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10.1517/13543784.2015.1021919

http://scihub22266oqcxt.onion/10.1517/13543784.2015.1021919
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C4433440!4433440!25727893
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suck abstract from ncbi


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pmid25727893      Expert+Opin+Investig+Drugs 2015 ; 24 (6): 743-60
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  • Investigational agents for treatment of traumatic brain injury #MMPMID25727893
  • Xiong Y; Zhang Y; Mahmood A; Chopp M
  • Expert Opin Investig Drugs 2015[Jun]; 24 (6): 743-60 PMID25727893show ga
  • 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 aim of this review is to provide an overview of select cell-based and pharmacological therapies under early development for the treatment of TBI, which seek to enhance cognitive and neurological functional recovery through neuroprotective and neurorestorative strategies. Expert?s 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.
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