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    30 July 2016, Volume 11 Issue 7 Previous Issue    Next Issue
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    Lim kinase, a bi-functional effector in injury-induced structural plasticity of synapses
    Weiwei Wang, Ellen Townes-Anderson
    2016, 11 (7):  1029-1032.  doi: 10.4103/1673-5374.187018
    Abstract ( 228 )   PDF (395KB) ( 376 )   Save

    The structural plasticity of synaptic terminals contributes to normal nervous system function but also to neural degeneration, in the form of terminal retraction, and regeneration, due to process growth. Synaptic morphological change is mediated through the actin cytoskeleton, which is enriched in axonal and dendritic terminals. Whereas the three RhoGTPases, RhoA, Cdc42 and Rac, function as upstream signaling nodes sensitive to extracellular stimuli, LIMK-cofilin activity serves as a common downstream effector to up-regulate actin turnover, which is necessary for both polymerization and depolymerization. The dual effects of LIMK activity make LIMK a potential target of therapeutic intervention for injury-induced synaptic plasticity, as LIMK inhibition can stabilize actin cytoskeleton and preserve existing structure. This therapeutic benefit of LIMK inhibition has been demonstrated in animal models of injury-induced axon retraction and neuritic sprouting by rod photoreceptors. A better understanding of the regulation of LIMK-cofilin activity and the interaction with the microtubular cytoskeleton may open new ways to promote synaptic regeneration that can benefit neuronal degenerative disease.

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    Repair of traumatic plasmalemmal damage to neurons and other eukaryotic cells
    George D. Bittner, Christopher S. Spaeth§, Andrew D. Poon, Zachary S. Burgess, Christopher H. McGill
    2016, 11 (7):  1033-1042.  doi: 10.4103/1673-5374.187019
    Abstract ( 219 )   PDF (1055KB) ( 337 )   Save

    The repair (sealing) of plasmalemmal damage, consisting of small holes to complete transections, is critical for cell survival, especially for neurons that rarely regenerate cell bodies. We first describe and evaluate different measures of cell sealing. Some measures, including morphological/ultra-structural observations, membrane potential, and input resistance, provide very ambiguous assessments of plasmalemmal sealing. In contrast, measures of ionic current flow and dye barriers can, if appropriately used, provide more accurate assessments. We describe the effects of various substances (calcium, calpains, cytoskeletal proteins, ESCRT proteins, mUNC-13, NSF, PEG) and biochemical pathways (PKA, PKC, PLC, Epac, cytosolic oxidation) on plasmalemmal sealing probability, and suggest that substances, pathways, and cellular events associated with plasmalemmal sealing have undergone a very conservative evolution. During sealing, calcium ion influx mobilizes vesicles and other membranous structures (lysosomes, mitochondria, etc.) in a continuous fashion to form a vesicular plug that gradually restricts diffusion of increasingly smaller molecules and ions over a period of seconds to minutes. Furthermore, we find no direct evidence that sealing occurs through the collapse and fusion of severed plasmalemmal leaflets, or in a single step involving the fusion of one large wound vesicle with the nearby, undamaged plasmalemma. We describe how increases in perikaryal calcium levels following axonal transection account for observations that cell body survival decreases the closer an axon is transected to the perikaryon. Finally, we speculate on relationships between plasmalemmal sealing, Wallerian degeneration, and the ability of polyethylene glycol (PEG) to seal cell membranes and rejoin severed axonal ends – an important consideration for the future treatment of trauma to peripheral nerves. A better knowledge of biochemical pathways and cytoplasmic structures involved in plasmalemmal sealing might provide insights to develop treatments for traumatic nerve injuries, stroke, muscular dystrophy, and other pathologies.

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    Aldynoglia cells and modulation of RhoGTPase activity as useful tools for spinal cord injury repair
    Ernesto Doncel-Pérez, Manuel Nieto-Sampedro
    2016, 11 (7):  1043-1045.  doi: 10.4103/1673-5374.187020
    Abstract ( 164 )   PDF (557KB) ( 332 )   Save

    A combined approach in spinal cord injury (SCI) therapy is the modulation of the cellular and molecular processes involved in glial scarring. Aldaynoglial cells are neural cell precursors with a high capacity to differentiate into neurons, promote axonal growth, wrapping and myelination of resident neurons. These important characteristics of aldaynoglia can be combined with specific inhibition of the RhoGTPase activity in astroglia and microglia that cause reduction of glial proliferation, retraction of glial cell processes and myelin production by oligodendrocytes. Previously we used experimental central nervous system (CNS) injury models, like spinal cord contusion and striatal lacunar infarction and observed that administration of RhoGTPase glycolipid inhibitor or aldaynoglial cells, respectively, produced a significant gain of functional recovery in treated animals. The combined therapy with neuro-regenerative properties strategy is highly desirable to treat SCI for functional potentiation of neurons and oligodendrocytes, resulting in better locomotor recovery. Here we suggest that treatment of spinal lesions with aldaynoglia from neurospheres plus local administration of a RhoGTPase inhibitor could have an additive effect and promote recovery from SCI.

