Down-regulation of adenylate kinase 5 in temporal lobe epilepsy patients and rat model.

Abstract:

:Adenylate kinase 5 (AK5) is one member of the AK family and plays a critical role in maintaining cellular homeostasis. Different from the other AKs, AK5 is almost exclusively expressed in the brain. However, its exact biological functions remain unclear. The aim of the present study is to explore the expression pattern of AK5 in patients with refractory epilepsy and in a chronic pilocarpine-induced epileptic rat model. Using Western blot, immunofluorescence and immunoprecipitation analysis, we found that AK5 protein was mainly expressed in neurons, demonstrated by colocalization with the dendritic marker, MAP2, which were similar to the corresponding controls. However, the expression of AK5 decreased remarkably in epileptic patients and experimental rats. Furthermore, immunoprecipitation analysis showed that the interaction of AK5 with copine VI (CPNE6, a brain specific protein) increased in epileptic patients and rat models. Our results are the first to indicate that the expression of AK5 in epileptic brain tissue may play important roles in epilepsy, especially refractory epilepsy.

journal_name

J Neurol Sci

authors

Lai Y,Hu X,Chen G,Wang X,Zhu B

doi

10.1016/j.jns.2016.04.037

subject

Has Abstract

pub_date

2016-07-15 00:00:00

pages

20-26

eissn

0022-510X

issn

1878-5883

pii

S0022-510X(16)30230-1

journal_volume

366

pub_type

杂志文章
  • Congenital fiber type disproportion myopathy caused by LMNA mutations.

    abstract::A boy, who had shown muscle weakness and hypotonia from early childhood and fiber type disproportion (FTD) with no dystrophic changes on muscle biopsy, was initially diagnosed as having congenital fiber type disproportion (CFTD). Subsequently, he developed cardiac conduction blocks. We reconsidered the diagnosis as po...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2014.02.036

    authors: Kajino S,Ishihara K,Goto K,Ishigaki K,Noguchi S,Nonaka I,Osawa M,Nishino I,Hayashi YK

    更新日期:2014-05-15 00:00:00

  • White matter changes and the development of motor phenotypes in de novo Parkinson's Disease.

    abstract:BACKGROUND:Parkinson's Disease (PD) patients are usually divided into Tremor Dominant (TD) and Postural Instability/Gait Difficulty (PIGD) subtypes. The latter is characterized by axial motor symptoms and worse outcomes, possibly also because of comorbid white matter disease. Therefore, the current study investigated t...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2016.06.015

    authors: Moccia M,Tedeschi E,Ugga L,Erro R,Picillo M,Caranci F,Barone P,Brunetti A

    更新日期:2016-08-15 00:00:00

  • Imaging correlates of apathy and depression in Parkinson's disease.

    abstract::Though the core symptoms of Parkinson's disease (PD) are motor-related, a majority of patients also have neuropsychiatric symptoms concerning mood, behavior and cognition. Apathy and depression are considered among the most frequent ones, and have a negative impact on global functioning and quality of life. Recent neu...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章,评审

    doi:10.1016/j.jns.2011.07.006

    authors: Benoit M,Robert PH

    更新日期:2011-11-15 00:00:00

  • Dipyridamole and headache--a pilot study of initial dose titration.

    abstract::Headache is reported by about one third of patients using dipyridamole (DP) after stroke or TIA. No study has systematically examined if initial dipyridamole titration may affect this headache. We therefore randomised patients to (1) standard aspirin and dipyridamole treatment b.i.d. for 2 weeks or (2) titration with ...

    journal_title:Journal of the neurological sciences

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1016/j.jns.2004.05.011

    authors: Lindgren A,Husted S,Staaf G,Ziegler B

    更新日期:2004-08-30 00:00:00

  • Characterization of multi-joint upper limb movements in a single task to assess bradykinesia.

    abstract::Bradykinesia is a disabling symptom of Parkinson's disease (PD) which presents with slowness of movement. Visual assessment using clinical rating scales is currently the gold standard to assess bradykinesia. Such assessments require multiple separate movements, are subjective, and rely on the ability of the rater to d...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2016.07.056

    authors: Delrobaei M,Tran S,Gilmore G,McIsaac K,Jog M

    更新日期:2016-09-15 00:00:00

  • Cytokine and chemokine mRNA expressing cells in muscle tissues of experimental autoimmune myasthenia gravis.

    abstract::In-situ hybridization with labeled oligonucleotide probes was applied to explore cytokine and chemokine mRNA expression in sections of striated muscle, the target organ in experimental autoimmune myasthenia gravis (EAMG), induced in Lewis rats by immunization with acetylcholine receptor (AChR) and complete Freund's ad...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/s0022-510x(98)00181-6

    authors: Li H,Shi FD,Bai X,Huang Y,Diab A,He B,Link H

    更新日期:1998-11-26 00:00:00

  • Immunological relationship between a demyelinating RNA enveloped budding virus (Semliki Forest) and brain glycolipids.

