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Pathol Res Pract ; 210(3): 135-41, 2014 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24314812

RESUMO

We examined the effects of vitamin E supplementation (VES) on osteoclast (OC) resorbing activity and cytomorphometry in Walker 256/B tumor osteolytic rats. Twenty-four aged male rats were randomized into 3 groups: 6 were sham operated; 9 were injected in the right hind limb with Walker 256/B cells (W256 group); and 9 were injected as above and supplemented with VE (45mg/kg BW) (W256VE group). Twenty days later, bone mass (BV/TV) and some microarchitectural parameters were assessed. Some histodynamic parameters, cellular and nuclear form factors (FFC and FFN), and nuclear-cytoplasmic ratio (N/C) of OC were measured for each group. W256 group exhibited osteolytic lesions in the operated femora. Walker 256/B induced trabecular perforation and decreased BV/TV associated with significant increases in OC numbering (N.Oc/B.Ar and Oc.N/B.Pm) and activity (ES/BS and Oc.S/BS). While FFN remain unchanged, the FFC and N/C ratio increased in the W256 group. W256VE showed less osteolytic lesions. Moreover, disruption of bone microarchitecture and OC activity in W256VE group decreased. VES reduced the malignant Walker 256/B-induced enhanced OC resorbing activity with cytoinhibition rate reaching 41%. The protective effect of VE may be due to its modulation of OC cytomorphometry and subsequently their activity.


Assuntos
Remodelação Óssea/efeitos dos fármacos , Neoplasias da Mama Masculina/tratamento farmacológico , Suplementos Nutricionais , Fêmur/efeitos dos fármacos , Osteoclastos/efeitos dos fármacos , Osteólise/prevenção & controle , Vitaminas/farmacologia , alfa-Tocoferol/farmacologia , Fosfatase Ácida/metabolismo , Animais , Biomarcadores/metabolismo , Neoplasias Ósseas/metabolismo , Neoplasias Ósseas/prevenção & controle , Neoplasias Ósseas/secundário , Neoplasias da Mama Masculina/complicações , Neoplasias da Mama Masculina/patologia , Fêmur/metabolismo , Fêmur/patologia , Isoenzimas/metabolismo , Masculino , Osteoclastos/metabolismo , Osteoclastos/patologia , Osteólise/etiologia , Osteólise/metabolismo , Osteólise/patologia , Ratos , Ratos Sprague-Dawley , Fosfatase Ácida Resistente a Tartarato , Fatores de Tempo
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