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    Points regarding cell transplantation for the treatment of spinal cord injury
    Chizuka Ide, Kenji Kanekiyo
    2016, 11 (7):  1046-1049.  doi: 10.4103/1673-5374.187021
    Abstract ( 144 )   PDF (30328KB) ( 319 )   Save
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    Reactive astrocyte scar and axon regeneration: suppressor or facilitator?
    Yosuke Ohtake, George M. Smith, Shuxin Li
    2016, 11 (7):  1050-1051.  doi: 10.4103/1673-5374.187022
    Abstract ( 200 )   PDF (168KB) ( 415 )   Save
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    The complex contribution of the astrocyte scar
    Melinda Fitzgerald
    2016, 11 (7):  1052-1053.  doi: 10.4103/1673-5374.187023
    Abstract ( 130 )   PDF (159KB) ( 307 )   Save
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    The astrocyte scar – not so inhibitory after all?
    Bor Luen Tang
    2016, 11 (7):  1054-1055.  doi: 10.4103/1673-5374.187024
    Abstract ( 155 )   PDF (165KB) ( 373 )   Save
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    Mitochondrial translocator protein (TSPO), astrocytes and neuroinflammation
    Olga V. Chechneva, Wenbin Deng
    2016, 11 (7):  1056-1057.  doi: 10.4103/1673-5374.187027
    Abstract ( 359 )   PDF (309KB) ( 435 )   Save
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    Novel rehabilitation paradigm for restoration of hand functions after tetraplegia
    Ashraf S. Gorgey, Mina P. Ghatas
    2016, 11 (7):  1058-1059.  doi: 10.4103/1673-5374.187025
    Abstract ( 173 )   PDF (159KB) ( 392 )   Save
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    Aligned carbon nanotube containing scaffolds for neural tissue regeneration
    Pallavi Gupta, Debrupa Lahiri
    2016, 11 (7):  1062-1063.  doi: 10.4103/1673-5374.187028
    Abstract ( 245 )   PDF (708KB) ( 367 )   Save
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    Resveratrol effects on neural connectivity during aging
    Gonzalo Flores, Rubén Antonio Vázquez-Roque, Alfonso Diaz
    2016, 11 (7):  1067-1068.  doi: 10.4103/1673-5374.187029
    Abstract ( 244 )   PDF (546KB) ( 400 )   Save
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    How does zebrafish support new strategies for neuroprotection and neuroregeneration in hypoxia-related diseases?
