Structure-activity relationship and biological evaluation of berberine derivatives as PCSK9 down-regulating agents

Bioorg Chem. 2021 Aug:113:104994. doi: 10.1016/j.bioorg.2021.104994. Epub 2021 May 18.

Abstract

Proprotein convertase subtilisin/kexin type 9 (PCSK9) is a secreted protein and its deficiency markedly enhanced the survival rate of patient with cardiovascular diseases (CVDs). Forty berberine (BBR) derivatives were synthesized and evaluated for their activities on down-regulating the transcription of PCSK9 in HepG2 cells, taking BBR as the lead. Structure-activity relationship (SAR) analysis revealed that 2,3-dimethoxy moiety might be beneficial for activity. Among them, 9k displayed the most potent activity with IC50 value of 9.5 ± 0.5 μM, better than that of BBR. Also, it significantly decreased PCSK9 protein level at cellular level, as well as in the liver and serum of mice in vivo. Furthermore, 9k markedly increased LDLR expression and LDL-C clearance via down-regulating PCSK9 protein. The mechanism of action of 9k is targeting HNF1α and/or Sp1 cluster modulation upstream of PCSK9, a different one from BBR. Therefore, 9k might have the potential to be a novel PCSK9 transcriptional inhibitor for the treatment of atherosclerosis, worthy for further investigation.

Keywords: Berberine; LDL-C; PCSK9; Structure–activity relationship; Transcriptional inhibition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Berberine / chemical synthesis
  • Berberine / chemistry
  • Berberine / pharmacology*
  • Dose-Response Relationship, Drug
  • Down-Regulation / drug effects*
  • Enzyme Inhibitors / chemical synthesis
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Molecular Structure
  • PCSK9 Inhibitors*
  • Proprotein Convertase 9 / metabolism
  • Structure-Activity Relationship

Substances

  • Enzyme Inhibitors
  • PCSK9 Inhibitors
  • Berberine
  • PCSK9 protein, human
  • Proprotein Convertase 9