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Table of Content

    15 January 2016, Volume 11 Issue 1 Previous Issue    Next Issue
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    Letter from the Editors-in-Chief
    Kwok-fai So and Xiao-ming Xu
    2016, 11 (1):  5-5. 
    Abstract ( 242 )   PDF (166KB) ( 1196 )   Save
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    Magnetic resonance imaging and cell-based neurorestorative therapy after brain injury
    Quan Jiang
    2016, 11 (1):  7-14.  doi: 10.4103/1673-5374.169603
    Abstract ( 211 )   PDF (1265KB) ( 679 )   Save

    Restorative cell-based therapies for experimental brain injury, such as stroke and traumatic brain injury, substantially improve functional outcome. We discuss and review state of the art magnetic resonance imaging methodologies and their applications related to cell-based treatment after brain injury. We focus on the potential of magnetic resonance imaging technique and its associated challenges to obtain useful new information related to cell migration, distribution, and quantitation, as well as vascular and neuronal remodeling in response to cell-based therapy after brain injury. The noninvasive nature of imaging might more readily help with translation of cell-based therapy from the laboratory to the clinic.

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    A brief report on MRI investigation of experimental traumatic brain injury
    Timothy Q. Duong, Lora T. Watts
    2016, 11 (1):  15-17.  doi: 10.4103/1673-5374.169604
    Abstract ( 198 )   PDF (170KB) ( 541 )   Save

    Traumatic brain injury is a major cause of death and disability. This is a brief report based on a symposium presentation to the 2014 Chinese Neurotrauma Association Meeting in San Francisco, USA. It covers the work from our laboratory in applying multimodal MRI to study experimental traumatic brain injury in rats with comparisons made to behavioral tests and histology. MRI protocols include structural, perfusion, manganese-enhanced, diffusion-tensor MRI, and MRI of blood-brain barrier integrity and cerebrovascular reactivity.

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    The potential of neural transplantation for brain repair and regeneration following traumatic brain injury
    Dong Sun
    2016, 11 (1):  18-22.  doi: 10.4103/1673-5374.169605
    Abstract ( 247 )   PDF (278KB) ( 578 )   Save

    Traumatic brain injury is a major health problem worldwide. Currently, there is no effective treatment to improve neural structural repair and functional recovery of patients in the clinic. Cell transplantation is a potential strategy to repair and regenerate the injured brain. This review article summarized recent development
    in cell transplantation studies for post-traumatic brain injury brain repair with varying types of cell sources. It also discussed the potential of neural transplantation to repair/promote recovery of the injured brain following traumatic brain injury.

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    RhoA/Rho kinase in spinal cord injury
    Xiangbing Wu, Xiao-ming Xu
    2016, 11 (1):  23-27.  doi: 10.4103/1673-5374.169601
    Abstract ( 276 )   PDF (734KB) ( 996 )   Save

    A spinal cord injury refers to an injury to the spinal cord that is caused by a trauma instead of diseases.Spinal cord injury includes a primary mechanical injury and a much more complex secondary injury process involving inflammation, oxidation, excitotoxicity, and cell death. During the secondary injury, many signal pathways are activated and play important roles in mediating the pathogenesis of spinal cord injury.Among them, the RhoA/Rho kinase pathway plays a particular role in mediating spinal degeneration and regeneration. In this review, we will discuss the role and mechanism of RhoA/Rho kinase-mediated spinal cord pathogenesis, as well as the potential of targeting RhoA/Rho kinase as a strategy for promoting both neuroprotection and axonal regeneration.

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    Direct reprogramming of somatic cells into neural stem cells or neurons for neurological disorders
    Shaoping Hou, Paul Lu
    2016, 11 (1):  28-31.  doi: 10.4103/1673-5374.169602
    Abstract ( 403 )   PDF (373KB) ( 842 )   Save

    Direct reprogramming of somatic cells into neurons or neural stem cells is one of the most important frontier
    fields in current neuroscience research. Without undergoing the pluripotency stage, induced neurons or induced neural stem cells are a safer and timelier manner resource in comparison to those derived from induced pluripotent stem cells. In this prospective, we review the recent advances in generation of induced neurons and induced neural stem cells in vitro and in vivo and their potential treatments of neurological disorders.

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    The progress in optic nerve regeneration, where are we?
    Jennifer Wei Huen Shum,Kai Liu, Kwok-fai So
    2016, 11 (1):  32-36.  doi: 10.4103/1673-5374.175038
    Abstract ( 404 )   PDF (205KB) ( 876 )   Save

    Optic nerve regeneration is an important area of research. It can be used to treat patients suffering from optic neuropathy and provides insights into the treatment of numerous neurodegenerative diseases. There are many hurdles impeding optic regeneration in mammals. The mammalian central nervous system is non-permissive to regeneration and intrinsically lacks the capacity for axonal regrowth. Any axonal injury also triggers a vicious cycle of apoptosis. Understanding these hurdles provides us with a rough framework to appreciate the essential steps to bring about optic nerve regeneration: enhancing neuronal survival, axon regeneration, remyelination and establishing functional synapses to the original neuronal targets. In this review article, we will go through current potential treatments for optic nerve regeneration, which includes neurotrophic factor provision, inflammatory stimulation, growth inhibition suppression, intracellular signaling
    modification and modeling of bridging substrates.

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    Glucocorticoids and nervous system plasticity
    Kathryn M. Madalena, Jessica K. Lerch
    2016, 11 (1):  37-41.  doi: 10.4103/1673-5374.175039
    Abstract ( 370 )   PDF (552KB) ( 858 )   Save

    Glucocorticoid and glucocorticoid receptor (GC/GR) interactions alter numerous aspects of neuronal function. These consequences (e.g., anti-inflammatory vs. pro-inflammatory) can vary depending on the duration of GC exposure or central nervous system (CNS) injury model. In this review we discuss how GC/GR interactions impact neuronal recovery after a central or peripheral nerve injury and discuss how GC exposure duration can produce divergent CNS neuronal growth responses. Finally we consider how new findings on gender specific immune cell responses after a nerve injury could intersect with GC/GR interactions to impact pain processing.

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    SCYL pseudokinases in neuronal function and survival
    Stephane Pelletier
    2016, 11 (1):  42-44.  doi: 10.4103/1673-5374.175040
    Abstract ( 259 )   PDF (246KB) ( 695 )   Save

    The generation of mice lacking SCYL1 or SCYL2 and the identification of Scyl1 as the causative gene in the motor neuron disease mouse model muscle deficient (Scyl1mdf/mdf) demonstrated the importance of the SCY1-like family of protein pseudokinases in neuronal function and survival. Several essential cellular processes such as intracellular trafficking and nuclear tRNA export are thought to be regulated by SCYL proteins. However,whether deregulation of these processes contributes to the neurodegenerative processes associated with the loss of SCYL proteins is still unclear. Here, I briefly review the evidence supporting that SCYL proteins play a role in these processes and discuss their possible involvement in the neuronal functions of SCYL proteins.I also propose ways to determine the importance of these pathways for the functions of SCYL proteins in vivo.

