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1.
Orthod Craniofac Res ; 16(1): 20-7, 2013 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-23311656

RESUMO

OBJECTIVES: The dental follicle plays an important role in tooth eruption by providing key regulators of osteogenesis and bone resorption. Patients with cleidocranial dysplasia (CCD) exhibit delayed tooth eruption in combination with increased bone density in the maxilla and mandible, suggesting disturbances in bone remodeling. The aim of this study was to determine the expression of genes relevant for tooth eruption and bone remodeling in the dental follicles of patients with CCD and normal subjects. MATERIAL AND METHODS: Thirteen dental follicles were isolated from five unrelated patients with CCD, and fourteen dental follicles were obtained from 10 healthy individuals. All teeth were in the intraosseous phase of eruption. The expression of RANK, RANKL, OPG, and CSF-1 was determined by quantitative RT-PCR. RESULTS: In patients with CCD, the mRNA levels of RANK, OPG, and CSF-1 were significantly elevated compared with the control group. Accordingly, the ratios of RANKL/OPG and RANKL/RANK mRNAs were significantly decreased in patients with CCD. CONCLUSION: The observed alterations in the expression and ratios of the aforementioned factors in the dental follicle of CCD individuals suggest a disturbed paracrine signaling for bone remodeling that could be responsible for the impaired tooth eruption seen in these patients.


Assuntos
Displasia Cleidocraniana/genética , Displasia Cleidocraniana/fisiopatologia , Erupção Dentária/genética , Adolescente , Adulto , Remodelação Óssea/genética , Estudos de Casos e Controles , Saco Dentário/metabolismo , Feminino , Expressão Gênica , Humanos , Fator Estimulador de Colônias de Macrófagos/genética , Masculino , Osteoprotegerina/genética , Ligante RANK/genética , Receptor Ativador de Fator Nuclear kappa-B/genética , Estatísticas não Paramétricas , Adulto Jovem
2.
Int Endod J ; 46(2): 160-8, 2013 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22889382

RESUMO

AIM: To investigate the expression of two endoplasmic reticulum (ER)-resident key chaperone proteins, ERdj5 and BiP, under the influence of resinous monomers and its relationship with the inhibition of mineralization caused by the monomer 2-hydroxyethyl methacrylate (HEMA). METHODOLOGY: The ERdj5 and BiP expression was studied in vitro, in primary human pulp cell cultures after treatment with three different HEMA concentrations at different time periods. Subsequently, the expression of both the odontoblast markers dentine sialoprotein (DSP) and osteonectin (OSN) was studied in human pulp cells under the same conditions. RESULTS: The ERdj5 and BiP expression was upregulated in the pulp cells. DSP and OSN were largely dispersed in the cytoplasm in control cell cultures but accumulated in a perinuclear area after exposure to HEMA. Their expression levels were not affected. CONCLUSIONS: The increased expression of ERdj5 and BiP may reflect activation of ER stress. DSP and OSN accumulation into the cells may lead to their secretion arrest and inhibition of dentine matrix formation. These events may elucidate the mechanism by which HEMA inhibits the mineralization process.


Assuntos
Polpa Dentária/efeitos dos fármacos , Estresse do Retículo Endoplasmático , Metacrilatos/efeitos adversos , Chaperonas Moleculares/metabolismo , Odontoblastos/efeitos dos fármacos , Estresse Fisiológico , Calcificação de Dente/efeitos dos fármacos , Adolescente , Células Cultivadas , Polpa Dentária/citologia , Análise do Estresse Dentário , Chaperona BiP do Retículo Endoplasmático , Matriz Extracelular/efeitos dos fármacos , Proteínas da Matriz Extracelular/antagonistas & inibidores , Proteínas da Matriz Extracelular/metabolismo , Proteínas de Choque Térmico HSP40/metabolismo , Proteínas de Choque Térmico/metabolismo , Humanos , Odontoblastos/metabolismo , Osteonectina/antagonistas & inibidores , Osteonectina/metabolismo , Fosfoproteínas/antagonistas & inibidores , Fosfoproteínas/metabolismo , Sialoglicoproteínas/antagonistas & inibidores , Sialoglicoproteínas/metabolismo
3.
Neuroscience ; 167(3): 741-9, 2010 May 19.
Artigo em Inglês | MEDLINE | ID: mdl-20219646

