RESUMO
BACKGROUND: X-linked dystonia-deafness syndrome (DDS) is characterized by early-onset deafness followed by progressive dystonia in adulthood. Only 4 families with the syndrome have been reported, and all were white. OBJECTIVE: To describe the first nonwhite family with X-linked DDS, involving 5 affected males in 4 generations. RESULTS: Clinical features of the family members, who were Japanese, were mostly consistent with reports of DDS in whites except for a lack of visual disturbances. Whereas microdeletions in the deafness-dystonia peptide (DDP) gene were found in 2 white DDS families, our patients showed a novel mutation (arg80ter) in exon 2 of the DDP gene. CONCLUSION: The existence of a DDS family of Japanese origin with a new kind of mutation in the DDP gene provides additional evidence that the DDP gene is a causative gene for X-linked DDS.
Assuntos
Surdez/genética , Distonia/genética , Ligação Genética , Proteínas de Membrana Transportadoras , Mutação/genética , Proteínas/genética , Cromossomo X/genética , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Humanos , Japão , Masculino , Proteínas do Complexo de Importação de Proteína Precursora Mitocondrial , Linhagem , Análise de Sequência de DNA/métodos , Aberrações dos Cromossomos Sexuais/genéticaRESUMO
BACKGROUND: Mutations in the SOD1 gene are responsible for approximately 25% of all familial amyotrophic lateral sclerosis (ALS) cases. However, the correlation between the clinical and pathological features and the various SOD1 gene mutations has not been well characterized. OBJECTIVES: To screen the SOD1 gene in search of potential mutations and to obtain clinical and pathological data for 2 Japanese families with ALS. DESIGN: Clinical histories and neurological findings, gross and microscopic pathological features, and DNA analysis of the SOD1 gene. RESULTS: The 2 families with ALS showed a novel missense mutation in the SOD1 gene, which was heterozygous for point mutation TTG to TCG, causing substitution of leucine for serine at codon 126 (Leu126Ser) in exon 5. Clinically, patients showed slower disease progression and lack of upper motor neuron signs. Neuropathologically, the autopsied patient showed the form of familial ALS with posterior column involvement, and the pontocerebellar tract and the dentate nuclei of the cerebellum were also involved. Furthermore, abundant Lewy body-like hyaline inclusions were observed in the affected motor and nonmotor neurons. CONCLUSIONS: Familial ALS with a novel Leu126Ser mutation in the SOD1 gene showed mild clinical features and lack of upper motor neuron signs. We believe that Leu126Ser might be associated with the clinical features and that the mutation site in the SOD1 gene and disease duration might be associated with the formation of Lewy body-like hyaline inclusions.
Assuntos
Esclerose Lateral Amiotrófica/genética , Esclerose Lateral Amiotrófica/patologia , Hialina/ultraestrutura , Corpos de Inclusão/ultraestrutura , Corpos de Lewy/ultraestrutura , Mutação Puntual/genética , Superóxido Dismutase/genética , Adulto , Idoso , Substituição de Aminoácidos , Encéfalo/patologia , Feminino , Humanos , Masculino , Pessoa de Meia-IdadeRESUMO
OBJECTIVE: To investigate the relationship between oxidative stress and apoE phenotype in dementia of Alzheimer type (DAT). MATERIAL AND METHODS: Hydroxyl radical content in blood, superoxide dismutase (SOD) activity in red blood cells (RBC) and plasma, Cu,Zn-SOD protein content in RBC, and apoE phenotype were determined in 24 DAT patients and 25 controls. RESULTS: DAT patients with the apoE4 phenotype showed higher hydroxyl radical levels than DAT patients without the apoE4 phenotype or controls. SOD activities and Cu,Zn-SOD protein levels in RBC of DAT patients with and without the apoE4 phenotype showed no significant differences, but values in both patient groups were lower than in controls. The apoE4 phenotype was more prevalent in DAT patients than in controls. DAT patients with the apoE4 phenotype were younger at disease onset than DAT patients without the apoE4 phenotype. CONCLUSION: Our findings suggest that apoE4 and SOD individually influence oxidative stress in DAT.