    Emerson S. Silva, João Batista T. Rocha, Diogo O. Souza, Marcos M. Braga
    2016, 11 (7):  1069-1070.  doi: 10.4103/1673-5374.187030
    Abstract ( 187 )   PDF (536KB) ( 362 )   Save
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    Beneficial effects of date palm fruits on neurodegenerative diseases
    Musthafa Mohamed Essa, Mohammed Akbar, Mohammed Abdul Sattar Khan
    2016, 11 (7):  1071-1072.  doi: 10.4103/1673-5374.187032
    Abstract ( 151 )   PDF (436KB) ( 360 )   Save
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    Novel role for transcranial magnetic stimulation to study post-traumatic respiratory neuroplasticity
    Stéphane Vinit, Michel Petitjean
    2016, 11 (7):  1073-1074.  doi: 10.4103/1673-5374.187034
    Abstract ( 197 )   PDF (327KB) ( 399 )   Save
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    Endogenous neural progenitor cells in the repair of the injured spinal cord
    Yilin Mao, Tara Nguyen, Theresa Sutherland, Catherine Anne Gorrie
    2016, 11 (7):  1075-1076.  doi: 10.4103/1673-5374.187035
    Abstract ( 144 )   PDF (390KB) ( 403 )   Save
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    NLRP3 inflammasome in retinal ganglion cell loss in optic neuropathy
    Liang Feng, Xiaorong Liu
    2016, 11 (7):  1077-1078.  doi: 10.4103/1673-5374.187036
    Abstract ( 260 )   PDF (171KB) ( 439 )   Save
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    Avoiding experimental bias by systematic antibody validation
    Sara B. Jager, Christian Bjerggaard Vaegter
    2016, 11 (7):  1079-1080.  doi: 10.4103/1673-5374.187037
    Abstract ( 148 )   PDF (588KB) ( 396 )   Save
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    Effect of ischemic preconditioning on antioxidant status in the gerbil hippocampal CA1 region after transient forebrain ischemia
    Seung Min Park, Chan Woo Park, Tae-Kyeong Lee, Jeong Hwi Cho, Joon Ha Park, Jae-Chul Lee, Bai Hui Chen, Bich-Na Shin, Ji Hyeon Ahn, Hyun-Jin Tae, Myoung Cheol Shin, Taek Geun Ohk, Jun Hwi Cho, Moo-Ho Won, Soo Young Choi, In Hye Kim
    2016, 11 (7):  1081-1089.  doi: 10.4103/1673-5374.187039
    Abstract ( 231 )   PDF (2655KB) ( 615 )   Save
    Ischemic preconditioning (IPC) is a condition of sublethal transient global ischemia and exhibits neuroprotective effects against subsequent lethal ischemic insult. We, in this study, examined the neuroprotective effects of IPC and its effects on immunoreactive changes of antioxidant enzymes including superoxide dismutase (SOD) 1 and SOD2, catalase (CAT) and glutathione peroxidase (GPX) in the gerbil hippocampal CA1 region after transient forebrain ischemia. Pyramidal neurons of the stratum pyramidale (SP) in the hippocampal CA1 region of animals died 5 days after lethal transient ischemia without IPC (8.6% (ratio of remanent neurons) of the sham-operated group); however, IPC prevented the pyramidal neurons from subsequent lethal ischemic injury (92.3% (ratio of remanent neurons) of the sham-operated group). SOD1, SOD2, CAT and GPX immunoreactivities in the sham-operated animals were easily detected in pyramidal neurons in the stratum pyramidale (SP) of the hippocampal CA1 region, while all of these immunoreactivities were rarely detected in the stratum pyramidale at 5 days after lethal transient ischemia without IPC. Meanwhile, their immunoreactivities in the sham-operated animals with IPC were similar to (SOD1, SOD2 and CAT) or higher (GPX) than those in the sham-operated animals without IPC. Furthermore, their immunoreactivities in the stratum pyramidale of the ischemia-operated animals with IPC were steadily maintained after lethal ischemia/reperfusion. Results of western blot analysis for SOD1, SOD2, CAT and GPX were similar to immunohistochemical data. In conclusion, IPC maintained or increased the expression of antioxidant enzymes in the stratum pyramidale of the hippocampal CA1 region after subsequent lethal transient forebrain ischemia and IPC exhibited neuroprotective effects in the hippocampal CA1 region against transient forebrain ischemia.
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    Electroacupuncture alleviates cerebral ischemia and reperfusion injury via modulation of the ERK1/2 signaling pathway
    Xiao-lu Jin, Peng-fei Li, Chun-bing Zhang, Jin-ping Wu, Xi-lian Feng, Ying Zhang, Mei-hong Shen
    2016, 11 (7):  1090-1098.  doi: 10.4103/1673-5374.187041
    Abstract ( 281 )   PDF (2507KB) ( 616 )   Save
    Electroacupuncture (EA) has anti-oxidative and anti-inflammatory actions, but whether the neuroprotective effect of EA against cerebral ischemia-reperfusion (I/R) injury involves modulation of the extracellular regulated kinase 1/2 (ERK1/2) signaling pathway is unclear. Middle cerebral artery occlusion (MCAO) was performed in Sprague-Dawley rats for 2 hours followed by reperfusion for 24 hours. A 30-minute period of EA stimulation was applied to both Baihui (DU20) and Dazhui (DU14) acupoints in each rat (10 mm EA penetration depth, continuous wave with a frequency of 3 Hz, and a current intensity of 1–3 mA) when reperfusion was initiated. EA significantly reduced infarct volume, alleviated neuronal injury, and improved neurological function in rats with MCAO. Furthermore, high mRNA expression of Bax and low mRNA expression of Bcl-2 induced by MCAO was prevented by EA. EA substantially restored total glutathione reductase (GR), glutathione (GSH) and glutathione peroxidase (GSH-Px) levels. Additionally, Nrf2 and glutamylcysteine synthetase (GCS) expression levels were markedly increased by EA. Interestingly, the neuroprotective effects of EA were attenuated when ERK1/2 activity was blocked by PD98059 (a specific MEK inhibitor). Collectively, our findings indicate that activation of the ERK1/2 signaling pathway contributes to the neuroprotective effects of EA. Our study provides a better understanding of the regulatory mechanisms underlying the therapeutic effectiveness of EA.
