Summary
The action of thyroid hormones on hepatic glucose-6-phos-phatase was studied in rats.
Fed and 24-h fasted rats received T3 (10 ug/day) or T4 (25 ug/day) 1 h, 1 or 3 days before sacrificing. In addition a group of fed rats
was treated with T4 for 7 and 14 days. The glucose-6-phosphatase activity was measured in the isolated
microsomes prepared from the liver. The intactness of the microsomal preparation was
checked using 2 mM mannose-6-phosphate as a substrate.
In fed rats a single injection of T3 or T4 augmented the activities of the translocase and hydrolase components of glucose-6-phosphatase
provided that the rats were killed 24 h after the administration of hormone. This
effect was more pronounced in animals treated for 3-14 days. As expected, fasting
per se increased the activities of both components of the enzyme. Moreover, in fasted
rats treatment with T3 and T4 for 3 days further augmented the activities of the translocase and the hydrolase
components of glucose-6-phosphatase. In fed animals T3 and T4 increased the latency of the enzyme whereas in fasted animals thyroid hormones increased
the activities of the trans-locase and hydrolase components in parallel, maintaining
the level of latency of the enzyme system. Administration of T3 and T4 increased blood glucose level in fasted rats after one day, while in fed rats a significant
hyperglycaemia appeared after 7-14 days of treatment. In conclusion, T3 and T4 increase the activities of the translocase and hydrolase components of hepatic glucose-6-phosphatase
in fed and fasted rats. This in turn may mediate the enhanced flow of glucose through
the glucose cycle (glucose- > glucose-6-P- > glucose.
Key-Words
Fasting
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Glucose-6-Phosphate Translocase
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Glucose-6-Phsophate Hydrolase
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Glucose Cycle