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1.
Adv Exp Med Biol ; 949: 311-332, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27714696

RESUMO

The aim of this work was to combine our previously published results with our new data to show how galectin-3 (Gal-3) controls myelin integrity and function, promotes oligodendroglial cell differentiation, and regulates microglial responses to limit cuprizone- (CPZ)-induced demyelination and foster remyelination. In this study, 8-week-old Gal-3-deficient (Lgals3 -/-) and wild type (WT) mice were fed a diet containing 0.2 % CPZ w/w for 6 weeks, after which CPZ was withdrawn in order to allow remyelination. Our results show that remyelination was less efficient in Lgals3 -/- than in WT mice. Electron microscopic images from remyelinated sections in Lgals3 -/- mice revealed collapsed axons with a defective myelin wrap, while remyelinated WT mice had normal axons without relevant myelin wrap disruption. MMP-3 expression increased during remyelination in WT but not in Lgals3 -/- mice. The number of CD45+, TNFα+ and TREM-2b+ cells decreased only in WT mice only, with no alterations in Lgals3 -/- mice during demyelination and remyelination. Therefore, Gal-3 influences remyelination by mechanisms involving the tuning of microglial cells, modulation of MMP activity, and changes in myelin architecture.


Assuntos
Astrócitos/patologia , Doenças Desmielinizantes/genética , Galectina 3/genética , Microglia/patologia , Oligodendroglia/patologia , Regeneração/genética , Animais , Astrócitos/metabolismo , Axônios/metabolismo , Axônios/patologia , Encéfalo/metabolismo , Encéfalo/patologia , Diferenciação Celular , Cuprizona , Doenças Desmielinizantes/induzido quimicamente , Doenças Desmielinizantes/patologia , Doenças Desmielinizantes/reabilitação , Galectina 3/deficiência , Regulação da Expressão Gênica , Proteína Glial Fibrilar Ácida/genética , Proteína Glial Fibrilar Ácida/metabolismo , Antígenos Comuns de Leucócito/genética , Antígenos Comuns de Leucócito/metabolismo , Masculino , Metaloproteinase 3 da Matriz/genética , Metaloproteinase 3 da Matriz/metabolismo , Camundongos , Camundongos Knockout , Microglia/metabolismo , Proteína Básica da Mielina/genética , Proteína Básica da Mielina/metabolismo , Oligodendroglia/metabolismo , Fagocitose , Receptores Imunológicos/genética , Receptores Imunológicos/metabolismo , Fator de Necrose Tumoral alfa/genética , Fator de Necrose Tumoral alfa/metabolismo
3.
Ann Neurol ; 66(4): 559-64, 2009 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19816926

RESUMO

Measuring in vivo spinal cord injury and repair remains elusive. Using magnetic resonance spectroscopy (MRS) we examined brainstem N-acetyl-aspartate (NAA) as a surrogate for spinal cord injury in two mouse strains with different reparative phenotypes following virus-induced demyelination. Swiss Jim Lambert (SJL) and Friend Virus B (FVB) mice progressively demyelinate with axonal loss. FVB mice demyelinate similarly but eventually remyelinate coincident with functional recovery. Brainstem NAA levels drop in both but recover in FVB mice. Chronically infected SJL mice lost 30.5% of spinal cord axons compared to FVB mice (7.3%). In remyelination-enhancing or axon-preserving clinical trials, brainstem MRS may be a viable endpoint to represent overall spinal cord dysfunction.


Assuntos
Ácido Aspártico/análogos & derivados , Tronco Encefálico/patologia , Tronco Encefálico/virologia , Doenças Desmielinizantes/patologia , Doenças Desmielinizantes/virologia , Traumatismos da Medula Espinal/patologia , Traumatismos da Medula Espinal/virologia , Animais , Ácido Aspártico/metabolismo , Biomarcadores/líquido cefalorraquidiano , Tronco Encefálico/fisiologia , Doenças Desmielinizantes/reabilitação , Vírus da Leucemia Murina de Friend/crescimento & desenvolvimento , Vírus da Leucemia Murina de Friend/isolamento & purificação , Espectroscopia de Ressonância Magnética/métodos , Camundongos , Prótons , Traumatismos da Medula Espinal/reabilitação
4.
Neuroimage ; 15(3): 708-18, 2002 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-11848714

