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1.
Placenta ; 130: 42-45, 2022 12.
Artigo em Inglês | MEDLINE | ID: mdl-36375223

RESUMO

Induction of diabetes mellitus by streptozotocin (STZ) in rats at birth is of high mortality and low success rate when male puppies are separated from females, prioritizing females breastfeeding. Cross-parental care of the entire litter and SZT-induced diabetes up to 12 h post-birth become with high success rate, low animal death, and females with glycaemia >140 mg/dL on the 90 postnatal day. Cross-parental care is more effective in STZ-induction of diabetes, which is maintained during pregnancy (diabetes in pregnancy), than the conventional protocol of male separation at birth.


Assuntos
Glicemia , Diabetes Mellitus Experimental , Gravidez , Feminino , Ratos , Animais , Cães , Masculino , Estreptozocina/efeitos adversos , Diabetes Mellitus Experimental/terapia
2.
Mol Biol Rep ; 47(4): 2475-2486, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-32124173

RESUMO

Classical methods used for culture of adipose-derived mesenchymal stromal cells (ADSCs) use xenobiotic components, which may present a potential risk for biological contamination and/or elicit immunological reactions. Therefore, the aim of this study was to establish a xeno-free methodology for the isolation and proliferation of human ADSCs (hADSCs). hADSCs were isolated by enzymatic digestion or mechanical dissociation and cultured in the presence of fetal bovine serum or human platelet lysate. Proliferation curves were performed as a function of time from the cell culture and used to calculate the population doubling time. Immunophenotyping and differentiation tests were used to identify and characterize the hADSCs. Human ADSCs isolated and cultured in conventional or xenobiotic-free conditions peaked at different days but achieved similar maximum proliferation. The hADSCs differentiation ability was similar in all groups. The characterization of hADSCs by flow cytometry showed low contamination of the cultures by other cell types. The xenobiotic-free methodology described in this study is a feasible and reproducible alternative for isolation and proliferation of hADSCs. This methodology is in accordance with the recommendations of the National Health Surveillance Agency, which proposes avoidance of xenobiotic products.


Assuntos
Técnicas de Cultura de Células/métodos , Células-Tronco Mesenquimais/metabolismo , Tecido Adiposo/citologia , Diferenciação Celular/fisiologia , Proliferação de Células , Células Cultivadas , Meios de Cultura , Citometria de Fluxo/métodos , Humanos , Imunofenotipagem/métodos , Xenobióticos
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