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1.
J Environ Sci Health B ; 49(12): 966-70, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25310812

RESUMO

Abstract The objective of this study was to evaluate the efficacy of oral sodium chlorate administration on reducing total coliform populations in ewes. A 30% sodium chlorate product or a sodium chloride placebo was administered to twelve lactating Dorper X Blackbelly or Pelibuey crossbred ewes averaging 65 kg body weight. The ewes were adapted to diet and management. Ewes were randomly assigned (4/treatment) to one of three treatments which were administered twice daily by oral gavage for five consecutive days: a control (TC) consisting of 3 g sodium chloride/animal/d, a T3 treatment consisting of 1.8 g of sodium chlorate/animal/d, and a T9 treatment consisting of 5.4 g sodium chlorate/animal/d; the latter was intended to approximate a lowest known effective dose. Ruminal samples collected by stomach tube and freshly voided fecal samples were collected daily beginning 3 days before treatment initiation and for 6 days thereafter. Contents were cultured quantitatively to enumerate total coliforms. There were no significant differences in total coliform numbers (log10 cfu/g) in the feces between treatments (P = 0.832). There were differences (P < 0.02) in ruminal coliform counts (log10 cfu/mL) between treatments (4.1, 4.3 and 5.0 log10/mL contents in TC, T3 and T9 Treatments, respectively) which tended to increase from the beginning of treatment until the 5th day of treatment (P < 0.05). Overall, we did not obtain the expected results with oral administration of sodium chloride at the applied doses. By comparing the trends in coliform populations in the rumen contents in all treatments, there was an increase over the days. The opposite trend occurred in the feces, due mainly to differences among rumen contents and feces in ewes administered the T9 treatment (P = 0.06). These results suggest that the low chlorate doses used here were suboptimal for the control of coliforms in the gastrointestinal tract of ewes.


Assuntos
Ração Animal , Anti-Infecciosos/farmacologia , Cloratos/administração & dosagem , Cloratos/farmacologia , Fezes/microbiologia , Rúmen/microbiologia , Administração Oral , Animais , Anti-Infecciosos/administração & dosagem , Escherichia coli/efeitos dos fármacos , Feminino , Rúmen/efeitos dos fármacos , Ovinos
2.
Int J Dev Neurosci ; 20(7): 563-71, 2002 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-12485624

RESUMO

Proteoglycans are considered to be important molecule in cell-microenvironment interactions. They are overexpressed in neoplastic cells modifying their growth and migration in hosts. In this work we verified that undersulfation of proteoglycans and other sulfated molecules, induced by sodium chlorate treatment, inhibited C6 glioma cells proliferation in a dose-dependent way. This effect was restored by the addition of exogenous heparin. We could not detect significant cell mortality in our culture condition. The treatment also impaired in a dose-dependent manner, C6 cell adhesion to extracellular matrix (ECM) proteins (collagen IV, laminin and fibronectin). In addition, sodium chlorate treatment altered C6 glioma cell morphology, from the fibroblast-like to a more rounded one. This effect was accompanied by increased synthesis of fibronectin and alterations in its extracellular network organization. However, we could not observe modifications on laminin organization and synthesis. The results suggest an important connection between sulfation degree with important tumor functions, such as proliferation and adhesion. We suggest that proteoglycans may modulate the glioma microenvironment network during tumor cell progression and invasion.


Assuntos
Cloratos/metabolismo , Glioblastoma/metabolismo , Glioblastoma/patologia , Proteínas/metabolismo , Proteoglicanas/metabolismo , Animais , Adesão Celular/fisiologia , Diferenciação Celular/efeitos dos fármacos , Divisão Celular/efeitos dos fármacos , Cloratos/administração & dosagem , Matriz Extracelular/efeitos dos fármacos , Fibronectinas/ultraestrutura , Glioma/metabolismo , Glioma/patologia , Laminina/ultraestrutura , Ratos , Valores de Referência , Sulfatos/metabolismo , Células Tumorais Cultivadas
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