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Acta Histochem ; 120(6): 505-512, 2018 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-29907324

RESUMO

OBJECTIVE: Evaluate the effects of doses of caffeine administered to pregnant rats on the articular cartilage chondrocytes of their offspring. METHODS: Twenty-four adult Wistar rats were randomly assigned to four groups, with one control group and three groups being treated with caffeine at doses of 25, 50 and 100 mg/kg throughout pregnancy. At birth, three offspring/females were euthanized so that the chondrocytes could be extracted. At 7, 14 and 21 days of culture, the chondrocytes were subjected to the MTT cell viability assay and an evaluation of their alkaline phosphatase activity and collagen synthesis. Chondrocytes were also stained by Hematoxylin-eosin, PAS, Safranin-O and Alcian Blue. The Sox-9, Runx-2, aggrecan, collagen-II and alkaline phosphatase gene transcript levels were also evaluated. Mean comparisons were performed by the Student-Newman-Keuls test. RESULTS: Chondrocyte cultures from the 25 mg/kg group had the lowest results, as chondrocytes from this group had reduced viability, percentage of cells, alkaline phosphatase activity and collagen and chondrogenic matrix synthesis. A reduced expression of Sox-9, alkaline phosphatase and collagen-II was also detected in the 25 mg/kg group. Chondrocyte cultures of the group treated with 50 mg/kg caffeine showed reduced collagen synthesis and Sox-9 expression. The caffeine dose of 100 mg/kg also reduced collagen and Sox-9 and alkaline phosphatase expression. CONCLUSION: Caffeine administered to pregnant rats negatively alters the articular cartilage chondrocytes of their offspring, reducing the synthesis of collagen and Sox-9 expression regardless of the dose. This study also concluded that the effects of caffeine are not linear or dose-dependent.


Assuntos
Cafeína/efeitos adversos , Cartilagem Articular/metabolismo , Condrócitos/metabolismo , Colágeno/biossíntese , Regulação da Expressão Gênica/efeitos dos fármacos , Exposição Materna/efeitos adversos , Animais , Animais Recém-Nascidos , Cafeína/farmacologia , Cartilagem Articular/patologia , Sobrevivência Celular/efeitos dos fármacos , Condrócitos/patologia , Feminino , Gravidez , Ratos , Ratos Wistar , Fatores de Transcrição SOX9/metabolismo
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