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    Unmasking the responses of the stem cells and progenitors in the subventricular zone after neonatal and pediatric brain injuries
    Mariano Guardia Clausi, Ekta Kumari, Steven W. Levison
    2016, 11 (1):  45-48.  doi: 10.4103/1673-5374.175041
    Abstract ( 312 )   PDF (530KB) ( 741 )   Save

    There is great interest in the regenerative potential of the neural stem cells and progenitors that populate the subventricular zone (SVZ). However, a comprehensive understanding of SVZ cell responses to brain injuries has been hindered by the lack of sensitive approaches to study the cellular composition of this niche. Here we review progress being made in deciphering the cells of the SVZ gleaned from the use of a recently designed flow cytometry panel that allows SVZ cells to be parsed into multiple subsets of progenitors as well as putative stem cells. We review how this approach has begun to unmask both the heterogeneity of SVZ cells as well as the dynamic shifts in cell populations with neonatal and pediatric brain injuries. We also discuss how flow cytometric analyses also have begun to reveal how specific cytokines, such as Leukemia inhibitory factor are coordinating SVZ responses to injury.

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    Tracking of iron-labeled human neural stem cells by magnetic resonance imaging in cell replacement therapy for Parkinson’s disease
    Milagros Ramos-Gómez, Alberto Martínez-Serrano
    2016, 11 (1):  49-52.  doi: 10.4103/1673-5374.169628
    Abstract ( 223 )   PDF (602KB) ( 546 )   Save

    Human neural stem cells (hNSCs) derived from the ventral mesencephalon are powerful research tools and candidates for cell therapies in Parkinson’s disease. However, their clinical translation has not been fully realized due, in part, to the limited ability to track stem cell regional localization and survival over long periods of time after in vivo transplantation. Magnetic resonance imaging provides an excellent non-invasive method to study the fate of transplanted cells in vivo. For magnetic resonance imaging cell tracking, cells need to be labeled with a contrast agent, such as magnetic nanoparticles, at a concentration high enough to be easily detected by magnetic resonance imaging. Grafting of human neural stem cells labeled with magnetic nanoparticles allows cell tracking by magnetic resonance imaging without impairment of cell survival, proliferation,self-renewal, and multipotency. However, the results reviewed here suggest that in long term grafting, activated microglia and macrophages could contribute to magnetic resonance imaging signal by engulfing dead labeled cells or iron nanoparticles dispersed freely in the brain parenchyma over time.

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    Macrophage polarization in nerve injury: do Schwann cells play a role?
    Jo Anne Stratton, Prajay T. Shah
    2016, 11 (1):  53-57.  doi: 10.4103/1673-5374.175042
    Abstract ( 444 )   PDF (548KB) ( 889 )   Save

    In response to peripheral nerve injury, the inflammatory response is almost entirely comprised of infiltrating macrophages. Macrophages are a highly plastic, heterogenic immune cell, playing an indispensable role in peripheral nerve injury, clearing debris and regulating the microenvironment to allow for efficient regeneration.There are several cells within the microenvironment that likely interact with macrophages to support their function – most notably the Schwann cell, the glial cell of the peripheral nervous system. Schwann cells express several ligands that are known to interact with receptors expressed by macrophages, yet the effects of Schwann cells in regulating macrophage phenotype remains largely unexplored. This review discusses macrophages in peripheral nerve injury and how Schwann cells may regulate their behavior.

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    Spinal cord concussion: studying the potential risks of repetitive injury
    Itzhak Fischer, Christopher Haas, Ramesh Raghupathi, Ying Jin
    2016, 11 (1):  58-60.  doi: 10.4103/1673-5374.169634
    Abstract ( 371 )   PDF (377KB) ( 1635 )   Save

    Spinal cord concussion is a variant of mild spinal cord injury, clinically designated as transient paraplegia or neurapraxia, and characterized by variable degrees of sensory impairment and motor weakness that typically resolves within 24–72 hours without permanent deficits. Ideally, a model of spinal concussion should use a closed injury to more accurately model the stretching or axial loading seen in clinical cord concussion, as injuries typically occur as a result of hyperextension or hyperflexion of the spinal cord exacerbated by smaller cervical canals or stenosis. The need for reproducible, quantitative injury models, however, makes the direct application of forces on the exposed spinal cord a necessary trade off for most of animal models of SCI. Our model is designed to represent spinal cord concussion, and to highlight the susceptibility and functional consequences of repeated injury. This study, however, is only a first step in preclinical work on the risks associated with spinal concussion, which will provide a mechanistic framework for understanding the etiology of the injury as well as better guide clinical decision-making for RTP following contact sports injuries. We anticipate that future work from our laboratory and others will elucidate the key parameters of spinal vulnerability following spinal concussion with respect to the time, location, and severity of the injury. To maximize the effectiveness of this work the basic research with animal models should be coordinated with clinical observations and studies of both spinal and brain contusion injuries.

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    Promoting neuronal regeneration using extracellular vesicles loaded with superparamagnetic iron oxide nanoparticles
    Jenni Neubert, Jana Glumm
    2016, 11 (1):  61-63.  doi: 10.4103/1673-5374.175043
    Abstract ( 227 )   PDF (367KB) ( 658 )   Save

    Intercellular communication between neurons and glial cells via extracellular vesicles (EVs) as a novel mechanism of information transfer has been shown to be involved in regeneration processes within the central nervous system (CNS). Hence, to take advantage of EV signaling for therapeutic applications appears to be a completely new approach to promote regeneration. One fundamental reason why influencing neuronal recovery after damage remains problematic is due to limited access to molecular processes, which are essential for the transcription of growth-promoting cues. EVs are currently under investigation for their use as hybrid vectors containing both therapeutic agents and superparamagnetic iron oxide nanoparticles (SPIOs) that can be remote guided using an external magnetic field. SPIO binding and accumulation at the extracellular membrane and the subsequent internalization in EVs have to be ensured. It is also certainly necessary to characterize SPIO behavior under standardized conditions in cell cultures of individual cells as well as mixed cell cultures, for instance, containing neurons, astrocytes and microglial cells. Under these conditions, the possibility of influencing EV cargos and their delivery could indeed open up new strategies for affecting information transfer within the brain to promote neuroregeneration.

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    Developmental transcription factors in age-related CNS disease: a phoenix rising from the ashes?
    Robert B. White*, Meghan G. Thomas
    2016, 11 (1):  64-65.  doi: 10.4103/1673-5374.175044
    Abstract ( 302 )   PDF (186KB) ( 584 )   Save

    The Pax6 gene belongs to the highly functionally and structurally conserved Pax gene family (Pax1–9) of tissue-specific transcription factors. The Pax family are instrumental in development and have a critical role in brain regionalisation and specification of subtypes of neurons within brain regions. Pax6 is one of the earliest gene products expressed in the developing embryo. Pax6 is a key neurogenic factor and a well-accepted neurogenic determinant. Indeed, Pax6 is frequently used as a marker of neural precursor status and recent studies have demonstrated that overexpression of both Pax6 and another transcription factor, Sox2, is sufficient to transdifferentiate fibroblast cells into induced neuronal progenitors (Maucksch et al., 2012), in line with it having been demonstrated that Pax6 alone induces neuronal specification of postnatal forebrain astrocytes.

