Investigational agents for treatment of traumatic brain injury

被引:70
作者
Xiong, Ye [1 ]
Zhang, Yanlu [1 ]
Mahmood, Asim [1 ]
Chopp, Michael [2 ,3 ]
机构
[1] Henry Ford Hosp, Dept Neurosurg, Educ & Res Bldg,Room 3096,2799 West Grand Blvd, Detroit, MI 48202 USA
[2] Henry Ford Hosp, Dept Neurol, Detroit, MI 48202 USA
[3] Oakland Univ, Dept Phys, Rochester, MI 48309 USA
关键词
angiogenesis; cell therapy; exosomes; microRNAs; neurogenesis; neuroprotection; neurorestoration; traumatic brain injury; MARROW STROMAL CELLS; NERVE GROWTH-FACTOR; INTERLEUKIN-1 RECEPTOR ANTAGONIST; TISSUE-PLASMINOGEN ACTIVATOR; CONTROLLED CORTICAL IMPACT; VASCULAR OCCLUSIVE EVENTS; MESENCHYMAL STEM-CELLS; SEX STEROID-HORMONES; TRANEXAMIC ACID; CYCLOSPORINE-A;
D O I
10.1517/13543784.2015.1021919
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Traumatic brain injury (TBI) is a major cause of death and disability worldwide. To date, there are no pharmacologic agents proven to improve outcomes from TBI because all the Phase III clinical trials in TBI have failed. Thus, there is a compelling need to develop treatments for TBI. Areas covered: The following article provides an overview of select cell-based and pharmacological therapies under early development for the treatment of TBI. These therapies seek to enhance cognitive and neurological functional recovery through neuroprotective and neurorestorative strategies. Expert opinion: TBI elicits both complex degenerative and regenerative tissue responses in the brain. TBI can lead to cognitive, behavioral, and motor deficits. Although numerous promising neuroprotective treatment options have emerged from preclinical studies that mainly target the lesion, translation of preclinical effective neuroprotective drugs to clinical trials has proven challenging. Accumulating evidence indicates that the mammalian brain has a significant, albeit limited, capacity for both structural and functional plasticity, as well as regeneration essential for spontaneous functional recovery after injury. A new therapeutic approach is to stimulate neurovascular remodeling by enhancing angiogenesis, neurogenesis, oligodendrogenesis, and axonal sprouting, which in concert, may improve neurological functional recovery after TBI.
引用
收藏
页码:743 / 760
页数:18
相关论文
共 191 条
[1]   Tissue Plasminogen Activator (tPA) and Matrix Metalloproteinases in the Pathogenesis of Stroke: Therapeutic Strategies [J].
Adibhatla, Rao Muralikrishna ;
Hatcher, James F. .
CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS, 2008, 7 (03) :243-253
[2]   Structural characterization of cyclosporin A, C and microbial bio-transformed cyclosporin A analog AM6 using HPLC-ESI-ion trap-mass spectrometry [J].
Ahn, Eun Young ;
Shrestha, Anil ;
Nguyen Huu Hoang ;
Nguyen Lan Huong ;
Yoon, Yeo Joon ;
Park, Je Won .
TALANTA, 2014, 123 :89-94
[3]   Beta Blockers for Acute Traumatic Brain Injury: A Systematic Review and Meta-analysis [J].
Alali, Aziz S. ;
McCredie, Victoria A. ;
Golan, Eyal ;
Shah, Prakesh S. ;
Nathens, Avery B. .
NEUROCRITICAL CARE, 2014, 20 (03) :514-523
[4]   Intranasal delivery of neurotrophic factors BDNF, CNTF, EPO, and NT-4 to the CNS [J].
Alcala-Barraza, Sandra R. ;
Lee, Michael S. ;
Hanson, Leah R. ;
McDonald, Abby A. ;
Frey, William H., II ;
McLoon, Linda K. .
JOURNAL OF DRUG TARGETING, 2010, 18 (03) :179-190
[5]   Traumatic Brain Injury Pathophysiology and Treatments: Early, Intermediate, and Late Phases Post-Injury [J].
Algattas, Hanna ;
Huang, Jason H. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2014, 15 (01) :309-341
[6]   Nerve growth factor: from the early discoveries to the potential clinical use [J].
Aloe, Luigi ;
Rocco, Maria Luisa ;
Bianchi, Patrizia ;
Manni, Luigi .
JOURNAL OF TRANSLATIONAL MEDICINE, 2012, 10
[7]  
Aminmansour Bahram, 2014, Adv Biomed Res, V3, P35, DOI 10.4103/2277-9175.125031
[8]   Effect of tranexamic acid in traumatic brain injury: a nested randomised, placebo controlled trial (CRASH-2 Intracranial Bleeding Study) [J].
不详 .
BMJ-BRITISH MEDICAL JOURNAL, 2011, 343
[9]  
[Anonymous], 2006, COCHRANE DATABASE SY
[10]  
[Anonymous], JEMS