Blood-Brain Barrier Permeable and NO-Releasing Multifunctional Nanoparticles for Alzheimer's Disease Treatment: Targeting NO/cGMP/CREB Signaling Pathways

J Med Chem. 2021 Sep 23;64(18):13853-13872. doi: 10.1021/acs.jmedchem.1c01240. Epub 2021 Sep 13.

Abstract

The development of novel therapeutic strategies for combating Alzheimer's disease (AD) is challenging but imperative. Multifunctional nanoparticles are promising tools for regulating complex pathological dysfunctions for AD treatment. Herein, we constructed multifunctional nanoparticles consisting of regadenoson (Reg), nitric oxide (NO) donor, and YC-1 in a single molecular entity that can spontaneously self-assemble into nanoparticles and load donepezil to yield Reg-nanoparticles (Reg-NPs). The Reg moiety enabled the Reg-NPs to effectively regulate tight junction-associated proteins in the blood-brain barrier, thus facilitating the permeation of donepezil through the barrier and its accumulation in the brain. Moreover, the released NO and YC-1 activated the NO/cGMP/CREB signaling pathway by stimulating soluble guanylyl cyclase and inhibiting phosphodiesterase activity, which finally reduced cytotoxicity induced by aggregated Aβ in the neurons and was beneficial for synaptic plasticity and memory formation.

MeSH terms

  • Alzheimer Disease / drug therapy*
  • Alzheimer Disease / metabolism
  • Animals
  • Apoptosis / drug effects
  • Cell Line, Tumor
  • Donepezil / chemistry
  • Donepezil / pharmacology
  • Drug Carriers / chemistry
  • Drug Liberation
  • Humans
  • Indazoles / chemistry
  • Indazoles / pharmacology
  • Male
  • Memory / drug effects
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Multifunctional Nanoparticles / chemistry*
  • Neuronal Plasticity / drug effects
  • Neurons / drug effects
  • Neuroprotective Agents / chemistry
  • Neuroprotective Agents / pharmacology*
  • Nitric Oxide / metabolism
  • Nitric Oxide Donors / chemistry
  • Nitric Oxide Donors / pharmacology*
  • Nootropic Agents / chemistry
  • Nootropic Agents / pharmacology*
  • Oxadiazoles / chemistry
  • Oxadiazoles / pharmacology
  • Purines / chemistry
  • Purines / pharmacology
  • Pyrazoles / chemistry
  • Pyrazoles / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction / drug effects*

Substances

  • Drug Carriers
  • Indazoles
  • Neuroprotective Agents
  • Nitric Oxide Donors
  • Nootropic Agents
  • Oxadiazoles
  • Purines
  • Pyrazoles
  • regadenoson
  • Nitric Oxide
  • Donepezil