Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Purchase individual online access for 1 year to this journal.
Price: EUR 230.00Impact Factor 2024: 1.9
This interdisciplinary journal publishes papers relating the plasticity and response of the nervous system to accidental or experimental injuries and their interventions, transplantation, neurodegenerative disorders and experimental strategies to improve regeneration or functional recovery and rehabilitation.
Experimental and clinical research papers adopting fresh conceptual approaches are encouraged. The overriding criteria for publication are novelty, significant experimental or clinical relevance and interest to a multidisciplinary audience.
Authors: Hubacher, Martina | DeLuca, John | Weber, Peter | Steinlin, Maja | Kappos, Ludwig | Opwis, Klaus | Penner, Iris-Katharina
Article Type: Research Article
Abstract: Purpose: To assess possible effects of working memory (WM) training on cognitive functionality, functional MRI and brain connectivity in patients with juvenile MS. Methods: Cognitive status, fMRI and inter-network connectivity were assessed in 5 cases with juvenile MS aged between 12 and 18 years. Afterwards they received a computerized WM training for four weeks. Primary cognitive outcome measures were WM (visual and verbal) and alertness. Activation patterns related to WM were assessed during fMRI using an N-Back task with increasing difficulty. Inter-network connectivity analyses were focused on fronto-parietal (left and right), default-mode (dorsal and ventral) …and the anterior salience network. Cognitive functioning, fMRI and inter-network connectivity were reassessed directly after the training and again nine months following training. Results: Response to treatment was seen in two patients. These patients showed increased performance in WM and alertness after the training. These behavioural changes were accompanied by increased WM network activation and systematic changes in inter-network connectivity. The remaining participants were non-responders to treatment. Effects on cognitive performance were maintained up to nine months after training, whereas effects observed by fMRI disappeared. Conclusions: Responders revealed training effects on all applied outcome measures. Disease activity and general intelligence may be factors associated with response to treatment. Show more
Keywords: Connectivity, cognitive rehabilitation, working memory, juvenile multiple sclerosis
DOI: 10.3233/RNN-150497
Citation: Restorative Neurology and Neuroscience, vol. 33, no. 5, pp. 713-725, 2015
Authors: Subramanian, Sandeep K | Chilingaryan, Gevorg | Sveistrup, Heidi | Levin, Mindy F.
Article Type: Research Article
Abstract: Purpose: Sensorimotor impairments and depressive symptoms (PSD) influence arm motor recovery post-stroke. Feedback provision improves upper limb motor learning in patients with chronic stroke but factors including PSD may affect ability to use feedback. We evaluated the influence of PSD on the ability to use auditory feedback for upper limb recovery and motor learning in patients with chronic stroke. Methods: Participants (n = 24) practiced 72 pointing movements/session (6 targets, 12 sessions, randomized) with auditory feedback on movement speed and trunk displacement. The presence of PSD (Beck’s Depression Inventory; BDI-II) was assessed at pre-intervention (PRE). Arm …motor impairment (Fugl-Meyer Assessment, shoulder horizontal adduction, shoulder flexion, elbow extension ranges, trunk displacement) and arm use (Motor Activity Log) were assessed at PRE, immediately after (POST) and retention (3mos; RET). Participants were divided into two groups based on BDI-II scores: ≥14/63 (DEP group; n = 8; score: 20.5 ± 7.5) and ≤13/63 (no PSD (ND) group; n = 16; score: 5.0 ± 3.8). Changes in impairment and arm use levels were assessed (mixed-model ANOVAs). Results: All participants improved arm use. DEP had lower Fugl-Meyer scores, used more compensatory trunk displacement and had lower shoulder horizontal adduction range compared to ND. Conclusion: The presence of PSD diminished the ability to use auditory feedback for arm motor recovery and motor learning. Show more
Keywords: Rehabilitation, kinematics, upper limb, mood, knowledge of performance, knowledge of results, cerebrovascular accident
DOI: 10.3233/RNN-150508
Citation: Restorative Neurology and Neuroscience, vol. 33, no. 5, pp. 727-740, 2015
Authors: Zhang, Rui | Yang, Nan | Ji, Chao | Zheng, Ji | Liang, Zhen | Hou, Chun-Ying | Liu, Yan-Yong | Zuo, Ping-Ping
Article Type: Research Article
Abstract: Purpose: To investigate the effect and underlying mechanism of Aceglutamide on motor dysfunction in rats after cerebral ischemia-reperfusion. Methods: Adult male Sprague-Dawley rats were subjected to 2 h transient middle cerebral artery occlusion (MCAO). Aceglutamide or vehicle was intraperitoneally given to rats at 24 h after reperfusion and lasted for 14 days. Subsequently functional recovery was assessed and number of tyrosine hydroxylase (TH)-positive neurons in substantia nigra (SN) was analyzed. Tumor necrosis factor receptor-associated factor 1(TRAF1), P-Akt and Bcl-2/Bax were determined in mesencephalic tissue by Western blot method. PC12 cells and primary cultured mesencephalic neurons were employed …to further investigate the mechanism of Aceglutamide. Results: Aceglutamide treatment improved behavioral functions, reduced the infarction volume, and elevated the number of TH-positive neurons in the SN. Moreover, Aceglutamide significantly attenuated neuronal apoptosis in the SN. Meanwhile Aceglutamide treatment significantly inhibited the expression of TRAF1 and up-regulated the expression of P-Akt and Bcl-2/Bax ratio both in vitro and in vivo . Conclusions: Aceglutamide ameliorated motor dysfunction and delayed neuronal death in the SN after ischemia, which involved the inhibition of pro-apoptotic factor TRAF1 and activation of Akt/Bcl-2 signaling pathway. These data provided experimental information for applying Aceglutamide to ischemic stroke treatment. Show more
Keywords: Aceglutamide, neuroprotection, cerebral ischemia and reperfusion, motor function, substantia nigra, TNF receptor associated factor 1 (TRAF1), apoptosis
DOI: 10.3233/RNN-150509
Citation: Restorative Neurology and Neuroscience, vol. 33, no. 5, pp. 741-759, 2015
Authors: Sergeeva, Elena G. | Henrich-Noack, Petra | Gorkin, Alexander G. | Sabel, Bernhard A.