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    Mechanisms of electroacupuncture effects on acute cerebral ischemia/reperfusion injury: possible association with upregulation of transforming growth factor beta 1
    Wen-biao Wang, Lai-fu Yang, Qing-song He, Tong Li, Yi-yong Ma, Ping Zhang, Yi-sheng Cao
    2016, 11 (7):  1099-1101.  doi: 10.4103/1673-5374.187042
    Abstract ( 280 )   PDF (238KB) ( 385 )   Save

    Electroacupuncture at the head acupoints Baihui (GV20) and Shuigou (GV26) improves recovery of neurological function following ischemic cerebrovascular events, but its mechanism remains incompletely understood. We hypothesized that the action of electroacupuncture at these acupoints is associated with elevated serum levels of transforming growth factor beta 1 (TGF-β1). To test this, we established a rat model of cerebral ischemia by middle cerebral artery occlusion. Electroacupuncture was performed at Baihui and Shuigou with a “dispersedense” wave at an alternating frequency of 2 and 150 Hz, and at a constant intensity of 3 mA. Each electroacupuncture session lasted 30 minutes and was performed every 12 hours for 3 days. Neurological severity scores were lower in injured rats after acupuncture than in those not subjected to treatment. Furthermore, serum level of TGF-β1 was greater after electroacupuncture than after no treatment. Our results indicate that electroacupuncture at Baihui and Shuigou increases the serum level of TGF-β1 in rats with acute cerebral ischemia/ reperfusion injury, and exerts neuroprotective effects.

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    Neuroprotective effect of angiotensin II type 2 receptor during cerebral ischemia/reperfusion
    Chun-ye Ma, Lin Yin
    2016, 11 (7):  1102-1107.  doi: 10.4103/1673-5374.187044
    Abstract ( 322 )   PDF (2248KB) ( 692 )   Save
    "Angiotensin II type 2 receptor (AT2R) activation has been shown to protect against stroke, but its precise mechanism remains poorly understood. We investigated whether the protective effect of AT2R against ischemia/reperfusion injury is mediated by the suppression of immune and inflammatory responses. Rat models of middle cerebral artery occlusion were intraperitoneally injected with physiological saline, the AT2R agonist CGP42112 (1 mg/kg per day) or antagonist PD123319 (1 mg/kg per day). In the CGP42112 group, AT2R expression increased, the infarct area decreased, interleukin-1β and tumor necrosis factor-α expression decreased, and interleukin-10 expression increased compared with the saline group. Antagonisin AT2R using PD123319 produced the opposite effects. These results indicate that AT2R activation suppresses immune and inflammatory responses, and protects against cerebral ischemia/reperfusion injury."
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    Dynamic changes in neuronal autophagy and apoptosis in the ischemic penumbra following permanent ischemic stroke
    Yi-hao Deng, Hong-yun He, Li-qiang Yang, Peng-yue Zhang
    2016, 11 (7):  1108-1114.  doi: 10.4103/1673-5374.187045
    Abstract ( 311 )   PDF (1088KB) ( 686 )   Save
    The temporal dynamics of neuronal autophagy and apoptosis in the ischemic penumbra following stroke remains unclear. Therefore, in this study, we investigated the dynamic changes in autophagy and apoptosis in the penumbra to provide insight into potential therapeutic targets for stroke. An adult Sprague-Dawley rat model of permanent ischemic stroke was prepared by middle cerebral artery occlusion. Neuronal autophagy and apoptosis in the penumbra post-ischemia were evaluated by western blot assay and immunofluorescence staining with antibodies against LC3-II and cleaved caspase-3, respectively. Levels of both LC3-II and cleaved caspase-3 in the penumbra gradually increased within 5 hours post-ischemia. Thereafter, levels of both proteins declined, especially LC3-II. The cerebral infarct volume increased slowly 1–4 hours after ischemia, but subsequently increased rapidly until 5 hours after ischemia. The severity of the neurological deficit was positively correlated with infarct volume. LC3-II and cleaved caspase-3 levels were high in the penumbra within 5 hours after ischemia, and after that, levels of these proteins decreased at different rates. LC3-II levels were reduced to a very low level, but cleaved caspase- 3 levels remained high 72 hours after ischemia. These results indicate that there are temporal differences in the activation status of the autophagic and apoptotic pathways. This suggests that therapeutic targeting of these pathways should take into consideration their unique temporal dynamics.
