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1.
Ophthalmic Genet ; 39(6): 717-724, 2018 12.
Artigo em Inglês | MEDLINE | ID: mdl-30484747

RESUMO

BACKGROUND: The purpose of this study was to screen juvenile open angle glaucoma (JOAG) patients from Brazil for variants within the MYOC and CYP1B1 genes. MATERIAL AND METHODS: In this study, we evaluated the coding regions of MYOC and CYP1B1 genes in 100 non-related patients with JOAG and 200 controls through Sanger sequencing. We also tested the most frequent single nucleotide variants of CYP1B1 for association with JOAG. RESULTS: Sixteen different sequence variants in the MYOC gene were observed in JOAG patients: eight variants were described as neutral and eight were identified in 34 out of 100 patients with JOAG and no controls, thus being considered damaging. In the CYP1B1 gene, nine neutral variants and two damaging alterations were found among JOAG patients. No association between CYP1B1 variants and JOAG was detected. CONCLUSION: While MYOC damaging alterations were highly prevalent (34%), CYP1B1 damaging variants were less frequent (2%) in this cohort of Brazilian JOAG patients.


Assuntos
Citocromo P-450 CYP1B1/genética , Proteínas do Citoesqueleto/genética , Proteínas do Olho/genética , Variação Genética , Glaucoma de Ângulo Aberto/genética , Glicoproteínas/genética , Adulto , Brasil/epidemiologia , Estudos de Coortes , Éxons/genética , Feminino , Glaucoma de Ângulo Aberto/diagnóstico , Glaucoma de Ângulo Aberto/epidemiologia , Gonioscopia , Humanos , Pressão Intraocular , Masculino , Mutação , Reação em Cadeia da Polimerase em Tempo Real , Acuidade Visual
2.
Arch Endocrinol Metab ; 59(3): 210-4, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-26154087

RESUMO

OBJECTIVE: The aim of this study was to evaluate the genetic expression of adipokines in the adipocytes of monosodium glutamate (MSG)-treated obese rats submitted to physical activity. MATERIALS AND METHODS: Obesity was induced by neonatal MSG administration. Exercised rats (MSG and control) were subjected to swim training for 30 min for 10 weeks, whereas their respective controls remained sedentary. Total RNA was obtained from sections of the mesenteric adipose tissue of the rats. mRNA levels of adiponectin (Adipoq), tumor necrosis factor alpha (Tnf), peroxisome proliferator-activated receptor alpha (Ppara), and peroxisome proliferator-activated receptor gamma (Pparg) adipokines were quantified by quantitative Real-Time Polymerase Chain Reaction (qRT-PCR). RESULTS: In the exercise-trained control group, the expression of Adipoq increased compared to the sedentary control, which was not observed in the MSG-obese rats. Increased levels of Tnf in MSG-obese rats were not reversed by the swim training. The expression of Ppara was higher in sedentary MSG-obese rats compared to the sedentary control. Swimming increased this adipokine expression in the exercise-trained control rats compared to the sedentary ones. mRNA levels of Pparg were higher in the sedentary MSG-rats compared to the sedentary control; however, the exercise did not influenced its expression in the groups analyzed. CONCLUSIONS: In conclusion, regular physical activity was not capable to correct the expression of proinflammatory adipokines in MSG-obese rat adipocytes.


Assuntos
Adipocinas/genética , Expressão Gênica/fisiologia , Obesidade/genética , Condicionamento Físico Animal/fisiologia , Natação/fisiologia , Adipocinas/análise , Tecido Adiposo/química , Animais , Modelos Animais de Doenças , Terapia por Exercício , Aromatizantes , Obesidade/induzido quimicamente , Obesidade/metabolismo , RNA Mensageiro/análise , Ratos , Reação em Cadeia da Polimerase em Tempo Real , Reprodutibilidade dos Testes , Comportamento Sedentário , Glutamato de Sódio , Fatores de Tempo , Fator de Necrose Tumoral alfa/análise , Fator de Necrose Tumoral alfa/genética
3.
Arch. endocrinol. metab. (Online) ; 59(3): 210-214, 06/2015. tab, graf
Artigo em Inglês | LILACS | ID: lil-751317

RESUMO

Objective The aim of this study was to evaluate the genetic expression of adipokines in the adipocytes of monosodium glutamate (MSG)-treated obese rats submitted to physical activity.Materials and methods Obesity was induced by neonatal MSG administration. Exercised rats (MSG and control) were subjected to swim training for 30 min for 10 weeks, whereas their respective controls remained sedentary. Total RNA was obtained from sections of the mesenteric adipose tissue of the rats. mRNA levels of adiponectin (Adipoq), tumor necrosis factor alpha (Tnf), peroxisome proliferator-activated receptor alpha (Ppara), and peroxisome proliferator-activated receptor gamma (Pparg) adipokines were quantified by quantitative Real-Time Polymerase Chain Reaction (qRT-PCR).Results In the exercise-trained control group, the expression of Adipoq increased compared to the sedentary control, which was not observed in the MSG-obese rats. Increased levels of Tnf in MSG-obese rats were not reversed by the swim training. The expression of Ppara was higher in sedentary MSG-obese rats compared to the sedentary control. Swimming increased this adipokine expression in the exercise-trained control rats compared to the sedentary ones. mRNA levels of Pparg were higher in the sedentary MSG-rats compared to the sedentary control; however, the exercise did not influenced its expression in the groups analyzed.Conclusions In conclusion, regular physical activity was not capable to correct the expression of proinflammatory adipokines in MSG-obese rat adipocytes.


Assuntos
Animais , Humanos , Adjuvantes Imunológicos , Mimetismo Molecular/imunologia , Fatores de Necrose Tumoral , Vacinas Sintéticas/imunologia , Vacinas/química , Vacinas/imunologia , Adjuvantes Imunológicos/química , /imunologia , /química , /metabolismo , Vacinas Anticâncer/química , Vacinas Anticâncer/imunologia , Vetores Genéticos/genética , Vetores Genéticos/imunologia , Imunoterapia , Ligantes , Lentivirus/genética , Lentivirus/imunologia , Macaca mulatta , Neoplasias/imunologia , Neoplasias/terapia , Multimerização Proteica , Ligante Indutor de Apoptose Relacionado a TNF/química , Receptores Toll-Like/agonistas , Fatores de Necrose Tumoral/química , Vacinas Sintéticas/química , Proteínas da Matriz Viral/imunologia
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