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1.
Neurosci Res ; 39(4): 463-8, 2001 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11274745

RESUMO

Veratridine is a neurotoxin that induces persistent activation of sodium channels in excitable cells. We investigated the effects of this toxin on excitatory synaptic transmission in CA3 neurons of juvenile rat hippocampus using whole-cell patch-clamp and field-potential recordings. The population spikes evoked by electrical stimulation of the mossy fiber were gradually enhanced after washout of veratridine (0.3 microM), but they were not enhanced by the co-application of veratridine and an N-methyl-D-aspartate (NMDA) receptor antagonist (D-APV, 30 microM). When a pipette solution contained QX-314 that antagonized the effect of veratridine in the recorded neuron, oscillatory membrane depolarization appeared in the early stage during bath-application of veratridine and gradually decreased in the late stage. After washout of veratridine, however, the oscillatory depolarization was gradually restored and maintained for at least 3 h. This oscillatory depolarization was also abolished by D-APV. We suggest that the activation of NMDA receptors is involved in the veratridine-induced long-lasting enhancement in the excitatory synaptic transmission in rat CA3 hippocampal neurons.


Assuntos
Hipocampo/efeitos dos fármacos , Potenciação de Longa Duração/efeitos dos fármacos , Neurotoxinas/farmacologia , Células Piramidais/efeitos dos fármacos , Transmissão Sináptica/efeitos dos fármacos , Veratridina/farmacologia , 2-Amino-5-fosfonovalerato/farmacologia , 6-Ciano-7-nitroquinoxalina-2,3-diona/farmacologia , Animais , Relógios Biológicos/efeitos dos fármacos , Relógios Biológicos/fisiologia , Membrana Celular/efeitos dos fármacos , Membrana Celular/metabolismo , Estimulação Elétrica , Potenciais Evocados/efeitos dos fármacos , Potenciais Evocados/fisiologia , Antagonistas de Aminoácidos Excitatórios/farmacologia , Hipocampo/citologia , Hipocampo/metabolismo , Potenciação de Longa Duração/fisiologia , Potenciais da Membrana/efeitos dos fármacos , Potenciais da Membrana/fisiologia , Fibras Musgosas Hipocampais/efeitos dos fármacos , Fibras Musgosas Hipocampais/metabolismo , Técnicas de Cultura de Órgãos , Células Piramidais/citologia , Células Piramidais/metabolismo , Ratos , Ratos Wistar , Receptores de AMPA/efeitos dos fármacos , Receptores de AMPA/metabolismo , Receptores de N-Metil-D-Aspartato/antagonistas & inibidores , Receptores de N-Metil-D-Aspartato/metabolismo , Canais de Sódio/efeitos dos fármacos , Canais de Sódio/metabolismo , Transmissão Sináptica/fisiologia
2.
J Virol Methods ; 3(5): 293-301, 1981 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-6277975

RESUMO

The envelope glycoproteins of influenza virus (HA and NA) and paramyxovirus (HN and F) were visualized on the surface of infected cells by immunoelectron microscopy using the indirect immunoperoxidase technique. In X7 influenza virus-infected fibroblasts, the hemagglutinin (HA) and the neuraminidase (NA) were observed on the cell membrane respectively 2 and 3--4 h after infection. The antigens were initially seen as discrete patches and later evenly distributed along the plasma membrane prior to budding. Antibody induction of HA and NA was observed as cytoplasmic inclusions, with peroxidase-positive activity, attributed to endocytosis. The redistribution of HA and NA supports the hypothesis of lateral mobility of the viral glycoproteins in cellular membranes as visualized by the immunoperoxidase method. The glycoproteins of Sendai virus, in infected Madin--Darby bovine kidney cells, were found to be evenly distributed along the plasma membrane and endoplasmic reticulum, the latter by the indirect microperoxidase method. The immunoperoxidase methods may be useful for investigating the polarized distribution of envelope glycoproteins.


