85 research outputs found
Reactive Astrocyte Gliosis: Production of Inhibitory Molecules
The astrocytic cell responses to injury have been extensively studied in a variety of experimental models, and the term “astrogliosis” is often used to describe the astrocyte reactions to injury. Cells responding in these ways to injury are often referred to as “reactive astrocytes.” Glial scarring appears to be a critical feature of wound healing in the central nervous system (CNS), since elimination of the mitotically active contingent of reactive astrocytes leads to increase in the size of the wound. Reactive astrogliosis is a term coined for the morphological and functional events seen in astrocytes responding to CNS injury. The concept of reactive astrogliosis and its molecular and cellular definition in spinal cord injury (SCI) is still incomplete. Producing several inhibitory molecules discourages regeneration of axons in the injured spinal cord. This inhibition is compounded by the poor regenerative ability of most CNS axons. This is probably a more achievable therapeutic target than axon regeneration, and an effective treatment would be of assistance to the majority of patients with partial cord injuries. Of course, understanding about astrogliosis and producing mediators and inhibitory molecules such as signaling pathways help us to develop new treatment strategies for SCI
Genistein inhibits aggregation of exogenous amyloid-beta1-40 and alleviates astrogliosis in the hippocampus of rats. Brain Res
Abstract We addressed the question of whether injection of Aβ in the rat brain is associated with pathology in the hippocampus, and if genistein has any protective effect against the neuronal damage caused by Aβ 1-40 . Genistein is a plant-derived compound with a structure similar to that of the female sex hormone oestrogen and it was recently shown that pretreatment with a single dose of genistein ameliorated learning and memory deficits in an amyloid beta (Aβ) 1-40 rat model of Alzheimer's disease. Here, we report that injection of the amyloid peptide into the hippocampus of rats led to formation of Aβ 1-40 positive aggregates close to the lateral blade of the dentate gyrus (DGlb). We also observed the following in the hippocampus: extensive cell death in the DGlb (P < 0.0001), CA1 (P = 0.03), and CA3 (P = 0.002); an increased number of iNOS-expressing cells (P = 0.01) and gliosis. Genistein given to rats by gavage one hour before Key words: amyloid-beta, Alzheimer's disease, genistein, neuronal degeneration 1 1 Abbreviations: AD, Alzheimer's disease; iNOS, inducible nitric oxide synthase; nNOS, neuronal nitric oxide synthase; CA1, cornu ammonis 1; CA2, cornu ammonis 2; CA3, cornu ammonis 3; Aβ, amyloid beta; DGlb, lateral blade of dentate gyrus; DGmb, medial blade of dentate gyrus; GFAP, glial fibrillary acidic protein; CC, corpus callosum; MAP, mitogenactivated protein; NFĸB, nuclear factor kappa B; MnSOD, manganese superoxide dismutase; APP, amyloid precursor protein; CrEL, Cremophor E
Contra-lateral Auditory Brainstem Responses in Dyslexia
How to Cite This Article: Akbari M, Joghataei MT, Poorbakhat A, Jenabi MS. Contra-lateral auditory Brainstem Responses in Dyslexia. Iran J Child Neurol. Autumn 2016; 10(4): 10-15. AbstractObjectiveDyslexia is a neurological dysfunction (also known as a learning disability) that characterized by disability in reading in spite of normal intelligence. Bothe genetic and environmental risk factors are contributing into the condition.Diagnosis of dyslexia is based on examination and investigation of the patient’s memorial, spelling, visual, and reading skills. It is the most common learning disability, affecting 3%–10% of the school population. Modern neuroimaging techniques such as