Peptides Derived from Growth Factors to Treat Alzheimer's Disease

Int J Mol Sci. 2021 Jun 4;22(11):6071. doi: 10.3390/ijms22116071.

Abstract

Alzheimer's disease (AD) is a devastating neurodegenerative disease characterized by progressive neuron losses in memory-related brain structures. The classical features of AD are a dysregulation of the cholinergic system, the accumulation of amyloid plaques, and neurofibrillary tangles. Unfortunately, current treatments are unable to cure or even delay the progression of the disease. Therefore, new therapeutic strategies have emerged, such as the exogenous administration of neurotrophic factors (e.g., NGF and BDNF) that are deficient or dysregulated in AD. However, their low capacity to cross the blood-brain barrier and their exorbitant cost currently limit their use. To overcome these limitations, short peptides mimicking the binding receptor sites of these growth factors have been developed. Such peptides can target selective signaling pathways involved in neuron survival, differentiation, and/or maintenance. This review focuses on growth factors and their derived peptides as potential treatment for AD. It describes (1) the physiological functions of growth factors in the brain, their neuronal signaling pathways, and alteration in AD; (2) the strategies to develop peptides derived from growth factor and their capacity to mimic the role of native proteins; and (3) new advancements and potential in using these molecules as therapeutic treatments for AD, as well as their limitations.

Keywords: MAPK; PI3K/AKT; amyloid-β peptide; bone morphogenetic proteins; cholinergic neurons; metabolic pathway; neurotrophin; tau protein.

Publication types

  • Review

MeSH terms

  • Alzheimer Disease / drug therapy*
  • Alzheimer Disease / metabolism
  • Animals
  • Humans
  • Intercellular Signaling Peptides and Proteins / pharmacology*
  • Peptide Fragments / pharmacology*

Substances

  • Intercellular Signaling Peptides and Proteins
  • Peptide Fragments