1. Academic Validation
  2. L-leucine promotes axonal outgrowth and regeneration via mTOR activation

L-leucine promotes axonal outgrowth and regeneration via mTOR activation

  • FASEB J. 2021 May;35(5):e21526. doi: 10.1096/fj.202001798RR.
Chao Ma  # 1 Long Teng  # 1 Ge Lin 1 Beibei Guo 1 Run Zhuo 1 Xiaowei Qian 1 Tuchen Guan 1 Ronghua Wu 1 Yan Liu 1 Mei Liu 1
Affiliations

Affiliation

  • 1 Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-innovation Center of Neuroregeneration, Nantong University, Nantong, China.
  • # Contributed equally.
Abstract

Discovering safe and effective drugs that promote neuron regeneration is an essential strategy for the recovery of central nervous system injuries. In this study, we found that L-leucine, an essential amino acid obtained from both supplements and food sources, could dramatically boost axonal outgrowth and regeneration. First, the effects of L-leucine on neurons were evaluated by cell Apoptosis, survival, and death assays, and the results showed no changes in these processes after treatment. By live cell imaging, L-leucine was found to remarkably increase axonal length and growth velocity after axotomy. We also verified that L-leucine enhanced p-mTOR/p-S6K activation in neurons by testing with an mTOR Inhibitor, rapamycin. Thereafter, we investigated the effects of L-leucine on the spinal cord injury in vivo. A mouse model of spinal cord hemi-section was established, and L-leucine was administered by tail intravenous injection. Basso mouse scale values revealed that L-leucine could improve functional recovery after injury. It was also notable that L-leucine treatment promoted axon growth across chondroitin sulfate proteoglycan (CSPG) areas. Furthermore, we used CSPGs as inhibitory environmental cues and clarified that L-leucine significantly enhanced axonal outgrowth and regeneration by promoting p-mTOR and p-S6K activation. Therefore, our study is the first to report that L-leucine promotes axonal regeneration in vitro and in vivo and could be candidate drug for axonal re-growth and nervous functional recovery.

Keywords

CSPGs; L-Leucine; axonal outgrowth; mTOR pathway; spinal cord injury.

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