The effect of mixed bovine brain gangliosides on hypoxic conduction block in control and streptozotocin-diabetic rats.

Abstract:

:This study describes the electrophysiological responses of endoneurial preparations derived from rat sciatic nerve to acute hypoxia in vitro. Preparations from control rats exhibited a 40% decline in compound action potential (CAP) amplitude after 40 min exposure to medium gassed with 8% O2. In preparations from 4 week streptozotocin-diabetic rats CAP declined by only 29%, indicating a resistance to hypoxic conduction blockade. Treating diabetic rats with mixed bovine brain gangliosides (10 mg/kg/day i.p.) exaggerated this resistance to hypoxic conduction blockade as CAP amplitude fell to only 18% of initial values. In a separate experiment, treating non-diabetic rats with gangliosides (10 mg/kg/day i.p.) or adding gangliosides (400 micrograms/ml) directly to the medium in which control nerves were maintained during in vitro recording also significantly attenuated the decline in CAP amplitude after 40 min hypoxia, thus effectively inducing a resistance to hypoxic conduction blockade similar to that observed in nerves from diabetic rats. These studies demonstrate that the systemic or acute local administration of gangliosides induces a resistance to hypoxic conduction block in normal nerve and exaggerates the resistance to hypoxic conduction block of diabetic rats.

journal_name

J Neurol Sci

authors

Calcutt NA,Carrington AL,Ettlinger CB,Tomlinson DR

doi

10.1016/0022-510x(92)90100-y

subject

Has Abstract

pub_date

1992-05-01 00:00:00

pages

96-101

issue

1

eissn

0022-510X

issn

1878-5883

pii

0022-510X(92)90100-Y

journal_volume

109

pub_type

杂志文章
  • White matter changes mimicking a leukodystrophy in a patient with Mucopolysaccharidosis: characterization by MRI.

    abstract::Mucopolysaccharidosis (MPS) type I (alpha-iduronidase deficiency) is characterized by storage and massive urinary excretion of dermatan sulfate and heparan sulfate; it may be distinguished into three different subtypes based on age at onset and severity of the clinical symptoms. We report on progressive white matter i...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/s0022-510x(02)00014-x

    authors: Barone R,Parano E,Trifiletti RR,Fiumara A,Pavone P

    更新日期:2002-03-30 00:00:00

  • Tumefactive demyelinating lesions as a first clinical event: Clinical, imaging, and follow-up observations.

    abstract:BACKGROUND:Tumefactive demyelinating lesions (TDLs) are associated with a variety of demyelinating diseases in the central nervous system (CNS). However, there are no current guidelines describing how to classify and treat patients with this rare phenotype. Thus, the present study aimed to determine the long-term evolu...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2015.08.034

    authors: Jeong IH,Kim SH,Hyun JW,Joung A,Cho HJ,Kim HJ

    更新日期:2015-11-15 00:00:00

  • Neuronal NOS is dislocated during muscle atrophy in amyotrophic lateral sclerosis.

    abstract::Previously, we demonstrated that neuronal nitric oxide synthase (nNOS) is activated and promotes muscle atrophy in skeletal muscle during tail suspension, a model of unloading and denervation. Here, we examined patients with amyotrophic lateral sclerosis (ALS) and mutant (H46R) SOD1 transgenic (Tg) mice model using im...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2010.03.022

    authors: Suzuki N,Mizuno H,Warita H,Takeda S,Itoyama Y,Aoki M

    更新日期:2010-07-15 00:00:00

  • Tumorigenicity of six clones of a cultured neoplastic cell line derived from a spontaneous murine astrocytoma: morphology and immunocytochemistry of tumours.

    abstract::Six clones obtained from the neoplastic, astrocytic murine cell line VMDk P497 were injected intracerebrally into syngeneic hosts and the tumorigenicity of each clone was established. Five of the 6 clones produced tumours with incidences ranging from 25% to 100% and mean latencies of 43-100 days, according to the clon...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(88)90071-8

    authors: Koppel H,Pilkington GJ,Lantos PL

    更新日期:1988-02-01 00:00:00

  • A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype.