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    The concentration game: differential effects of bioactive signaling in 2D and 3D culture
    Laura A. Smith Callahan
    2016, 11 (1):  66-68.  doi: 10.4103/1673-5374.165303
    Abstract ( 407 )   PDF (384KB) ( 610 )   Save

    Traumatic injuries to the central nervous system trigger a series of secondary biochemical and cellular responses that ultimately lead to cellular death and maintenance of an unsupportive extracellular matrix (ECM) for tissue regeneration. Artificial ECM or scaffolds represent a way to alter this unsupportive environment to improve the efficacy of stem cell therapies and enhance neural tissue regeneration. The inclusion of basic scaffolds with stem cell therapy treatments have shown increased efficacy in rodent models. More advanced scaffolds could better mimic the chemical, physical and mechanical properties of the ECM to promote survival, adhesion, proliferation and differentiation altering the injured ECM to mitigate the barriers to axon invasion, myelination and cellular maturation. Changes in IKVAV concentration have been implicated in altering cellular attachment and neural differentiation. In 2D culture, maximal neurite extension and neural gene expression occurred on hydrogels. While in 3D culture, neurite extension was delayed. The common thread to many of the changes between 2D and 3D culture is a real or perceived change in the concentration of elements (cytokines, tethered bioactive signaling, etc.) by the cell in its extracellular milieu. The complexity of how the concentration changes interact with cells to change cellular survival, attachment, and differentiation throughout central nervous system development is not yet well understood. Unraveling the effects of these concentration changes will ultimately lead to a better understanding of tissue development allowing us to begin to effectively manipulate the extracellular environment with scaffolds, drugs, stem cells, etc. to restore neurological function after traumatic brain and spinal cord injuries.

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    Skeletal muscle activity and CNS neuro-plasticity
    Rachel Zhorne, Shauna Dudley-Javoroski, Richard K. Shields
    2016, 11 (1):  69-70.  doi: 10.4103/1673-5374.169623
    Abstract ( 305 )   PDF (330KB) ( 935 )   Save

    The systemic health benefits of regular skeletal muscle activity are well documented. Increased skeletal muscle activity is associated with an improved systemic metabolic rate, reduced incidence of diabetes and obesity, and improved function with age. Despite these known systemic benefits, many healthy people do not meet the recommended daily dose of skeletal muscle activity (exercise) needed to prevent metabolic disease. People with central nervous system (CNS) damage (from complete spinal cord injury, for example), are even further compromised as they are unable to activate their own musculature. In this perspective paper, we discuss recent findings relating skeletal muscle activity and CNS signaling. A central theme is that appropriately prescribed skeletal muscle activity (rehabilitation) may have important implications for optimizing neural plasticity, enhancing stem cell proliferation and differentiation, and improving the overall environment for regenerative approaches for people with CNS damage (spinal cord injury, stroke, multiple sclerosis, closed cranial trauma, etc.). One method to induce skeletal muscle activity in people with paralysis is by activating the skeletal muscle electrically. Neuromuscular electrical stimulation directly activates peripheral nerves (not muscle), which consist of the motor and sensory axons that communicate with the muscle from the spinal cord. Most people with traumatic spinal cord injury, for example, have an upper motor neuron injury. A complete upper motor neuron injury prevents any voluntary signal from the motor cortex to the muscle; but the lower motor neuron and its associated axons are retained, allowing peripheral communication between the spinal cord and the muscle.

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    Exploiting kinase polypharmacology for nerve regeneration
    Hassan Al-Ali*, John L. Bixby, Vance P. Lemmon
    2016, 11 (1):  71-72.  doi: 10.4103/1673-5374.169614
    Abstract ( 271 )   PDF (837KB) ( 1205 )   Save

    The humancentral nervous system (CNS) has a markedly poor capacity for regenerating its axons following injury. This appears to be due to two main causes: 1) a developmentally regulated decline in regenerative capacity within mature CNS neurons, and 2) the presence of biological components that constitute barriers to axon regeneration (e.g., growth-inhibitory molecules). Intrinsic alterations have been elucidated by studies that show causative links between developmental changes in gene expression programs and growth-signaling states on one hand, and changes in regenerative capacity on the other. In addition to these neuron-intrinsic factors, several molecular species that are native to the CNS microenvironment, such as myelin associated proteins, and others that are secreted by injury-activated astrocytes, such as chondroitin sulfate proteoglycans (CSPGs), exert extrinsic inhibitory influences on growing axons.

    Given the various factors that negatively influence axon regrowth in the adult CNS, achieving clinically relevant regeneration to promote recovery from traumatic injury has been difficult. Experimental manipulation of individual inhibitory factors, or their mediators, has resulted in some improvement of regeneration/sprouting. However, manipulations that simultaneously target intrinsic growth capacity while also blocking inhibition from extrinsic factors appear to produce the most pronounced effects in vivo. Development of effective therapies thus requires agents that simultaneously modulate multiple sources of regeneration failure. This could be achieved with drugs that engage multiple targets (polypharmacology) within various relevant signaling networks. The use of multi-target drugs to treat complex polygenic disorders is not a new concept; however,the lack of appropriate methodologies have hindered systematic exploitation of polypharmacology. Interestingly though, it appears that polypharmacologyis important for the therapeutic efficacy of many approved drugs.
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    Schwannomas provide insight into the role of p75NTR and merlin in Schwann cells following nerve injury and during regeneration
    Elise Cheng, Marlan R. Hansen
    2016, 11 (1):  73-74.  doi: 10.4103/1673-5374.175045
    Abstract ( 238 )   PDF (455KB) ( 618 )   Save

    Recent publications have begun to elucidate how merlin regulates responses of Schwann cells to nerve injury and how dysregulation of these responses in the absence of merlin likely contributes to schwannoma cell tumorigenesis. When Schwann cells lose contact with axons, merlin becomes phosphorylated leading to increased p75NTR expression and ultimately to schwannoma cell apoptosis and loss. However, in the absence of functional merlin, Schwann cells become resistant to p75NTR-mediated apoptosis. Further, p75NTR signaling elicits a prosurvival response in schwannoma cells, likely contributing to their ability to proliferate and survive in the absence of axons. This pro-survival response may contribute to the relative resistance of vestibular schwannomas cells to chemotherapeutic agents such as kinase inhibitors. Thus, simultaneously targeting p75NTR and/or NF-kB may sensitize vestibular schwannomas cells to other classes of chemotherapeutic agents. Interestingly, the mechanisms by which vestibular schwannomas cells escape cell death also inform our understanding of normal Schwann cell behavior following nerve injury.

