Insulin-like Effects of Vanadate on Rat Liver 6-Phosphofructo-2-Kinase/Fructose-2, 6-Bisphosphatase mRNA and Protein Inductions in Diabetic Rats
Effects of vanadate on liver 6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase (6PF-2-K/F-2, 6-P2ase) mRNA and protein inductions were examined in streptozotocin (STZ)-induced diabetic rats. In diabetic rats at one week after STZ (60mg/kg body weight), the liver 6PF-2-K activity was decreased to...
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Published in | Endocrine Journal Vol. 41; no. 1; pp. 75 - 82 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Tokyo
The Japan Endocrine Society
1994
Japan Endocrine Society |
Subjects | |
Online Access | Get full text |
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Summary: | Effects of vanadate on liver 6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase (6PF-2-K/F-2, 6-P2ase) mRNA and protein inductions were examined in streptozotocin (STZ)-induced diabetic rats. In diabetic rats at one week after STZ (60mg/kg body weight), the liver 6PF-2-K activity was decreased to 22% of the control. The enzyme protein was also decreased to 31% of the control, but the reduction in mRNA was not significant. Treatment of diabetes with vanadate (10mg/kg BW, i.v., every 8h), as well as insulin (10u/kg BW, s.c., every 8h), increased the 6PF-2-K activity and theenzyme protein content, though it was not completely restored to the control level. 68% of the control was the figure for enzyme activity and 65% of the control for protein content after 24-h of treatment. On the other hand, vanadate, like insulin, increased enzyme mRNA content to a higher level than the control (140% of the control). The present results indicate that vanadate, like insulin, modulates the liver 6PF-2-K/Fru-2, 6-P2ase gene expression, and stimulated protein induction contribu tes to the regulation of its enzyme activity, resulting in amelioration of the deranged carbohydrate metabolism in the diabetic state. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0918-8959 1348-4540 |
DOI: | 10.1507/endocrj.41.75 |