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1.
Ann Nutr Aliment ; 33(3): 395-404, 1979.
Article in French | MEDLINE | ID: mdl-294836

ABSTRACT

When Wistar and Sprague-Dawley rats fed from weaning on a vitamin A and provitamin A deficient diet are supplemented with retinoic acid, they mature into adults whose general physical conditions and weight are comparable with those of retinol supplemented animals. However, the adrenal cortex, testes and ovaries delta 5-3 beta hydroxysteroid deshydrogenases-delta 5-delta 4-3-oxosteroide isomerases are in all cases strongly decreased compared with those of retinol supplemented animals. These results are reproducible only if the mothers' reserves in vitamin A are about 50 gamma/g of hepatic tissue and if the animals are weaned between the 19th and 21st day. These results obtained under these strictly defined conditions demonstrate the importance of the "biochemical lesion" which causes steroidogenesis perturbations induced by the vitamin A deficiency. The experimental data are discussed in the light of the recent findings concerning the direct role of the vitamin A in the transglycosylation reactions (Luigi M. de Luca, Vitamins and Hormones, 1977, 35, 1-57).


Subject(s)
Steroids/biosynthesis , Tretinoin/pharmacology , Vitamin A Deficiency/metabolism , 3-Hydroxysteroid Dehydrogenases/metabolism , Adrenal Glands/drug effects , Adrenal Glands/enzymology , Animals , Female , Male , Organ Size/drug effects , Ovary/drug effects , Ovary/enzymology , Rats , Testis/drug effects , Testis/enzymology , Vitamin A/pharmacology
2.
C R Seances Soc Biol Fil ; 170(1): 168-75, 1976.
Article in French | MEDLINE | ID: mdl-134769

ABSTRACT

A rapidly migrating variant of albumin has been discovered in a 28-year-old breton woman. At least eight relatives also bear the trait. This new variant is described in terms of its electrophoretic mobilities, immunological properties and heat- and storage stability. Two other reports of the slow type are presented, but no family study was performed in these cases. It is suggested that bisalbuminaemia could be a relatively common inherited condition in Brittany.


Subject(s)
Blood Protein Disorders/genetics , Serum Albumin , Adult , Blood Protein Disorders/congenital , Blood Protein Electrophoresis , Electrophoresis, Polyacrylamide Gel , Female , France , Humans , Immunoelectrophoresis , Pedigree , Serum Albumin/analysis , Serum Albumin/immunology
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