Improving peripheral nerve regeneration: From molecular mechanisms to potential therapeutic targets

被引:143
作者
Chan, K. Ming [1 ,2 ]
Gordon, Tessa [1 ,2 ,3 ]
Zochodne, Douglas W. [4 ]
Power, Hollie A. [5 ]
机构
[1] Univ Alberta, Div Phys Med & Rehabil, Edmonton, AB T6G 2E1, Canada
[2] Univ Alberta, Ctr Neurosci, Edmonton, AB T6G 2E1, Canada
[3] Univ Toronto, Div Plast Surg, Toronto, ON, Canada
[4] Univ Calgary, Dept Clin Neurosci, Calgary, AB, Canada
[5] Univ Alberta, Div Plast Surg, Edmonton, AB T6G 2E1, Canada
关键词
Peripheral nerve injury; Nerve regeneration; Therapeutics; Molecular mechanisms; Animal studies; ACETYL-L-CARNITINE; POOR FUNCTIONAL RECOVERY; GENE-RELATED PEPTIDE; SCHWANN-CELL; AXONAL REGENERATION; DOUBLE-BLIND; GROWTH CONE; CYCLIC-AMP; WALLERIAN DEGENERATION; NEUROTROPHIC FACTOR;
D O I
10.1016/j.expneurol.2014.09.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Peripheral nerve injury is common especially among young individuals. Although injured neurons have the ability to regenerate, the rate is slow and functional outcomes are often poor. Several potential therapeutic agents have shown considerable promise for improving the survival and regenerative capacity of injured neurons. These agents are reviewed within the context of their molecular mechanisms. The PI3K/Akt and Ras/ERK signaling cascades play a key role in neuronal survival. A number of agents that target these pathways, including erythropoietin, tacrolimus, acetyl-L-carnitine, n-acetylcysteine and geldanamycin have been shown to be effective. Trk receptor signaling events that up-regulate cAMP play an important role in enhancing the rate of axonal outgrowth. Agents that target this pathway including rolipram, testosterone, fasudil, ibuprofen and chondroitinase ABC hold considerable promise for human application. A tantalizing prospect is to combine different molecular targeting strategies in complementary pathways to optimize their therapeutic effects. Although further study is needed prior to human trials, these modalities could open a new horizon in the clinical arena that has so far been elusive. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:826 / 835
页数:10
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