functional magnetic resonance imaging (fMRI) have shown a correlation between both functional and structural differences in the brains of children with reading difficulties. Hence, to address this issue, the auditory brainstem responses of children with dyslexia were investigated. Materials &Methods Fifty two children with dyslexia (30 males, 22 females) were selected after examination by speech therapist. In addition, fifty two control children were included as well. The IPSI and contralateral ABR tests were conducted on both cases and controls. Click stimuli were used at 75 nHL intensity. The study focused on absolute latency of wave V in both groups. ResultsAbsolute latency of wave V in contralateral showed differences between children with dyslexia and control group, but no significant results were found in IPSI testing. ConclusionThe current data provide an evidence for brainstem and its function in signal processing and the role of brainstem nucleus on processing and delivering the information to each hemisphere. References1. Lyon GR, Shaywitz SE, Shaywitz BA. A definition of dyslexia: partI - defining dyslexia, comorbidity, teachers’ knowledge of language and reading. Ann Dyslexia; 2003: 53:1-14.2. Vellutino, F, Fletcher, J,Snowling, M, &Scalon, D. Specific reading disability (dyslexia): what have we learnt in the past four decades? Child Psychology and Psychiatry; 2004: 45: 2–403. Demonet JF, Taylor MJ, Chaix Y. Developmental dyslexia. Lancet; 2004.4. Wible B, NicolT, Kraus N. Correlation between brainstem and cortical auditory Brain. 2005; 128: 417–42.5. Tzounopoulos T, Kraus N. Neuron. Learning to Encode Timing: Mechanisms of Plasticity in the Auditory Brainstem 2009; 62(4): 463–469.6. Jeffery A, Winer.Decoding the auditory corticofugal systems Hearing Research (2005).207; 1–9.7. Kraus N, Nicol T. Brainstem origins for cortical “what” and “where” pathways in the auditory system. Trends in Neurosciences. 2005; 28: 176-181.8. KrishnanaA, XuaY, Gandoura J, Carianib P. Encoding of pitch in the human brainstem is sensitive to language experience. Cognitive Brain Research. 2005; 161 – 168.9. Adams, M. Beginning to read: thinking and learning about print. Cambridge, Mass. MIT Press. 1990.10. Demb, JB, Boynton G, M., &Heeger, D. J. Functional magnetic resonance imaging of early visual pathways in dyslexia. Neurosci. 1998; 18(17): 6939-6951.11. Fiez, JA,Petersen, SE. Neuroimaging studies of word reading. PNAS. 1998; 95:914-921.12. Hinshelwood J. Congenital word blindness. London: Lewis. 1917.13. Morgan, WP. A case of congenital word blindness. The British Medical Journal. 1896; 2: 1378.14. Dejerine, Suruncas de cectieverbale avec agraphie, suivid’autopsie. CR Soc. 1891; 43: 197–201.15. Drake WE. Clinical and pathological findings in a child with a developmental learning disability. J Learn Disabil. 1968; 1: 486–502.16. Orton ST. Reading, writing, and speech problems in children and selected papers. Austin: ProEd. 1937.17. Geschwind, N, Galaburda, AM. Cerebral lateralization: Biological mechanisms, associations, and pathology. Cambridge, MA: MIT Press. 1987.18. Weintraub S, Mesulam MM. Developmental learning disabilities. Arch Neurol. 1983;40(8):463-8.19. Cohen L, Dehaene S. Neuroimage Specialization within the ventral stream.2004; 22(1):466-76.20. Simos PG1, Fletcher JM, Bergman E, Breier JI, Foorman BR, Castillo EM, Davis RN, Fitzgerald M, Papanicolaou AC. Neurology. 2002;58(8):1203-13.21. Wible, B, Nicol, T, Kraus N. Correlation between brainstem and cortical auditoryprocesses in normal and language-impaired children. Brain. 2005; 128: 417–423.22. Starr A, Picton T, Sininger Y, Hood I, Berlin C. Auditory neuropathy. Brain. 1996; 119:741-753.23. Zhang, Y. and Suga, N. Corticofugal feedback for collicular plasticity evoked by electric stimulation of the inferior colliculus. Neurophysiol. 