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    Role of neuronal gap junctions in NMDA receptor-mediated excitotoxicity and ischemic neuronal death
    Andrei B. Belousov, Joseph D. Fontes
    2016, 11 (1):  75-76.  doi: 10.4103/1673-5374.169630
    Abstract ( 275 )   PDF (257KB) ( 800 )   Save

    In the mammalian CNS coupling of neurons by gap junctions and the expression of neuronal gap junction protein, connexin 36 (Cx36) rapidly increase (usually during 1-2 hours) following a wide range of neuronal injuries, including ischemia, traumatic brain injury (TBI), spinal cord injury, epilepsy and inflammation. Pharmacological blockade or genetic elimination of Cx36-containing gap junctions dramatically reduce neuronal death in animal models of ischemia, TBI and epilepsy and prevent NMDA receptor (NMDAR)-mediated excitotoxicity. This suggests a critical role for neuronal gap junctions in the mechanisms of neuronal death. In our recent study, we addressed the following three questions. Are changes in the expression of Cx36 directly affect neuronal death? Is the contribution of Cx36 to neuronal death depends on channel activity of gap junctional complexes among neurons or it is channel-independent? Do neuronal hemichannels contribute to neuronal death? In conclusion, this study provided insight into the mechanisms of contribution of neuronal gap junctions in NMDAR-dependent excitotoxicity and ischemic neuronal death. Because clinical trials for NMDAR antagonists as neuroprotective agents largely failed, the study suggested that another important therapeutic target for the development of new neuroprotective agents can be neuronal gap junction coupling.

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    Lipid mediators of inflammation in neurological injury: shifting the balance toward resolution
    Jordan L. Harrison, Rachel K. Rowe, Jonathan Lifshitz
    2016, 11 (1):  77-78.  doi: 10.4103/1673-5374.175046
    Abstract ( 365 )   PDF (349KB) ( 964 )   Save

    Acquired neurological injuries initiate a pathological cascade of secondary injury processes, including inflammation, which continue for days to weeks following injury. Injury-induced neuroinflammation acts as a host defense mechanism contributing to the neutralization of the insult (removing offending factors) and restoring structure and function of the brain (establish homeostasis). The timing of these protective functions of the immune response is vital, since chronic inflammation has been associated with progressive cell loss and neurotoxicity. A separate sub-class of lipid mediators, termed specialized pro-resolving mediators (SPMs), functions to resolve inflammation. Endogenous SPMs, notably those derived from omega-3 fatty acids, may represent a valuable target in shifting the balance of neuroinflammatory processes from inflammation-driving to inflammation-resolving conditions in the injured CNS. Enthusiasm for a therapeutic approach involving SPMs comes from the natural routes of administration, such as dietary supplementation of their metabolic precursors, exogenous SPMs, and adjunctive interventions focused on increasing the availability of SPMs after injury. SPMs provide a cellular target for therapeutic approaches to limit secondary injury processes after acquired neurological injury. The potent anti-inflammatory properties of SPMs in peripheral diseases and the therapeutic efficacy of their fatty acid precursors in neurological disease provide a sound basis for further exploration of their neuroprotective efficacy in acquired neurological injury. Of particular value to the clinical problems of stroke and TBI are therapies which are rapid and accessible. The endogenous nature of SPMs makes them promising candidates for readily accessible therapies, which could shift the inflammatory balance toward resolution of cellular pathophysiology and limit the extent of injury.

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    Nootropics with potential to (re)build neuroarchitecture
    Kyoko Koshibu
    2016, 11 (1):  79-80.  doi: 10.4103/1673-5374.169635
    Abstract ( 289 )   PDF (172KB) ( 2023 )   Save

    Development of effective treatments for neurodegenerative disorders is a clinical conundrum that has puzzled many researchers. Currently available drugs target symptomatic relief rather than suppressing, ceasing or repairing the devastating neural damages. For Alzheimer’s disease, there are two classes of procognitive compounds that are approved as a treatment of the disease. Acetylcholinesterase (AChE) inhibitors, such as tacrine, donepezil, galantamine and rivastigmine, inhibit the hydrolysis of acetylcholine and elevate the acetylcholine neurotransmitter level. The other class of drug is N-methyl-D-aspartate (NMDA) receptor antagonists, such as memantine, intended to suppress ?-amyloid induced excitotoxicity. These compounds have produced only modest improvements in cognitive and behavioral symptoms in some Alzheimer’s patients. Thus, tremendous efforts are being made to discover and develop more effective treatments for Alzheimer’s disease. In the midst of the intense investigation for new treatments, there have been increasing effort to understand the cellular effects of the existing nootropic compounds on neurogenesis and neuritogenesis, a central process for the formation of neural networks during brain plasticity and (re)growth, to determine their potential for molding neuroarchitecture. Interestingly, studies have shown that selective procognitive compounds indeed possess such properties. We have recently shown that an AChE inhibitor donepezil can significantly promote neurite outgrowth in a primary cortical culture system. The cellular effects of AChE inhibitors conceivably include stimulation of neurogenesis, because cholinergic receptors are expressed on neuronal progenitors and are coupled to cell proliferation. However, the actual molecular targets of donepezil that promotes neuritogenesis may differ from AChE in light of the lack of effect of tacrine in our study. Donepezil is known to have various other targets in addition to AChE. In particular, donepezil binds sigma1 receptors with high affinity at a low nanomolar range in vitro and behave as an effective sigma1 receptor agonist. Neuroprotective effects of donepezil have been reported to involve a sigma1 interaction in a mouse model and in rodent cortical culture. The authors have reported that donepezil and sigma1 receptor agonist Pre-084 provide a complete neuroprotection in mice treated with β-amyloid peptide 25–35 while only a partial neuroprotection can be achieved with AChE inhibitor tacrine. Furthermore, pre-administration of the sigma1 receptor antagonist BD1047 or in vivo antisense probe treatment blocks the memory-enhancing effect of donepezil. These studies suggest that the procognitive and neuroprotective activities of donepezil are at least partially mediated by sigma1 receptor.

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    Polarizing the immune system towards neuroprotection in brain ischemia
    Diana Amantea
    2016, 11 (1):  81-82.  doi: 10.4103/1673-5374.169633
    Abstract ( 207 )   PDF (334KB) ( 814 )   Save

    The evolution of ischemic brain damage is dramatically affected by the immune system, whose activation occurs immediately after the insult and may last for several days, involving a complex interplay between soluble and cellular mediators. Accordingly, recent expression profiling studies have revealed that the majority of the genes modulated in the blood of stroke patients participate to the regulation of innate immune responses. Moreover, in the clinical setting, serum levels of markers of acute inflammation correlate with the severity of ischemic brain damage and neurological deficit. Brain resident microglia and blood-borne immune cells crucially contribute to the acute and chronic processes implicated in tissue injury, as well as to the regenerative and reparative mechanisms that limit the damage and provide tissue healing and recovery. In this context, an attractive approach to improve successful clinical translation of stroke therapeutics would consist in achieving a rational modulation of the immune system, by blocking its detrimental inflammatory responses while promoting its beneficial components. This perspective commentary will focus on the most recent findings regarding relevant targets and drugs for immunomodulation in stroke and their potential application in patients.