Assuntos
Doença de Alzheimer/genética , Apolipoproteínas E/genética , Estresse Oxidativo , Superóxido Dismutase/metabolismo , Idoso , Idoso de 80 Anos ou mais , Doença de Alzheimer/fisiopatologia , Estudos de Casos e Controles , Eritrócitos/fisiologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , FenótipoRESUMO
This study was designed to establish a role for cAMP-responsive element (CRE) binding protein (CREB) in signal transduction cascade in the hippocampus associated with kindling. Male Sprague-Dawley rats were kindled from the left amygdala until they exhibited Racine's class 5 generalized seizures [Racine (1972). EMBO J. 11, 3337-3346] Nuclear proteins were extracted from dorsal hippocampi obtained from 0 to 24 h after final kindling stimulation. From these, we evaluated the temporal pattern of CRE DNA-binding activity by use of a gel mobility-shift assay with a 32P-labeled CREB oligonucleotide probe. CRE-binding activity in the hippocampus was enhanced significantly at 2 h and returned to baseline level within 4 h after the stimulation. Our results suggest that CREB may be involved in the hippocampal signal transduction pathway of rats activated in response to a kindling stimulation to the amygdala. However, the transient elevation of CRE-binding activity following a seizure in a kindled animal also suggests that persistent activation of CREB may not be required for maintenance of the kindling phenomenon.
Assuntos
Proteína de Ligação ao Elemento de Resposta ao AMP Cíclico/metabolismo , Hipocampo/metabolismo , Excitação Neurológica/metabolismo , Fator de Transcrição AP-1/metabolismo , Animais , Masculino , Ratos , Ratos Sprague-DawleyRESUMO
Hydroxyl radical (.OH) levels in blood, superoxide dismutase (SOD) activity in plasma (plasma-SOD) and in red blood cells (RBC) relative to Cu,Zn-SOD (SOD1) protein (RBC-SOD/SOD1), SOD1 protein in RBC (SOD1/RBC) and plasma (SOD1/plasma), and Mn-SOD protein in plasma (SOD2/plasma) were measured in patients with Parkinson's disease (PD), multiple-system atrophy (MSA) with parkinsonism, and in control subjects. Patients with PD had significantly higher.OH and plasma-SOD values and significantly lower RBC-SOD/SOD1 and SOD1/RBC values than the corresponding MSA and control values. In PD, RBC-SOD/SOD1 values were significantly lower in older patients and were negatively correlated with age.OH levels were significantly higher in PD patients with early onset, a long period of illness or severe Yahr stage, and were negatively correlated with onset and positively correlated with duration of illness. RBC-SOD/SOD1 values in PD patients who received pergolide therapy were significantly higher than those in PD patients who received neither pergolide nor bromocriptine therapy. Therefore, the higher.OH level and the lower SOD1 activity may play a role in the onset and progression of PD, and pergolide may act neuroprotectively by inducing SOD1 activity.
Assuntos
Radical Hidroxila/sangue , Doença de Parkinson/sangue , Superóxido Dismutase/sangue , Fatores Etários , Idade de Início , Idoso , Antiparkinsonianos/uso terapêutico , Bromocriptina/uso terapêutico , Progressão da Doença , Eritrócitos/enzimologia , Humanos , Levodopa/uso terapêutico , Pessoa de Meia-Idade , Atrofia de Múltiplos Sistemas/sangue , Doença de Parkinson/tratamento farmacológico , Doença de Parkinson/patologia , Pergolida/uso terapêutico , Índice de Gravidade de Doença , Estatística como Assunto , Fatores de TempoRESUMO
UNLABELLED: Iodine-123 MIBG is a biochemical marker that can be used to monitor pulmonary norepinephrine (NE) metabolism. The purpose of this study was to characterize pulmonary I-123 MIBG kinetics in relation to age and gender. MATERIALS AND METHODS: Seventeen healthy volunteers and 14 patients with no cardiac or pulmonary disorders were included in this study (age range: 24 to 88 years, mean age 50.2 +/- 17.6 years; 16 males, 15 females). Planar images were obtained 15 min (early) and 3 h (delayed) after injection of I-123 MIBG (111 MBq). Pulmonary uptake of I-123 MIBG was quantified based on the lung-to-mediastinum ratio (LMR) on early and delayed images. The lung clearance rate (LCR) was calculated form both the early and delayed images. RESULTS: Both early and delayed LMR values increased slightly, although they showed no significant correlations with age. There was a significant inverse correlation between LCR and age (r = -0.57, p < 0.001). Neither LCR nor LMR differed significantly between male and female patients, but the mean age of the men was lower than that of the women. CONCLUSIONS: Pulmonary I-123 MIBG kinetics may reflect age-dependent changes in NE metabolism. The effects of age should be taken into account when assessing pulmonary NE metabolism with I-123 MIBG.