2005; 94: 2676–2682.24. Hood L J. Clinical applications of the auditory brainstem response. Singular Publishing Group. 1998; 49-63.25. Dobie R A, Berlin C I. Binaural interaction in human auditory evoked responses. Archives of Otolaryngology. 1979; 105: 391-398.26. MollerA R, Jannetta P J. Auditory evoked potentials recorded from the cochlearnucleus and its vicinity in man. Journal of Neurosurgery. 1983; 59(6): 1013–1018.27. Moller A R, Jho H D, Yokota M, Janetta P J. Contribution from crossed and uncrossed brainstem structures to the brainstem auditory evoked potentials: a study in humans. Laryngoscope. 1995; 105(6): 596–605.28. Wible B, Nicol T, Kraus N. Correlation between brainstem and cortical auditory processes in normal and language-impaired children. Brain. 2005; 128, 417–423.29. Stone J L, Calderon-Arnulphi M, Watson K S. Brainstem auditory evoked potentials- a review and modified studies in healthy subjects. Journal of Clinical Neurophysiology. 2009; 26(3): 167–175.30. Parkkonen L, Fujiki N, Mäkelä J P. Sources of auditory brainstem responses21 revisited: contribution by magnetoencephalography. Human Brain Mapping. 2009; 30(6): 1772–1782.31. Møller AR, Jho HD, Yokota M, Jannetta PJ. Contribution from crossed and uncrossed brainstem structures to the brainstem auditory evoked potentials: a study in humans. Laryngoscope. 1995; 105(6):596–605.32. Voordecker P, Brunko E, Beyl Z D. Selective unilateral absence or attenuationof wave V of brain-stem auditory evoked potentials with intrinsic brain-stem lesions. Archives of Neurology.1988; 45(11), 1272–1276.33. Litovsky R Y, Fligor B J, Tramo M J. Functional role of the human inferiorcolliculus in binaural hearing. Hearing Research.2002; 165(1–2): 177–188.34. Tzounopoulos T, Kraus N. Learning to encode timing: mechanisms of plasticity in the auditory brainstem. Neuron. 2009; 62(4): 463–469.35. Hatanaka T, Shuto H, Yasuhara A, Kobayashi Y. Ipsilateral and contralateral recordings of auditory brainstem responses to monaural stimulation. Pediatric Neurology. 1988; 4(6): 354–357
Prevention of diagnostic errors in position of conus medullaris in adult patients
Background: Finding the safe location of spinal cord for cerebrospinal fluid (CSF) during surgical procedures is very important due to its various nature for each patient as well as its potential peripheral nervous system hazards. The aim of this study was to find the relationship between the location of conus medullaris (CM) and gender, age and body mass index (BMI) in order to minimize the potential diagnostic errors. Methods: Magnetic resonance imaging (MRI) with T1-weighted sagittal spin echo sequences of the lumbar spine was studied in 350 patients older than 20 years, whom had been referred for imaging in order to assess the potential causes of low back pain of the lumbar spine, and were referred to Shahid Chamran MRI center in Sanandaj, located in the west of Iran in 2014. The results were compared with international standards to reveal the potential errors. Results: In different age groups, the mean position was variable ranging from T12-L1 intervertebral disc to upper part of L1 middle third, not clinically significant. The inter canal position of the spinal cord was toward dorsal. No significant relationship was found between CM and gender, age as well as BMI. Similar relationship was found for the spinal cord position in spinal column. Conclusion: There is a safe region of 2–4 vertebral bodies and intervertebral spaces during spinal block. It means that the variation of CM position and its end level could be a guidance to realize that why neurological symptoms may vary in different patients
COVID-19 AND FEAR, WHICH COMES FIRST?