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    Future needs for informed consent in stem cell clinical trials in neurodegenerative diseases
    Natalie Hellmers, Yaa Obeng-Aduasare,Inmaculada de Melo-Martín, Claire Henchcliffe
    2016, 11 (1):  83-85.  doi: 10.4103/1673-5374.169632
    Abstract ( 289 )   PDF (264KB) ( 614 )   Save

    Translation of recent advances in stem cell research into clinical trials for restorative therapies for human disease is dramatically accelerating. There is a strong focus upon neurodegenerative disorders such as Parkinson’s disease (PD), Huntington’s disease (HD), and amyotrophic lateral sclerosis (ALS). In particular, first-in-human intracerebral transplantation of cells derived from human embryonic stem cells (hESC) and inducible pluripotent cells (iPS) is likely within the next few years and intraspinal transplantation of hESC-derived cells has been recently reported in ALS. As clinical trials are planned and implemented, it will be critical to attend to the ethical framework necessary for responsible translation of scientifically compelling, but risky, interventions in humans. In particular, these clinical trials will present a variety of challenges to the informed consent process. We therefore review barriers to obtaining a truly informed consent in early phase stem cell clinical trials in neurodegenerative conditions, and examine procedures and interventions that have been investigated to potentially address and overcome these barriers. A variety of neurodegenerative disorders are thought to be amenable to restorative therapies using stem cell-based interventions. However, many studies raise concerns that “standard” consent processes may be insufficient to ensure that potential study participants’ decisions to enroll in such trials are indeed autonomous and made voluntarily, based upon their understanding of adequately disclosed information about the trial. Although some of these concerns are common to all trials, the important uncertainty regarding the risks and potential benefits of stem cell trials in neurodegeneration makes the need for development of guidelines for researchers imperative. We suggest that conveying complex and nuanced scientific information and reducing the effects of the therapeutic misconception could be addressed by extended consent procedures that might take place over time, and that can incorporate tablet-based or web-based materials. Researchers will need support in the use of expanded consent processes that may involve multiple media. The recognized need for long term follow up also necessitates changes in how capacity is assessed over time, and how to address a situation in which a subject loses capacity, for example due to progressive cognitive decline associated with some neurodegenerative disorders. As the field as a whole works towards consensus, we recommend close collaborations, not only between preclinical and clinical research teams, but also with bioethicists and individuals (usually psychiatrists) skilled in assessing capacity, and local IRBs familiar with issues particular to a given geographic region or culture.

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    How does resveratrol influence the genesis of some neurodegenerative diseases?
    Ester Tellone, Antonio Galtieri, Annamaria Russo, Silvana Ficarra
    2016, 11 (1):  86-87.  doi: 10.4103/1673-5374.175047
    Abstract ( 272 )   PDF (389KB) ( 596 )   Save

    In recent century, the advancing age and increased lifespan of the world’s population have led to a significant increase in the incidence of neurodegenerative diseases that are a major cause of disability and death for most of those affected. These findings put the neurodegeneration as a major public health problem in modern society also because effective pharmacological interventions for prevention and treatment of the disease, are lacking. Based on the premise that oxidative stress underlies a number of neurodegenerative diseases, the identification of novel antioxidants as potential therapeutics is a prolific area of neuroscience research. In fact, although the different neurodegenerative diseases manifest in distinct neuronal cell types, oxidative stress and suppression of neuronal survival signals are common to many of these pathological conditions and appear to be highly relevant targets for treatment. Growing evidences suggest that at the pathological level, almost all neurodegenerative diseases share common features such as the iron accumulation and the generation of misfolded protein deposits. Furthermore, it was shown that the oxidative stress markers precede the pathological lesions of neurodegeneration

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    Lingo-1: a novel target in therapy for Alzheimer’s disease?
    Francesca Fernandez-Enright, Jessica L. Andrews
    2016, 11 (1):  88-89.  doi: 10.4103/1673-5374.175048
    Abstract ( 363 )   PDF (619KB) ( 668 )   Save

    Alzheimer’s disease (AD) is a progressive, neurodegenerative disease characterized clinically by gradual cognitive decline including loss of memory, orientation and reasoning, and is pathologically characterized by accumulation of neurofibrillary tangles and amyloid plaques in the brain. The rate of growth of these amyloid plaques differs throughout neocortical and hippocampal regions, and are formed from oligomers of amyloid-β (Aβ) in the intracellular and extracellular space. Aβ is the result of proteolysis of amyloid precursor protein (APP) by β and γ-secretase enzymes. The accumulation of Aβ oligomers becomes progressively toxic and triggers the start of neurodegenerative processes. Here we discuss the role of Lingo-1, or LERN1 (leucine-rich repeat neuronal protein 1) in this process, a transmembrane protein which is highly abundant in the brain and is implicated in numerous neurodegenerative disorders, and demonstrate reasons suggesting its potential for a role in future AD therapy. It appears that Lingo-1 plays a critical role in the AD pathophysiology by both favoring the β-cleavage of APP and the generation of Aβ fragment, but also by the activation of key molecular signaling pathways leading to the inhibition of neuronal outgrowth and survival. An antibody targeting Lingo-1 (BIIB033 produced by Biogen®), has been engineered to be able to cross the blood brain barrier and to antagonize Lingo-1 within the central nervous system. This Lingo-1 antagonist is currently in phase II clinical trials for treating multiple sclerosis and may prove to be a promising treatment option for future AD therapies.

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    Mesenchymal stem cells require the peripheral immune system for immunomodulating effects in animal models of multiple sclerosis
    Laura Salinas Tejedor, Thomas Skripuletz, Martin Stangel,Viktoria Gudi
    2016, 11 (1):  90-91.  doi: 10.4103/1673-5374.175050
    Abstract ( 318 )   PDF (531KB) ( 599 )   Save

    Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) that affects oligodendrocytes and myelin. Loss of myelin leads to progressive axonal damage and neuronal death resulting in neurodenegeration and functional disability. Several inflammatory factors influence the development of this neurological disorder. It is generally accepted that autoreactive T lymphocytes migrate towards the CNS then initiating an immune reaction upon encountering the specific myelin antigen. Remyelination is the natural repair mechanism and is important to restore the fast saltatory nerve conduction. In addition it restores the axon-myelin unit and may thus preserve the axon from secondary degeneration. This regenerative process implies the migration of oligodendroglial precursors cells (OPC) towards demyelinated regions and their differentiation into mature myelinating oligodendrocytes. Unfortunately, this process is often incomplete in MS patients and current treatments are based on the use of immunomodulatory drugs, which diminish the inflammatory reaction, but they do not repair existing damage.  For this reason, extensive research is being conducted in the area of remyelinating therapies in order to stop disease progression and restore neurological disabilities.

