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1.
Cell Biochem Funct ; 31(2): 173-9, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-22972462

RESUMEN

This study aimed to investigate the functional relationship of sialic acid in regressing and remodelling organs such as the tail, small intestine and liver during the metamorphosis of Pelophylax ridibundus. For this purpose, four groups were composed according to developmental periods by considering Gosner's criteria (1964). Our findings showed that the sialic acid content of the larval tail has an opposite profile to cell death process. Although the sialic acid content of the small intestine and liver did not change evidently during metamorphosis, it increased after the completion of metamorphosis. Frog tail extensively exhibited cell death process and decreased proliferative activity and underwent complete degeneration during metamorphic climax. In spite of increased apoptotic index, a decreased sialic acid level in the tail tissues during climax can be the indication of a death cell removal process. However, the intestine and the liver included both cell death and proliferative process and remodelling in their adult forms. Thus, their sialic acid profiles during metamorphosis were different from the tail's profile. These data show that sialic acid may be an indicator of the presence of some cellular events during metamorphosis and that it can have different roles in the developmental process depending on the organ's fate throughout metamorphosis.


Asunto(s)
Metamorfosis Biológica , Ácido N-Acetilneuramínico/metabolismo , Especificidad de Órganos , Ranidae/crecimiento & desarrollo , Ranidae/metabolismo , Humedales , Animales , Apoptosis , Proliferación Celular , Etiquetado Corte-Fin in Situ , Intestino Delgado/citología , Larva/citología , Larva/metabolismo , Hígado/citología , Antígeno Nuclear de Célula en Proliferación/metabolismo , Cola (estructura animal)/citología
2.
Mol Cell Biochem ; 294(1-2): 37-44, 2007 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-17124636

RESUMEN

In this study, 12 months old female Swiss albino rats were used. They were randomly divided into four groups. The animals of group I were fed with pellet chow. Group II were fed with pellet chow and treated with 250 microg/kg CrCl3 x 6H2O and 100 mg/kg niacin for 45 days. Group III were fed a lipogenic diet consisting of 2% cholesterol, 0.5% cholic acid and 2% sunflower oil added to the pellet chow, and given 3%alcoholic water for 60 days. Group IV were fed with the same lipogenic diet for 60 day sand treated by gavage technique to rats at a dose of 250 micro/kg CrCl3 x 6H2O and 100 mg/kg niacin for 45 days, 15 days after experimental animals were rendered hyperlipidemic. At the 60th day, renal tissue and blood samples were taken from the animals. The sections were examined under light and electron microscopy. The degenerative changes were much more in the hyperlipidemic rats than the control group. The changes in renal tissue were also observed in hyperlipidemic animals given niacin and chromium. In the hyperlipidemic rats, renal glutathione levels decreased and renal lipid peroxidation levels, and serum urea and creatinine levels were increased. But, renal glutathione levels increased and lipid peroxidation levels and serum urea and creatinine levels decreased in hyperlipidemic rats given niacin and chromium. The purpose of this study was to investigate whether a protective effect of a combination of niacin and chromium is present on the renal tissue of hyperlipidemic rats or not. In conclusion, we can say that niacin and chromium do not have a protective effect on the morphology of the renal tissue of hyperlipidemic rats, except a protective effect on their biochemical parameters.


Asunto(s)
Cromo/uso terapéutico , Hiperlipidemias/tratamiento farmacológico , Hiperlipidemias/metabolismo , Hipolipemiantes/uso terapéutico , Riñón/metabolismo , Niacina/uso terapéutico , Animales , Cromo/administración & dosificación , Creatinina/sangre , Grasas de la Dieta/administración & dosificación , Grasas de la Dieta/farmacología , Quimioterapia Combinada , Femenino , Glutatión/sangre , Hiperlipidemias/patología , Hipolipemiantes/administración & dosificación , Riñón/efectos de los fármacos , Riñón/patología , Riñón/ultraestructura , Peroxidación de Lípido , Niacina/administración & dosificación , Distribución Aleatoria , Ratas , Urea/sangre
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