    abstract::Mutations in the gene encoding 27-kDa small heat-shock protein B1 (HSPB1) have been reported in association with Charcot-Marie-Tooth disease type 2F or dHMN type II. We describe an Italian patient with wasting and weakness of distal muscles, involving primarily and mostly the lower limbs and later the upper limbs, in ...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2010.09.008

    authors: Luigetti M,Fabrizi GM,Madia F,Ferrarini M,Conte A,Del Grande A,Tasca G,Tonali PA,Sabatelli M

    更新日期:2010-11-15 00:00:00

  • Epstein-Barr virus and multiple sclerosis.

    abstract::Epstein-Barr virus (EBV) is a human DNA herpesvirus infecting more than 90% of the world's population. EBV is the etiological agent of infectious mononucleosis (Pfeiffer's disease). Furthermore, diverse malignancies such as Burkitt and Hodgkin lymphoma have been associated with EBV. More recently, a possible role for ...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章,评审

    doi:10.1016/j.jns.2009.03.028

    authors: Pohl D

    更新日期:2009-11-15 00:00:00

  • The MPTP model: versatile contributions to the treatment of idiopathic Parkinson's disease.

    abstract::In human and subhuman primates, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) produces irreversible clinical, biochemical and neuropathological alterations highly reminiscent of those observed in Parkinson's disease. The MPTP model has provided the best available tool to date for the assessment of efficacy and s...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章,评审

    doi:10.1016/0022-510x(90)90225-c

    authors: Bloem BR,Irwin I,Buruma OJ,Haan J,Roos RA,Tetrud JW,Langston JW

    更新日期:1990-07-01 00:00:00

  • Polymyositis in solid organ transplant recipients receiving tacrolimus.

    abstract::Tacrolimus, also known as FK506, is an immunosuppressive agent widely used for the prevention of acute allograft rejection in organ transplantation and for the treatment of immunological diseases. This study reports two male patients who underwent solid organ transplantation (liver and kidney). After transplant, the p...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2014.07.036

    authors: Vattemi G,Marini M,Di Chio M,Colpani M,Guglielmi V,Tomelleri G

    更新日期:2014-10-15 00:00:00

  • Steroids and brain atrophy in multiple sclerosis.

    abstract::In this review, we focus on different pathogenetic mechanisms of corticosteroids that induce short- and long-term brain volume fluctuations in a variety of systemic conditions and disorders, as well as on corticosteroid-induced immunomodulatory, immunosuppressive and anti-inflammatory mechanisms that contribute to the...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章,评审

    doi:10.1016/j.jns.2005.03.006

    authors: Zivadinov R

    更新日期:2005-06-15 00:00:00

  • Postural control, falls and fear of falling in people with multiple sclerosis without mobility aids.

    abstract::The purpose of the study was to determine the relationship between static postural control parameters to fear of falling and falling history in people with multiple sclerosis (MS) without mobility assistive devices. One-hundred and seven relapsing-remitting patients diagnosed with MS, 62 women aged 42.8 (S.D.=12.0), p...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2013.09.029

    authors: Kalron A,Achiron A

    更新日期:2013-12-15 00:00:00

  • Hemichorea in a patient with diabetic ketoacidosis.

    abstract:BACKGROUND:Chorea is a common presenting feature of metabolic disorders, including nonketotic hyperglycemia in patients with type 2 diabetes mellitus, but rarely has been reported in diabetic ketoacidosis, hypothyroidism and vitamin B12 deficiency. METHODS:Review the literature for reported cases of chorea as a presen...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2014.04.038

    authors: Yassin AM,Shroff S,Patel SD,Paker AM,Berman MA,Jackson GR

    更新日期:2014-07-15 00:00:00

  • Mouse nerve growth factor promotes neurological recovery in patients with acute intracerebral hemorrhage: A proof-of-concept study.