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    Absence of galectin-3 attenuates neuroinflammation improving functional recovery after spinal cord injury
    Caio Andrade Prins, Fernanda Martins Almeida, Ana Maria Blanco Martinez
    2016, 11 (1):  92-93.  doi: 10.4103/1673-5374.175051
    Abstract ( 267 )   PDF (429KB) ( 583 )   Save

    After spinal cord injury, a cascade of events begins. At first, there is physical damage with disruption of the blood brain barrier (BBB) and the integrity of the nervous tissue. The disruption of central nervous system BBB alters the endothelial permeability, the protein and chemokines expression and the propensity to in situ release of inflammatory cytokines overcoming anti-inflammatory signals, facilitating the attraction and entry of immune system cells into the injured spinal cord parenchyma. As a result there is a neuroinflammatory response with changes in blood flow, edema, cell infiltration, apoptosis and release of axonal growth inhibitory factors. Nerve function loss occurs when the nerve impulse propagation is interrupted and do not reach its target. This disorder encompasses neuron and glia apoptosis, accompanied by Wallerian Degeneration of disconnected axons, and central nervous system cells exposure to a hostile microenvironment that hampers axon regeneration. Additionally, the damage spreads further in a phenomenon called progressive hemorrhagic necrosis – PHN, with the appearance of petechial hemorrhagic foci and deterioration in areas outside the lesion epicenter during the next 2 – 24 hours after the trauma. Our laboratory investigates the role of galectin-3, a protein linked to mechanisms of inflammation, behind the cellular mechanisms of neural degeneration/regeneration with perspectives of a novel treatment.

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    Neuroprotective effect of Shenqi Fuzheng injection pretreatment in aged rats with cerebral ischemia/reperfusion injury
    Ying-min Cai, Yong Zhang, Peng-bo Zhang, Lu-ming Zhen, Xiao-ju Sun, Zhi-ling Wang, Ren-yan Xu, Rong-liang Xue
    2016, 11 (1):  94-100.  doi: 10.4103/1673-5374.175052
    Abstract ( 285 )   PDF (1602KB) ( 618 )   Save

    Shenqi Fuzheng injection is extracted from the Chinese herbs Radix Astragali and Radix Codonopsis. The aim of the present study was to investigate the neuroprotective effects of Shenqi Fuzheng injection in cerebral ischemia and reperfusion. Aged rats (20–22 months) were divided into three groups: sham, model, and treatment. Shenqi Fuzheng injection or saline (40 mL/kg) was injected into the tail vein daily for 1 week, after which a cerebral ischemia/reperfusion injury model was established. Compared with model rats that received saline, rats in the treatment group had smaller infarct volumes, lower brain water and malondialdehyde content, lower brain Ca2+ levels, lower activities of serum lactate dehydrogenase and creatine kinase, and higher superoxide dismutase activity. In addition, the treatment group showed less damage to the brain tissue ultrastructure and better neurological function. Our findings indicate that Shenqi Fuzheng injection
    exerts neuroprotective effects in aged rats with cerebral ischemia/reperfusion injury, and that the underlying mechanism relies on oxygen free radical scavenging and inhibition of brain Ca2+ accumulation.

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    Verbascoside promotes the regeneration of tyrosine hydroxylase-immunoreactive neurons in the substantia nigra
    Jian-qing Liang, Li Wang, Jian-cheng He, Xian-dong Hua
    2016, 11 (1):  101-106.  doi: 10.4103/1673-5374.175053
    Abstract ( 216 )   PDF (965KB) ( 1008 )   Save

    Tyrosine hydroxylase is a key enzyme in dopamine biosynthesis. Change in tyrosine hydroxylase expression in the nigrostriatal system is closely related to the occurrence and development of Parkinson’s disease. Verbascoside, an extract from Radix Rehmanniae Praeparata has been shown to be clinically effective in treating Parkinson’s disease. However, the underlying mechanisms remain unclear. It is hypothesized that the effects of verbascoside on Parkinson’s disease are related to tyrosine hydroxylase expression change in the nigrostriatal system. Rat models of Parkinson’s disease were established and verbascoside (60 mg/kg) was administered intraperitoneally once a day. After 6 weeks of verbascoside treatment, rat rotational behavior was alleviated; tyrosine hydroxylase mRNA and protein expression and the number of tyrosine hydroxylase-immunoreactive neurons in the rat right substantia nigra were significantly higher than the Parkinson’s model group. These findings suggest that the mechanism by which verbascoside treats Parkinson’s disease is related to the regeneration of tyrosine hydroxylase-
    immunoreactive neurons in the substantia nigra.

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    Umbilical cord-derived mesenchymal stem cell transplantation combined with hyperbaric oxygen treatment for repair of traumatic brain injury
    Hai-xiao Zhou, Zhi-gang Liu, Xiao-jiao Liu, Qian-xue Chen
    2016, 11 (1):  107-113.  doi: 10.4103/1673-5374.175054
    Abstract ( 172 )   PDF (1067KB) ( 831 )   Save

    Transplantation of umbilical cord-derived mesenchymal stem cells (UC-MSCs) for repair of traumatic brain injury has been used in the clinic. Hyperbaric oxygen (HBO) treatment has long been widely used as an adjunctive therapy for treating traumatic brain injury. UC-MSC transplantation combined with HBO treatment is expected to yield better therapeutic effects on traumatic brain injury. In this study, we established rat models of severe traumatic brain injury by pressurized fluid (2.5–3.0 atm impact force). The injured rats were then administered UC-MSC transplantation via the tail vein in combination with HBO treatment. Compared with monotherapy, aquaporin 4 expression decreased in the injured rat brain, but growth-associated protein-43 expression, calaxon-like structures, and CM-Dil-positive cell number increased. Following combination therapy, however, rat cognitive and neurological function significantly improved. UC-MSC transplantation combined with HBO therapyfor repair of traumatic brain injury shows better therapeutic effects than monotherapy and significantly promotes recovery of neurological functions.

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    Specific effects of c-Jun NH2-terminal kinase-interacting protein 1 in neuronal axons
    Shu Tang, Qiang Wen, Xiao-jian Zhang, Quan-cheng Kan
    2016, 11 (1):  114-118.  doi: 10.4103/1673-5374.175055
    Abstract ( 148 )   PDF (816KB) ( 507 )   Save

    c-Jun NH2-terminal kinase (JNK)-interacting protein 3 plays an important role in brain-derived neurotrophic factor/tropomyosin-related kinase B (TrkB) anterograde axonal transport. It remains unclear whether JNK-interacting protein 1 mediates similar effects, or whether JNK-interacting protein 1 affects the regulation of TrkB anterograde axonal transport. In this study, we isolated rat embryonic hippocampus and cultured hippocampal neurons in vitro. Coimmunoprecipitation results demonstrated that JNK-interacting protein 1 formed TrkB complexes in vitro and in vivo. Immunocytochemistry results showed that when JNK-interacting protein 1 was highly expressed, the distribution of TrkB gradually increased in axon terminals. However, the distribution of TrkB reduced in axon terminals after knocking out JNK-interacting protein 1. In addition, there were differences in distribution of TrkB after JNK-interacting protein 1 was knocked out compared with not. However, knockout of JNK-interacting protein 1 did not affect the distribution of TrkB in dendrites. These findings confirm that JNK-interacting
    protein 1 can interact with TrkB in neuronal cells, and can regulate the transport of TrkB in axons, but not in dendrites.

