Abstract

Alzheimer’s disease (AD) has become a major world health problem as the population ages. There is still no available treatment that can stop or reverse the progression of AD. Human amnion epithelial cells (hAECs), an alternative source for stem cells, have shown neuroprotective and neurorestorative potentials when transplanted in vivo. Besides, studies have suggested that stem cell priming with plant-derived bioactive compounds can enhance stem cell proliferation and differentiation and improve the disease-treating capability of stem cells. Verbenalin is an iridoid glucoside found in medicinal herbs of Verbenaceae family. In the present study, we have conducted microarray gene expression profiling of verbenalin-treated hAECs to explore its therapeutic potential for AD. Gene set enrichment analysis revealed verbenalin treatment significantly enriched AD-associated gene sets. Genes associated with lysosomal dysfunction, pathologic angiogenesis, pathologic protein aggregation, circadian rhythm, age-related neurometabolism, and neurogenesis were differentially expressed in the verbenalin-treated hAECs compared to control cells. Additionally, the neuroprotective effect of verbenalin was confirmed against amyloid beta-induced neurotoxicity in human neuroblastoma SH-SY5Y cells. Our present study is the first to report the therapeutic potential of verbenalin for AD; however, further in-depth research in the in vitro and in vivo models are required to confirm our preliminary findings.

Highlights

  • Alzheimer’s disease (AD) is a prevalent neurodegenerative disorder accounting for at least twothirds of cases of dementia in people aged 65 and over

  • Control Human amnion epithelial cells (hAECs) spheroids were maintained in the placental basal medium, and the treatment hAEC spheroids were treated with 20 μM of verbenalin for seven days

  • In the www.aging-us.com microarray analysis, we found that verbenalin treatment significantly downregulated the expression of epidermal growth factor (EGF) receptor (EGFR), and vascular endothelial growth factor B (VEGFB)

Read more

Summary

Introduction

Alzheimer’s disease (AD) is a prevalent neurodegenerative disorder accounting for at least twothirds of cases of dementia in people aged 65 and over. AD is characterized by progressive deterioration of cognitive function and memory [1]. Increasing age is the most important known risk factor for AD, a combination of genetic, lifestyle, and environmental factors contribute to the pathologic progress of AD [2]. It is projected that by 2050, the number of people living with AD and dementia would www.aging-us.com be over 100 million [3]. Continuing efforts are still required to develop medicines as well as novel, practical strategies that would slow the progression, halt, or prevent AD and other dementias and recover cognitive functions

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call