Today people have a few unanswered questions in their mind, such as "Do negative emotions will co-survive with the COVID-19
pandemic? Which one is worse? Which one will disappear quicker? Is there any connection between negative emotions and being
infected by COVID-19 or the severity of infected individual\u27s symptoms ? How are we supposed to live with COVID-19 and adapt our
emotional system to the virus for more than one upcoming year?
These uncertainties could result in massive pressure on people. While there is no clear consensus regarding what establishes
psychological stress on an individual, the effect of negative affect and psychological stress on increased susceptibility to disease due
to altered immune functions is well established. Here we are going through the possible effect of emotions associated with the
present pandemic on COVID-19 course of disease and severity of symptoms
Mesenchymal Stem Cell Therapies for Paraplegia: Preclinical and Clinical Studies
Paraplegia is the damage or loss of function in motor and/or sensory abilities. This insult can be observed in the thoracic, lumbar, or sacral parts of spinal column. Besides, paraplegia may be occurring because of any injuries or diseases of the lower segments or peripheral nerves or by cerebral palsy (CP). This damage can be seen as a result of a tumor or blood clot on the spinal cord. By now, there is not any curative treatment for paraplegia. Using mesenchymal stem cells (MSCs) in the treatment of spinal cord injury is a promising tested strategy because of their simplicity of isolation/preservation and their properties. Several preclinical studies in this field can be found; however, MSCs showed weak and conflicting outcomes in trials. In this chapter book, we will discuss about the therapeutic role of these cells in the treatment of paraplegia, with emphasis on their characterization, relevance, boundaries, and prospect views
COVID-19 AND FEAR, WHICH COMES FIRST?
Today people have a few unanswered questions in their mind, such as "Do negative emotions will co-survive with the COVID-19
pandemic? Which one is worse? Which one will disappear quicker? Is there any connection between negative emotions and being
infected by COVID-19 or the severity of infected individual\u27s symptoms ? How are we supposed to live with COVID-19 and adapt our
emotional system to the virus for more than one upcoming year?
These uncertainties could result in massive pressure on people. While there is no clear consensus regarding what establishes
psychological stress on an individual, the effect of negative affect and psychological stress on increased susceptibility to disease due
to altered immune functions is well established. Here we are going through the possible effect of emotions associated with the
present pandemic on COVID-19 course of disease and severity of symptoms
Evaluating a new verbal working memory-balance program: a double-blind, randomized controlled trial study on Iranian children with dyslexia
Abstract: Background: It is important to improve verbal Working Memory (WM) in reading disability, as it is a key factor in learning. There are commercial verbal WM training programs, which have some short-term effects only on the verbal WM capacity, not reading. However, because of some weaknesses in current verbal WM training programs, researchers suggested designing and developing newly structured programs that particularly target educational functions such as reading skills. In the current double-blind randomized clinical trial study, we designed a new Verbal Working Memory-Balance (VWM-B) program which was carried out using a portable robotic device. The short-term effects of the VWM-B program, on verbal WM capacity, reading skills, and postural control were investigated in Iranian children with developmental dyslexia. Results: The effectiveness of the VWM-B program was compared with the VWM-program as a traditional verbal WM training. In comparison with VWM-program, the participants who received training by the VWM-B program showed superior performance on verbal WM capacity, reading skills, and postural control after a short-term intervention. Conclusions: We proposed that the automatized postural control resulting from VWM-B training had a positive impact on improving verbal WM capacity and reading ability. Based on the critical role of the cerebellum in automatizing skills, our findings support the cerebellar deficit theory in dyslexia. Trial registration: This trial was (retrospectively) registered on 8 February 2018 with the Iranian Registry of Clinical Trials (IRCT20171219037953N1)