Assuntos
3-Iodobenzilguanidina/farmacocinética , Pulmão/metabolismo , Compostos Radiofarmacêuticos/farmacocinética , Adulto , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Radioisótopos do Iodo , Pulmão/diagnóstico por imagem , Masculino , Pessoa de Meia-Idade , Cintilografia , Fatores SexuaisRESUMO
We studied brain synapsin I and II mRNA levels using the amygdala kindling model of epilepsy. There were significant increases in the synapsin I mRNA level in the granule cell layer of the hippocampal bilateral dentate gyrus. One to 8 h after seizures, the level in the dentate gyrus ipsilateral to stimulation increased by 44.2-73.2%, compared with the control level. Of the time points investigated, the greatest increase in expression was observed 8 h after the kindled seizures. Furthermore, the synapsin I mRNA levels in the dentate gyrus contralateral to stimulation increased by 28.0% and 51.1%, 2 and 8 h, respectively, after the kindled seizures. Expression of this mRNA, however, did not change significantly in other areas examined, including CA1, CA2, CA3 and the polymorphic layer of the hippocampus and the perirhinal and temporal cortices. Synapsin II mRNA levels did not change significantly in any of the regions studied for up to 24 h after the seizures and synapsin II was presumed to have little involvement in kindling. We considered the locally elevated synapsin I mRNA levels in the bilateral dentate gyrus associated with kindling indicate that excitatory changes occur in the synaptic circuit in which the dentate granule cells participate. Synapsin I may be involved in the presynaptic molecular mechanisms underlying the neuronal plasticity in kindling.
Assuntos
Tonsila do Cerebelo/metabolismo , Excitação Neurológica , RNA Mensageiro/análise , Convulsões/metabolismo , Sinapsinas/genética , Tonsila do Cerebelo/patologia , Análise de Variância , Animais , Modelos Animais de Doenças , Estimulação Elétrica , Expressão Gênica , Hipocampo/metabolismo , Hibridização In Situ , Masculino , Ratos , Ratos Sprague-Dawley , Convulsões/classificação , Transmissão Sináptica/fisiologiaRESUMO
We studied the time-dependent changes in synapsin I mRNA levels after hippocampal long-term potentiation (LTP) in rats in vivo. Following LTP induction by stimulating the perforant path, synapsin I mRNA expression in the granule cell layer of the dentate gyrus ipsilateral to stimulation increased significantly in a time-dependent manner. From 2 to 8 h after stimulation, the synapsin I mRNA levels in the ipsilateral dentate gyrus were significantly higher than those of controls subjected to a sham procedure. The synapsin I mRNA level (157.4+/-7.1% of the control level, mean+/-SEM) was at a maximum 8 h after stimulation. The synapsin I mRNA level of animals that received only test pulses did not increase significantly, compared with the control level. These results suggest that the increased level of synapsin I mRNA is related to persistent enhancement of synaptic activity within the neural networks in which dentate granule cells participate in LTP.
Assuntos
Hipocampo/metabolismo , Potenciação de Longa Duração , RNA Mensageiro/biossíntese , Sinapsinas/genética , Animais , Hibridização In Situ , Masculino , Ratos , Ratos Sprague-Dawley , Fatores de TempoRESUMO
We compared the time-dependent changes in messenger ribonucleic acid (mRNA) levels for two neurotrophic factors after amygdala-kindled seizures and hippocampal long-term potentiation (LTP) in rats in vivo. The brain-derived neurotrophic factor (BDNF) mRNA levels in the bilateral granule cell layer of the dentate gyrus, increased significantly 1-4 h after stage 5 kindled seizures. Nerve growth factor (NGF) mRNA levels increased throughout the bilateral limbic regions more gradually than those of BDNF mRNA. The maximum levels in the dentate gyrus ipsilateral to stimulation (BDNF mRNA: 493%, NGF mRNA: 199% of control levels) occurred 2 h after seizures. As observed with kindling, BDNF and NGF mRNA expression increased in the dentate gyrus ipsilateral to stimulation also increased following LTP induced by the perforant path stimulation, with maximum levels occurring 2 h and 4 h, respectively, after stimulation, when they reached 284% and 189% of the control levels, respectively. These results suggest that BDNF and NGF are involved in enhancement of synaptic efficacy in the granule cells of the dentate gyrus in the hippocampus in kindling, not related to the neuronal excitability associated with seizure activity.