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    Magnetic resonance diffusion tensor imaging following major ozonated autohemotherapy for treatment of acute cerebral infarction
    Xiao-na Wu, Tao Zhang, Jun Wang, Xiao-yan Liu, Zhen-sheng Li, Wei Xiang, Wei-qing Du, Hong-jun Yang, Tie-gen Xiong, Wen-ting Deng, Kai-run Peng, Su-yue Pan
    2016, 11 (7):  1115-1121.  doi: 10.4103/1673-5374.187046
    Abstract ( 218 )   PDF (1002KB) ( 431 )   Save
    Major ozonated autohemotherapy has been shown to promote recovery of upper limb motor function in patients with acute cerebral infarction, but whether major ozonated autohemotherapy affects remote injury remains poorly understood. Here, we assumed that major ozonated autohemotherapy contributes to recovery of clinical function, possibly by reducing remote injury after acute cerebral infarction. Sixty acute cerebral infarction patients aged 30–80 years were equally and randomly allocated to ozone treatment and control groups. Patients in the ozone treatment group received medical treatment and major ozonated autohemotherapy (47 mg/L, 100 mL ozone) for 10 ± 2 days. Patients in the control group received medical treatment only. National Institutes of Health Stroke Scale score, modified Rankin scale score, and reduced degree of fractional anisotropy values of brain magnetic resonance diffusion tensor imaging were remarkably decreased, brain function improved, clinical efficiency significantly increased, and no obvious adverse reactions detected in the ozone treatment group compared with the control group. These findings suggest that major ozonated autohemotherapy promotes recovery of neurological function in acute cerebral infarction patients by reducing remote injury, and additionally, exhibits high safety.
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    CD163 promotes hematoma absorption and improves neurological functions in patients with intracerebral hemorrhage
    Wen-jing Xie, Hong-quan Yu, Yu Zhang, Qun Liu, Hong-mei Meng
    2016, 11 (7):  1122-1127.  doi: 10.4103/1673-5374.187047
    Abstract ( 305 )   PDF (895KB) ( 626 )   Save
    Clinical outcomes are positively associated with hematoma absorption. The monocyte-macrophage scavenger receptor, CD163, plays an important role in the metabolism of hemoglobin, and a soluble form of CD163 is present in plasma and other tissue fluids; therefore, we speculated that serum CD163 affects hematoma absorption after intracerebral hemorrhage. Patients with intracerebral hemorrhage were divided into high- and low-level groups according to the average CD163 level (1,977.79 ± 832.91 ng/mL). Compared with the high-level group, the low-level group had a significantly slower hematoma absorption rate, and significantly increased National Institutes of Health Stroke Scale scores and modified Rankin Scale scores. These results suggest that CD163 promotes hematoma absorption and the recovery of neurological function in patients with intracerebral hemorrhage.
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    Apelin-13 as a novel target for intervention in secondary injury after traumatic brain injury
    Hai-jun Bao, Hai-yang Qiu, Jin-xia Kuai, Cheng-jie Song, Shao-xian Wang, Chao-qun Wang, Hua-bin Peng, Wen-can Han, Yong-ping Wu
    2016, 11 (7):  1128-1133.  doi: 10.4103/1673-5374.187049
    Abstract ( 417 )   PDF (1159KB) ( 386 )   Save

    The adipocytokine, apelin-13, is an abundantly expressed peptide in the nervous system. Apelin-13 protects the brain against ischemia/ reperfusion injury and attenuates traumatic brain injury by suppressing autophagy. However, secondary apelin-13 effects on traumatic brain injury-induced neural cell death and blood-brain barrier integrity are still not clear. Here, we found that apelin-13 significantly decreases cerebral water content, mitigates blood-brain barrier destruction, reduces aquaporin-4 expression, diminishes caspase-3 and Bax expression in the cerebral cortex and hippocampus, and reduces apoptosis. These results show that apelin-13 attenuates secondary injury after traumatic brain injury and exerts a neuroprotective effect.