Subcutaneous granulocyte colony-stimulating factor administration for subacute traumatic spinal cord injuries, report of neurological and functional outcomes: a double-blind randomized controlled clinical trial
OBJECTIVEGranulocyte-colony stimulating factor (G-CSF) is a major cytokine that has already been clinically verified for chronic traumatic spinal cord injuries (TSCIs). In this study, the authors set out to determine the safety and efficacy of G-CSF administration for neurological and functional improvement in subacute, incomplete TSCI.METHODSThis phase II/III, prospective, double-blind, placebo-controlled, parallel randomized clinical trial was performed in 60 eligible patients (30 treatment, 30 placebo). Patients with incomplete subacute TSCIs with American Spinal Injury Association Impairment Scale (AIS) grades B, C, and D were enrolled. Patients were assessed using the International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI) scale, Spinal Cord Independence Measure (SCIM-III) and International Association of Neurorestoratology Spinal Cord Injury Functional Rating Scale (IANR-SCIFRS), just before intervention and at 1, 3, and 6 months, after 7 daily subcutaneous administrations of 300 μg/day of G-CSF in the treatment group and placebo in the control group.RESULTSAmong 60 participants, 28 patients (93.3%) in the G-CSF group and 26 patients (86.6%) in the placebo group completed the study protocol. After 6 months of follow-up, the AIS grade remained unchanged in the placebo group, while in the G-CSF group 5 patients (45.5%) improved from AIS grade B to C, 5 (45.5%) improved from AIS grade C to grade D, and 1 patient (16.7%) improved from AIS grade D to E. The mean ± SEM change in ISNCSCI motor score in the G-CSF group was 14.9 ± 2.6 points, which was significantly greater than in the placebo group (1.4 ± 0.34 points, p < 0.001). The mean ± SEM light-touch and pinprick sensory scores improved by 8.8 ± 1.9 and 10.7 ± 2.6 points in the G-CSF group, while those in the placebo group improved by 2.5 ± 0.60 and 1.2 ± 0.40 points, (p = 0.005 and 0.002, respectively). Evaluation of functional improvement according to the IANR-SCIFRS instrument revealed significantly more functional improvement in the G-CSF group (10.3 ± 1.3 points than in the placebo group (3.0 ± 0.81 points; p < 0.001). A significant difference was also observed between the 2 groups as measured by the SCIM-III instrument (29.6 ± 4.1 vs 10.3 ± 2.2, p < 0.001).CONCLUSIONSIncomplete subacute TSCI is associated with significant motor, sensory, and functional improvement after administration of G-CSF.Clinical trial registration no.: IRCT201407177441N3 (www.irct.ir
Clinimetrics of the Freezing of Gait Questionnaire for Parkinson Disease During the "off" State
Introduction: Freezing of gait, a common PD motor symptom, could increase the risk of falling. This study aimed to investigate the clinimetric attributes of the Freezing of Gait Questionnaire (FOGQ) for people with Parkinson disease in the "off" state. Methods: A total of 115 patients with Parkinson disease (PD; mean age, 60.25 years) were included. Acceptability, internal consistency (by the Cronbach alpha, and test-retest by Intraclass Correlation [ICC]), and reliability of the Persian-translated version of the FOGQ were examined. Dimensionality was estimated by Exploratory Factor Analysis (EFA). Fall efficacy scale-international, unified Parkinson disease rating scale-II, Berg balance scale, functional reach test, and Parkinson disease questionnaire-39 were applied to determine the convergent validity. Diagnostic accuracy for obtaining optimal cutoff point, separating faller and non-faller groups, was analyzed by Receiver Operating Characteristics (ROC) curve analysis and Area Under the Curve (AUC). All tests were carried out in an "off" state. Results: The Cronbach alpha was high (α=0.92). The test-retest showed high reliability (ICC=0.89). The FOGQ was unidimensional according to the EFA and had acceptable convergent validity with moderate to high correlation with other clinical scales. The optimal cutoff point to discriminate fallers from non-fallers during the "off" state was 9/10, with an AUC of 0.92. Conclusion: Our results suggest that the FOGQ has appropriate reliability, validity, and discriminative ability for measuring FOG in patients with PD during the "off" state.S
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