Non-polyphenolic natural inhibitors of amyloid aggregation

Eur J Med Chem. 2020 Apr 15:192:112197. doi: 10.1016/j.ejmech.2020.112197. Epub 2020 Mar 5.

Abstract

Protein misfolding diseases (PMDs) are chronic and progressive, with no effective therapy so far. Aggregation and misfolding of amyloidogenic proteins are closely associated with the onset and progression of PMDs, such as amyloid-β (Aβ) in Alzheimer's disease, α-Synuclein (α-Syn) in Parkinson's disease and human islet amyloid polypeptide (hIAPP) in type 2 diabetes. Inhibiting toxic aggregation of amyloidogenic proteins is regarded as a promising therapeutic approach in PMDs. The past decade has witnessed the rapid progresses of this field, dozens of inhibitors have been screened and verified in vitro and in vivo, demonstrating inhibitory effects against the aggregation and misfolding of amyloidogenic proteins, together with beneficial effects. Natural products are major sources of small molecule amyloid inhibitors, a number of natural derived compounds have been identified with great bioactivities and translational prospects. Here, we review the non-polyphenolic natural inhibitors that potentially applicable for PMDs treatment, along with their working mechanisms. Future directions are proposed for the development and clinical applications of these inhibitors.

Keywords: Amyloidogenic protein; Inhibitor; Non-polyphenolic natural products; Protein aggregation; Protein misfolding disease.

Publication types

  • Review

MeSH terms

  • Amyloidogenic Proteins / antagonists & inhibitors*
  • Amyloidogenic Proteins / metabolism
  • Biological Products / chemistry
  • Biological Products / pharmacology*
  • Humans
  • Molecular Structure
  • Protein Aggregates / drug effects
  • Proteostasis Deficiencies / drug therapy*
  • Proteostasis Deficiencies / metabolism

Substances

  • Amyloidogenic Proteins
  • Biological Products
  • Protein Aggregates