    abstract:BACKGROUND:ew drugs were confirmed to be effective in the treatments of neurological dysfunction caused by acute intracerebral hemorrhage (ICH). The present prospective clinical trial aims to evaluate the effect of mouse nerve growth factor (mNGF) on neurological function in patients with acute ICH. METHODS:60 patient...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2020.117069

    authors: An S,Jia Y,Tian Y,Sun J,Wei Y,Yue S,Lin L,Wei Y,Li Y,Lei P,Zhang J,Jiang R

    更新日期:2020-11-15 00:00:00

  • Baló's concentric sclerosis and tumefactive demyelination: a shared immunopathogenesis?

    abstract::Baló's concentric sclerosis (BCS) and tumefactive demyelination (TD) are considered atypical forms of multiple sclerosis (MS). Baló lesions are characterized by concentric rings corresponding to alternating bands of demyelination and relatively preserved myelin (Hu and Lucchinetti, 2009). Tumefactive lesions are pseud...

    journal_title:Journal of the neurological sciences

    pub_type: 信件

    doi:10.1016/j.jns.2014.11.024

    authors: Hardy TA,Beadnall HN,Sutton IJ,Mohamed A,Jonker BP,Buckland ME,Barnett MH

    更新日期:2015-01-15 00:00:00

  • Multiple sclerosis in Iraq: does it have the same features encountered in Western countries?

    abstract:OBJECTIVES:To characterize the clinical, demographic and epidemiological features of MS patients from the only specialised MS centre in Iraq. METHODS:Data for consecutive Iraqi MS patients attending the Baghdad Multidiscipline MS Clinic between 2000 and 2002 who fulfilled Poser et al. criteria for clinically definite ...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2005.03.033

    authors: Al-Araji A,Mohammed AI

    更新日期:2005-07-15 00:00:00

  • Frontal-lobe syndrome and psychosis after damage to the brainstem dopaminergic nuclei.

    abstract::A patient developed frontal-lobe syndrome and psychotic symptoms after infarction in the pontomesencephalic junction. Stereotaxic lesion localization on magnetic resonance imaging and statistical analyses of regional cerebral blood flow (rCBF) disclosed an involvement of the rostral brainstem dopaminergic nuclei and h...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2007.04.021

    authors: Nishio Y,Ishii K,Kazui H,Hosokai Y,Mori E

    更新日期:2007-09-15 00:00:00

  • Acute loss of spatial navigational skills in a case of a right posterior hippocampus stroke.

    abstract::The ability to accurately navigate within an environment (known or new) is not fully understood but involves a number of highly complicated cognitive process related to both central and peripheral nervous system structures and neuronal networks. We describe a patient who developed loss of his spatial navigational skil...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2011.06.026

    authors: Aradillas E,Libon DJ,Schwartzman RJ

    更新日期:2011-09-15 00:00:00

  • Myophosphorylase deficiency associated with a defect in complex I of the mitochondrial respiratory chain.

    abstract::We studied a 21-year-old patient with clinical, biochemical and histochemical evidence of myophosphorylase deficiency and unusual repetitive episodes of pigmenturia. His muscle biopsy also revealed morphological signs of mitochondrial proliferation and a defect of complex I of the respiratory chain. His mother had exe...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/s0022-510x(98)00263-9

    authors: Rubio JC,Martín MA,Bautista J,Campos Y,Segura D,Cabello A,Chinchón I,Arenas J

    更新日期:1998-12-11 00:00:00

  • Stroke severity, early recovery and outcome are each related with clinical classification of stroke: data from the 'Tinzaparin in Acute Ischaemic Stroke Trial' (TAIST).

    abstract:INTRODUCTION:Baseline severity and clinical stroke syndrome (Oxford Community Stroke Project, OCSP) classification are predictors of outcome in stroke. We used data from the 'Tinzaparin in Acute Ischaemic Stroke Trial' (TAIST) to assess the relationship between stroke severity, early recovery, outcome and OCSP syndrome...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章,随机对照试验

    doi:10.1016/j.jns.2006.12.016

    authors: Sprigg N,Gray LJ,Bath PM,Lindenstrøm E,Boysen G,De Deyn PP,Friis P,Leys D,Marttila R,Olsson JE,O'Neill D,Ringelstein EB,van der Sande JJ,Turpie AG,TAIST Investigators.