Assuntos
Fator Neurotrófico Derivado do Encéfalo/biossíntese , Potenciais Pós-Sinápticos Excitadores/fisiologia , Hipocampo/fisiologia , Excitação Neurológica/fisiologia , Potenciação de Longa Duração/fisiologia , Convulsões/fisiopatologia , Transcrição Gênica , Tonsila do Cerebelo/fisiologia , Tonsila do Cerebelo/fisiopatologia , Animais , Estimulação Elétrica , Hipocampo/fisiopatologia , Masculino , RNA Mensageiro/biossíntese , Ratos , Ratos Sprague-Dawley , Fatores de TempoRESUMO
DNA binding by transcripton factor AP-1 was enhanced remarkably following kindling stimulation in rat amygdala. Maximum increase occurred 2 h after stimulation with return to baseline within 24 h. Supershift and western analyses revealed that 38,000 mol. wt Fos-related antigen and JunD were the main components of the evoked AP-1 complexes at the time their induction reached maximum. AP-1 induction 2 h after the last kindling stimulation was more prominent in samples from previously kindled rats than in those from non-kindled rats. This study sought to establish the role of AP-1 in plastic changes of the hippocampus associated with kindling. Male Sprague-Dawley rats were kindled from the left amygdala until they exhibited Racine15 class 5 generalized seizures. Nuclear proteins were extracted from dorsal hippocampi obtained from 0 to 24 h after final stimulations. From these, we evaluated the temporal pattern of DNA binding by AP-1 using a gel mobility-shift assay with a 32P-labelled AP-1 probe. Supershift and western analyses were added to investigate components of the seizure-evoked AP-1 complexes. Our results suggest that the basal level of AP-1 complexes is not associated with the seizure susceptibility in kindling. However, development of kindling appears to facilitate stimulus-evoked AP-1 induction, probably via plastic changes in the central nervous system. AP-1 may mediate such changes by regulating expression of certain genes.
Assuntos
Proteínas de Ligação a DNA/biossíntese , Hipocampo/metabolismo , Excitação Neurológica/fisiologia , Convulsões/metabolismo , Fator de Transcrição AP-1/biossíntese , Análise de Variância , Animais , Sequência de Bases , Núcleo Celular/metabolismo , Sequência Consenso , Hipocampo/fisiologia , Hipocampo/fisiopatologia , Cinética , Masculino , Proteínas Nucleares/biossíntese , Sondas de Oligonucleotídeos , Ratos , Ratos Sprague-Dawley , Valores de Referência , Convulsões/fisiopatologia , Fatores de Tempo , Transcrição GênicaRESUMO
A 72-year-old woman with Parkinson's disease and autonomic dysfunction underwent I-123 MIBG cardiac imaging to study sympathetic neuronal integrity. This revealed a defect in the infero-posterior wall. Tc-99m sestamibi myocardial perfusion imaging revealed no abnormalities. On follow-up I-123 MIBG SPECT, the defect was less prominent and the parkinsonian symptoms were ameliorated by drug therapy. Cardiac I-123 MIBG imaging may be a promising new method for evaluating drug therapy in patients with Parkinson's disease.
Assuntos
3-Iodobenzilguanidina , Antiparkinsonianos/uso terapêutico , Coração/diagnóstico por imagem , Radioisótopos do Iodo , Doença de Parkinson/tratamento farmacológico , Compostos Radiofarmacêuticos , Tomografia Computadorizada de Emissão de Fóton Único , Idoso , Doenças do Sistema Nervoso Autônomo/diagnóstico por imagem , Circulação Coronária , Droxidopa/uso terapêutico , Feminino , Seguimentos , Imagem do Acúmulo Cardíaco de Comporta , Cardiopatias/diagnóstico por imagem , Humanos , Pergolida/uso terapêutico , Volume Sistólico , Sistema Nervoso Simpático/diagnóstico por imagem , Tecnécio Tc 99m Sestamibi , Tomografia Computadorizada de Emissão de Fóton Único/métodosRESUMO
The free radical levels in the cerebrospinal fluid of 8 patients with neurological diseases and 9 undergoing lumbar anesthesia for surgery were measured. The ascorbate free radical level 10 min after lumbar puncture showed a positive correlation with the hydroxyl radical level. In the patient with mitochondrial encephalomyopathy, the levels of hydroxyl and ascorbate free radicals increased upon discontinuation of treatment and decreased upon its resumption, and the ascorbate free radical levels without therapy fell after lumbar puncture. The free radical levels in the cerebrospinal fluid may reflect the degree of oxidative stress in the central nervous system.