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    Heat shock protein 70 protects PC12 cells against ischemia-hypoxia/reoxygenation by maintaining intracellular Ca2+ homeostasis
    Yuan Liu, Xue-chun Wang, Dan Hu, Shu-ran Huang, Qing-shu Li, Zhi Li, Yan Qu
    2016, 11 (7):  1134-1140.  doi: 10.4103/1673-5374.187051
    Abstract ( 420 )   PDF (926KB) ( 608 )   Save
    Heat shock protein 70 (HSP70) maintains Ca2+ homeostasis in PC12 cells, which may protect against apoptosis; however, the mechanisms of neuroprotection are unclear. Therefore, in this study, we examined Ca2+ levels in PC12 cells transfected with an exogenous lentiviral HSP70 gene expression construct, and we subsequently subjected the cells to ischemia-hypoxia/reoxygenation injury. HSP70 overexpression increased neuronal viability and ATPase activity, and it decreased cellular reactive oxygen species levels and intracellular Ca2+ concentration after hypoxia/reoxygenation. HSP70 overexpression enhanced the protein and mRNA expression levels of sarcoplasmic/ endoplasmic reticulum Ca2+-ATPase (SERCA), but it decreased the protein and mRNA levels of inositol 1,4,5-trisphosphate receptor (IP3R), thereby leading to decreased intracellular Ca2+ concentration after ischemia-hypoxia/reoxygenation. These results suggest that exogenous HSP70 protects against ischemia-hypoxia/reoxygenation injury, at least in part, by maintaining cellular Ca2+ homeostasis, by upregulating SERCA expression and by downregulating IP3R expression.
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    Magnetic stimulation at Neiguan (PC6) acupoint increases connections between cerebral cortex regions
    Hong-li Yu, Gui-zhi Xu, Lei Guo, Ling-di Fu, Shuo Yang, Shuo Shi, Hua Lv
    2016, 11 (7):  1141-1146.  doi: 10.4103/1673-5374.187053
    Abstract ( 186 )   PDF (2235KB) ( 762 )   Save
    Stimulation at specific acupoints can activate cortical regions in human subjects. Previous studies have mainly focused on a single brain region. However, the brain is a network and many brain regions participate in the same task. The study of a single brain region alone cannot clearly explain any brain-related issues. Therefore, for the present study, magnetic stimulation was used to stimulate the Neiguan (PC6) acupoint, and 32-channel electroencephalography data were recorded before and after stimulation. Brain functional networks were constructed based on electroencephalography data to determine the relationship between magnetic stimulation at the PC6 acupoint and cortical excitability. Results indicated that magnetic stimulation at the PC6 acupoint increased connections between cerebral cortex regions.
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    Detection of Ca2+-dependent acid phosphatase activity identifies neuronal integrity in damaged rat central nervous system after application of bacterial melanin.
    Tigran R. Petrosyan, Anna S. Ter-Markosyan, Anna S. Hovsepyan
    2016, 11 (7):  1147-1152.  doi: 10.4103/1673-5374.187055
    Abstract ( 133 )   PDF (1290KB) ( 385 )   Save
    The study aims to confirm the neuroregenerative effects of bacterial melanin (BM) on central nervous system injury using a special staining method based on the detection of Ca2+-dependent acid phosphatase activity. Twenty-four rats were randomly assigned to undergo either unilateral destruction of sensorimotor cortex (group I; n = 12) or unilateral rubrospinal tract transection at the cervical level (C3–4) (group II; n = 12). In each group, six rats were randomly selected after surgery to undergo intramuscular injection of BM solution (BM subgroup) and the remaining six rats were intramuscularly injected with saline (saline subgroup). Neurological testing confirmed that BM accelerated the recovery of motor function in rats from both BM and saline subgroups. Two months after surgery, Ca2+-dependent acid phosphatase activity detection in combination with Chilingarian’s calcium adenoside triphosphate method revealed that BM stimulated the sprouting of fibers and dilated the capillaries in the brain and spinal cord. These results suggest that BM can promote the recovery of motor function of rats with central nervous system injury; and detection of Ca2+-dependent acid phosphatase activity is a fast and easy method used to study the regeneration- promoting effects of BM on the injured central nervous system.