    abstract::A monoclonal antibody (MAb) raised against central nervous system (CNS) myelin (212) and a MAb (308) raised against brain with Semliki Forest virus (SFV) were both found to react against the same CNS glycolipids. Both these MAbs were also found to react strongly with SFV and against certain brain glycolipid fractions ...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(86)90144-9

    authors: Khalili-Shirazi A,Gregson N,Webb HE

    更新日期:1986-11-01 00:00:00

  • Fingerprint inclusions. Ultrastructural demonstration of muscle fiber type specificity.

    abstract::Fingerprint inclusions were identified in the skeletal muscle of a child with severe hypotonia. The mean Z-line and M-line widths from each of 19 muscle fibers containing the fingerprint inclusions were calculated. The mean Z-line widths were 85-99 nm, and the mean M-line widths were 75-101 nm. According to out presen...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(77)90216-7

    authors: Payne CM,Curless RG

    更新日期:1977-04-01 00:00:00

  • Practical issues in measuring autoantibodies to neuronal cell-surface antigens in autoimmune neurological disorders: 190 cases.

    abstract:OBJECTIVES:To address practical issues in measuring autoantibodies to neuronal cell-surface antigens (NSAs) in various autoimmune neurological disorders (ANDs). METHODS:We retrospectively reviewed the clinical information of 221 patients with clinically suspected ANDs who underwent antibody testing for NSAs between Ja...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2018.04.009

    authors: Kaneko J,Kanazawa N,Tominaga N,Kaneko A,Suga H,Usui R,Ishima D,Kitamura E,Akutsu T,Yoshida K,Nishiyama K,Iizuka T

    更新日期:2018-07-15 00:00:00

  • Controlled studies on the effects of alcohol ingestion on peripheral nerves of macaque monkeys.

    abstract::In two different studies, monkeys were fed diets with 50% and 30% of calories replaced with alcohol for 5 and 3 years, respectively. Nerves were studied with electrophysiological and quantitative histological methods, but no deleterious effect of alcohol was identified. ...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(87)90221-8

    authors: Hallett M,Fox JG,Rogers AE,Nicolosi R,Schoene W,Goolsby HA,Landis DM,Pezeshkpour G

    更新日期:1987-08-01 00:00:00

  • Accuracy of CSF and MRI criteria for dissemination in space in the diagnosis of multiple sclerosis.

    abstract::Demonstration of lesion dissemination in space (DIS) and time (DIT) is necessary for the diagnosis of multiple sclerosis (MS) in clinically isolated syndromes (CIS). The McDonald criteria accepted two methods to demonstrate DIS. The fulfillment of at least three of four MRI Barkhof criteria (MRI-BC) or, alternatively,...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2007.08.030

    authors: Villar LM,García-Barragán N,Sádaba MC,Espiño M,Gómez-Rial J,Martínez-San Millán J,González-Porqué P,Alvarez-Cermeño JC

    更新日期:2008-03-15 00:00:00

  • The significance of cerebral atrophy for the symptomatology of Parkinson's disease.

    abstract::Hitherto published results on the impact of brain atrophy on the neurological and psychopathological sympion of this problem without risk of complications. We investigated 173 parkinsonian patients (89 men, 84 women) aged 37--83 years. Besides CT in all patients a standardized neurological and psychopathological inves...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(79)90050-9

    authors: Schneider E,Fischer PA,Jacobi P,Becker H,Hacker H

    更新日期:1979-07-01 00:00:00

  • Risk factors for mental disorders in patients with hypertensive intracerebral hemorrhage following neurosurgical treatment.

    abstract:BACKGROUND:Mental disorders are commonly observed among surgically treated patients with hypertensive intracerebral hemorrhage (HICH), leading to serious negative impacts on the patient's treatment, rehabilitation, and prognosis. The study aimed to establish the prevalence rates and risk factors for mental disorders fo...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2014.04.021

    authors: Li F,Chen QX

    更新日期:2014-06-15 00:00:00

  • Increased amyloid beta protein levels in children and adolescents with Down syndrome.

    abstract:BACKGROUND:Persons with Down syndrome (DS) (40 years and older) have neuropathological changes characteristic of Alzheimer disease (AD). Soluble forms of amyloid beta (Abeta) peptide generated from amyloid precursor protein (APP) end at C-terminal residues 40 and 42. The presence of the apolipoprotein E (ApoE) epsilon4...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2006.12.010

    authors: Mehta PD,Capone G,Jewell A,Freedland RL

    更新日期:2007-03-15 00:00:00

  • Analyses of mitochondrial respiratory chain function and mitochondrial DNA deletion in human skeletal muscle: effect of ageing.