Assuntos
Ácido Ascórbico/líquido cefalorraquidiano , Radical Hidroxila/líquido cefalorraquidiano , Encefalomiopatias Mitocondriais/líquido cefalorraquidiano , Doenças do Sistema Nervoso/líquido cefalorraquidiano , Idoso , Espectroscopia de Ressonância de Spin Eletrônica , Feminino , Humanos , Masculino , Pessoa de Meia-IdadeRESUMO
We studied levels of mRNA for the alpha- and beta-subunits of calmodulin (CaM) kinase II using the amygdaloid kindling model of epilepsy. There were significant increases in mRNA for the beta-subunit of CaM kinase II in the hippocampus 4-24 h after stage 5-kindled seizures. Moreover, this mRNA was significantly increased by 20.0-26.5% in the bilateral dentate gyrus 8 to 24 h after kindled seizures. The beta-subunit mRNA was also significantly increased by 13.5-19.0% in the CA3 on the side ipsilateral to the stimulation, 4 to 8 h after kindled seizures. mRNA for the alpha-subunit of CaM kinase II was not significantly changed in the regions examined for up to 24 h after the kindled seizures. These results suggest that CaM kinase II mediates the molecular processes that follow kindled seizures. It is possible that increases in CaM kinase II-dependent protein phosphorylation are associated with the plastic changes in kindling.
Assuntos
Encéfalo/metabolismo , Proteínas Quinases Dependentes de Cálcio-Calmodulina/metabolismo , Epilepsia/enzimologia , Animais , Proteína Quinase Tipo 2 Dependente de Cálcio-Calmodulina , Modelos Animais de Doenças , Hibridização In Situ , Excitação Neurológica , Masculino , RNA Mensageiro/metabolismo , Ratos , Ratos Sprague-DawleyRESUMO
Povidone-iodine (PVP-I) is generally very safe, but cases of thyroid dysfunction induced by PVP-I have been reported. The effect of long-term treatment with PVP-I on thyroid function was to be assessed. In 40 inpatients of the department of neurology, the status of the use of PVP-I preparations and their effects on serum inorganic iodine levels and thyroid functions were investigated. In 27 patients treated with PVP-I for a long term, inorganic iodine levels were significantly increased as compared to those in 13 patients without PVP-I treatment. Out of 27 patients treated with PVP-I in the long term, subclinical hypothroidism was seen in 3 patients, mild hyperthroidism was seen in 1 patient, and subclinical hyperthyroidism was suspected in 7 patients. Patients treated with PVP-I for a long time should be observed carefully for any manifestation of thyroid dysfunction.
Assuntos
Anti-Infecciosos Locais/uso terapêutico , Iodóforos/uso terapêutico , Povidona-Iodo/uso terapêutico , Glândula Tireoide/efeitos dos fármacos , Esclerose Lateral Amiotrófica/complicações , Anti-Infecciosos Locais/efeitos adversos , Cateterismo Venoso Central/instrumentação , Feminino , Gastrostomia/instrumentação , Humanos , Hipertireoidismo/induzido quimicamente , Hipotireoidismo/induzido quimicamente , Iodo/sangue , Iodóforos/efeitos adversos , Estudos Longitudinais , Masculino , Pessoa de Meia-Idade , Mucosa Nasal/efeitos dos fármacos , Nutrição Parenteral/instrumentação , Povidona-Iodo/efeitos adversos , Segurança , Úlcera Cutânea/tratamento farmacológico , Degenerações Espinocerebelares/complicações , Glândula Tireoide/fisiologia , Tireotropina/sangue , Tiroxina/sangue , Traqueotomia , Tri-Iodotironina/sangue , Uretra/efeitos dos fármacosRESUMO
We measured hydroxyl radical (.OH) levels in blood, superoxide dismutase (SOD) activity in red blood cells (RBC) relative to both total protein (RBC-SOD/P) and Cu,Zn-SOD protein (RBC-SOD/SOD), SOD activity in plasma (plasma-SOD), and Cu,Zn-SOD protein relative to total RBC protein (Cu,Zn-SOD/P) in 22 patients with probable dementia of the Alzheimer type (DAT group, mean age 74.8+/-9.4 years), 16 with probable vascular dementia (VAD group, mean age 76.9+/-6.7 years) and 19 non-demented controls (control group, mean age 73.5+/-6.2 years). Levels of .OH in the DAT and VAD groups were significantly (P<0.01 and P<0.001, respectively) higher, whereas the values of RBC-SOD/P and RBC-SOD/SOD in these two groups (both P<0.001) and Cu,Zn-SOD/P in the DAT group (P<0.001) were significantly lower than the corresponding control values. Members of the VAD group with risk factors for stroke (RF+ group) showed significantly higher .OH levels than members of the VAD group without risk factors (RF- group; P<0.01) and the control group (P<0.001). RBC-SOD/P and RBC-SOD/SOD values in the RF+ group were significantly (both P<0.01) lower than the corresponding control values. There were no significant differences among the VAD, RF+ and control groups with respect to Cu,Zn-SOD/P values, or between the RF- and control groups for any measured parameter. We conclude that oxidative stress plays a role in the brain damage seen in both DAT and VAD, and that the causes of decreased SOD activity in RBC differ between DAT and VAD patients.
Assuntos
Doença de Alzheimer/sangue , Demência Vascular/sangue , Superóxido Dismutase/sangue , Idoso , Idoso de 80 Anos ou mais , Progressão da Doença , Feminino , Radicais Livres/sangue , Humanos , Masculino , Pessoa de Meia-Idade , Estresse Oxidativo/fisiologia , Fatores de RiscoRESUMO
We studied mRNA levels for neurotrophic factors using the amygdaloid k indling model of epilepsy. One hour after stage 5 kindled seizures, there were four-to fivefold increases in brain-derived neurotrophic factor (BDNF) mRNA in rat dentate gyrus and perirhinal cortex. Nerve growth factor (NGF) mRNA levels were increased bilaterally in some (but not all) limbic areas. There were no detectable changes in acidic fibroblast GF (aFGF) mRNA or basic fibroblast GF (bFGF) mRNA for 24 h after the kindled seizures. During kindling, levels of BDNF mRNA in the dentate gyrus correlated with projection to generalized seizures, whereas NGF mRNA in the limbic regions continued to increase during seizure development. These results indicate that the induction of mRNAs for neurotrophic factors, especially for BDNF mRNA in the dentate gyrus, corresponds to the increases in metabolic and electrical ictal discharge associated with kindled seizures. The persistent increase observed in NGF mRNA may be related to enhanced synaptic efficacy during kindling, but aFGF and bFGF are presumed to have little relation to the kindling process.
Assuntos
Tonsila do Cerebelo/metabolismo , Encéfalo/metabolismo , Fator 1 de Crescimento de Fibroblastos/análise , Fator 2 de Crescimento de Fibroblastos/análise , Excitação Neurológica/metabolismo , Fatores de Crescimento Neural/análise , Proteínas do Tecido Nervoso/análise , Tonsila do Cerebelo/química , Animais , Sequência de Bases , Química Encefálica , Fator Neurotrófico Derivado do Encéfalo , Fator 1 de Crescimento de Fibroblastos/biossíntese , Fator 2 de Crescimento de Fibroblastos/biossíntese , Hipocampo/química , Hipocampo/metabolismo , Hibridização In Situ , Masculino , Dados de Sequência Molecular , Fatores de Crescimento Neural/biossíntese , Proteínas do Tecido Nervoso/biossíntese , RNA Mensageiro/metabolismo , Ratos , Ratos Sprague-Dawley , Distribuição TecidualRESUMO
We studied the relationships between the superoxide dismutase (SOD) activity, free radical (FR) levels and clinical data in patients with sporadic amyotrophic lateral sclerosis (SALS). The SOD activities and blood FR levels of 16 patients with SALS (mean age 58.6 +/- 10.2 years), 11 with other neurological disease, including myotonic dystrophy (ND, mean age 53.5 +/- 9.1 years), and 15 normal control subjects (mean age 56.2 +/- 7.3 years) were measured. The mean levels of FR in blood from the patients with SALS and ND and the SOD activities in red blood cells (RBC) from those with ND were significantly higher than the corresponding control values. There was a positive correlation between the SOD activities in RBC and blood hydroxyl radical levels in the patients with ND, but neither the patients with SALS nor the controls showed such a correlation. The SALS patients without pyramidal signs showed slow disease progression and their mean RBC SOD activity was significantly higher than the corresponding control value. We compared the FR levels and SOD activities of 8 patients who needed a respirator within 40 months after the onset of SALS (SALS40, mean age 58.7 +/- 9.4 years), 3 who needed a respirator over 100 months after the onset of SALS (SALS100, mean age 58.3 +/- 15.9 years) and the controls. The mean blood FR levels of the SALS40 and SALS100 patients were significantly higher than the corresponding control values. The mean SOD activity in RBC from the SALS100 group was significantly higher than the SALS40 and control group values. Therefore, we concluded that elevated blood FR levels do not induce RBC SOD in SALS patients and that the disease progressed more rapidly in SALS patients with low than high RBS SOD activities.
Assuntos
Esclerose Lateral Amiotrófica/diagnóstico , Esclerose Lateral Amiotrófica/metabolismo , Periodicidade , Superóxido Dismutase/metabolismo , Idoso , Esclerose Lateral Amiotrófica/enzimologia , Técnicas de Laboratório Clínico , Feminino , Radicais Livres , Humanos , Masculino , Pessoa de Meia-IdadeRESUMO
We confirmed a homozygous type of relatively small expansion of CAG triplet repeats (57 repeats) in the short arm of chromosome 12 in a male patient with dentatorubral-pallidoluysian atrophy (DRPLA) by polymerase chain reaction. He showed early onset (age, 17 years) of DRPLA. There was good correlation of the age of onset with the number of triplet repeats. The homozygous state of the expansion of the triplet repeats was responsible for the early onset and severity of his DRPLA.
Assuntos
Giro Denteado/patologia , Globo Pálido/patologia , Degenerações Espinocerebelares/genética , Adulto , Idade de Início , Atetose/genética , Atrofia/genética , Ataxia Cerebelar/genética , Demência/genética , Epilepsias Mioclônicas/genética , Humanos , Masculino , Linhagem , Sequências Repetitivas de Ácido NucleicoRESUMO
Autonomic functions were studied in 10 respiratory-support patients with motor neuron disease (MND) at its most advanced stage by means of hemodynamic function tests. The mean duration of disease was 83.4 months (SD 28.0, range 50-140 months). All the patients in this study had lost their ability to breathe spontaneously and were ventilated by respirator. Hemodynamic function tests were performed in 8 out of 10 patients. These patients showed exaggerated sympathetic vasomotor reflexes, increased reflex hypertension and tachycardia in response to the cold pressor test and increased response to administration of adrenaline. However, the responses to both the Aschner eyeball pressure test and injection of atropine were normal, indicating normal parasympathetic nervous system function. Plasma and urine levels of norepinephrine, epinephrine and their metabolites were almost normal in all 10 patients, as were serum dopamine-beta-hydroxylase levels. In patients with the most advanced stage of MND, hyperfunction of the adrenergic sympathetic nervous system was observed, and this was considered to be a symptom characteristic of MND.
Assuntos
Doenças do Sistema Nervoso Autônomo/etiologia , Doença dos Neurônios Motores/complicações , Idoso , Doenças do Sistema Nervoso Autônomo/diagnóstico , Doenças do Sistema Nervoso Autônomo/fisiopatologia , Monoaminas Biogênicas/análise , Ácidos Carboxílicos/análise , Dopamina beta-Hidroxilase/sangue , Epinefrina , Feminino , Hemodinâmica/fisiologia , Humanos , Hidrocortisona/análise , Ácido Hidroxi-Indolacético/análise , Masculino , Pessoa de Meia-Idade , Exame FísicoRESUMO
We reported a 16-year-old boy who had Guillain-Barré syndrome (GBS) after suffering diarrhea. Campylobacter jejuni was isolated from his stool, and the serotype belonged to PEN 43. Neurologic examination revealed distal-dominant muscle weakness atrophy, and mild sensory disturbance. Motor and sensory nerve conduction velocities were normal, but compound muscle action potentials were markedly reduced. Serum from the patient had high titers of anti-FalNAc-GD1a antibodies. He had HLA-A24, B51, DRB1*04 and DRB1*09. His elder sister showed diarrhea and serum anti-C. jejuni antibody, but did not showed GBS and serum anti-ganglioside antibody. Her HLA types were A24, B51, DRB1*09 and DRB1*14.