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    Genistein suppresses the mitochondrial apoptotic pathway in hippocampal neurons in rats with Alzheimer’s disease
    Yan Wang, Biao Cai, Jing Shao, Ting-ting Wang, Run-ze Cai, Chang-ju Ma, Tao Han, Jun Du
    2016, 11 (7):  1153-1158.  doi: 10.4103/1673-5374.187056
    Abstract ( 227 )   PDF (1908KB) ( 365 )   Save
    Genistein is effective against amyloid-β toxicity, but the underlying mechanisms are unclear. We hypothesized that genistein may protect neurons by inhibiting the mitochondrial apoptotic pathway, and thereby play a role in the prevention of Alzheimer’s disease. A rat model of Alzheimer’s disease was established by intraperitoneal injection of D-galactose and intracerebral injection of amyloid-β peptide (25–35). In the genistein treatment groups, a 7-day pretreatment with genistein (10, 30, 90 mg/kg) was given prior to establishing Alzheimer’s disease model, for 49 consecutive days. Terminal deoxyribonucleotidyl transferase-mediated dUTP nick end labeling assay demonstrated a reduction in apoptosis in the hippocampus of rats treated with genistein. Western blot analysis showed that expression levels of capase-3, Bax and cytochrome c were decreased compared with the model group. Furthermore, immunohistochemical staining revealed reductions in cytochrome c and Bax immunoreactivity in these rats. Morris water maze revealed a substantial shortening of escape latency by genistein in Alzheimer’s disease rats. These findings suggest that genistein decreases neuronal loss in the hippocampus, and improves learning and memory ability. The neuroprotective effects of genistein are associated with the inhibition of the mitochondrial apoptotic pathway, as shown by its ability to reduce levels of caspase-3, Bax and cytochrome c.
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    Protective effects of ginsenoside Rg1 against hydrogen peroxide-induced injury in human neuroblastoma cells
    Zhi-gao Sun, Li-ping Chen, Fa-wei Wang, Cheng-yong Xu, Miao Geng
    2016, 11 (7):  1159-1164.  doi: 10.4103/1673-5374.187057
    Abstract ( 207 )   PDF (749KB) ( 643 )   Save
    The active ingredient of ginseng, ginsenosides Rg1, has been shown to scavenge free radicals and improve antioxidant capacity. This study hypothesized that ginsenosides Rg1 has a protective role in human neuroblastoma cells injured by H2O2. Ginsenosides Rg1 at different concentrations (50 and 100 μM) was used to treat H2O2 (150 μM)-injured SH-SY5Y cells. Results demonstrated that ginsenoside Rg1 elevated the survival rate of SH-SY5Y cells injured by H2O2, diminished the amount of leaked lactate dehydrogenase, and increased superoxide dismutase activity. Ginsenoside Rg1 effectively suppressed caspase-3 immunoreactivity, and contributed to heat shock protein 70 gene expression, in a dose-dependent manner. These results indicate that ginsenoside Rg1 has protective effects on SH-SY5Y cells injured by H2O2 and that its mechanism of action is associated with anti-oxidation and the inhibition of apoptosis.
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    Differential temporal expression of matrix metalloproteinases following sciatic nerve crush
    Jing Qin, Guang-bin Zha, Jun Yu, Hong-hong Zhang, Sheng Yi
    2016, 11 (7):  1165-1171.  doi: 10.4103/1673-5374.187059
    Abstract ( 262 )   PDF (1073KB) ( 508 )   Save
    We previously performed transcriptome sequencing and found that genes for matrix metalloproteinases (MMPs), such as MMP7 and 12, seem to be highly upregulated following peripheral nerve injury, and may be involved in nerve repair. In the present study, we systematically determined the expression levels of MMPs and their regulators at 1, 4, 7 and 14 days after sciatic nerve crush injury. The number of differentially expressed genes was elevated at 4 and 7 days after injury, but decreased at 14 days after injury. Among the differentially expressed genes, those most up-regulated showed fold changes of more than 214, while those most down-regulated exhibited fold changes of more than 2?10. Gene sequencing showed that, at all time points after injury, a variety of MMP genes in the “Inhibition of MMPs” pathway were up-regulated, and their inhibitor genes were down-regulated. Expression of key up- and down-regulated genes was verified by quantitative real-time polymerase chain reaction analysis and found to be consistent with transcriptome sequencing. These results suggest that MMP-related genes are strongly involved in the process of peripheral nerve regeneration.
