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J Biomed Mater Res A ; 108(4): 871-881, 2020 04.
Artigo em Inglês | MEDLINE | ID: mdl-31846170

RESUMO

Combining collagen, an established regenerative biomaterial, and copper (Cu) with its known antibacterial and angiogenic effects could improve wound healing. However, Cu is also cytotoxic. Thus, this study aimed at examining the tissue reactions after simultaneous intramuscular implantation of collagen discs either without Cu (controls) or impregnated in 2, 20, or 200 mmol/L Cu acetate in 24 rats. After 7, 14, and 56 days, implants with peri-implant tissue were retrieved from 8 rats/day for immunohistochemical detection of CD68+ monocytes/macrophages and CD163+ macrophages, MHC-II+ cells, T lymphocytes and nestin as tissue regeneration marker. CD68+ monocytes/macrophages around implants increased with Cu amount but decreased over time except for the highest Cu amount, while CD163+ macrophages increased over time around and within implants. MHC-II+ cells were similar to CD68+ monocytes/macrophages. T lymphocyte numbers around implants were higher for Cu-impregnated samples vs. controls on day 7 and highest on day 14, but declined afterwards. Nestin expression around and within implants was largely unaffected by Cu. In conclusion, pro-inflammatory reactions around implants were dose-dependently influenced by Cu but mostly decreased over time, while Cu did not negatively affect anti-inflammatory and regenerative reactions. These results suggest that Cu-impregnated collagen could be beneficial in wound treatment.


Assuntos
Anti-Inflamatórios/farmacologia , Colágeno/farmacologia , Cobre/farmacologia , Próteses e Implantes , Implantação de Prótese , Regeneração/efeitos dos fármacos , Animais , Antígenos CD/metabolismo , Membrana Celular/efeitos dos fármacos , Membrana Celular/metabolismo , Antígenos de Histocompatibilidade Classe II/metabolismo , Macrófagos/efeitos dos fármacos , Macrófagos/metabolismo , Masculino , Músculos/efeitos dos fármacos , Nestina/metabolismo , Ratos Endogâmicos Lew , Suínos , Linfócitos T/efeitos dos fármacos , Linfócitos T/imunologia
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