The combination of peripheral nerve grafts and acidic fibroblast growth factor enhances arginase I and polyamine spermine expression in transected rat spinal cords

被引:35
作者
Kuo, Huai-Sheng
Tsai, May J.
Huang, Ming-Chao
Huang, Wen-Cheng
Lee, Meng-Jen
Kuo, Wen-Chun
You, Li-Hua
Szeto, Ka-Chun
Tsai, I-Lun
Chang, Wen-Chi
Chiu, Chuan-Wen
Ma, Hsu
Chak, Kin-Fu
Cheng, Henrich
机构
[1] Taipei Vet Gen Hosp, Neurol Inst, Dept Neurosurg, Neural Regenerat Lab, Taipei, Taiwan
[2] Taipei Vet Gen Hosp, Dept Neurosurg, Ctr Neural Regenerat, Taipei, Taiwan
[3] Taipei Med Univ, Sch Med, Taipei, Taiwan
[4] Natl Yang Ming Univ, Sch Med, Fac Med, Taipei 112, Taiwan
[5] Chaoyang Univ Technol, Grad Inst Biotechnol, Taichung, Taiwan
[6] Taipei Vet Gen Hosp, Dept Plast Surg, Taipei, Taiwan
[7] Natl Yang Ming Univ, Inst Biochem, Taipei 112, Taiwan
[8] Natl Yang Ming Univ, Sch Med, Dept Pharmacol, Taipei 112, Taiwan
[9] Natl Yang Ming Univ, Sch Med, Inst Pharmacol, Taipei 112, Taiwan
关键词
spinal cord; arginase I; acid fibroblast growth factor; peripheral nerve graft; alternatively activated macrophage; polyamine spermine; regeneration; neuron; rat;
D O I
10.1016/j.bbrc.2007.02.167
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Treatment with a combination of peripheral nerve grafts and acidic fibroblast growth factor improves hind limb locomotor function after spinal cord transection. This study examined the effect of treatment on expression of arginase I (Arg I) and polyamines. Arg I expression was low in the spinal cords of normal rats but increased following spinal injury. Only fully repaired spinal cords expressed higher Arg I levels, 6-14 days following repair. In 10-day repaired spinal cords, high Arg I immunoreactivity was detected in motoneurons and alternatively activated macrophages in the graft area and graft-stump edges, and high levels of the polyamine spermine were expressed by macrophages within the intercostal nerve graft. Thus, in addition to enhancing the expression of Arg I and spermine in repaired spinal cords, our treatment may recruit activated macrophages and create a more favorable environment for axonal regrowth. (c) 2007 Elsevier Inc All rights reserved.
引用
收藏
页码:1 / 7
页数:7
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