RESUMO

The results of in vivo neuroimaging studies assessing whether and where brain white matter damage occurs in alcoholic women is controversial. To address this controversy, we examined regional white matter macrostructure and microstructure, the latter of which may be more sensitive to the detection of subtle fiber disruption than gross measures of size. Accordingly, we used conventional magnetic resonance imaging (MRI) to quantify regional callosal size and diffusion tensor imaging (DTI) to examine intravoxel coherence (fractional anisotropy, FA) and intervoxel coherence (C) of white matter of the genu and splenium of the corpus callosum and of the centrum semiovale in 12 detoxified alcoholic women and 18 control women. Additional analyses examined sex differences in FA and C in alcoholic women compared with alcoholic men. Despite absence of group differences in regional areas of callosal macrostructure, the alcoholic women had lower FA and C in genu and centrum semiovale than the control group of women. These measures also correlated with total lifetime consumption of alcohol and performance on a test of visual search in the alcoholic women. Sex comparisons revealed similar extents of FA abnormality in the genu and centrum semiovale in alcoholic men and women and differential effects in other DTI measures, with abnormalities present in splenium FA and C in the men and abnormalities present in centrum C in the women. These results provide in vivo evidence for disruption of white matter microstructure in alcoholic women not necessarily detectable with coarser measures of white matter mass and perhaps antedating its appearance.


Assuntos
Alcoolismo/diagnóstico , Encéfalo/patologia , Doenças Desmielinizantes/diagnóstico , Imageamento por Ressonância Magnética , Fibras Nervosas Mielinizadas/patologia , Adulto , Idoso , Alcoolismo/reabilitação , Doenças Desmielinizantes/reabilitação , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Mielinólise Central da Ponte/diagnóstico , Mielinólise Central da Ponte/reabilitação , Fatores Sexuais
5.
Arch Phys Med Rehabil ; 81(3 Suppl 1): S20-6; quiz S36-44, 2000 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-10721757

RESUMO

This self-directed learning module provides an updated tool for establishing the differential diagnosis and subsequently designing a cost-effective workup for patients with peripheral neuropathy. It is part of the chapter on neuromuscular rehabilitation and electrodiagnosis in the Self-Directed Physiatric Education Program for practitioners and trainees in physical medicine and rehabilitation. Medication intervention for neuropathic pain is reviewed by medication class with recommendations for starting doses and review of side-effect profiles. This article also reviews the current treatment standards for a patient with juvenile-onset diabetes, including recommendations for glucose control, management of nephropathy and retinopathy, and care of foot complications.


Assuntos
Diabetes Mellitus Tipo 1/complicações , Neuropatias Diabéticas/diagnóstico , Neuropatias Diabéticas/reabilitação , Doenças do Sistema Nervoso Periférico/diagnóstico , Doenças do Sistema Nervoso Periférico/reabilitação , Algoritmos , Análise Custo-Benefício , Doenças Desmielinizantes/diagnóstico , Doenças Desmielinizantes/reabilitação , Eletrodiagnóstico , Humanos , Planejamento de Assistência ao Paciente/economia , Doenças do Sistema Nervoso Periférico/etiologia
7.
J Neurol ; 246(8): 700-5, 1999 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-10460448

RESUMO

The findings in 44 patients (42 of whom were chronic alcoholics) with central pontine myelinolysis show that the outcome does not depend on the severity of neurological deficits during the acute phase of the condition or on concomitant internal diseases, including the degree of hyponatremia. Of the 34 patients for whom follow-up data were available, 32 survived. Of these 11 completely recovered, 11 had some deficits but were independent, and 10 were dependent (4 through disorders of memory or cognition, 3 with tetraparesis, 2 with cerebellar ataxia, 1 with polyneuropathy). The electrophysiological findings did not contribute usefully to the prediction of outcome. Additional neuroradiological diagnostic testing with magnetic resonance imaging was also of no prognostic significance. The extent of the initial pontine lesion was not correlated with the severity of clinical findings during the acute phase of disease, nor was persistence of the pontine lesion as usually seen on magnetic resonance imaging correlated with clinical improvement. We conclude that patients with cerebral myelinolysis survive if the nonspecific secondary complications of transient illnesses such as aspiration pneumonia, ascending urinary tract infection with subsequent septicemia, deep venous thrombosis, and pulmonary embolism can be avoided.


