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Membrane-Free Stem Cells and Pyridoxal 5′-Phosphate Synergistically Enhance Cognitive Function in Alzheimer’s Disease Mouse Model
Accumulation of amyloid beta (Aβ) is a major pathological hallmark of Alzheimer’s disease (AD). In this study, we evaluated the protective effect of membrane-free stem cell extract (MFSCE), which is a component of adipose-tissue-derived stem cells, on cognitive impairment in Aβ(25–35)-injected AD mi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945526/ https://www.ncbi.nlm.nih.gov/pubmed/35326251 http://dx.doi.org/10.3390/antiox11030601 |
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author | Choi, Ji Myung Park, Hye Sook He, Mei Tong Kim, Young Sil Kim, Hyun Young Lee, Ah Young Cho, Eun Ju |
author_facet | Choi, Ji Myung Park, Hye Sook He, Mei Tong Kim, Young Sil Kim, Hyun Young Lee, Ah Young Cho, Eun Ju |
author_sort | Choi, Ji Myung |
collection | PubMed |
description | Accumulation of amyloid beta (Aβ) is a major pathological hallmark of Alzheimer’s disease (AD). In this study, we evaluated the protective effect of membrane-free stem cell extract (MFSCE), which is a component of adipose-tissue-derived stem cells, on cognitive impairment in Aβ(25–35)-injected AD mice. The ICR mice were i.c.v. injected with Aβ(25–35) and then treated with MFSCE for 14 days (i.p.). The Aβ(25–35)-injected mice showed deficits in spatial and object perception abilities, whereas treatment with MFSCE inhibited Aβ(25–35)-induced learning and memory impairment in the T-maze, novel object recognition, and Morris water maze tests. Moreover, Aβ(25–35)-induced lipid peroxidation and nitric oxide overproduction were attenuated by treatment with MFSCE. These antioxidant effects of MFSCE were related to the inhibition of the apoptotic signaling pathway. In particular, the combination treatment of MFSCE and pyridoxal 5′-phosphate (PLP) showed greater suppression of Bax and cleaved caspase-3 protein expression compared to the MFSCE- or PLP-only treatment. Furthermore, the MFSCE and PLP combination significantly downregulated the amyloidogenic-pathway-related protein expressions, such as amyloid precursor protein, presenilin 1, and presenilin 2. Therefore, the MFSCE and PLP combination may synergistically prevent Aβ(25–35)-induced neuronal apoptosis and amyloidogenesis, which contributes to cognitive improvement and has potential therapeutic implications for AD patients. |
format | Online Article Text |
id | pubmed-8945526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89455262022-03-25 Membrane-Free Stem Cells and Pyridoxal 5′-Phosphate Synergistically Enhance Cognitive Function in Alzheimer’s Disease Mouse Model Choi, Ji Myung Park, Hye Sook He, Mei Tong Kim, Young Sil Kim, Hyun Young Lee, Ah Young Cho, Eun Ju Antioxidants (Basel) Article Accumulation of amyloid beta (Aβ) is a major pathological hallmark of Alzheimer’s disease (AD). In this study, we evaluated the protective effect of membrane-free stem cell extract (MFSCE), which is a component of adipose-tissue-derived stem cells, on cognitive impairment in Aβ(25–35)-injected AD mice. The ICR mice were i.c.v. injected with Aβ(25–35) and then treated with MFSCE for 14 days (i.p.). The Aβ(25–35)-injected mice showed deficits in spatial and object perception abilities, whereas treatment with MFSCE inhibited Aβ(25–35)-induced learning and memory impairment in the T-maze, novel object recognition, and Morris water maze tests. Moreover, Aβ(25–35)-induced lipid peroxidation and nitric oxide overproduction were attenuated by treatment with MFSCE. These antioxidant effects of MFSCE were related to the inhibition of the apoptotic signaling pathway. In particular, the combination treatment of MFSCE and pyridoxal 5′-phosphate (PLP) showed greater suppression of Bax and cleaved caspase-3 protein expression compared to the MFSCE- or PLP-only treatment. Furthermore, the MFSCE and PLP combination significantly downregulated the amyloidogenic-pathway-related protein expressions, such as amyloid precursor protein, presenilin 1, and presenilin 2. Therefore, the MFSCE and PLP combination may synergistically prevent Aβ(25–35)-induced neuronal apoptosis and amyloidogenesis, which contributes to cognitive improvement and has potential therapeutic implications for AD patients. MDPI 2022-03-21 /pmc/articles/PMC8945526/ /pubmed/35326251 http://dx.doi.org/10.3390/antiox11030601 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Choi, Ji Myung Park, Hye Sook He, Mei Tong Kim, Young Sil Kim, Hyun Young Lee, Ah Young Cho, Eun Ju Membrane-Free Stem Cells and Pyridoxal 5′-Phosphate Synergistically Enhance Cognitive Function in Alzheimer’s Disease Mouse Model |
title | Membrane-Free Stem Cells and Pyridoxal 5′-Phosphate Synergistically Enhance Cognitive Function in Alzheimer’s Disease Mouse Model |
title_full | Membrane-Free Stem Cells and Pyridoxal 5′-Phosphate Synergistically Enhance Cognitive Function in Alzheimer’s Disease Mouse Model |
title_fullStr | Membrane-Free Stem Cells and Pyridoxal 5′-Phosphate Synergistically Enhance Cognitive Function in Alzheimer’s Disease Mouse Model |
title_full_unstemmed | Membrane-Free Stem Cells and Pyridoxal 5′-Phosphate Synergistically Enhance Cognitive Function in Alzheimer’s Disease Mouse Model |
title_short | Membrane-Free Stem Cells and Pyridoxal 5′-Phosphate Synergistically Enhance Cognitive Function in Alzheimer’s Disease Mouse Model |
title_sort | membrane-free stem cells and pyridoxal 5′-phosphate synergistically enhance cognitive function in alzheimer’s disease mouse model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945526/ https://www.ncbi.nlm.nih.gov/pubmed/35326251 http://dx.doi.org/10.3390/antiox11030601 |
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