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    Connectivity differences between adult male and female patients with attention deficit hyperactivity disorder according to resting-state functional MRI
    Bo-yong Park, Hyunjin Park
    2016, 11 (1):  119-125.  doi: 10.4103/1673-5374.175056
    Abstract ( 227 )   PDF (525KB) ( 801 )   Save

    Attention deficit hyperactivity disorder (ADHD) is a pervasive psychiatric disorder that affects both children and adults. Adult male and female patients with ADHD are differentially affected, but few studies have explored the differences. The purpose of this study was to quantify differences between adult male and female patients with ADHD based on neuroimaging and connectivity analysis. Resting-state functional magnetic resonance imaging scans were obtained and preprocessed in 82 patients. Group-wise differences between male and female patients were quantified using degree centrality for different brain regions. The medial-, middle-, and inferior-frontal gyrus, superior parietal lobule, precuneus, supramarginal gyrus, superior- and middle-temporal gyrus, middle occipital gyrus, and cuneus were identified as regions with significant group-wise differences. The identified regions were correlated with clinical scores reflecting depression
    and anxiety and significant correlations were found. Adult ADHD patients exhibit different levels of depression and anxiety depending on sex, and our study provides insight into how changes in brain circuitry might differentially impact male and female ADHD patients.

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    Does hemispheric lateralization influence therapeutic effects of transcranial direct current stimulation?
    Yong Hyun Kwon, Kyung Woo Kang, Na Kyung Lee, Sung Min Son
    2016, 11 (1):  126-129.  doi: 10.4103/1673-5374.175057
    Abstract ( 297 )   PDF (399KB) ( 567 )   Save

    This study investigated the effect of transcranial direct current stimulation (tDCS) polarity depending on lateralized function of task property in normal individuals performing visuomotor and simple repetitive tasks. Thirty healthy participants with no neurological disorders were recruited to participate in this study. Participantswere randomly allocated into active or control condition. For the active condition, tDCS intensity was 2 mA with stimulation applied for 15 minutes to the right hemisphere (tDCS condition). For the sham control, electrodes were placed in the same position, but the stimulator was turned off after 30 seconds (sham condition).The tapping and tracking task tests were performed before and after for both conditions. Univariate analysis revealed significant difference only in the tracking task. For direct comparison of both tasks within each group, the tracking task had significantly higher Z score than the tapping task in the tDCS group (P < 0.05). Thus, our study indicates that stimulation of the right hemisphere using tDCS can effectively improve visuomotor (tracking) task over simple repetitive (tapping) task.

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    Spatiotemporal expression of Nogo-66 receptor after focal cerebral ischemia
    Yue Cao, Ya-xian Dong, Jie Xu, Guo-liang Chu, Zhi-hua Yang, Yan-ming Liu
    2016, 11 (1):  132-136.  doi: 10.4103/1673-5374.175059
    Abstract ( 179 )   PDF (2775KB) ( 577 )   Save

    NgR, the receptor for the neurite outgrowth inhibitor Nogo-66, plays a critical role in the plasticity and regeneration of the nervous system after injury such as ischemic stroke. In the present study, we used immunohistochemistry to investigate the regional expression of NgR in rat brain following middle cerebral artery occlusion (MCAO). NgR protein expression was not observed in the center of the lesion, but was elevated in the marginal zone compared with control and sham-operated rats. The cerebral cortex and hippocampus (CA1, CA2, and CA3) showed the greatest expression of NgR. Furthermore, NgR expression was higher in the ipsilesional hemisphere than on the control side in the same coronal section. Although time-dependent changes in NgR expression across brain regions had their own characteristics, the overall trend complied with the following rules: NgR expression changes with time showed two peaks and one trough; the first peak in expression appeared between 1 and 3 days after MCAO; expression declined at 5 days; and the second peak occurred at 28 days.

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    Time representation of mitochondrial morphology and function after acute spinal cord injury
    Zhi-qiang Jia, Gang Li, Zhen-yu Zhang, Hao-tian Li, Ji-quan Wang, Zhong-kai Fan, Gang Lv
    2016, 11 (1):  137-143.  doi: 10.4103/1673-5374.175061
    Abstract ( 279 )   PDF (1417KB) ( 651 )   Save

    Changes in mitochondrial morphology and function play an important role in secondary damage after acute spinal cord injury. We recorded
    the time representation of mitochondrial morphology and function in rats with acute spinal cord injury. Results showed that mitochondria had an irregular shape, and increased in size. Mitochondrial cristae were disordered and mitochondrial membrane rupture was visible at 2–24 hours after injury. Fusion protein mitofusin 1 expression gradually increased, peaked at 8 hours after injury, and then decreased to its lowest level at 24 hours. Expression of dynamin-related protein 1, amitochondrial fission protein, showed the opposite kinetics. At 2–24 hours after acute spinal cord injury, malondialdehyde content, cytochrome c levels and caspase-3 expression were increased,but glutathione content, adenosine triphosphate content, Na+-K+-ATPase activity and mitochondrial membrane potential were gradually reduced. Furthermore, mitochondrial morphology altered during the acute stage of spinal cord injury. Fusion was important within the first 8 hours, but fission played a key role at 24 hours. Oxidative stress was inhibited, biological productivity was diminished, and mitochondrial membrane potential and permeability were reduced in the acute stage of injury. In summary, mitochondrial apoptosis is activated when the time of spinal cord injury is prolonged.

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    Treatment with analgesics after mouse sciatic nerve injury does not alter expression of wound healing-associated genes
    Matt C. Danzi, Dario Motti, Donna L. Avison, John L. Bixby, Vance P. Lemmon
    2016, 11 (1):  144-149.  doi: 10.4103/1673-5374.169637
    Abstract ( 306 )   PDF (432KB) ( 626 )   Save

    Animal models of sciatic nerve injury are commonly used to study neuropathic pain as well as axon regeneration.
    Administration of post-surgical analgesics is an important consideration for animal welfare, but the actions of the analgesic must not interfere with the scientific goals of the experiment. In this study, we show that treatment with either buprenorphine or acetaminophen following a bilateral sciatic nerve crush surgery does not alter the expression in dorsal root ganglion (DRG) sensory neurons of a panel of genes associated with wound healing. These findings indicate that the post-operative use of buprenorphine or acetaminophen at doses commonly suggested by Institutional Animal Care and Use Committees does not change the intrinsic gene expression response of DRG neurons to a sciatic nerve crush injury, for many wound healing-associated genes. Therefore, administration of post-operative analgesics may not confound the results of transcriptomic studies employing this injury model.

