Inhibitory activities of kukoamines A and B from Lycii Cortex on amyloid aggregation related to Alzheimer's disease and type 2 diabetes

J Nat Med. 2020 Jan;74(1):247-251. doi: 10.1007/s11418-019-01337-0. Epub 2019 Jul 2.

Abstract

Alzheimer's diseases (AD) and type 2 diabetes (T2D) are two age-related diseases characterized by amyloid fibrillogenesis. Prevention of amyloid aggregation is a promising therapeutic strategy for AD and T2D. Two spermine alkaloids, kukoamines A and B, isolated from Lycii Cortex (LyC) were investigated for their inhibitory effect on amyloid aggregation. Both kukoamines A and B inhibited aggregation of amyloid β (Aβ) and human islet amyloid polypeptide (hIAPP) in a dose-dependent manner. Kukoamine B showed stronger inhibitory activity than kukoamine A. These results on the inhibitory activity of kukoamines A and B on Aβ and hIAPP indicate that the catechol moiety is essential for inhibition of amyloid aggregation.

Keywords: Alzheimer’s disease; Amyloid aggregation; Kukoamines A and B; Lycii Cortex; Type 2 diabetes.

MeSH terms

  • Alzheimer Disease / pathology*
  • Amyloid beta-Peptides / metabolism*
  • Caffeic Acids / metabolism*
  • Catechols / chemistry
  • Diabetes Mellitus, Type 2 / pathology*
  • Humans
  • Islet Amyloid Polypeptide / metabolism*
  • Spermine / analogs & derivatives*
  • Spermine / metabolism

Substances

  • Amyloid beta-Peptides
  • Caffeic Acids
  • Catechols
  • Islet Amyloid Polypeptide
  • kukoamine A
  • kukoamine B
  • Spermine
  • catechol