Assuntos
Doenças Desmielinizantes/diagnóstico , Mielinólise Central da Ponte/diagnóstico , Adulto , Idoso , Idoso de 80 Anos ou mais , Doenças Desmielinizantes/reabilitação , Potenciais Evocados/fisiologia , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Mielinólise Central da Ponte/reabilitação , Estudos Retrospectivos , Resultado do Tratamento
8.
J Spinal Cord Med ; 21(2): 142-7, 1998 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-9697091

RESUMO

Although arsenic poisoning was a common cause of homicide in the past, it is seldom suspected today; thus there may be serious delays in diagnosis and treatment of arsenic ingestion. Rehabilitation specialists have traditionally dealt with the debilitating consequences of the classic arsenic-induced sensorimotor peripheral neuropathy; however, a knowledge of the presentation of acute toxicity combined with the effects of chronic exposure is essential for proper treatment, particularly in the event of ongoing exposure. This case report demonstrates the wide spectrum of medical complications associated with arsenic poisoning and briefly reviews its pathophysiology and treatment from both the medical and psychosocial perspective.


Assuntos
Intoxicação por Arsênico , Doenças Desmielinizantes/induzido quimicamente , Equipe de Assistência ao Paciente , Doenças do Sistema Nervoso Periférico/induzido quimicamente , Intoxicação/reabilitação , Quadriplegia/induzido quimicamente , Adulto , Doença Crônica , Doenças Desmielinizantes/reabilitação , Humanos , Masculino , Exame Neurológico/efeitos dos fármacos , Doenças do Sistema Nervoso Periférico/reabilitação , Quadriplegia/reabilitação , Medidas de Segurança
10.
Artigo em Russo | MEDLINE | ID: mdl-8585370

RESUMO

120 patients with Guillain-Barre syndrome and other peripheral myelinopathies were randomly assigned to three treatment groups. One of the group was exposed to pulsed high frequency electric field (47 patients), the other group to continuous current (52 patients), and the third group received the imitation of therapy (21 patients). Pulsed current therapy caused the greatest regress of the neurological deficit (45 from 47 cases). The electroneuromyography of paretic limbs nerves showed that the acceleration of remyelinization process turn to be the background of pulsed high frequency electric field medical action. Both the rheovasography and isotope muscle flow measurements did not confirm the hypothesis about preferential mediation of the healing potency of pulsed short wave diathermy through vascular mechanism. It was suggested the direct influence of pulsed short wave diathermy on protein synthesis process in the spinal alpha-motoneurone and myocyte.


Assuntos
Doenças Desmielinizantes/reabilitação , Terapia por Estimulação Elétrica/métodos , Polirradiculoneuropatia/reabilitação , Adolescente , Glândulas Suprarrenais/fisiopatologia , Adulto , Idoso , Velocidade do Fluxo Sanguíneo , Doenças Desmielinizantes/fisiopatologia , Terapia por Estimulação Elétrica/instrumentação , Terapia por Estimulação Elétrica/estatística & dados numéricos , Eletromiografia , Feminino , Pé/irrigação sanguínea , Antebraço/irrigação sanguínea , Humanos , Masculino , Pessoa de Meia-Idade , Músculo Esquelético/irrigação sanguínea , Polirradiculoneuropatia/fisiopatologia , Estatísticas não Paramétricas
11.
Pediatr Neurol ; 11(1): 57-8, 1994 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-7986295

RESUMO

An infant with acute demyelinating encephalomyelitis resulting from California virus infection presented with a neurodegenerative clinical picture. The clinical course was complicated by infantile spasms which responded to treatment with corticotropin. Acute demyelinating encephalomyelitis should be included in the diagnostic evaluation of patients who present with subacute regression of developmental milestones.


Assuntos
Doenças Desmielinizantes/diagnóstico , Encefalite da Califórnia/diagnóstico , Hormônio Adrenocorticotrópico/administração & dosagem , Encéfalo/patologia , Terapia Combinada , Doenças Desmielinizantes/reabilitação , Diagnóstico Diferencial , Eletroencefalografia/efeitos dos fármacos , Encefalite da Califórnia/reabilitação , Humanos , Lactente , Imageamento por Ressonância Magnética , Masculino , Exame Neurológico/efeitos dos fármacos , Modalidades de Fisioterapia , Espasmos Infantis/diagnóstico , Espasmos Infantis/reabilitação
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