Article Type: Research Article
Abstract: Purpose: Transcorneal alternating current stimulation (tACS) has become a promising tool to modulate brain functions and treat visual diseases. To understand the mechanisms of action a suitable animal model is required. However, because existing animal models employ narcosis, which interferes with brain oscillations and stimulation effects, we developed an experimental setup where current stimulation via the eye and flicker light stimulation can be applied while simultaneously recording local field potentials in awake rats. Method: tACS was applied in freely-moving rats (N = 24) which had wires implanted under their upper eye lids. Field potential recordings were made in …visual cortex and superior colliculus. To measure visual evoked responses, rats were exposed to flicker-light using LEDs positioned in headset spectacles. Results: Corneal electrodes and recording assemblies were reliably operating and well tolerated for at least 4 weeks. Transcorneal stimulation without narcosis did not induce any adverse reactions. Stable head stages allowed repetitive and long-lasting recordings of visual and electrically evoked potentials in freely moving animals. Shape and latencies of electrically evoked responses measured in the superior colliculus and visual cortex indicate that specific physiological responses could be recorded after tACS. Conclusions: Our setup allows the stimulation of the visual system in unanaesthetised rodents with flicker light and transcorneally applied current travelling along the physiological signalling pathway. This methodology provides the experimental basis for further studies of recovery and restoration of vision. Show more
Keywords: Noninvasive brain stimulation, animal model, freely-moving animal, vision restoration, visual evoked potential, electrically evoked response
DOI: 10.3233/RNN-150513
Citation: Restorative Neurology and Neuroscience, vol. 33, no. 5, pp. 761-769, 2015
Authors: Zhang, Qihui | Yang, Ying | Saver, Jeffrey L.
Article Type: Research Article
Abstract: Purpose: Final global disability 3 months post-stroke is the cardinal endpoint in acute stroke clinical trials. The most similar variable available in administrative datasets is discharge destination at end of the acute hospitalization. We investigated the predictive value of discharge destination for final global disability. Methods: In the public dataset of the two NINDS-TPA trials, we characterized discharge destination as a 4 level ordinal variable. Correlation coefficients and logistic models probed the relation with the modified Rankin Scale (mRS) of global disability at 3 months. Results: Among the 624 ischemic stroke patients, discharge destination was …home in 42.1% , rehabilitation in 33.0% , skilled nursing facility in 9.8% , and in hospital-death in 12.4% . A strong correlation was noted between hospital discharge destination and 3 month mRS, r = 0.71, P < 0.001. Length of stay showed a weaker correlation with 3 month mRS, r = 0.29, p < 0.0001. A multiple logistic regression model identified 4 categories of independent predictors of 3 month global disability outcome, with discharge destination as the strongest independent variable. Conclusions: Discharge destination is a powerful predictor of final 3 month global disability outcomes and a valid outcome measure for use in local and national quality improvement programs. Show more
Keywords: Hospital discharge destination, Ischemic stroke, Modified rankin score
DOI: 10.3233/RNN-150531
Citation: Restorative Neurology and Neuroscience, vol. 33, no. 5, pp. 771-775, 2015
Authors: Koyuncuoglu, Turkan | Turkyilmaz, Mesut | Goren, Bulent | Cetinkaya, Merih | Cansev, Mehmet | Alkan, Tulin
Article Type: Research Article
Abstract: Purpose: A significant cause of neurological disability in newborns is hypoxic-ischemic encephalopathy (HIE), a disorder which involves an enhancement in histone deacetylase (HDAC) activity among underlying pathological mechanisms. We showed recently that exogenous administration of uridine to newborn rats with HIE reduced brain injury in a dose-dependent manner. The present study was performed to investigate whether uridine modulates histone acetylation/deacetylation balance in a neonatal rat model of HIE. Methods: Newborn rats that were subjected to hypoxic-ischemic (HI) insult on postnatal day 7 (P7) were injected intraperitoneally with either saline or uridine (500 mg/kg) for three consecutive days. One …day after completion of treatment, brains of pups were collected for evaluation of brain infarct volume, apoptosis, HDAC activity and acetylated-Histone H3 (Ac-H3) and H4 (Ac-H4) protein levels. Results: Results revealed that uridine administration reduced infarct volume, active Caspase-3 levels and HDAC activity while increasing the expressions of Ac-H3 and Ac-H4 proteins. Conclusions: We conclude that one mechanism by which uridine provides neuroprotection in neonatal rat HIE model involves reduction in HDAC activity. Show more
Keywords: Hypoxic-ischemic encephalopathy, neonatal, rat, uridine, histone deacetylase, neuroprotection
DOI: 10.3233/RNN-150549
Citation: Restorative Neurology and Neuroscience, vol. 33, no. 5, pp. 777-784, 2015
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
[email protected]
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office [email protected]
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
如果您在出版方面需要帮助或有任何建, 件至: [email protected]