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    A novel bioactive nerve conduit for the repair of peripheral nerve injury
    Bin-bin Li, Yi-xia Yin, Qiong-jiao Yan, Xin-yu Wang, Shi-pu Li
    2016, 11 (1):  150-155.  doi: 10.4103/1673-5374.175062
    Abstract ( 202 )   PDF (2263KB) ( 607 )   Save

    The use of a nerve conduit provides an opportunity to regulate cytokines, growth factors and neurotrophins in peripheral nerve regeneration
    and avoid autograft defects. We constructed a poly-D-L-lactide (PDLLA)-based nerve conduit that was modified using poly{(lactic acid)-co-[(glycolic acid)-alt-(L-lysine)]} and β-tricalcium phosphate. The effectiveness of this bioactive PDLLA-based nerve conduit was compared to that of PDLLA-only conduit in the nerve regeneration following a 10-mm sciatic nerve injury in rats. We observed the nerve morphology in the early period of regeneration, 35 days post injury, using hematoxylin-eosin and methylene blue staining. Compared with the PDLLA conduit, the nerve fibers in the PDLLA-based bioactive nerve conduit were thicker and more regular in size. Muscle fibers in the soleus muscle had greater diameters in the PDLLA bioactive group than in the PDLLA only group. The PDLLA-based bioactive nerve conduit is a promising strategy for repair after sciatic nerve injury.

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    Cerebrolysin improves sciatic nerve dysfunction in a mouse model of diabetic peripheral neuropathy
    Han-yu Dong, Xin-mei Jiang, Chun-bo Niu, Lin Du, Jun-yan Feng, Fei-yong Jia
    2016, 11 (1):  156-162.  doi: 10.4103/1673-5374.175063
    Abstract ( 225 )   PDF (1096KB) ( 1114 )   Save

    To examine the effects of Cerebrolysin on the treatment of diabetic peripheral neuropathy, we first established a mouse model of type 2 diabetes mellitus by administering a high-glucose, high-fat diet and a single intraperitoneal injection of streptozotocin. Mice defined as diabetic in this model were then treated with 1.80, 5.39 or 8.98 mL/kg of Cerebrolysin via intraperitoneal injections for 10 consecutive days. Our results demonstrated that the number, diameter and area of myelinated nerve fibers increased in the sciatic nerves of these mice after administration of Cerebrolysin. The results of several behavioral tests showed that Cerebrolysin dose-dependently increased the slope angle in the inclined plane test (indicating an improved ability to maintain body position), prolonged tail-flick latency and foot-licking time (indicating enhanced sensitivity to thermal and chemical pain, respectively, and reduced pain thresholds), and increased an index of sciatic nerve function in diabetic mice compared with those behavioral results in untreated diabetic mice. Taken together, the anatomical and functional results suggest that Cerebrolysin ameliorated peripheral neuropathy in a mouse model of type 2 diabetes mellitus.

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    Dexamethasone prevents vascular damage in early-stage non-freezing cold injury of the sciatic nerve
    Hao Li, Lei Zhang, Min Xu
    2016, 11 (1):  163-167.  doi: 10.4103/1673-5374.175064
    Abstract ( 275 )   PDF (1286KB) ( 767 )   Save

    Non-freezing cold injury is a prevalent cause of peripheral nerve damage, but its pathogenic mechanism is poorly understood, and treatment
    remains inadequate. Glucocorticoids have anti-inflammatory and lipid peroxidation-inhibiting properties. We therefore examined whether dexamethasone, a synthetic glucocorticoid compound, would alleviate early-stage non-freezing cold injury of the sciatic nerve. We established Wistar rat models of non-freezing cold injury by exposing the left sciatic nerve to cold (3–5°C) for 2 hours, then administered dexamethasone (3 mg/kg intraperitoneally) to half of the models. One day after injury, the concentration of Evans blue tracer in the injured sciatic nerve of rats that received dexamethasone was notably lower than that in the injured sciatic nerve of rats that did not receive dexamethasone; neither Evans blue dye nor capillary stenosis was observed in the endoneurium, but myelinated nerve fibers were markedly degenerated in the injured sciatic nerve of animals that received dexamethasone. After dexamethasone administration, however, endoneurial vasculopathy was markedly improved, although damage to the myelinated nerve fiber was not alleviated. These findings suggest that dexamethasone protects the blood-nerve barrier, but its benefit in non-freezing cold injury is limited to the vascular system.

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    Angiogenesis in tissue-engineered nerves evaluated objectively using MICROFIL perfusion and micro-CT scanning
    Hong-kui Wang, Ya-xian Wang, Cheng-bin Xue, Zhen-mei-yu Li, Jing Huang, Ya-hong Zhao, Yu-min Yang, Xiao-song Gu
    2016, 11 (1):  168-173.  doi: 10.4103/1673-5374.175065
    Abstract ( 306 )   PDF (632KB) ( 957 )   Save

    Angiogenesis is a key process in regenerative medicine generally, as well as in the specific field of nerve regeneration. However, no convenient
    and objective method for evaluating the angiogenesis of tissue-engineered nerves has been reported. In this study, tissue-engineered nerves were constructed in vitro using Schwann cells differentiated from rat skin-derived precursors as supporting cells and chitosan nerve conduits combined with silk fibroin fibers as scaffolds to bridge 10-mm sciatic nerve defects in rats. Four weeks after surgery, three-dimensional blood vessel reconstructions were made through MICROFIL perfusion and micro-CT scanning, and parameter analysis of the tissue-engineered nerves was performed. New blood vessels grew into the tissue-engineered nerves from three main directions: the proximal end, the distal end, and the middle. The parameter analysis of the three-dimensional blood vessel images yielded several parameters, including the number, diameter, connection, and spatial distribution of blood vessels. The new blood vessels were mainly capillaries and microvessels, with diameters ranging from 9 to 301 μm. The blood vessels with diameters from 27 to 155 μm accounted for 82.84% of the new vessels. The microvessels in the tissue-engineered nerves implanted in vivo were relatively well-identified using the MICROFIL perfusion and micro-CT scanning method, which allows the evaluation and comparison of differences and changes of angiogenesis in tissue-engineered nerves implanted in vivo.

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    Vascular endothelial growth factor: an attractive target in the treatment of hypoxic/ischemic brain injury
    Hui Guo, Hui Zhou, Jie Lu, Yi Qu, Dan Yu, Yu Tong
    2016, 11 (1):  174-179.  doi: 10.4103/1673-5374.175067
    Abstract ( 309 )   PDF (253KB) ( 723 )   Save

    Cerebral hypoxia or ischemia results in cell death and cerebral edema, as well as other cellular reactions such as angiogenesis and the reestablishment of functional microvasculature to promote recovery from brain injury. Vascular endothelial growth factor is expressed in the central nervous system after hypoxic/ischemic brain injury, and is involved in the process of brain repair via the regulation of angiogenesis, neurogenesis, neurite outgrowth, and cerebral edema, which all require vascular endothelial growth factor signaling. In this review, we focus on the role of the vascular endothelial growth factor signaling pathway in the response to hypoxic/ischemic brain injury, and discuss potential therapeutic interventions.

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    Information for Authors -Neural Regeneration Research
    2016, 11 (1):  180-184. 
    Abstract ( 316 )   PDF (262KB) ( 1003 )   Save
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