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Nicotinamide phosphoribosyltransferase‑related signaling pathway in early Alzheimer's disease mouse models

  • Authors:
    • Sanli Xing
    • Yiran Hu
    • Xujiao Huang
    • Dingzhu Shen
    • Chuan Chen
  • View Affiliations / Copyright

    Affiliations: Shanghai Geriatric Institute of Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 200031, P.R. China
    Copyright: © Xing et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 5163-5171
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    Published online on: October 30, 2019
       https://doi.org/10.3892/mmr.2019.10782
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Abstract

Alzheimer's disease (AD) is a neurodegenerative disease of the central nervous system that is characterized by progressive cognitive dysfunction and which ultimately leads to dementia. Studies have shown that energy dysmetabolism contributes significantly to the pathogenesis of a variety of aging‑associated diseases and degenerative diseases of the nervous system, including AD. One focus of research thus has been how to regulate the expression of nicotinamide phosphoribosyltransferase (NAMPT) to prevent against neurodegenerative diseases. Therefore, the present study used 6‑month‑old APPswe/PS1ΔE9 (APP/PS1) transgenic mice as early AD mouse models and sought to evaluate nicotinamide adenine dinucleotide (NAD+) and FK866 (a NAMPT inhibitor) treatment in APP/PS1 mice to study NAMPT dysmetabolism in the process of AD and elucidate the underlying mechanisms. As a result of this treatment, the expression of NAMPT decreased, the synthesis of ATP and NAD+ became insufficient and the NAD+/NADH ratio was reduced. The administration of NAD+ alleviated the spatial learning and memory of APP/PS1 mice and reduced senile plaques. Administration of NAD+ may also increase the expression of the key protein NAMPT and its related protein sirtuin 1 as well as the synthesis of NAD+. Therefore, increasing NAMPT expression levels may promote NAD+ production. Their regulation could form the basis for a new therapeutic strategy.
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Copy and paste a formatted citation
Spandidos Publications style
Xing S, Hu Y, Huang X, Shen D and Chen C: Nicotinamide phosphoribosyltransferase‑related signaling pathway in early Alzheimer's disease mouse models. Mol Med Rep 20: 5163-5171, 2019.
APA
Xing, S., Hu, Y., Huang, X., Shen, D., & Chen, C. (2019). Nicotinamide phosphoribosyltransferase‑related signaling pathway in early Alzheimer's disease mouse models. Molecular Medicine Reports, 20, 5163-5171. https://doi.org/10.3892/mmr.2019.10782
MLA
Xing, S., Hu, Y., Huang, X., Shen, D., Chen, C."Nicotinamide phosphoribosyltransferase‑related signaling pathway in early Alzheimer's disease mouse models". Molecular Medicine Reports 20.6 (2019): 5163-5171.
Chicago
Xing, S., Hu, Y., Huang, X., Shen, D., Chen, C."Nicotinamide phosphoribosyltransferase‑related signaling pathway in early Alzheimer's disease mouse models". Molecular Medicine Reports 20, no. 6 (2019): 5163-5171. https://doi.org/10.3892/mmr.2019.10782
Copy and paste a formatted citation
x
Spandidos Publications style
Xing S, Hu Y, Huang X, Shen D and Chen C: Nicotinamide phosphoribosyltransferase‑related signaling pathway in early Alzheimer's disease mouse models. Mol Med Rep 20: 5163-5171, 2019.
APA
Xing, S., Hu, Y., Huang, X., Shen, D., & Chen, C. (2019). Nicotinamide phosphoribosyltransferase‑related signaling pathway in early Alzheimer's disease mouse models. Molecular Medicine Reports, 20, 5163-5171. https://doi.org/10.3892/mmr.2019.10782
MLA
Xing, S., Hu, Y., Huang, X., Shen, D., Chen, C."Nicotinamide phosphoribosyltransferase‑related signaling pathway in early Alzheimer's disease mouse models". Molecular Medicine Reports 20.6 (2019): 5163-5171.
Chicago
Xing, S., Hu, Y., Huang, X., Shen, D., Chen, C."Nicotinamide phosphoribosyltransferase‑related signaling pathway in early Alzheimer's disease mouse models". Molecular Medicine Reports 20, no. 6 (2019): 5163-5171. https://doi.org/10.3892/mmr.2019.10782
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