1. Academic Validation
  2. Membrane-Free Stem Cells and Pyridoxal 5'-Phosphate Synergistically Enhance Cognitive Function in Alzheimer's Disease Mouse Model

Membrane-Free Stem Cells and Pyridoxal 5'-Phosphate Synergistically Enhance Cognitive Function in Alzheimer's Disease Mouse Model

  • Antioxidants (Basel). 2022 Mar 21;11(3):601. doi: 10.3390/antiox11030601.
Ji Myung Choi 1 2 Hye Sook Park 1 3 Mei Tong He 1 Young Sil Kim 3 Hyun Young Kim 4 Ah Young Lee 4 Eun Ju Cho 1
Affiliations

Affiliations

  • 1 Department of Food Science and Nutrition, Pusan National University, Busan 46241, Korea.
  • 2 Department of Food Science and Biotechnology, Kyungsung University, Busan 48434, Korea.
  • 3 T-Stem Co., Ltd., Changwon 51573, Korea.
  • 4 Department of Food Science and Nutrition, Gyeongsang National University, Jinju 52828, Korea.
Abstract

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 Aβ25-35-injected AD mice. The ICR mice were i.c.v. injected with Aβ25-35 and then treated with MFSCE for 14 days (i.p.). The Aβ25-35-injected mice showed deficits in spatial and object perception abilities, whereas treatment with MFSCE inhibited Aβ25-35-induced learning and memory impairment in the T-maze, novel object recognition, and Morris water maze tests. Moreover, Aβ25-35-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 Aβ25-35-induced neuronal Apoptosis and amyloidogenesis, which contributes to cognitive improvement and has potential therapeutic implications for AD patients.

Keywords

Alzheimer’s disease; amyloid beta; cognitive ability; membrane-free stem cell; pyridoxal 5′-phosphate.

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