ABSTRACT
The present study analyzed the action of sodium trimetaphosphate (TMP) and/or fluoride on hydroxyapatite. Hydroxyapatite powder was suspended in different solutions: deionized water, 500 µg F/mL, 1,100 µg F/mL, 1%TMP, 3%TMP, 500 µg F/mL plus 1%TMP and 500 µg F/mL plus 3%TMP. The pH value of the solutions was reduced to 4.0 and after 30 min, raised to 7.0 (three times). After pH-cycling, the samples were analyzed by X-ray diffraction and infrared spectroscopy. The concentrations of calcium fluoride, fluoride, calcium and phosphorus were also determined. Adding 1% or 3% TMP to the solution containing 500 µg F/mL produced a higher quantity of calcium fluoride compared to samples prepared in a 1,100 µg F/mL solution. Regarding the calcium concentration, samples prepared in solutions of 1,100 µg F/mL and 500 µg F/mL plus TMP were statistically similar and showed higher values. Using solutions of 1,100 µg F/mL and 500 µg F/mL plus TMP resulted in a calcium/phosphorus ratio close to that of hydroxyapatite. It is concluded that the association of TMP and fluoride favored the precipitation of a more stable hydroxyapatite.
O presente estudo avaliou a ação do trimetafosfato de sódio (TMP) e/ou fluoreto sobre a hidroxiapatita. Pó de hidroxiapatita foi suspenso em diferentes soluções: água deionizada, 500 µg F/mL, 1100 µg F/mL, 1%TMP, 3%TMP, 500 µg F/mL adicionado a 1%TMP e 500 µg F/mL associado a 3%TMP. O pH das soluções foi reduzido para 4,0 e depois de 30 min, elevado para 7,0 (três vezes). Depois do processo de ciclagem de pH, as amostras foram analisadas por difração de raios-X e espectroscopia por infravermelho. As concentrações de fluoreto de cálcio, fluoreto, cálcio e fósforo também foram determinadas. A adição de 1% ou 3% TMP na solução contendo 500 µg F/mL produziu uma maior quantidade de fluoreto de cálcio comparado às amostras tratadas com uma solução de 1100 µg F/mL. A respeito da concentração de cálcio, amostras tratadas com soluções de 1100 µg F/mL e 500 µg F/mL adicionado ao TMP foram estatisticamente similares e mostraram maiores valores. Soluções de 1100 µg F/mL e 500 µg F/mL adicionado ao TMP resultaram em uma proporção molar Ca/P mais próxima à da hidroxiapatita. Conclui-se que a associação de TMP e F favoreceu a precipitação de uma hidroxiapatita mais estável.
Subject(s)
Animals , Mice , Bacterial Infections/microbiology , Endotoxins/toxicity , Escherichia coli/pathogenicity , Intestinal Mucosa/microbiology , Tungsten Compounds , Allopurinol/pharmacology , Gentamicins/pharmacology , Ileum/microbiology , Ileum/pathology , Polymyxin B/pharmacology , Quinolinium Compounds/pharmacology , Tungsten/pharmacology , Xanthine Oxidase/antagonists & inhibitorsABSTRACT
Wistar male rats, 3 months of age were given ad-libitum a nutritionally adequate diet and demineralized drinking water. The Molybdenum (Mo) and Tungsten (W) were provided in the drinking water at 200 ppm concentration. Intestinal tumors were induced by 1,2-dimethylhydrazine (DMH) given subcutaneously as 16 weekly doses at 20 mg/kg body weight. Mo in the form of (NH4)6 Mo7O24 4H2O or W in the form of (Na2WO4) were provided in the drinking water two months before the first DMH treatment and were continued during 4 months more until the last DMH treatment. Three months after the last carcinogen injection, all animals were sacrificed and examined for intestinal tumors. The number, size and location of the tumors were recorded and the pathology was examined. The addition of Mo to the drinking water induced an increase of hepatic Mo content. At the end of the second month, the hepatic content of Mo was 5.61 ppm, compared with control and W groups (2.18 and 0.96 ppm, respectively). A significantly lower incidence of tumors was observed in the Mo group (47), compared with the control group given DMH alone (105) and W group (113). On the other hand, the Mo group showed a significant decrease in the numbers of multiple tumors per rat.
Subject(s)
Male , /pharmacology , Molybdenum/administration & dosage , Molybdenum/pharmacology , Intestinal Neoplasms/chemically induced , Intestinal Neoplasms/prevention & control , Diet , Cell Division/drug effects , Molybdenum/therapeutic use , Intestinal Neoplasms/drug therapy , Intestinal Neoplasms/pathology , Body Weight/drug effects , Rats , Rats, Wistar , Tungsten/pharmacologyABSTRACT
Se determinaron receptores estrogénicos testiculares en presencia de inhibidores de fosfatasas, molibdato (Mo04), wolframato (W04) y fluoruro (F-), bajo diferentes condiciones experimentales. A 0-4-C el Mo04 mimetizó parcialmente la acción estabilizadora del ditiotreitol (DTT) sobre la unión del estrógeno a su receptor citosólico, sugiriendo un efecto protector sobre los grupos sulfhidrilo reducidos. Por otra parte, a 25-C, en presencia de DTT, el efecto de Mo04 fue observado en homogenato y sobrenadante de baja velocidad, pero no se evidenció en citosol. Un posible mecanismo protector de la actividad de unión basado en la inhibición de la actividad de fosfatasas fue corroborado mediante el uso de W04. La actividad fosfatasa ácida resultó inhibida por estos agentes, mientras que la fosfatasa alcalina no presentó modificaciones. El agregado de Mo04 y W04, provocó, además, una inhibición siginificativa de la actividad proteolítica. Estos resultados sugieren que el Mo04 podría estabilizar la unión de estrógenos a sus receptores testiculares, a través de tres posibles mecanismos: 1) protección de grupos sulfhidrilo reducidos; 2) inhibición de la fosfatasa ácida y 3) inhibición de la actividad protelítica