    更新日期:2007-03-15 00:00:00

  • A comparison of community-residing older adults with frontal and parkinsonian gaits.

    abstract::Frontal gaits (FG) and parkinsonian gaits (PG) are common neurological gait abnormalities in older adults. It may be difficult to distinguish these gaits as they share common clinical characteristics such as unsteadiness, slowing, and shuffling. Of 488 community-residing subjects in an aging study, 11 were diagnosed w...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2006.05.035

    authors: Ambrose A,Levalley A,Verghese J

    更新日期:2006-10-25 00:00:00

  • The psychological impact of MND on patients and carers.

    abstract::Nineteen patients with Motor Neurone Disease (MND) who had been living with their partners for at least two years prior to the onset of their illness, together with their partners, completed self-report questionnaires to investigate the impact of MND on both patients and carers. Physical disability and impact of the i...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/s0022-510x(98)00209-3

    authors: Goldstein LH,Adamson M,Jeffrey L,Down K,Barby T,Wilson C,Leigh PN

    更新日期:1998-10-01 00:00:00

  • Invalidation of Parkinson's disease diagnosis after years of follow-up based on clinical, radiological and neurophysiological examination.

    abstract:INTRODUCTION:Diagnosis of Parkinson's disease (PD) is mainly based on clinical features. Accurate neurological examination is required but dopamine transporter (DaT) single photon emission computed tomography (SPECT) could be perfomed to support the diagnosis in ambiguous cases. The aim of this work is to describe the ...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2019.116454

    authors: Coarelli G,Garcin B,Roze E,Vidailhet M,Degos B

    更新日期:2019-11-15 00:00:00

  • Superficial siderosis due to dural defect with thoracic spinal cord herniation.

    abstract::Superficial siderosis (SS) of the central nervous system is a rare disorder caused by chronic or recurrent hemorrhages into the subarachnoid space with hemosiderin and ferritin deposition, which leads to neuronal damage. The source of bleeding remains unknown in 50% of cases. Recently, attention has been focused on fl...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2011.07.034

    authors: Boncoraglio GB,Ballabio E,Erbetta A,Prada F,Savoiardo M,Parati EA

    更新日期:2012-01-15 00:00:00

  • Relation between MRI features and dementia in cerebrovascular disease patients with leukoaraiosis: a longitudinal study.

    abstract::We examined selective MRI features (localization and degree of white matter abnormalities, cortical and subcortical atrophy) in relation to cognitive decline in patients with cerebrovascular disease (CVD) and leukoaraiosis (LA). We enrolled 6 female and 18 male CVD patients (mean age 66.2 +/- 6.6 years) whose Magnetic...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(93)90263-x

    authors: Bracco L,Campani D,Baratti E,Lippi A,Inzitari D,Pracucci G,Amaducci L

    更新日期:1993-12-15 00:00:00

  • Profound cerebrospinal fluid pleocytosis and Froin's Syndrome secondary to widespread necrotizing vasculitis in an HIV-positive patient with varicella zoster virus encephalomyelitis.

    abstract::Demonstration of the direct involvement of cranial blood vessels by varicella zoster virus (VZV) is facilitated by immunohistochemistry (IHC), in situ hybridization (ISH) and polymerase chain reaction (PCR) techniques. The extent to which an inflammatory vasculitis serves as the pathogenic mechanism for VZV encephalom...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/s0022-510x(98)00171-3

    authors: Kleinschmidt-DeMasters BK,Mahalingam R,Shimek C,Marcoux HL,Wellish M,Tyler KL,Gilden DH

