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1.
Braz J Biol ; 84: e248411, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35544785

RESUMO

The dopamine content in cerebral structures has been related to neuronal excitability and several approaches have been used to study this phenomenon during seizure vulnerability period. In the present work, we describe the effects of dopamine depletion after the administration of 6-hidroxidopamine (6-OHDA) into the substantia nigra pars compacta of male rats submitted to the pilocarpine model of epilepsy. Susceptibility to pilocarpine-induced status epilepticus (SE), as well as spontaneous and recurrent seizures (SRSs) frequency during the chronic period of the model were determined. Since the hippocampus is one of main structures in the development of this experimental model of epilepsy, the dopamine levels in this region were also determined after drug administration. In the first experiment, 62% (15/24) of 6-OHDA pre-treated rats and 45% (11/24) of those receiving ascorbic acid as control solution progressed to motor limbic seizures evolving to SE, after the administration of pilocarpine. Severeness of seizures during the model´s the acute period, was significantly higher in epileptic experimental rats (56.52%), than in controls (4.16%). In the second experiment, the frequency of seizures in the model's chronic phase did not significantly change between groups. Our data show that dopamine may play an important role on seizure severity in the pilo's model acute period, which seems to be due to dopamine inhibitory action on motor expression of seizure.


Assuntos
Epilepsia , Estado Epiléptico , Animais , Dopamina/efeitos adversos , Epilepsia/induzido quimicamente , Masculino , Agonistas Muscarínicos/efeitos adversos , Oxidopamina/efeitos adversos , Pilocarpina/toxicidade , Ratos , Ratos Wistar , Convulsões/induzido quimicamente , Convulsões/metabolismo , Estado Epiléptico/induzido quimicamente
2.
J Control Release ; 320: 180-200, 2020 04 10.
Artigo em Inglês | MEDLINE | ID: mdl-31978444

RESUMO

Standard cancer therapies sometimes fail to deliver chemotherapeutic drugs to tumor cells in a safe and effective manner. Nanotechnology takes the lead in providing new therapeutic options for cancer due to major potential for selective targeting and controlled drug release. Antibodies and antibody fragments are attracting much attention as a source of targeting ligands to bind specific receptors that are overexpressed on cancer cells. Therefore, researchers are devoting time and effort to develop targeting strategies based on nanoparticles functionalized with antibodies, which hold great promise to enhance therapeutic efficacy and circumvent severe side effects. Several methods have been described to immobilize antibodies on the surface of nanoparticles. However, selecting the most appropriate for each application is challenging but also imperative to preserve antigen binding ability and yield stable antibody-conjugated nanoparticles. From this perspective, we aim to provide considerable knowledge on the most widely used methods of functionalization that can be helpful for decision-making and design of conjugation protocols as well. This review summarizes adsorption, covalent conjugation (carbodiimide, maleimide and "click" chemistries) and biotin-avidin interaction, while discussing the advantages, limitations and relevant therapeutic approaches currently under investigation.


Assuntos
Imunoconjugados , Nanopartículas , Neoplasias , Anticorpos , Humanos , Nanotecnologia , Neoplasias/tratamento farmacológico
3.
Genetics ; 156(2): 535-47, 2000 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11014804

RESUMO

Strong evidence indicates that transcription elongation by RNA polymerase II (pol II) is a highly regulated process. Here we present genetic results that indicate a role for the Saccharomyces cerevisiae Rtf1 protein in transcription elongation. A screen for synthetic lethal mutations was carried out with an rtf1 deletion mutation to identify factors that interact with Rtf1 or regulate the same process as Rtf1. The screen uncovered mutations in SRB5, CTK1, FCP1, and POB3. These genes encode an Srb/mediator component, a CTD kinase, a CTD phosphatase, and a protein involved in the regulation of transcription by chromatin structure, respectively. All of these gene products have been directly or indirectly implicated in transcription elongation, indicating that Rtf1 may also regulate this process. In support of this view, we show that RTF1 functionally interacts with genes that encode known elongation factors, including SPT4, SPT5, SPT16, and PPR2. We also show that a deletion of RTF1 causes sensitivity to 6-azauracil and mycophenolic acid, phenotypes correlated with a transcription elongation defect. Collectively, our results suggest that Rtf1 may function as a novel transcription elongation factor in yeast.


Assuntos
Proteínas Fúngicas/metabolismo , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/genética , Proteína de Ligação a TATA-Box , Fatores de Transcrição , Transcrição Gênica , Proteínas Fúngicas/genética , Deleção de Genes , Regulação Fúngica da Expressão Gênica , Genes Letais , Genótipo , Inositol/metabolismo , Mutagênese , Fenótipo , RNA Polimerase II/metabolismo , Saccharomyces cerevisiae/crescimento & desenvolvimento
4.
Clin Phys Physiol Meas ; 13 Suppl A: 201-7, 1992.
Artigo em Inglês | MEDLINE | ID: mdl-1587102

RESUMO

A data interchange format is described to allow groups working on electrical impedance tomography (EIT) with disparate algorithms and instruments to compare results. The procedure has been tested by exchanging data by e-mail. The format is defined in the appendix.


Assuntos
Comunicação , Cooperação Internacional , Tomografia/métodos , Condutividade Elétrica , Humanos
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