THE EFFECT OF CORTISOL ADMINISTRATION ON THE ACTIVITIES OF URIDINE AND DEOXYURIDINE PHOSPHORYLASES OF NORMAL AND REGENERATING RAT LIVER

1964 ◽  
Vol 42 (3) ◽  
pp. 317-325 ◽  
Author(s):  
Esther W. Yamada

The phosphorolysis of uridine and deoxyuridine by homogenates of normal and regenerating liver of rats was assayed by a modification of the method of Canellakis (J. Biol. Chem. 227, 701 (1957)). By this assay the Kmvalues for uridine and deoxyuridine were 1.035 × 10−3 M and 2.95 × 10−4 M, respectively. The activities at an arsenate concentration of 0.114 M were 87 to 95% of the activities at an equivalent phosphate concentration.Forty-eight hours after partial hepatectomy the activity of uridine phosphorylase of regenerating liver was 1.1 times that of normal liver, and the activity of deoxyuridine phosphorylase of regenerating liver was 0.75 times that of normal liver. After a single injection of 9 mg of cortisol sodium succinate ester per 100 g of body weight there was a 1.8-fold increase in the activity of uridine phosphorylase but no significant increase in the activity of deoxyuridine phosphorylase of regenerating liver. After a single injection of 9 mg of cortisol per 100 g of body weight into normal rats there was a 1.6-fold increase in the activity of uridine phosphorylase and a 1.4-fold increase in the activity of deoxyuridine phosphorylase of normal liver. Thus, the phosphorolysis of uridine and deoxyuridine increases at different rates in liver after partial hepatectomy, or after cortisol, and this finding lends support to the view of others that the activities are due to two enzymes. The effect of cortisol, whether direct or indirect, in increasing the activities of the two enzymes in normal or regenerating liver would aid in the regulation of concentrations of intermediates of nucleic acid metabolism.

1964 ◽  
Vol 47 (1) ◽  
pp. 85-94
Author(s):  
W. de Loecker

ABSTRACT Normal and hepatoma bearing rats were treated with cortisol in order to study the effect of adrenal steroids on nucleic acid metabolism of different tissues. Normal liver, precancerous liver, hepatoma nodules and skeletal muscle were used in these experiments. The incorporation of 14C from glycine-2-14C into RNA and DNA fractions of different tissues was examined. The incorporation of glycine carbon into RNA of normal and precancerous liver was found to be stimulated by cortisol treatment. The RNA fraction of hepatoma tissue of non treated animals showed a higher incorporation level than that observed in liver, but incorporation was drastically inhibited by cortisol. The DNA fraction of hepatoma tissue showed a higher incorporation than the DNA fraction from the other tissues examined, and followed the same incorporation pattern as RNA. The incorporation of 14C into the nucleic acids of skeletal muscle was not affected by cortisol treatment.


1963 ◽  
Vol 9 (3) ◽  
pp. 337-341 ◽  
Author(s):  
MICHIO OISHI ◽  
SHIGERU KITAYAMA ◽  
HAJIME TAKAHASHI ◽  
BUNJI MARUO

1992 ◽  
Vol 25 (11) ◽  
pp. 341-345 ◽  
Author(s):  
C. Furihata ◽  
M. Yamashita ◽  
N. Kinae ◽  
T. Matsushima

MX is a strong direct acting mutagen on Salmonella typhimurium TA100 and is present in chlorinated tap water which contains organic compounds. MX was administered orally to 7-week-old male F344 rats, and its geno-toxicity in the pyloric mucosa of stomach was examined by analysis of DNA single strand scissions by the alkaline elution method. The effect of MX on cell proliferation was examined by assays of the inductions of replicative DNA synthesis and ornithine decarboxylase. MX at closes of 20-48 mg/kg body weight induced DNA single strand scissions dose-dependently (p<0.02) in the pyloric mucosa of the stomach 2 h after its administration. Moreover at doses of 10-60 mg/kg body weight, it induced up to 21-fold increase in replicative DNA synthesis (p<0.01) 16 h after its administration. At doses of 10-60 mg/kg body weight, it induced up to 100-fold increase in ornithine decarboxylase activity with a maximum 16 h after its administration. These results suggest that MX is genotoxic and induces cell proliferation in the glandular stomach of rats.


2021 ◽  
Vol 138 ◽  
pp. 111516
Author(s):  
Andrey Elchaninov ◽  
Maria Nikitina ◽  
Polina Vishnyakova ◽  
Anastasia Lokhonina ◽  
Andrey Makarov ◽  
...  

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