Natural Dietary Supplementation of Anthocyanins via PI3K/Akt/Nrf2/HO-1 Pathways Mitigate Oxidative Stress, Neurodegeneration, and Memory Impairment in a Mouse Model of Alzheimer's Disease

Mol Neurobiol. 2018 Jul;55(7):6076-6093. doi: 10.1007/s12035-017-0798-6. Epub 2017 Nov 23.

Abstract

Well-established studies have shown an elevated level of reactive oxygen species (ROS) that induces oxidative stress in the Alzheimer's disease (AD) patient's brain and an animal model of AD. Herein, we investigated the underlying anti-oxidant neuroprotective mechanism of natural dietary supplementation of anthocyanins extracted from Korean black beans in the amyloid precursor protein/presenilin-1 (APP/PS1) mouse model of AD. Both in vivo (APP/PS1 mice) and in vitro (mouse hippocampal HT22 cells) results demonstrated that anthocyanins regulate the phosphorylated-phosphatidylinositol 3-kinase-Akt-glycogen synthase kinase 3 beta (p-PI3K/Akt/GSK3β) pathways and consequently attenuate amyloid beta oligomer (AβO)-induced elevations in ROS level and oxidative stress via stimulating the master endogenous anti-oxidant system of nuclear factor erythroid 2-related factor 2 (Nrf2) and heme oxygenase-1 (Nrf2/HO-1) pathways and prevent apoptosis and neurodegeneration by suppressing the apoptotic and neurodegenerative markers such as activation of caspase-3 and PARP-1 expression as well as the TUNEL and Fluoro-Jade B-positive neuronal cells in the APP/PS1 mice. In vitro ApoTox-Glo™ Triplex assay results also showed that anthocyanins act as a potent anti-oxidant neuroprotective agent and reduce AβO-induced neurotoxicity in the HT22 cells via PI3K/Akt/Nrf2 signaling. Importantly, anthocyanins improve memory-related pre- and postsynaptic protein markers and memory functions in the APP/PS1 mice. In conclusion, our data suggested that consumption and supplementation of natural-derived anti-oxidant neuroprotective agent such as anthocyanins may be beneficial and suggest new dietary-supplement strategies for intervention in and prevention of progressive neurodegenerative diseases, such as AD.

Keywords: APP/PS1; Alzheimer’s disease (AD); Anthocyanins; Memory functions; Neurodegeneration; Nrf2/HO-1 pathway; Oxidative stress; Pre- and postsynaptic protein markers; Reactive oxygen species (ROS); p-PI3K/Akt/GSK3β pathways.

MeSH terms

  • Alzheimer Disease / complications
  • Alzheimer Disease / drug therapy*
  • Alzheimer Disease / genetics
  • Alzheimer Disease / physiopathology
  • Amyloid beta-Peptides / metabolism
  • Animals
  • Anthocyanins / pharmacology
  • Anthocyanins / therapeutic use*
  • Biomarkers / metabolism
  • Cell Line
  • Cell Nucleus / metabolism
  • Dietary Supplements*
  • Disease Models, Animal
  • Gene Expression Regulation
  • Heme Oxygenase-1 / metabolism
  • Humans
  • Male
  • Memory Disorders / complications
  • Memory Disorders / drug therapy*
  • Memory Disorders / genetics
  • Memory Disorders / physiopathology
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • NF-E2-Related Factor 2 / metabolism
  • Nerve Degeneration / drug therapy*
  • Nerve Degeneration / pathology
  • Nerve Degeneration / physiopathology
  • Oxidative Stress* / drug effects
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Reactive Oxygen Species / metabolism
  • Signal Transduction*

Substances

  • Amyloid beta-Peptides
  • Anthocyanins
  • Biomarkers
  • NF-E2-Related Factor 2
  • Reactive Oxygen Species
  • Heme Oxygenase-1
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt