Abstract
We previously showed that a phosphate-deficient diet resulting in hypophosphatemia
upregulated the catalytic subunit p36 of rat liver glucose-6-phosphatase, which is
responsible for hepatic glucose production. A possible association between phosphate
and glucose homeostasis was now further evaluated in the Hyp mouse, a murine homologue
of human X-linked hypophosphatemia. We found that in the Hyp mouse as in the dietary
Pi deficiency model, serum insulin was reduced while glycemia was increased, and that
liver glucose-6-phosphatase activity was enhanced as a consequence of increased mRNA
and protein levels of p36. In contrast, the Hyp model had decreased mRNA and protein
levels of the putative glucose-6-phosphate translocase p46 and liver cyclic AMP was
not increased as in the phosphate-deficient diet rats. It is concluded that in genetic
as in dietary hypophosphatemia, elevated glucose-6-phosphatase activity could be partially
responsible for the impaired glucose metabolism albeit through distinct mechanisms.
Key words
Glucose Intolerance - Phosphate Homeostasis - Mouse Liver
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G. van de Werve, Ph.D.
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