Assuntos
Glicoproteínas/análise , Vírus da Influenza A/ultraestrutura , Vírus da Parainfluenza 1 Humana/ultraestrutura , Proteínas Virais/análise , Animais , Bovinos , Linhagem Celular , Membrana Celular/ultraestrutura , Embrião de Galinha , Glicoproteínas de Hemaglutininação de Vírus da Influenza , Hemaglutininas Virais/análise , Técnicas Imunoenzimáticas , Rim , Microscopia Eletrônica , Neuraminidase/análise , Proteínas do Envelope Viral
3.
Br J Radiol ; 72(863): 1046-51, 1999 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-10700819

RESUMO

The purpose of the study was to assess the signal intensities of arachnoid granulations within the dural sinuses using the FLAIR sequence for differentiation of space-occupying lesions in and adjacent to the dural sinuses. We retrospectively reviewed MR images of the brain of 1118 consecutive subjects, ranging in age from 0 to 93 years (mean 57.2 years). Nodules within the dural sinuses with signal intensities similar to that of cerebrospinal fluid (CSF) on both T1 and T2 weighted images were defined as arachnoid granulations. The location, signal intensity on T1 weighted spin echo (SE), T2 weighted fast SE and FLAIR images, the impression on the inner table of the skull, and the size of the lesion were assessed. 112 subjects (10.0%), age range 4-89 years old (mean 58.9 years), were found to have 134 arachnoid granulations. The commonest location was the transverse sinus, with 115 granulations (85.8%). The prevalence of the granulations showed a peak in the sixth decade of age. All granulations were isointense relative to CSF on T2 weighted images and almost all lesions were isointense relative to CSF on T1 weighted images. On FLAIR images, 90.3% of the granulations were isointense relative to CSF and the other 9.7% granulations were slightly hyperintense compared with the CSF. 21 (15.7%) subjects showed impressions on the inner table; one case involved the outer table. In conclusion, arachnoid granulations were isointense or slightly hyperintense relative to CSF on FLAIR. FLAIR images are helpful in differentiating arachnoid granulations from other dural sinus lesions or skull lesions which have an intensity similar to that of CSF on T1 weighted and T2 weighted images.


Assuntos
Veias Cerebrais/anatomia & histologia , Tecido de Granulação/anatomia & histologia , Angiografia por Ressonância Magnética/métodos , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Aracnoide-Máter/anatomia & histologia , Criança , Pré-Escolar , Dura-Máter/anatomia & histologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fluxo Pulsátil , Estudos Retrospectivos , Espaço Subaracnóideo/anatomia & histologia
4.
Jpn J Vet Res ; 49(2): 115-23, 2001 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-11590919

RESUMO

Our previous study established protein gene product 9.5 (PGP 9.5), a ubiquitin C-terminal hydrolase, as a specific cytochemical marker of synovial lining cells (type B synoviocytes) in the horse joint. The present study aimed to detect PGP 9.5 in the synovial fluid and shows that PGP 9.5 is a valuable marker of osteoarthritis in the horse. Immunohistochemical staining confirmed rich and consistent localization of PGP 9.5 immunoreactivity in the cytoplasm of synovial lining cells in the normal horse joint. Western blot analysis of synovial fluid from normal joints could detect a significant band corresponding to that contained in the brain and synovial membrane extracts. When 60 synovial fluid samples from normal and abnormal joints were assayed with an enzyme-linked immunosorbent assay (ELISA) system, the concentration of PGP 9.5 tended to be elevated in osteochondrosis dissecance, inflammatory arthropathy and intra-articular fracture, among which a statistically significant elevation was recognizable between the intra-articular fracture and the control. Thus, this study demonstrated the possibility that PGP 9.5, derived from synovial lining cells, may be a new biochemical marker for arthritic disorders of the horse.


Assuntos
Doenças dos Cavalos/metabolismo , Osteoartrite/veterinária , Líquido Sinovial/metabolismo , Tioléster Hidrolases/metabolismo , Animais , Western Blotting/veterinária , Ensaio de Imunoadsorção Enzimática/veterinária , Feminino , Cavalos , Imuno-Histoquímica/veterinária , Osteoartrite/diagnóstico , Ubiquitina Tiolesterase
6.
Kaibogaku Zasshi ; 41(2): 123-4, 1966 Apr 01.
Artigo em Japonês | MEDLINE | ID: mdl-5333539
7.
Nihon Rinsho ; 25(10): 2361-2, 1967 Oct.
Artigo em Japonês | MEDLINE | ID: mdl-5627574
10.
Nihon Kyobu Geka Gakkai Zasshi ; 39(12): 2140-4, 1991 Dec.
Artigo em Japonês | MEDLINE | ID: mdl-1774500

RESUMO

The efficacy and method of administration of recombinant human erythropoietin (EPO) in adult cardiac surgical patients when given preoperatively was evaluated. We used EPO intravenously (iv) with 40 mg ferric oxide for a total of consecutive 47 patients. The patients were divided into group A (n = 14; EPO 200 IU/kg iv 3 times a week from 3 weeks prior to surgery to 2 weeks after surgery, donation of 800 ml) and group B (n = 33; EPO 200 IU/kg iv everyday from 8 days prior to surgery to 2 weeks after surgery, donation of 400 ml). Control groups were group AO (n = 11; donation of 835 +/- 33 ml from 14.8 days prior to surgery) and group BO (n = 7; donation of 406 +/- 34 ml at 7.3 days prior to surgery). All the EPO-treated patients received no homologous blood transfusion while 2 of patients in group BO received some homologous blood transfusion. A hemoglobin change between pre-donation and surgery was +0.14 +/- 1.3 (g/dl) in group A, +0.04 +/- 1.0 (g/dl) in group B, -1.7 +/- 1.3 (g/dl) in group AO and -1.0 +/- 0.6 (g/dl) in group BO. In a comparison of post-surgical hemoglobin levels between group A and group B, we demonstrated that the level in group B, +2.1 +/- 1.8 (g/dl) was significantly higher than that in group A, +11.1 +/- 1.6 (g/dl) 2 weeks after surgery. There was no evidence to show an aggravation of anemia in the pre-surgical period in EPO-treated groups.(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Anemia/terapia , Transfusão de Sangue Autóloga , Procedimentos Cirúrgicos Cardíacos , Eritropoetina/uso terapêutico , Complicações Pós-Operatórias/terapia , Humanos , Proteínas Recombinantes/uso terapêutico
11.
Endocrinol Jpn ; 22(2): 175-80, 1975 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-168060

RESUMO

We have presented here a case of atypical insulinoma. Despite the recurrent episodes of hypoglycemic symptoms, the plasma level of insulin has never been excessive at fasting or by regular provocative tests. Detailed examination had demonstrated qualitative abnormality of insulin secretion. Hyposuppressibility of insulin secretion by hypoglycemia, borderline diabetic curve of glucose tolerance test, blunted response ot insulin to glucagon and leucine were the principle characteristics of these abnormalities. After removal of adenoma, insulin response to glucose, glucagon and leucine was improved. Only secretion provoked a high level of insulin and this abnormal elevation was no longer seen after the removal of adenoma. A removed elevation was no longer seen after the removal of adenoma. A removed insulinoma contained 25 U of immunoreactive insulin per gram tissue, but was negative for aldehyde-fuchsin staining. On electromicroscopy only atypical beta-cell granules were seen.


Assuntos
Adenoma de Células das Ilhotas Pancreáticas/fisiopatologia , Insulina/metabolismo , Neoplasias Pancreáticas/fisiopatologia , Adenoma/patologia , Adenoma/cirurgia , Adenoma de Células das Ilhotas Pancreáticas/cirurgia , Glicemia/metabolismo , Feminino , Glucagon , Teste de Tolerância a Glucose , Humanos , Hipoglicemia/metabolismo , Insulina/sangue , Secreção de Insulina , Leucina , Microscopia Eletrônica , Pessoa de Meia-Idade , Neoplasias Pancreáticas/patologia , Neoplasias Pancreáticas/cirurgia
12.
Phys Rev Lett ; 90(4): 041801, 2003 Jan 31.
Artigo em Inglês | MEDLINE | ID: mdl-12570410

RESUMO

The K2K experiment observes indications of neutrino oscillation: a reduction of nu(mu) flux together with a distortion of the energy spectrum. Fifty-six beam neutrino events are observed in Super-Kamiokande (SK), 250 km from the neutrino production point, with an expectation of 80.1(+6.2)(-5.4). Twenty-nine one ring mu-like events are used to reconstruct the neutrino energy spectrum, which is better matched to the expected spectrum with neutrino oscillation than without. The probability that the observed flux at SK is explained by statistical fluctuation without neutrino oscillation is less than 1%.

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