Roles of NAD in Protection of Axon against Degeneration via SIRT1 Pathways

Axonal degeneration is a common pathological change of neurogenical disease which often arises before the neuron death. But it had not found any effective method to protect axon from degeneration. In this study we intended to confirm the protective effect of nicotinamide adenine dinucleotide (NAD),...

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Published inChinese journal of physiology Vol. 59; no. 2; p. 78
Main Authors Zhang, Jing, Guo, Wei-Hua, Qi, Xiao-Xia, Li, Gui-Bao, Hu, Yan-Lai, Wu, Qi, Ding, Zhao-Xi, Li, Hong-Yu, Hao, Jing, Sun, Jin-Hao
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LanguageEnglish
Published India 30.04.2016
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Abstract Axonal degeneration is a common pathological change of neurogenical disease which often arises before the neuron death. But it had not found any effective method to protect axon from degeneration. In this study we intended to confirm the protective effect of nicotinamide adenine dinucleotide (NAD), investigate the optimal administration dosage and time of NAD, and identify the relationship between silence signal regulating factor 1 (SIRT1) and axonal degeneration. An axonal degeneration model was established using dorsal root ganglion (DRG) neurons injured by vincristine to observe the protective effects of NAD to the injured axons. In addition, the potential contribution of the SIRT1 in axonal degeneration was also investigated. Through the 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, immunochemistry staining, axons counting and length measuring, transmission electron microscope (TEM) observation, we demonstrated that NAD played an important role in preventing axonal degeneration. Further study revealed that the expression of SIRT1 and phosphorylated Akt1 (p-Akt1) was up-regulated when NAD was added into the culturing medium. Taking together, our results demonstrated that NAD might delay the axonal degeneration through SIRT1/Akt1 pathways.
AbstractList Axonal degeneration is a common pathological change of neurogenical disease which often arises before the neuron death. But it had not found any effective method to protect axon from degeneration. In this study we intended to confirm the protective effect of nicotinamide adenine dinucleotide (NAD), investigate the optimal administration dosage and time of NAD, and identify the relationship between silence signal regulating factor 1 (SIRT1) and axonal degeneration. An axonal degeneration model was established using dorsal root ganglion (DRG) neurons injured by vincristine to observe the protective effects of NAD to the injured axons. In addition, the potential contribution of the SIRT1 in axonal degeneration was also investigated. Through the 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, immunochemistry staining, axons counting and length measuring, transmission electron microscope (TEM) observation, we demonstrated that NAD played an important role in preventing axonal degeneration. Further study revealed that the expression of SIRT1 and phosphorylated Akt1 (p-Akt1) was up-regulated when NAD was added into the culturing medium. Taking together, our results demonstrated that NAD might delay the axonal degeneration through SIRT1/Akt1 pathways.
Author Wu, Qi
Zhang, Jing
Hao, Jing
Qi, Xiao-Xia
Li, Gui-Bao
Ding, Zhao-Xi
Sun, Jin-Hao
Hu, Yan-Lai
Guo, Wei-Hua
Li, Hong-Yu
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Snippet Axonal degeneration is a common pathological change of neurogenical disease which often arises before the neuron death. But it had not found any effective...
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StartPage 78
SubjectTerms Animals
Antineoplastic Agents, Phytogenic - toxicity
Axons - drug effects
Axons - pathology
Cell Count
Ganglia, Spinal - cytology
Ganglia, Spinal - drug effects
NAD - metabolism
Nerve Degeneration - metabolism
Neurites - drug effects
Neuroprotective Agents - pharmacology
Phosphorylation
Proto-Oncogene Proteins c-akt - metabolism
Rats
Rats, Wistar
Signal Transduction - drug effects
Sirtuin 1 - drug effects
Vincristine - toxicity
Title Roles of NAD in Protection of Axon against Degeneration via SIRT1 Pathways
URI https://www.ncbi.nlm.nih.gov/pubmed/27080463
Volume 59
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