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1.
Cell ; 170(4): 800-814.e18, 2017 Aug 10.
Artigo em Inglês | MEDLINE | ID: mdl-28802047

RESUMO

Improved methods for manipulating and analyzing gene function have provided a better understanding of how genes work during organ development and disease. Inducible functional genetic mosaics can be extraordinarily useful in the study of biological systems; however, this experimental approach is still rarely used in vertebrates. This is mainly due to technical difficulties in the assembly of large DNA constructs carrying multiple genes and regulatory elements and their targeting to the genome. In addition, mosaic phenotypic analysis, unlike classical single gene-function analysis, requires clear labeling and detection of multiple cell clones in the same tissue. Here, we describe several methods for the rapid generation of transgenic or gene-targeted mice and embryonic stem (ES) cell lines containing all the necessary elements for inducible, fluorescent, and functional genetic mosaic (ifgMosaic) analysis. This technology enables the interrogation of multiple and combinatorial gene function with high temporal and cellular resolution.


Assuntos
Marcação de Genes/métodos , Animais , Linhagem Celular , Células-Tronco Embrionárias , Camundongos , Camundongos Transgênicos
2.
Addict Biol ; 22(4): 1002-1009, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27001197

RESUMO

A mouse model has been developed to study the effect of dietary fat combined with food deprivation periods on palatable food seeking and on the expression of three potential addiction biomarkers in the nucleus accumbens: fumarate hydratase (FH), ATP synthase subunit alpha (ATP5a1) and transketolase (TKT). Forty C57BL/6 J male mice, four-week old, were fed either with a high-fat (HF) diet or standard diet along the experiment. After 3 weeks of differential feeding, animals underwent a two-week training period of two daily sessions where visual cues were paired either to palatable food (chocolate cereals) or no food at all. This training was prolonged one more week with similar, one daily sessions preceded by 12 hours of food deprivation. A behavioural test was finally conducted where mice were confined for 30 minutes either in food unpaired compartments or in compartments previously paired with cereals, but now with empty food trays. Total activity during this behavioural test and serum corticosterone levels right after it were similar in all experimental groups. Mice tested in food-paired compartments showed a marked preference for the empty food tray that gradually disappeared in standard diet-fed individuals but persisted in HF-fed mice. HF-fed mice also overexpressed FH, ATP5a1 and TKT, which positively correlated with the persistence of preference for the empty food tray. It is suggested that HF diets combined with food deprivation may enhance food seeking behaviours while upregulating FH/ATP5a1/TKT, which are further envisaged as biomarkers of addiction.


Assuntos
Comportamento Aditivo/sangue , Comportamento Aditivo/fisiopatologia , Comportamento Animal , Dieta Hiperlipídica/efeitos adversos , Comportamento Alimentar/fisiologia , Privação de Alimentos/fisiologia , Animais , Biomarcadores/sangue , Corticosterona/sangue , Modelos Animais de Doenças , Masculino , Camundongos , Camundongos Endogâmicos C57BL
3.
Int J Dev Neurosci ; 67: 1-5, 2018 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-29545097

RESUMO

Autism spectrum disorder diagnosis is currently based on clinical observations and behavioral evaluations exclusively, without any biological determination. Molecular biomarkers are usually obtained from biological fluids, such as blood or urine, generally through invasive and uncomfortable procedures. Patients with autism are characterized by sensory reactivity and behavioral difficulties which make sample collection problematic. Saliva has emerged as a feasible alternative to obtain relevant biological information and is especially indicated in the case of children with autism due to its painless and noninvasive sampling characteristics. Furthermore, saliva represents a valuable resource to study candidate biomarkers of autism. This has resulted in a number of interesting studies reported during the last 5 years that we have gathered and briefly discussed.


Assuntos
Transtorno Autístico/diagnóstico , Patologia Molecular/métodos , Patologia Molecular/tendências , Saliva/metabolismo , Transtorno Autístico/genética , Biomarcadores/metabolismo , Humanos
4.
J Nutr Biochem ; 37: 13-19, 2016 11.
Artigo em Inglês | MEDLINE | ID: mdl-27592201

RESUMO

Aldosterone plays a central role in the development of cardiac pathological states involving ion transport imbalances, especially sodium transport. We have previously demonstrated a cardioprotective effect of proanthocyanidins in aldosterone-treated rats. Our objective was to investigate for the first time the effect of proanthocyanidins on serum and glucocorticoid-regulated kinase 1 (SGK1), epithelial Na+ channel (γ-ENaC), neuronal precursor cells expressed developmentally down-regulated 4-2 (Nedd4-2) and phosphoNedd4-2 protein expression in the hearts of aldosterone-treated rats. Male Wistar rats received aldosterone (1mg kg-1day-1)+1% NaCl for 3weeks. Half of the animals in each group were simultaneously treated with the proanthocyanidins-rich extract (80% w/w) (PRO80, 5mg kg-1day-1). Hypertension and diastolic dysfunction induced by aldosterone were abolished by treatment with PRO80. Expression of fibrotic, inflammatory and oxidative mediators were increased by aldosterone-salt administration and blunted by PRO80. Antioxidant capacity was improved by PRO80. The up-regulated aldosterone mediator SGK1, ENaC and p-Nedd4-2/total Nedd4-2 ratio were blocked by PRO80. PRO80 blunted aldosterone-mineralocorticoid-mediated up-regulation of ENaC provides new mechanistic insight of the beneficial effect of proanthocyanidins preventing the cardiac alterations induced by aldosterone excess.


Assuntos
Suplementos Nutricionais , Complexos Endossomais de Distribuição Requeridos para Transporte/antagonistas & inibidores , Canais Epiteliais de Sódio/metabolismo , Ventrículos do Coração/metabolismo , Proteínas Imediatamente Precoces/antagonistas & inibidores , Proantocianidinas/uso terapêutico , Proteínas Serina-Treonina Quinases/antagonistas & inibidores , Ubiquitina-Proteína Ligases/antagonistas & inibidores , Disfunção Ventricular Esquerda/prevenção & controle , Animais , Anti-Inflamatórios não Esteroides/uso terapêutico , Anti-Hipertensivos/uso terapêutico , Antioxidantes/uso terapêutico , Biomarcadores/metabolismo , Cardiomegalia/etiologia , Cardiomegalia/prevenção & controle , Cardiotônicos/uso terapêutico , Complexos Endossomais de Distribuição Requeridos para Transporte/agonistas , Complexos Endossomais de Distribuição Requeridos para Transporte/metabolismo , Agonistas do Canal de Sódio Epitelial/antagonistas & inibidores , Agonistas do Canal de Sódio Epitelial/metabolismo , Bloqueadores do Canal de Sódio Epitelial/uso terapêutico , Canais Epiteliais de Sódio/química , Fibrose , Ventrículos do Coração/imunologia , Ventrículos do Coração/patologia , Ventrículos do Coração/fisiopatologia , Hipertensão/etiologia , Hipertensão/prevenção & controle , Proteínas Imediatamente Precoces/agonistas , Proteínas Imediatamente Precoces/metabolismo , Masculino , Antagonistas de Receptores de Mineralocorticoides/uso terapêutico , Ubiquitina-Proteína Ligases Nedd4 , Estresse Oxidativo , Proteínas Serina-Treonina Quinases/metabolismo , Ratos Wistar , Ubiquitina-Proteína Ligases/metabolismo , Disfunção Ventricular Esquerda/metabolismo , Disfunção Ventricular Esquerda/patologia , Disfunção Ventricular Esquerda/fisiopatologia
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