Combination of drug and stem cells neurotherapy: Potential interventions in neurotrauma and traumatic brain injury
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Elsevier Ltd
Abstract
Traumatic brain injury (TBI) has been recognized as one of the major public health issues that leads to devastating neurological disability. As a consequence of primary and secondary injury phases, neuronal loss following brain trauma leads to pathophysiological alterations on the molecular and cellular levels that severely impact the neuropsycho-behavioral and motor outcomes. Thus, to mitigate the neuropathological sequelae post-TBI such as cerebral edema, inflammation and neural degeneration, several neurotherapeutic options have been investigated including drug intervention, stem cell use and combinational therapies. These treatments aim to ameliorate cellular degeneration, motor decline, cognitive and behavioral deficits. Recently, the use of neural stem cells (NSCs) coupled with selective drug therapy has emerged as an alternative treatment option for neural regeneration and behavioral rehabilitation post-neural injury. Given their neuroprotective abilities, NSC-based neurotherapy has been widely investigated and well-reported in numerous disease models, notably in trauma studies. In this review, we will elaborate on current updates in cell replacement therapy in the area of neurotrauma. In addition, we will discuss novel combination drug therapy treatments that have been investigated in conjunction with stem cells to overcome the limitations associated with stem cell transplantation. Understanding the regenerative capacities of stem cell and drug combination therapy will help improve functional recovery and brain repair post-TBI. This article is part of the Special Issue entitled “Novel Treatments for Traumatic Brain Injury”. © 2018 Elsevier Ltd
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Cell therapy, Clinical trials, Drug-based therapy, Neurotrauma, Stem cells, Traumatic brain injury, Animals, Brain injuries, traumatic, Combined modality therapy, Humans, Neuroprotective agents, Stem cell transplantation, 4 (1 aminoethyl) n (4 pyridyl)cyclohexanecarboxamide, 4 phosphonomethylpipecolic acid, Abrineurin, Atorvastatin, Carbazole derivative, Cyclosporine, Dextrorphan, Epidermal growth factor receptor, Erythropoietin, Fasudil, Fenofibrate, Lithium, Molecular scaffold, Neurotrophin, Nimodipine, Progesterone, Recombinant granulocyte colony stimulating factor, Recombinant growth factor, Simvastatin, Somatomedin, Superoxide dismutase, Tirilazad, Valproic acid, Neuroprotective agent, Alzheimer disease, Antiinflammatory activity, Axonal injury, Behavior disorder, Bone marrow stroma cell, Brain edema, Brain necrosis, Cell regeneration, Cell reprogramming technique, Cerebrovascular disease, Cognitive defect, Disease course, Disease severity, Drug efficacy, Drug potentiation, Embryonic stem cell, Excitotoxicity, Human, Induced pluripotent stem cell, Mesenchymal stem cell transplantation, Microangiopathy, Motor dysfunction, Nervous system development, Nervous system inflammation, Nervous system injury, Neural stem cell transplantation, Neuropharmacology, Neuroprotection, Nonhuman, Oxidative stress, Priority journal, Process optimization, Review, Substitution therapy, Survival rate, Treatment failure, Treatment outcome, Umbilical cord blood cell, Animal, Multimodality cancer therapy