RESUMEN

The objective of this study was to evaluate whether demineralized bovine bone (Gen-ox®) alters bone neoformation in rats submitted to alcoholism. Forty male rats were separated into two groups of 20 rats and distributed as follows: Group E1, which received 25% ethanol and a surgical cavity filled only by a blood clot, and Group E2, which received 25% ethanol and a surgical cavity filled with Gen-ox®. The animals were euthanized at 10, 20, 40 and 60 days after surgery and necropsy was performed. The histomorphological and histometric analyses of the area of connective tissue and bone neoformation showed that the reorganization of the bone marrow and full repair of the surgical cavity in Group E1 occurred more quickly than in Group E2. It was also noted that in the final period the animals in Group E2 showed areas of connective tissue and thick bone trabeculae around the particles of the implant. It can be concluded that the use of Gen-ox® delayed the process of bone repair in alcoholic rats, although it can be used as filling material because it shows osteoconductive activity, as evidenced by bone tissue formation around the graft particles.

O objetivo deste trabalho foi avaliar se a matriz óssea bovina desmineralizada (Gen-ox®) altera a neoformação óssea em ratos submetidos ao alcoolismo. Foram utilizados 40 ratos machos, separados em dois grupos de 20 animais cada, assim distribuídos: Grupo E1, que recebeu etanol a 25% e cavidade cirúrgica preenchida por coágulo sanguíneo, e Grupo E2, que recebeu etanol a 25% e cavidade cirúrgica preenchida por Gen-ox®. Os animais foram eutanasiados aos 10, 20, 40 e 60 dias após a cirurgia. Os estudos histomorfológico e histométrico da quantidade de tecido conjuntivo presente e a quantidade de tecido ósseo neoformado demostraram que a reorganização da medula óssea e a reparação total da cavidade cirúrgica no Grupo E1 ocorreram em menor espaço de tempo do que no Grupo E2. Observou-se também que, no período final do experimento, os animais do Grupo E2 apresentaram áreas de tecido conjuntivo e trabéculas ósseas espessas ao redor das partículas do material implantado. Concluiu-se que a utilização do Gen-ox® retardou o processo de reparação óssea em ratos alcoolizados, muito embora o Gen-ox® possa ser utilizado como material de preenchimento, pois demonstra atividade osteocondutiva, com a formação de tecido ósseo ao redor das partículas do enxerto.

Asunto(s)

RESUMEN

The objective of this study was to evaluate whether demineralized bovine bone (Gen-ox®) alters bone neoformation in rats submitted to alcoholism. Forty male rats were separated into two groups of 20 rats and distributed as follows: Group E1, which received 25% ethanol and a surgical cavity filled only by a blood clot, and Group E2, which received 25% ethanol and a surgical cavity filled with Gen-ox®. The animals were euthanized at 10, 20, 40 and 60 days after surgery and necropsy was performed. The histomorphological and histometric analyses of the area of connective tissue and bone neoformation showed that the reorganization of the bone marrow and full repair of the surgical cavity in Group E1 occurred more quickly than in Group E2. It was also noted that in the final period the animals in Group E2 showed areas of connective tissue and thick bone trabeculae around the particles of the implant. It can be concluded that the use of Gen-ox® delayed the process of bone repair in alcoholic rats, although it can be used as filling material because it shows osteoconductive activity, as evidenced by bone tissue formation around the graft particles.(AU)

O objetivo deste trabalho foi avaliar se a matriz óssea bovina desmineralizada (Gen-ox®) altera a neoformação óssea em ratos submetidos ao alcoolismo. Foram utilizados 40 ratos machos, separados em dois grupos de 20 animais cada, assim distribuídos: Grupo E1, que recebeu etanol a 25% e cavidade cirúrgica preenchida por coágulo sanguíneo, e Grupo E2, que recebeu etanol a 25% e cavidade cirúrgica preenchida por Gen-ox®. Os animais foram eutanasiados aos 10, 20, 40 e 60 dias após a cirurgia. Os estudos histomorfológico e histométrico da quantidade de tecido conjuntivo presente e a quantidade de tecido ósseo neoformado demostraram que a reorganização da medula óssea e a reparação total da cavidade cirúrgica no Grupo E1 ocorreram em menor espaço de tempo do que no Grupo E2. Observou-se também que, no período final do experimento, os animais do Grupo E2 apresentaram áreas de tecido conjuntivo e trabéculas ósseas espessas ao redor das partículas do material implantado. Concluiu-se que a utilização do Gen-ox® retardou o processo de reparação óssea em ratos alcoolizados, muito embora o Gen-ox® possa ser utilizado como material de preenchimento, pois demonstra atividade osteocondutiva, com a formação de tecido ósseo ao redor das partículas do enxerto.(AU)

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RESUMEN

In the present article we show that supernatants derived from lipopolysaccharide (LPS) or phorbol 12-myristate 13-acetate (PMA)-stimulated A-20 B cell lymphoma are able to induce polyclonal immunoglobulin (Ig) secretion by normal B cells in a T-cell-dependent manner. This activity could be blocked by neutralizing monoclonal antibodies against interferon-gamma, but not by monoclonal antibodies against interleukin (IL)-2, IL-4, IL-5, IL-6, IL-10 and granulocyte macrophage colony-stimulating factor (GM-CSF) or even a polyclonal antibody against tumor necrosis factor (TNF)-alpha. Furthermore, A-20 supernatants induced the production of measurable amounts of interferon-gamma by normal murine spleen cells and activates natural killer (NK) cells. Fractionation of factor-rich supernatants on a Sephacryl S-200 column revealed that the factor activity is located in the fractions corresponding to a molecular mass of 160-150 kDa and 80-70 kDa. The biological activities found in the A-20 supernatant are very similar to the ones described for the recently cloned human IL-12/NK cell stimulatory factor. These results suggest the existence of a murine analogous factor for the human IL-12 produced by A-20 B cell lymphoma.

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