GSK-3 Inhibitor Promotes Neuronal Cell Regeneration and Functional Recovery in a Rat Model of Spinal Cord Injury

被引:17
|
作者
Lei, Fei [1 ,2 ]
He, Wen [3 ]
Tian, Xinggui [2 ]
Zhou, Qingzhong [2 ]
Zheng, Lipeng [2 ]
Kang, Jianping [2 ]
Song, Yueming [1 ]
Feng, Daxiong [2 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Orthoped Surg, 37 Guoxue St, Chengdu 610041, Sichuan, Peoples R China
[2] Southwest Med Univ, Dept Spine Surg, Affiliated Hosp, 25 Taiping St, Luzhou 646000, Sichuan, Peoples R China
[3] Southwest Med Univ, Dept Lib, 1 Xianglin Rd, Luzhou 646000, Sichuan, Peoples R China
关键词
AXONAL REGENERATION; INDUCED APOPTOSIS; GROWTH-FACTOR; PATHWAY; PROTEIN; INACTIVATION; INVOLVEMENT; MECHANISMS;
D O I
10.1155/2019/9628065
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The reparative process following spinal cord injury (SCI) is extremely complicated. Cells in the microenvironment express multiple inhibitory factors that affect axonal regeneration over a prolonged period of time. The axon growth inhibitory factor glycogen synthase kinase-3 (GSK-3) is an important factor during these processes. TDZD-8 (4-benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione) is the most effective and specific non-ATP-competitive inhibitor of GSK-3. Here, we show that administering TDZD-8 after SCI was associated with significantly inhibited neuronal apoptosis, upregulated GAP-43 expression, increased density of cortical spinal tract fibers around areas of injury, and increased Basso, Beattie, and Bresnahan (BBB) scores in the lower limbs. These findings support the notion that GSK-3 inhibitors promote neuronal cell regeneration and lower limb functional recovery.
引用
收藏
页数:8
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