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1.
Acta Physiol Lat Am ; 25(3): 197-203, 1975.
Artículo en Español | MEDLINE | ID: mdl-1232754

RESUMEN

Initial plasma disappearance rate and biliary excretion of intravenously injected sulfobromophthalein were studied in Wistar female rats fed a normal or a protein-free diet. Proteins and sulfobromophthalein distribution in the liver were studied by a gel filtration method. The results suggest that protein deficiency may produce an impaired sulfobromophthalein transference from plasma to liver cell due to a reduction of total hepatic proteins and of sulfobromophthalein-binding protein fraction responsible for liver uptake.


Asunto(s)
Hígado/metabolismo , Deficiencia de Proteína/metabolismo , Proteínas/metabolismo , Sulfobromoftaleína , Animales , Bilis/análisis , Proteínas en la Dieta/administración & dosificación , Femenino , Pruebas de Función Hepática , Unión Proteica , Ratas , Sulfobromoftaleína/análisis
2.
Acta Physiol Lat Am ; 25(3): 197-203, 1975.
Artículo en Español | BINACIS | ID: bin-48390

RESUMEN

Initial plasma disappearance rate and biliary excretion of intravenously injected sulfobromophthalein were studied in Wistar female rats fed a normal or a protein-free diet. Proteins and sulfobromophthalein distribution in the liver were studied by a gel filtration method. The results suggest that protein deficiency may produce an impaired sulfobromophthalein transference from plasma to liver cell due to a reduction of total hepatic proteins and of sulfobromophthalein-binding protein fraction responsible for liver uptake.

3.
Acta physiol. latinoam ; 25(3): 197-203, 1975.
Artículo en Español | LILACS-Express | BINACIS | ID: biblio-1158400

RESUMEN

Initial plasma disappearance rate and biliary excretion of intravenously injected sulfobromophthalein were studied in Wistar female rats fed a normal or a protein-free diet. Proteins and sulfobromophthalein distribution in the liver were studied by a gel filtration method. The results suggest that protein deficiency may produce an impaired sulfobromophthalein transference from plasma to liver cell due to a reduction of total hepatic proteins and of sulfobromophthalein-binding protein fraction responsible for liver uptake.

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