis causes high morbidity and mortality. Silibinin (SIL) is a secondary metabolite isolated from the seed extract of the milk thistle plant with various properties, including anti-inflammatory, anti-fibrotic, and anti-oxidative activities. This study, for the first time, examined the effects and mechanisms of SIL pretreatment, posttreatment and in combination with classical antibiotics in septic myocardial injury. The survival rate, sepsis score, anal temperature, routine blood parameters, blood biochemical parameters, cardiac function indicators, pathological indicators of myocardial injury, NR1H3 signaling pathway, and several sepsis-related signaling pathways were detected 8 h following cecal ligation and puncture (CLP). Our results showed that SIL pretreatment showed a significant protective effect on sepsis and septic myocardial injury, which was explained by the attenuation of inflammation, inhibition of oxidative stress, improvement of mitochondrial function, regulation of endoplasmic reticulum stress (ERS), and activation of the NR1H3 pathway. SIL posttreatment and the combination of SIL and azithromycin (AZI) showed a certain therapeutic effect. RNA-seq detection further clarified the myocardial protective mechanisms of SIL. Taken together, this study provides a theoretical basis for the application strategy and combination of SIL in septic myocardial injury.

Keywords: NR1H3; Posttreatment; Pretreatment; Sepsis; Septic myocardial injury; Silibinin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Endoplasmic Reticulum Stress
  • Heart Injuries* / pathology
  • Humans
  • Liver X Receptors / metabolism
  • Myocardium / metabolism
  • Sepsis* / complications
  • Silybin / metabolism
  • Silybin / pharmacology
  • Silybin / therapeutic use

Substances

  • Liver X Receptors
  • NR1H3 protein, human
  • Silybin