Angelica Injection Improves Functional Recovery and Motoneuron Maintenance with Increased Expression of Brain Derived Neurotrophic Factor and Nerve Growth Factor

被引:10
作者
Cui, Qin [1 ]
Zhang, Junjian [1 ]
Zhang, Lei [1 ]
Li, Ruiling [1 ]
Liu, Hui [1 ]
机构
[1] Wuhan Univ, Dept Neurol, Zhongnan Hosp, Wuhan 430071, Peoples R China
关键词
Sciatic nerve crush injury; angelica injection; sciatic function index; Brain Derived Neurotrophic Factor (BDNF); Nerve Growth Factor (NGF); DORSAL-ROOT GANGLION; RAT SCIATIC-NERVE; NEURITE OUTGROWTH; REGENERATION; MODEL; SINENSIS; NEURONS; INJURY;
D O I
10.2174/156720209788185641
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
This study assessed the neuroprotective effects of angelica injection in the rat sciatic nerve crush injury (SCI). Forty eight male Sprague Dawley rats were randomly divided into 4 groups: one was the sham group (S), which received sham surgery and given saline injection and the others were received SCI surgery and given saline injection, high and low dose angelica injection for 4 weeks, respectively. The sciatic functional index (SFI) in walking-track analysis, conductive velocity (CV), the number of fluorogold labeled motoneurons, and the expression patterns of brain derived neurotrophic factor (BDNF) and nerve growth factor (NGF) in the sciatic nerve and spine were examined. The results showed that SFI descended gradually on day 7, and dropped more quickly on day 28 in treatment groups (Low and High dose group). The CV in treatment groups was higher than control group (C). The numbers of motoneurons in treatment groups were larger than C group (P<0.05), but less than that in S group (P<0.01). The expressions of BDNF and NGF protein in the groups received SCI surgery were significantly lower than in S group, but the protein expressions in the groups received angelica injections were significantly higher than that in C group (P<0.01). These findings suggested that angelica injection can improve the sciatic nerve crush injury, and the mechanism might be through the increase of BDNF and NGF protein expression.
引用
收藏
页码:117 / 123
页数:7
相关论文
共 25 条
[1]   Induction of nerve growth factor mRNA in a rat dorsal root ganglion after application of a tourniquet [J].
Abe, S ;
Mizusawa, I ;
Kanno, K ;
Yabashi, A ;
Suto, M ;
Kuraya, M ;
Honda, T ;
Hiraiwa, K .
ACTA NEUROPATHOLOGICA, 2004, 108 (03) :183-188
[2]   NERVE CRUSH INJURIES - A MODEL FOR AXONOTMESIS [J].
BRIDGE, PM ;
BALL, DJ ;
MACKINNON, SE ;
NAKAO, Y ;
BRANDT, K ;
HUNTER, DA ;
HERTL, C .
EXPERIMENTAL NEUROLOGY, 1994, 127 (02) :284-290
[3]   Enhancing and regulating neurite outgrowth [J].
Calabrese, Edward J. .
CRITICAL REVIEWS IN TOXICOLOGY, 2008, 38 (04) :391-418
[4]   EFFECTS OF NERVE GROWTH-FACTOR ON CRUSHED SCIATIC-NERVE REGENERATION IN WATS [J].
CHEN, ZW ;
WANG, MS .
MICROSURGERY, 1995, 16 (08) :547-551
[5]   Brain-derived neurotrophic factor increases in the uninjured dorsal root ganglion neurons in selective spinal nerve ligation model [J].
Fukuoka, T ;
Kondo, E ;
Dai, Y ;
Hashimoto, N ;
Noguchi, K .
JOURNAL OF NEUROSCIENCE, 2001, 21 (13) :4891-4900
[6]   ENHANCEMENT OF MOTOR-NERVE REGENERATION BY NERVE GROWTH-FACTOR [J].
HE, CL ;
CHEN, ZW ;
CHEN, ZR .
MICROSURGERY, 1992, 13 (03) :151-154
[7]  
Liu Yu-min, 2004, Zhongguo Zhong Xi Yi Jie He Za Zhi, V24, P205
[8]   Long-term functional and morphological assessment of a standardized rat sciatic nerve crush injury with a non-serrated clamp [J].
Luis, A. L. ;
Amado, S. ;
Geuna, S. ;
Rodrigues, J. M. ;
Simoes, M. J. ;
Santos, J. D. ;
Fregnan, F. ;
Raimondo, S. ;
Veloso, A. Prieto ;
Ferreira, A. J. A. ;
Armada-da-Silva, P. A. S. ;
Varejao, A. S. P. ;
Mauricio, A. C. .
JOURNAL OF NEUROSCIENCE METHODS, 2007, 163 (01) :92-104
[9]   The role of neurotrophins in axonal growth, guidance, and regeneration [J].
Lykissas, Maricis G. ;
Batistatou, Anna K. ;
Charalabopoulos, Konstantinos A. ;
Beris, Alexandros E. .
CURRENT NEUROVASCULAR RESEARCH, 2007, 4 (02) :143-151
[10]   Immobilized concentration gradients of neurotrophic factors guide neurite outgrowth of primary neurons in macroporous scaffolds [J].
Moore, K ;
Macsween, M ;
Shoichet, M .
TISSUE ENGINEERING, 2006, 12 (02) :267-278