RESUMO

The estrogen-mimicking endocrine disrupter bisphenol A (BPA) which is used in the manufacture of plastic and epoxy resins, is one of the world's most heavily produced synthetic chemicals. BPA is detected in animal tissues, and its bio-accumulation has shown to be higher in the fetus than the mother. Exposure to doses below the daily safe limit has been reported to affect the sexual differentiation of the brain and modify the behavior of the exposed rodent offspring. The aim of the present study was to investigate in the rat the possible organizational effects of low BPA exposure on glucocorticoid-regulated responses. Female breeders were exposed to 40 microg/kg b.w. BPA daily throughout pregnancy and lactation. Plasma corticosterone levels and the two types of hippocampal corticosteroid receptors (GR and MR) were determined in mid-adolescent offspring under basal conditions and following a Y-maze task. BPA treated females had higher corticosterone levels than control females and BPA males and lower GR levels than BPA males, under basal conditions. Following the mildly stressful experience of Y-maze, corticosterone levels were increased in BPA-treated animals of both sexes, compared to the controls. GR levels were also increased in BPA-treated females compared to males. No effect of BPA was observed on MR levels, whereas the Y-maze experience significantly decreased receptors' levels in both female groups. The animals' performance in the task was also evaluated. BPA exposure significantly impaired the spatial recognition memory in both sexes, and modified the behavioural coping in a sex-dependent manner. Female BPA-treated offspring exhibited increased "anxiety-like" behaviour and dramatic loss of exploration attitude during the task, in comparison to males. This study provides for the first time evidence that corticosterone and its actions in the brain are sensitive to the programming effects of BPA at a dose below the currently acceptable daily intake.


Assuntos
Encéfalo/efeitos dos fármacos , Corticosterona/agonistas , Disruptores Endócrinos/toxicidade , Exposição Ambiental/efeitos adversos , Fenóis/toxicidade , Efeitos Tardios da Exposição Pré-Natal/induzido quimicamente , Adaptação Psicológica/efeitos dos fármacos , Adaptação Psicológica/fisiologia , Animais , Ansiedade/induzido quimicamente , Ansiedade/metabolismo , Ansiedade/fisiopatologia , Compostos Benzidrílicos , Encéfalo/metabolismo , Encéfalo/fisiopatologia , Corticosterona/metabolismo , Relação Dose-Resposta a Droga , Estrogênios não Esteroides/toxicidade , Comportamento Exploratório/efeitos dos fármacos , Comportamento Exploratório/fisiologia , Feminino , Hipocampo/efeitos dos fármacos , Hipocampo/metabolismo , Hipocampo/fisiopatologia , Sistema Hipotálamo-Hipofisário/efeitos dos fármacos , Sistema Hipotálamo-Hipofisário/fisiopatologia , Masculino , Aprendizagem em Labirinto/efeitos dos fármacos , Aprendizagem em Labirinto/fisiologia , Transtornos da Memória/induzido quimicamente , Transtornos da Memória/metabolismo , Transtornos da Memória/fisiopatologia , Sistemas Neurossecretores/efeitos dos fármacos , Sistemas Neurossecretores/metabolismo , Sistemas Neurossecretores/fisiopatologia , Sistema Hipófise-Suprarrenal/efeitos dos fármacos , Sistema Hipófise-Suprarrenal/fisiopatologia , Gravidez , Efeitos Tardios da Exposição Pré-Natal/metabolismo , Efeitos Tardios da Exposição Pré-Natal/fisiopatologia , Ratos , Ratos Wistar , Receptores de Esteroides/efeitos dos fármacos , Receptores de Esteroides/metabolismo , Caracteres Sexuais
4.
Int J Dev Neurosci ; 11(1): 1-9, 1993 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-7683839

RESUMO

The protein products of growth factor genes such as IGF-II and cellular oncogenes such as c-fos are believed to be necessary for the support of normal neuronal function. Steady-state levels of c-fos and IGF-II mRNA were determined in the brain of young and old rats, using Northern analysis. Both RNAs were found to be decreased in the brain of aged rats. Age-related decrease was detected in the hippocampus, hypothalamus, striatum, cerebral cortex and cerebellum, for IGF-II mRNA, and in the cerebral cortex and cerebellum for c-fos mRNA. Furthermore, changes in the degree and pattern of DNA methylation were noted at both gene loci, in the aged rat brain. Our results could reflect changes at the genomic level possibly related to the process of aging and the accompanying decline in brain function.


Assuntos
Envelhecimento/fisiologia , Encéfalo/crescimento & desenvolvimento , Regulação da Expressão Gênica/fisiologia , Genes fos , Fator de Crescimento Insulin-Like II/biossíntese , Animais , Northern Blotting , Southern Blotting , DNA/metabolismo , Sondas de DNA , Masculino , Metilação , Hibridização de Ácido Nucleico , RNA/biossíntese , Ratos , Ratos Wistar
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