中国神经再生研究(英文版) ›› 2019, Vol. 14 ›› Issue (11): 1961-1967.doi: 10.4103/1673-5374.259625

• 原著:脊髓损伤修复保护与再生 • 上一篇    下一篇

苦参碱促进神经环路重塑以改善慢性脊髓损伤小鼠的运动功能

  

  • 出版日期:2019-11-15 发布日期:2019-11-15
  • 基金资助:

    日本教育、文化、体育、科学和技术部的援助性探索性研究资助;富山大学自然医学研究所项目;日本富山县自然医学和生物技术研究项目

Matrine promotes neural circuit remodeling to regulate motor function in a mouse model of chronic spinal cord injury

Norio Tanabe, Tomoharu Kuboyama, Chihiro Tohda   

  1. Division of Neuromedical Science, Institute of Natural Medicine, University of Toyama, Toyama, Japan
  • Online:2019-11-15 Published:2019-11-15
  • Contact: Chihiro Tohda, PhD, chihiro@inm.u-toyama.ac.jp.
  • Supported by:

    This work was supported by a Grant-in-Aid for Challenging Exploratory Research (No. 26670044) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan (to CT), a Grant-in-Aid for a Cooperative Research Project from the Institute of Natural Medicine, University of Toyama, in 2014 and 2015 (to CT), and discretionary funds of the President of the University of Toyama, in 2014, 2015, and 2016 (to CT), and the Natural Medicine and Biotechnology Research of Toyama Prefecture, Japan (to CT).

摘要:

以往研究发现苦参碱通过直接激活细胞外热休克蛋白90诱导急性脊髓损伤小鼠的轴突生长和功能恢复,但其治疗慢性期脊髓损伤的效果尚未得到充分评估。为此,实验在小鼠脊髓损伤后28天开始每天一次灌胃苦参碱(100μmol/ kg /天),连续154天。结果发现苦参碱干预后,慢性脊髓损伤小鼠的后肢运动功能明显改善,受损脊髓中神经丝H阳性轴突的密度明显增加,与腰髓中胆碱乙酰转移酶阳性运动神经元bassoon阳性突触前密度也明显增加。结果显示出,苦参碱确实发挥了促进脊髓损伤小鼠神经回路重塑的作用,从而促进其后肢运动功能的恢复。

orcid: 0000-0002-5738-4258(Chihiro Tohda)

关键词: 苦参碱, 慢性脊髓损伤, 轴突生长, 突触, 后肢运动, 突触前, 免疫组化, Basso小鼠量表, 苦参

Abstract:

In chronic phase of spinal cord injury, functional recovery is more untreatable compared with early intervention in acute phase of spinal cord injury. In the last decade, several combination therapies successfully improved motor dysfunction in chronic spinal cord injury. However, their effectiveness is not sufficient. We previously found a new effective compound for spinal cord injury, matrine, which induced axonal growth and functional recovery in acute spinal cord injury mice via direct activation of extracellular heat shock protein 90. Although our previous study clarified that matrine was an activator of extracellular heat shock protein 90, the potential of matrine for spinal cord injury in chronic phase has not been sufficiently evaluated. Thus, this study aimed to investigate whether matrine ameliorates chronic spinal cord injury in mice. Once daily intragastric administration of matrine (100 μmol/kg per day) to spinal cord injury mice were starte at 28 days after injury, and continued for 154 days. Continuous matrine treatment improved hindlimb motor function in chronic spinal cord injury mice. In injured spinal cords of the matrine-treated mice, the density of neurofilament-H-positive axons was increased. Moreover, matrine treatment increased the density of bassoon-positive presynapses in contact with choline acetyltransferase-positive motor neurons in the lumbar spinal cord. These findings suggest that matrine promotes remodeling and reconnection of neural circuits to regulate hindlimb movement. All protocols were approved by the Committee for Animal Care and Use of the Sugitani Campus of the University of Toyama (approval No. A2013INM-1 and A2016INM-3) on May 7, 2013 and May 17, 2016, respectively.

Key words: matrine, chronic spinal cord injury, axonal growth, synaptogenesis, hindlimb locomotor, presynapse, immunohistochemistry, Basso Mouse Scale, Body Support Score, Sophora flavescens