Influência de variáveis metodológicas na resistência de união ao cisalhamento / The influence of the methodological variables on the shear bond strength

OBJETIVO: avaliar a influência de diferentes variáveis metodológicas sobre a resistência de união ao cisalhamento em estudos in vitro. MÉTODOS: foram utilizados 105 incisivos permanentes bovinos, seccionados ao nível do colo dentário. A porção coronária foi inclusa em tubos de PVC, com resina acrílica autopolimerizável, e com face vestibular voltada para cima. Todos os corpos de prova foram preparados para a colagem com profilaxia e condicionamento ácido na região central das coroas, onde foram posicionados braquetes Morelli® de incisivos centrais superiores, com resina Concise® Ortodôntico (3M/Unitek). Foram determinados três grupos de acordo com a variável estudada: (Grupo 1) - meio de armazenamento dos dentes, previamente à inclusão e à colagem, com solução de timol 0,1 por cento (a), água destilada (b) e congelamento (c); (Grupo 2) - velocidade da célula de carga da máquina de ensaio de 0,5 (a), 1,0 (b) e 2,0mm/min (c) e (Grupo 3) - diferentes marcas comerciais de ácidos fosfóricos a 37 por cento, 3M/Unitek (a), AcidGel (b) e Attack Tek (c). Os corpos de prova foram submetidos ao ensaio mecânico de resistência ao cisalhamento através da máquina Emic DL2000®. Os dados foram analisados estatisticamente por meio do Teste t Student para amostras independentes. RESULTADOS: os resultados demonstraram que no Grupo 1 o subgrupo de congelamento apresentou maiores valores em relação aos outros dois subgrupos, porém sem diferença estatisticamente significativa (p > 0,05). No Grupo 2, a força no momento da ruptura foi menor à medida que era aumentada a velocidade da célula de carga, porém sem diferença significativa entre os subgrupos. No Grupo 3, o ácido da 3M/Unitek apresentou a maior média em MPa, no entanto, também sem diferença significativa entre os subgrupos. CONCLUSÕES: conclui-se, portanto, que as variáveis analisadas neste trabalho não apresentaram influência suficiente para determinação de diferenças estatisticamente significativas...

AIM: Evaluate the influence of several methodological variables on the shear bond strength of in vitro studies. METHODS: 105 bovine incisors were sectioned at the cervical level. The coronary portion was included in PVC rings, fulfilled with auto polymerized acrylic resin, with its labial faces turned to the top. All the samples were prepared for bonding, cleaned and acid etched on the central area of the crowns. In this area, central incisors' MorelliÕ brackets were bonded with ConciseÕ (3M/Unitek). Three testing groups were established, according to the studied variable: Group 1 - storage previous to bonding (a-Thymol 0,1 percent; b- distilled water; c- freezing); Group 2 - crosshead speed of the universal testing machine (a- 0,5mm/min; b- 1,0mm/min; c- 2,00mm/min) and Group 3 - commercial brand of 37 percent phosphoric acid (a- 3M/Unitek; b- Acid Gel; c- Attack Tek). The shear bond strength test was performed at the Emic DL2000Õ universal testing machine. Data was analyzed through the Student's t test for independent samples. RESULTS: In Group 1, the freezing group showed the higher values of shear bond strength when compared to the others, although no statistical difference was observed (p>0,05). For Group 2, the higher the crosshead speed, the lower the shear bond strength, with no statistical difference. In Group 3, the 3M/Unitek brand showed the highest average of shear bond strength in MPa, but also no statistical difference was shown. CONCLUSIONS: The variable analyzed in this research had not presented enough influence to determine significant differences between the results.

Expression of Smad4 and Smad7 in human thyroid follicular carcinoma cell lines.

Smad proteins have been shown tomediate the signal transduction pathway downstream of the transforming growth factor beta (TGFbeta). TGFbeta induces the phosphorylation of Smad2 and Smad3 which associate with Smad4 and translocate to the nucleus where they regulate gene transcription; besides these stimulatory Smads, the inhibitory Smads, Smad6 and Smad7, oppose signaling by blocking receptors and interrupting the phosphorylation of Smads2/3. The loss of TGFbeta-sensitivity, caused by inactivation of components of TGFbeta signaling, as Smad4, underlies a wide variety of human disorders, including cancer. In addition, the overexpression of the inhibitory Smad7, which prevents the phosphorylation of Smad2/3 and consequently inhibits TGFbeta signaling pathways, was observed in some diseases. In the present study we investigated the expression of Smad4 and Smad7 in thyroid cell lines (NPA papillary carcinoma, WRO follicular carcinoma and ARO anaplastic carcinoma) by RT-PCR and immunocytochemistry. Our results show that Smad4 was expressed in all thyroid cell lines and controls analyzed, differently from other classes of tumors where Smad4 expression was deleted. On the other hand, Smad7 was overexpressed in ARO anaplastic cell line, the most malignant follicular thyroid carcinoma. Our data suggest that the abrogation of the TGFbeta response by Smad7 overexpression may be a mechanism for the tumor aggressiveness observed in undifferentiated thyroid tumors.