    更新日期:1998-08-14 00:00:00

  • Epidemiology of multiple sclerosis in Arabs in Kuwait: a comparative study between Kuwaitis and Palestinians.

    abstract::On December 31, 1988 there were 201 registered multiple sclerosis patients in Kuwait, an overall prevalence rate (PR) of 10.2 per 100,000; among them were 186 Arabs, of whom 72 were Palestinians and 51 Kuwaitis. Comparison of these two subgroups, who had a similar age distribution revealed that the disease was 2 1/2 t...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(90)90024-h

    authors: al-Din AS,Khogali M,Poser CM,al-Nassar KE,Shakir R,Hussain J,Behbahani K,Chadha G

    更新日期:1990-12-01 00:00:00

  • Herpes simplex virus antibodies in patients with Parkinson's disease.

    abstract::Sera from 40 patients with idiopathic Parkinson's disease and their age- and sex-matched controls were assayed for immunoglobulin G (IgG) antibodies against herpes simplex virus (HSV) type 1-induced cell surface antigens with the indirect immunofluorescent test. An increased level of HSV antibodies was found among the...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(78)90017-5

    authors: Marttila RJ,Rinne UK

    更新日期:1978-02-01 00:00:00

  • Absence of neuronal and glial proteins in human and rat leptomeninges in situ.

    abstract::Human leptomeningeal (arachnoid and pia mater) cells in culture have been demonstrated in replicated studies to express typical neuronal proteins such as neurofilament protein and neuron-specific enolase. In addition, they can express glial fibrillary acidic protein. The present study examines the possibility that neu...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/s0022-510x(96)00189-x

    authors: Calingasan NY,Bernstein JJ,Blass JP

    更新日期:1996-12-01 00:00:00

  • PDE4D and ALOX5AP genetic variants and risk for Ischemic Cerebrovascular Disease in Sweden.

    abstract:BACKGROUND:Genetic variants in Phosphodiesterase 4D (PDE4D) and 5-lipoxygenase activating protein (ALOX5AP) have been shown to confer risk of Ischemic Cerebrovascular Disease (ICVD) in Iceland. We investigated whether these variants associate with ICVD in Sweden. METHODS:Previously published PDE4D and ALOX5AP gene var...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2007.06.042

    authors: Kostulas K,Gretarsdottir S,Kostulas V,Manolescu A,Helgadottir A,Thorleifsson G,Gudmundsson LJ,Thorsteinsdottir U,Gulcher JR,Stefansson K,Hillert J

    更新日期:2007-12-15 00:00:00

  • Early expression of serum neutrophil gelatinase-associated lipocalin (NGAL) is associated with neurological severity immediately after traumatic brain injury.

    abstract:PURPOSE:Intracranial bleeding and inflammatory reactions are common consequences of traumatic brain injury (TBI). Neutrophil gelatinase-associated lipocalin (NGAL), an iron-handling and acute phase protein, may participate in the pathogenesis of TBI. Therefore, we hypothesize that NGAL may be of high diagnostic and the...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2016.07.060

    authors: Zhao J,Chen H,Zhang M,Zhang Y,Qian C,Liu Y,He S,Zou Y,Liu H

    更新日期:2016-09-15 00:00:00

  • A unique episode of REM sleep behavior disorder triggered during surgery for Parkinson's disease.

    abstract::REM sleep behavior disorder (RBD) is characterized by vigorous movements during REM sleep. Here, the authors report the case of a patient who presented such a disorder immediately after the implantation of the definitive electrode for left subthalamic stimulation. Interestingly, this was and has remained a unique epis...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2006.11.005

    authors: Piette T,Mescola P,Uytdenhoef P,Henriet M,Vanderkelen B,Jacquy J,Seeldrayers P,Godaux E

    更新日期:2007-02-15 00:00:00