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1.
Medisan ; 22(9)nov.-dic. 2018. tab, ilus
Artigo em Espanhol | LILACS | ID: biblio-976174

RESUMO

Se realizó un estudio descriptivo, observacional y transversal en 160 cortes histológicos de la fascia dentada del hipocampo de ratones BALB/c y ratas Wistar blancas, en el Laboratorio de Investigaciones Biomédicas de la Universidad de Ciencias Médicas de Santiago de Cuba, de septiembre de 2013 a igual mes de 2014, con vistas a determinar las transformaciones histológicas que ocurren en dicha fascia en el segundo y sexto días posnatales. La observación microscópica de estos cortes se realizó empleando del software Image J. La extensión de la fascia al sexto día de vida llegó a ser mayor en los ratones; los máximos incrementos del grosor en ambos tipos de roedores se encontraron en el hilus, y el estrato granuloso fue de menor crecimiento en las ratas. La celularidad en los roedores presentó mayores proporciones en las tres regiones del hilus al segundo día, pero disminuyó en el sexto día, mientras que las zonas relacionadas con el hilus mantuvieron una mayor cantidad de células; sin embargo, el número celular disminuyó en ambas regiones moleculares de la fascia de las ratas.


A descriptive, observational and cross-sectional study was carried out in 160 histological cuts of the hippocampus fascia dentata from mice BALB/c and rats white Wistar, in the Laboratory of Biomedical Investigations from Santiago de Cuba Medical University, from September, 2013 to the same month in 2014, with the aim of determining the histological transformations that take place in this fascia in the second and sixth posnatal days. The microscopic observation of these cuts was carried out using the software Image J. The extension of the fascia at the sixth day of life was larger in the mice; the maximum increases of thickness in both types of rodents were in the hilus, and the granular stratum was of smaller growth in rats. The celularity in the rodents presented larger proportions in the three regions from the hilus at the second day, but it decreased at the sixth day, while the areas related to the hilus maintained a greater quantity of cells; however, the cellular number diminished in both molecular regions of the rats fascia.


Assuntos
Animais , Masculino , Feminino , Recém-Nascido , Camundongos , Ratos , Ratos Wistar/anatomia & histologia , Giro Denteado/crescimento & desenvolvimento , Camundongos/anatomia & histologia , Ratos Wistar/crescimento & desenvolvimento , Giro Denteado/anatomia & histologia , Camundongos/crescimento & desenvolvimento
2.
Journal of Veterinary Science ; : 27-33, 2014.
Artigo em Inglês | WPRIM | ID: wpr-69673

RESUMO

In this study, we determined how rosiglitazone (RSG) differentially affected hippocampal neurogenesis in mice fed a low-fat diet (LFD) or high-fat diet (HFD; 60% fat). LFD and HFD were given to the mice for 8 weeks. Four weeks after initiating the LFD and HFD feeding, vehicle or RSG was administered orally once a day to both groups of mice. We measured cell proliferation and neuroblast differentiation in the subgranular zone of the dentate gyrus using Ki67 and doublecortin (DCX), respectively, as markers. In addition, we monitored the effects of RSG on the levels of DCX and brain-derived neurotrophic factor (BDNF) in hippocampal homogenates. At 8 weeks after the LFD feeding, the numbers of Ki67- and DCX-positive cells as well as hippocampal levels of DCX and BDNF were significantly decreased in the RSG-treated group compared to the vehicle-treated animals. In contrast, the numbers of Ki67- and DCX-positive cells along with hippocampal levels of DCX and BDNF in the HFD fed mice were significantly increased in the RSG-treated mice compared to the vehicle-treated group. Our data demonstrate that RSG can modulate the levels of BDNF, which could play a pivotal role in cell proliferation and neuroblast differentiation in the hippocampal dentate gyrus.


Assuntos
Animais , Masculino , Western Blotting , Fator Neurotrófico Derivado do Encéfalo/metabolismo , Diferenciação Celular/efeitos dos fármacos , Proliferação de Células/efeitos dos fármacos , Giro Denteado/crescimento & desenvolvimento , Dieta com Restrição de Gorduras , Dieta Hiperlipídica , Hipocampo/crescimento & desenvolvimento , Hipoglicemiantes/farmacologia , Imuno-Histoquímica , Antígeno Ki-67/metabolismo , Camundongos Endogâmicos C57BL , Proteínas Associadas aos Microtúbulos/metabolismo , Neurogênese/efeitos dos fármacos , Neuropeptídeos/metabolismo , Tiazolidinedionas/farmacologia
3.
Arq. neuropsiquiatr ; 66(3b): 731-735, set. 2008. ilus
Artigo em Inglês | LILACS | ID: lil-495543

RESUMO

OBJECTIVE: As axon outgrowth and dentate granule cell neurogenesis are hallmarks of hippocampal development and are also the two morphologic changes in the structure of the dentate gyrus after status epilepticus (SE), we hypothesized that molecules involved in normal development may also play a role during epileptogenesis. METHOD: Using in situ hybridization, we have characterized mRNA expression of myocyte-specific enhancer binding factor 2C (MEF2C) in the dentate gyrus during development (P0, P3, P7, P14 and P28) and at multiple time points following pilocarpine-induced SE (3, 7, 14, 28 days after SE). RESULTS: It was demonstrated that MEF2C is up-regulated during development (P0, P3, P7, P14 and P28) and in the adult rat dentate gyrus following SE (3, 7, 14, 28 days after SE). CONCLUSIONS: The molecules controlling cell-fate decisions in the developing dentate gyrus are also operative during epileptogenesis.


OBJETIVO: Como o crescimento axonal e a neurogênese do giro denteado são características intrínsecas do hipocampo durante o processo de desenvolvimento, e também são duas alterações morfológicas na estrutura do giro denteado após o status epilepticus (SE), nós hipotetizamos que as moléculas envolvidas no processo normal do desenvolvimento hipocampal também podem participar do processo de epileptogênese. MÉTODO: Utilizando hibridização in situ, caracterizamos a expressão do RNAm do fator de transcrição myocyte-specific enhancer binding factor 2C (MEF2C) no giro denteado durante o desenvolvimento (P0, P3, P7, P14 e P28) e em diferentes períodos após o SE (3, 7, 14, 28 dias após SE). RESULTADOS: Foi demonstrado um aumento da expressão de MEF2C no giro denteado durante o desenvolvimento e no giro denteado de animais adultos após o SE. CONCLUSÃO: As moléculas que controlam o destino celular durante o processo de desenvolvimento também estão operativas durante o processo de epileptogênese.


Assuntos
Animais , Masculino , Ratos , Giro Denteado/crescimento & desenvolvimento , Fatores de Regulação Miogênica/metabolismo , Estado Epiléptico/metabolismo , Giro Denteado/química , Hibridização In Situ , Pilocarpina/farmacologia , Ratos Sprague-Dawley , RNA Mensageiro/metabolismo , Estado Epiléptico/induzido quimicamente
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