    abstract::The analysis of human skeletal muscle mitochondria revealed a progressive decline in mitochondrial respiratory chain function with age. The activities affected to the greatest extent were those of complexes I and IV which were decreased by 59% and 47% respectively between the ages of 20-30 years and 60-90 years of age...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(92)90270-u

    authors: Cooper JM,Mann VM,Schapira AH

    更新日期:1992-11-01 00:00:00

  • Central and peripheral SEP defects in neurologically symptomatic and asymptomatic subjects with low vitamin B12 levels.

    abstract::Somatosensory evoked potentials (SEPs) following median nerve stimulation were abnormal in 7 patients with sensory impairment due to vitamin B12 deficiency. Extensor plantar reflexes indicated a central sensory pathway lesion in 4 cases and absent tendon jerks suggested peripheral neuropathy in 4, but median nerve SEP...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(87)90006-2

    authors: Jones SJ,Yu YL,Rudge P,Kriss A,Gilois C,Hirani N,Nijhawan R,Norman P,Will R

    更新日期:1987-12-01 00:00:00

  • Canine X-linked muscular dystrophy. An animal model of Duchenne muscular dystrophy: clinical studies.

    abstract::The progression of clinical disease and serum creatine kinase (CK) levels in canine X-linked muscular dystrophy (CXMD) was studied in 7 dogs from birth to 12-14 months and in 18 dogs at varying intervals from birth to 8 weeks. One affected male was studied from age 3.5 to 6 years, and all pups were descendants of this...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(88)90206-7

    authors: Valentine BA,Cooper BJ,de Lahunta A,O'Quinn R,Blue JT

    更新日期:1988-12-01 00:00:00

  • Calcium deposits in the perineurium and their relation to lipid accumulation.

    abstract::Calcification of the perineurium in sural nerves occurs in human adults. Deposits of calcium salts can be found focally in the middle and outer layers of the perineurium. Evidence indicates that this calcification is related to nerve fibre breakdown and to the local presence of lipids in the perineurium. The origin of...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(79)90016-9

    authors: Van Lis JM,Jennekens FG,Veldman H

    更新日期:1979-11-01 00:00:00

  • Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: two novel mutations in the NOTCH3 gene in Chinese.

    abstract:BACKGROUND:Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary disorder caused by NOTCH3 mutations, usually localized to exons 3 and 4, and characterized by recurrent subcortical infarctions, dementia and leukoencephalopathy. So far, there has been only l...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2006.02.011

    authors: Lee YC,Yang AH,Liu HC,Wong WJ,Lu YC,Chang MH,Soong BW

    更新日期:2006-07-15 00:00:00

  • Cerebrospinal fluid autoantibodies to myelin basic protein in multiple sclerosis patients. Detection during first exacerbations and kinetics of acute relapses and subsequent convalescent phases.

    abstract::In order to determine if free (F) and bound (B) levels of autoantibodies to myelin basic protein (anti-MBP) are present from the onset of multiple sclerosis (MS), 201 patients referred to our clinic were clinically divided into a group diagnosed as having an initial MS relapse and a group of non-MS controls. Ninety-fo...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(89)90083-x

    authors: Warren KG,Catz I

    更新日期:1989-06-01 00:00:00

  • Systemic thrombolytic therapy in acute ischemic stroke--new experiences in spreading network of stroke units in Croatia.

    abstract:BACKGROUND:The aims of this paper are: 1) to present the data of systemic thrombolysis for ischemic stroke in five Croatian centers from July 2008 till January 2010; 2) to compare the results between centers and; 3) to compare data with previously published results from 2006 to 2008 period from our center, and with the...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2011.10.008

    authors: Matijević V,Poljaković Z,Malojčić B,Mišmaš A,Bazina A,Boban M,Bilić I,Radanović B,Glavor KD,Kiđemet-Piskač S,Habek M

    更新日期:2012-03-15 00:00:00

  • A novel exon 5 mutation (N139H) in the SOD1 gene in a Spanish family associated with incomplete penetrance.

    abstract:BACKGROUND:Allelic heterogeneity and phenotype variability-especially in age at onset, penetrance and progression-are reported in ALS1 families. For this reason, SOD1 gene mutation data in ALS1 patients are currently being gathered to better understand the genotype-phenotype relationship in this disorder. Here, we repo...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2003.10.018

    authors: Nogales-Gadea G,Garcia-Arumi E,Andreu AL,Cervera C,Gamez J

    更新日期:2004-04-15 00:00:00

  • Zolpidem-induced sleep-related eating disorder.

    abstract::An association between zolpidem administration and sleep-related eating disorder (SRED) has been suggested. The authors observed zolpidem-induced SRED in restless legs syndrome (RLS). With the review of previous reports, we identified a common occurrence of RLS in zolpidem-induced SRED. ...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2009.09.026

    authors: Yun CH,Ji KH

    更新日期:2010-01-15 00:00:00

  • The mirror system, theory of mind and Parkinson's disease.

    abstract::The mirror system includes a group of neurons in the monkey cortex that discharge both when a movement is executed and when that same movement is observed. An equivalent system in humans has been proposed to mediate action and emotion understanding, being therefore related to theory of mind. Theory of mind (TOM) is th...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章,评审

    doi:10.1016/j.jns.2011.07.030

    authors: Alegre M,Guridi J,Artieda J

    更新日期:2011-11-15 00:00:00

  • Visual evoked responses and ophthalmological examination in optic neuritis. A follow-up study.

    abstract::Ophthalmological examination and visual evoked responses (VERs) were repeated at 6-120 (mean 46) months after the first attack of acute optic neuritis in 80 patients who had abnormal VERs in 98 symptomatic eyes at the initial examination. The wide field VER returned to within the normal range in 19/98 (19%) symptomati...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(86)90075-4

    authors: Hely MA,McManis PG,Walsh JC,McLeod JG

    更新日期:1986-10-01 00:00:00

  • Contraction tension and kinetics of the peroneus longus muscle in golden retriever muscular dystrophy.

    abstract::Contraction tension and kinetics of the peroneus longus muscle were studied in dogs with the Duchenne homologue, golden retriever muscular dystrophy (GRMD), in advance of evaluating localized therapies such as myoblast transplantation. Absolute and both muscle- and body-weight-corrected twitch tension in GRMD dogs wer...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(94)90210-0

    authors: Kornegay JN,Sharp NJ,Bogan DJ,Van Camp SD,Metcalf JR,Schueler RO

    更新日期:1994-05-01 00:00:00

  • Germanium intoxication with sensory ataxia.

    abstract::Sensory ataxia in inorganic germanium intoxication is rare. A 63-year-old housewife had taken inorganic germanium preparations at a dosage of 36 mg a day for about 6 years (total dose about 80 g). She subsequently developed difficulty in writing and gait disturbance with peripheral neuropathy and renal involvement. Ge...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(95)00032-w

    authors: Asaka T,Nitta E,Makifuchi T,Shibazaki Y,Kitamura Y,Ohara H,Matsushita K,Takamori M,Takahashi Y,Genda A

    更新日期:1995-06-01 00:00:00

  • (123)I-MIBG myocardial scintigraphy and neurocirculatory abnormalities in patients with dementia with Lewy bodies and Alzheimer's disease.

    abstract:BACKGROUND:Although adoption of new clinical criteria for dementia with Lewy bodies (DLB) leads to an increase in the proportion of patients diagnosed with probable DLB, the sensitivity of clinical diagnostic criteria of DLB is low, and there are no generally accepted clinical or imaging biomarkers to distinguish DLB f...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2015.07.025

    authors: Kim JS,Park HE,Oh YS,Song IU,Yang DW,Park JW,Lee KS

    更新日期:2015-10-15 00:00:00

  • Oxidative stress, mitochondrial dysfunction and cellular stress response in Friedreich's ataxia.

    abstract::There is significant evidence that the pathogenesis of several neurodegenerative diseases, including Parkinson's disease, Alzheimer's disease, Friedreich's ataxia (FRDA), multiple sclerosis and amyotrophic lateral sclerosis, may involve the generation of reactive oxygen species (ROS) and/or reactive nitrogen species (...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章,评审

    doi:10.1016/j.jns.2005.03.012

    authors: Calabrese V,Lodi R,Tonon C,D'Agata V,Sapienza M,Scapagnini G,Mangiameli A,Pennisi G,Stella AM,Butterfield DA

    更新日期:2005-06-15 00:00:00

  • Anhedonia and its correlation with clinical aspects in Parkinson's disease.

    abstract::Anhedonia is one of the non-motor symptoms observed in the Parkinson's disease (PD). However, there is no clear relationship between anhedonia and its correlation with other symptoms of PD. The aim of this study is to evaluate the characteristics of anhedonia and its correlation with clinical aspects of PD in a relati...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章,多中心研究

    doi:10.1016/j.jns.2016.10.051

    authors: Nagayama H,Maeda T,Uchiyama T,Hashimoto M,Nomoto N,Kano O,Takahashi T,Terashi H,Hamada S,Hasegawa T,Hatano T,Takahashi T,Baba Y,Sengoku R,Watanabe H,Inoue M,Kadowaki T,Kaneko S,Shimura H,Kubo SI,Young Japanese Exp

    更新日期:2017-01-15 00:00:00