The effect of insulin on the glycogen metabolism of isolated fat cells

Résumé (1) Des adipocytes isolés à partir du tissu adipeux épididymaire du rat ont été incubés dans des milieux contenant du glucose (1¹⁴C) et des concentrations variables d'insuline. La quantité de glucose (1¹⁴C) transformée en glycogène (¹⁴C), (¹⁴C)O₂ et triglycerides (¹⁴C) a été déterminée. (2) On démontre que la quantité de glucose (1¹⁴C) transformée en glycogène par des adipocytes peut être évaluée et qu'elle est fonction de la concentration d'insuline. (3) La comparaison entre les effets d'insuline sur les transformations du glucose (1¹⁴C) en glycogène (¹⁴C), en triglycerides (¹⁴C) ou (¹⁴C)O₂ révèle que l'insuline a une action apparemment directe sur l'incorporation du glucose au glycogène. (4) Ce fait serait donc dû à un effet direct de l'insuline sur une réaction dans la synthèse du glycogène par les adipocytes ou à une grande affinité des enzymes participant à la synthèse du glycogène pour le glucose-1-phosphate et à leur faible capacité pour la synthèse du glycogène.     

The effect of insulin on the glycolysis and glycogen content of beating rat heart cells in the primary culture

Zusammenfassung An pulsierenden Rattenherzzellen in der Primärkultur wurde die Insulinwirkung auf die Glykolyse und den Glykogengehalt untersucht.     

The effect of calcitonin on calcium uptake in mouse molars in vitro

Summary Mouse maxillary second molars were removed at either 24 or 96 h of age and maintained in vitro. Half of the teeth, of each age group, were treated with 50 m-units of synthetic salmon calcitonin. By comparing the initial and final calcium concentrations in the medium, the net uptake or release of calcium was inferred. The treated molars took up significantly more calcium than the untreated groups.     

The effect of 5-bromodeoxyuridine on mouse embryos during neurulation in vitro

Mouse embryos explanted at various stages during neurulation were cultured for 20-28 h in the presence of 25-900 micrograms/ml of 5-bromodeoxyuridine (BUdR). BUdR strongly inhibited closure of the cranial neural tube, which was found to be stage-dependent. When mouse embryos were exposed to BUdR after development of the concave curvature in the neuroepithelium of the midbrain to the upper hindbrain regions, they became insensitive to the drug-induced open cranial neural tube. Histological observations showed that BUdR interfered with interkinetic migration and cytokinesis of the neuroepithelial cells. These cellular abnormalities were not dependent on the morphological development of the cranial neural folds. The 3H-BUdR experiment confirmed that the label was mostly incorporated into the DNA fraction.     

The effect of 5-bromodeoxyuridine on mouse embryos during neurulation in vitro

Summary Mouse embryos explanted at various stages during neurulation were cultured for 20–28 h in the presence of 25–900 g/ml of 5-bromodeoxyuridine (BUdR). BUdR strongly inhibited closure of the cranial neural tube, which was found to be stage-dependent. When mouse embryos were exposed to BUdR after development of the concave curvature in the neuroepithelium of the midbrain to the upper hindbrain regions, they became insensitive to the drug-induced open cranial neural tube. Histological observations showed that BUdR interfered with interkinetic migration and cytokinesis of the neuroepithelial cells. These cellular abnormalities were not dependent on the morphological development of the cranial neural folds. The³H-BUdR experiment confirmed that the label was mostly incorporated into the DNA fraction.Acknowledgment. This work was supported by Grant-in-Aids for scientific research No. 557469 and 58480391 from the Ministry of Education, Japan.     

Prompt effect of insulin in vitro on the esterolytic activity of tissue homogenates not modified by actinomycin D

Zusammenfassung Die in vitro-Wirkung des Insulins (Konzentrationsbereich von 50–100 000µU/ml des Inkubationsmediums) auf die esterolytische Aktivität der Fettgewebe, Homogenate von Myokard, Lunge und Muskel wurde bei Ratten beschrieben. Es ergibt sich eine von der Enzym-Synthese unabhängige schnelle Insulinwirkung.     

The effect of uremic serum on carbohydrate metabolism in rat diaphragm

Zusammenfassung Das Serum von Uremikern inhibiert die Glukoseutilisation im Rattendiaphragma. Der Sauerstoffverbrauch ändert sich nicht trotz niedrigerer Glukoseutilisation, da dieselbe durch eine erhöhte Auswertung anderer Substrate im Diaphragma kompensiert wird. Ein erhöhter Glykogen-, Laktat- und -ketoglutarat-Verbrauch konnte bewiesen werden.     

Suppressor effect induced by sodium periodate on the antibody response of mouse splenic cells in vitro : inhibition of this effect by sodium borohydride]

Mild oxidation of mouse spleen cells by sodium periodate induces blastogenesis. Concomitantly, the in vitro response of these cells to sheep red blood cells is inhibited. Exposure of spleen cells to sodium borohydride following periodate treatment reduces blastogenesis and restores the immune response.     

The effect of cyproheptadine on insulin biosynthesis

Summary The effect of a potent antiserotonin-antithistaminic compound, cyproheptadine (CPH) on insulin biosynthesis was studied in pancreatic islets isolated from CPH-treated rats. Though insulin content of islets was markedly reduced in CPH-treated rats, the incorporation of radiolabeled leucine into proinsulin and insulin fractions was not affected with respect to the rate and amount. It is concluded that CPH may deplete insulin content of the islets through causing the leakage of insulin.     

The effect of cyproheptadine on insulin biosynthesis

The effect of a potent antiserotonin-antihistaminic compound, cyproheptadine (CPH) on insulin biosynthesis was studied in pancreatic islets isolated from CPH-treated rats. Though insulin content of islets was markedly reduced in CPH-treated rats, the incorporation of radiolabeled leucine into proinsulin and insulin fractions was not affected with respect to the rate and amount. It is concluded that CPH may deplete insulin content of the islets through causing the leakage of insulin.