Back to Search Start Over

Intranasal administration of human adipose-derived stem cell-conditioned media ameliorates cognitive performance in a rat model of Alzheimer’s disease.

Authors :
Shaker, Seyed Amir
Parsaei, Houman
Amini, Nasser
Nobakht, Maliheh
Babaei, Javad Fahanik
Dadseresht, Ali
Seidkhani, Elham
Eftekharzadeh, Mina
Source :
Physiology & Pharmacology. Mar2024, Vol. 28 Issue 1, p43-55. 13p.
Publication Year :
2024

Abstract

Introduction: Alzheimer’s disease (AD) is an age-related disorder, characterized by the gradual loss of memory and cognitive function owing to neuronal damage and brain shrinkage. This study aimed to investigate how intranasal injection of human adiposederived stem cell-conditioned media (hADSC-CM) ameliorates cognitive performance and affects the level of estrogen receptor beta (Erβ) in the hippocampus of rats in an AD model. Methods: A total of 32 male rats were divided into four groups, including the control, AD model, hADSC-CM, and vehicle groups. The Morris water maze was used to assess the animals’ behavioral changes. Moreover, Nissl and Thioflavin-S staining were performed to evaluate the histology of the hippocampus. Immunohistochemistry was also carried out to evaluate the expression level of Erβ. Results: The intranasal injection of hADSC-CM improved the rats’ cognitive performance by reducing the number of dark cells and beta-amyloid plaques in the hippocampus in the AD model. Besides, the intranasal injection of hADSC-CM increased the level of Erβ in this model. Conclusion: The present findings indicated that the intranasal injection of hADSC-CM ameliorated cognitive function. Amyloid plaques and dark cells also diminished in the CA1 area of the hippocampus. Moreover, the expression level of ERβ increased. It can be concluded that hADSC-CM has significant treatment benefits for AD in rats. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17350581
Volume :
28
Issue :
1
Database :
Academic Search Index
Journal :
Physiology & Pharmacology
Publication Type :
Academic Journal
Accession number :
177301956
Full Text :
https://doi.org/10.61186/phypha.28.1.43