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    Extracellular matrix from human umbilical cord-derived mesenchymal stem cells as a scaffold for peripheral nerve regeneration
    Bo Xiao, Feng Rao, Zhi-yuan Guo, Xun Sun, Yi-guo Wang, Shu-yun Liu, Ai-yuan Wang, Quan-yi Guo, Hao-ye Men, Qing Zhao, Jiang Peng, Yu Wang, Shi-bi Lu
    2016, 11 (7):  1172-1179.  doi: 10.4103/1673-5374.187061
    Abstract ( 263 )   PDF (3175KB) ( 753 )   Save
    The extracellular matrix, which includes collagens, laminin, or fibronectin, plays an important role in peripheral nerve regeneration. Recently, a Schwann cell-derived extracellular matrix with classical biomaterial was used to mimic the neural niche. However, extensive clinical use of Schwann cells remains limited because of the limited origin, loss of an autologous nerve, and extended in vitro culture times. In the present study, human umbilical cord-derived mesenchymal stem cells (hUCMSCs), which are easily accessible and more proliferative than Schwann cells, were used to prepare an extracellular matrix. We identified the morphology and function of hUCMSCs and investigated their effect on peripheral nerve regeneration. Compared with a non-coated dish tissue culture, the hUCMSC-derived extracellular matrix enhanced Schwann cell proliferation, upregulated gene and protein expression levels of brain-derived neurotrophic factor, glial cell-derived neurotrophic factor, and vascular endothelial growth factor in Schwann cells, and enhanced neurite outgrowth from dorsal root ganglion neurons. These findings suggest that the hUCMSC-derived extracellular matrix promotes peripheral nerve repair and can be used as a basis for the rational design of engineered neural niches.
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    Low-power laser therapy for carpal tunnel syndrome: effective optical power
    Yan Chen, Cheng-qiang Zhao, Gang Ye, Can-dong Liu, Wen-dong Xu
    2016, 11 (7):  1180-1184.  doi: 10.4103/1673-5374.187063
    Abstract ( 306 )   PDF (1040KB) ( 422 )   Save
    Low-power laser therapy has been used for the non-surgical treatment of mild to moderate carpal tunnel syndrome, although its efficacy has been a long-standing controversy. The laser parameters in low-power laser therapy are closely related to the laser effect on human tissue. To evaluate the efficacy of low-power laser therapy, laser parameters should be accurately measured and controlled, which has been ignored in previous clinical trials. Here, we report the measurement of the effective optical power of low-power laser therapy for carpal tunnel syndrome. By monitoring the backside reflection and scattering laser power from human skin at the wrist, the effective laser power can be inferred. Using clinical measurements from 30 cases, we found that the effective laser power differed significantly among cases, with the measured laser reflection coefficient ranging from 1.8% to 54%. The reflection coefficient for 36.7% of these 30 cases was in the range of 10–20%, but for 16.7% of cases, it was higher than 40%. Consequently, monitoring the effective optical power during laser irradiation is necessary for the laser therapy of carpal tunnel syndrome.
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    Dose response and time course of manganese-enhanced magnetic resonance imaging for visual pathway tracing in vivo
    Wei-ling Wang, Hui Xu, Ying Li, Zhi-zhong Ma, Xiao-dong Sun, Yun-tao Hu
    2016, 11 (7):  1185-1190.  doi: 10.4103/1673-5374.187065
    Abstract ( 347 )   PDF (854KB) ( 603 )   Save
    Axonal tracing is useful for detecting optic nerve injury and regeneration, but many commonly used methods cannot be used to observe axoplasmic flow and synaptic transmission in vivo. Manganese (Mn2+)-enhanced magnetic resonance imaging (MEMRI) can be used for in vivo longitudinal tracing of the visual pathway. Here, we explored the dose response and time course of an intravitreal injection of MnCl2 for tracing the visual pathway in rabbits in vivo using MEMRI. We found that 2 mM MnCl2 enhanced images of the optic nerve but not the lateral geniculate body or superior colliculus, whereas at all other doses tested (5–40 mM), images of the visual pathway from the retina to the contralateral superior colliculus were significantly enhanced. The images were brightest at 24 hours, and then decreased in brightness until the end of the experiment (7 days). No signal enhancement was observed in the visual cortex at any concentration of MnCl2. These results suggest that MEMRI is a viable method for temporospatial tracing of the visual pathway in vivo. Signal enhancement in MEMRI depends on the dose of MnCl2, and the strongest signals appear 24 hours after intravitreal injection.
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