Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros








Base de dados
Tipo de estudo
Intervalo de ano de publicação
1.
An Acad Bras Cienc ; 90(2 suppl 1): 2317-2329, 2018 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-29694498

RESUMO

Creatine acts intracellularly as energy buffer and storage, demonstrating protective effects in animal models of neurodegenerative diseases. However, its permeability throught blood-brain barrier (BBB) is reduced. The aim of the present study was developing a carrier to facilitate the delivery of creatine to the central nervous system. Creatine nanoliposomes were produced, characterized and assayed in models of toxicity in vitro and in vivo. Particles showed negative zeta potential (-12,5 mV), polydispersity index 0.237 and medium-size of 105 nm, which was confirmed by transmission electron microscopy (TEM) images. Toxicity assay in vitro was evaluated with blank liposomes (no drug) or creatine nanoliposomes at concentrations of 0.02 and 0.2 mg/mL, that did not influence the viability of Vero cells. The result. of the comet assay that the nanoliposomes are not genotoxic, togeher with cell viability demonstrated that the nanoliposomes are not toxic. Besides, in vivo assays not demonstrate toxicity in hematological and biochemical markers of young rats. Nevertheless, increase content of creatine in the cerebral cortex tissue after subchronic treatment was observed. Altogether, results indicate increase permeability of creatine to the BBB that could be used as assay for in vivo studies to confirm improved effect than free creatine.


Assuntos
Encéfalo/efeitos dos fármacos , Creatina/toxicidade , Lipossomos/toxicidade , Nanopartículas/toxicidade , Polissorbatos/toxicidade , Animais , Encéfalo/ultraestrutura , Chlorocebus aethiops , Microscopia Eletrônica de Transmissão , Modelos Animais , Ratos , Ratos Wistar , Células Vero
2.
Vet Parasitol ; 223: 102-10, 2016 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-27198785

RESUMO

Although Eurytrema coelomaticum is considered a parasite with low pathogenicity, it may be associated with mortality and loss of productive performance in animals due to chronic pancreatitis. The aim of this study was to evaluate the occurrence of oxidative stress caused by E. coelomaticum in naturally infected cattle, correlating the biochemical findings with the parasite load and histopathological changes. For this study, blood and pancreas samples from 51 cattle were collected, and levels of the thiobarbituric acid reactive substances (TBARS), advanced oxidation protein products (AOPP) and ferric reducing ability of plasma (FRAP) were measured in the serum and pancreas, and superoxide dismutase (SOD) activity was measured in total blood. Parasite burden was determined opening the pancreatic ducts, and then fragments of pancreas were collected and fixed in 10% buffered formalin and routinely processed for histopathology. From the 51 collected pancreas, 33 (63.5%) were parasitized. The average parasite burden per pancreas was 532 (12-2,578). TBARS and FRAP showed higher levels in serum and pancreas of infected animals (p<0.05), with a positive correlation between the histopathological changes and the number of parasites. SOD level in blood was 42% higher in parasitized group compared with control group (p<0.05), as well as AOPP in serum. Based on these results, we concluded that in natural infection by E. coelomaticum in cattle, oxidative stress occurs, characterized by the occurrence of protein oxidation, lipid peroxidation and activation of antioxidant system.


Assuntos
Doenças dos Bovinos/parasitologia , Estresse Oxidativo/fisiologia , Pâncreas/patologia , Pancreatopatias/veterinária , Trematódeos/classificação , Infecções por Trematódeos/veterinária , Animais , Sequência de Bases , Bovinos , Doenças dos Bovinos/patologia , DNA de Helmintos/genética , Pâncreas/parasitologia , Pancreatopatias/parasitologia , Pancreatopatias/patologia , Infecções por Trematódeos/parasitologia , Infecções por Trematódeos/patologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA