Emerging drugs for spinal cord injury

被引:45
作者
Baptiste, Darryl C. [3 ]
Fehlingst, Michael G. [1 ,2 ]
机构
[1] Univ Toronto, Toronto, ON M5T 2S8, Canada
[2] Toronto Western Res Inst, Krembil Neurosci Program, Toronto, ON M5T 2S8, Canada
[3] Univ Toronto, Toronto Western Hosp, Univ Hlth Network, Div Neurosurg,Krembil Neurosci Ctr, Toronto, ON M5T 2S8, Canada
关键词
acute spinal cord injury; apoptosis; clinical trials; neuroprotection; regeneration; pharmacological;
D O I
10.1517/14728214.13.1.63
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: This review summarizes several promising pharmacological approaches for the therapeutic management of traumatic spinal cord injury (SCI), which are either in early-phase clinical trials or nearing clinical translation. Objective: This review provides the reader with an understanding of the key pathophysiological mechanisms that contribute to neurological deficits after SCI. Through discussion of the mechanism(s) of action of the selected therapeutic approaches potentially important targets to aid further drug discovery will be highlighted. Methods: Systematic literature review of the pre-clinical literature and clinical SCI trials related to neuroprotective, immunomodulatory and regenerative therapeutic approaches. Results/conclusion: The next decade will witness an unprecedented number of clinical trials which will seek to translate key biomedical research discoveries. The promising drug-based therapeutic approaches include regenerative strategies to neutralize myelin-mediated neurite outgrowth inhibition, neuroprotective strategies to reduce apoptotic triggers, the targeting of cationic/glutamatergic toxicity, anti-inflammatory strategies and the use of approaches to stabilize disrupted cell membranes.
引用
收藏
页码:63 / 80
页数:18
相关论文
共 126 条
[1]   Inhibition of Fas-mediated apoptosis through administration of soluble Fas receptor improves functional outcome and reduces posttraumatic axonal degeneration after acute spinal cord injury [J].
Ackery, Alun ;
Robins, Sherri ;
Fehlings, Michael G. .
JOURNAL OF NEUROTRAUMA, 2006, 23 (05) :604-616
[2]  
AFTER S, 2004, J NEUROSCI, V24, P2182
[3]   The effect of the sodium channel blocker QX-314 on recovery after acute spinal cord injury [J].
Agrawal, SK ;
Fehlings, MG .
JOURNAL OF NEUROTRAUMA, 1997, 14 (02) :81-88
[4]  
Agrawal SK, 1996, J NEUROSCI, V16, P545
[5]   Targeting recovery: Priorities of the spinal cord-injured population [J].
Anderson, KD .
JOURNAL OF NEUROTRAUMA, 2004, 21 (10) :1371-1383
[6]  
[Anonymous], 2006, SPINAL CORD INJURY F
[7]  
AXONAL R, 1994, NEURON, V13, P757
[8]   Regeneration in the central nervous system [J].
Bandtlow, CE .
EXPERIMENTAL GERONTOLOGY, 2003, 38 (1-2) :79-86
[9]   Update on the treatment of spinal cord injury [J].
Baptiste, Darryl C. ;
Fehlings, Michael G. .
NEUROTRAUMA: NEW INSIGHTS INTO PATHOLOGY AND TREATMENT, 2007, 161 :217-233
[10]   Chondroitinase ABC promotes sprouting of intact and injured spinal systems after spinal cord injury [J].
Barritt, A. W. ;
Davies, M. ;
Marchand, F. ;
Hartley, R. ;
Grist, J. ;
Yip, P. ;
McMahon, S. B. ;
Bradbury, E. J. .
JOURNAL OF NEUROSCIENCE, 2006, 26 (42) :10856-10867