Journal
HORMONE AND METABOLIC RESEARCH
Volume 34, Issue 4, Pages 217-221Publisher
GEORG THIEME VERLAG KG
DOI: 10.1055/s-2002-26714
Keywords
type 2 diabetes; insulin secretion; fura-2 AM; pancreatic beta-cell; phlorizin
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Chronic hyperglycemia is known to lead to a progressively further impaired insulin response and to hasten the development of complications in patients with type 2 diabetes, a notion referred as glucose toxicity. T-1095, a derivative of phlorizin, is a newly developed oral hypoglycemic agent that acts as a specific inhibitor of renal Na+-glucose co-transporters, reducing circulating blood glucose levels by promoting glucose excretion into urine. The effects of glycemic improvement by T-1095 on secretory function and cytoplasmic calcium response in pancreatic beta-cells were investigated using spontaneously diabetic GK rats. After four weeks of treatment with T-1095 (age 4 to 8 week rats), serum glucose and HbA1c levels were significantly improved (serum glucose level, GK vs. GK T-1095, 277.3 +/- 11.8 vs. 204.7 +/- 6.4 mg/dl; HbA1c level, GK vs. GK T-1095, 6.2 +/- 0.2 vs. 4.8 +/- 0.1%). Insulin secretion induced by 16.7 mM glucose was also significantly increased in the T-1095-treated group compared to the untreated group. The [Ca2+]i response induced by 16.7 mM glucose in GK beta-cells was characterized by the loss of the steep First peak of [Ca2+]i elevation, and the lost first peak of [Ca2+]i reappeared in T-1095-treated beta-cells in 32 of 34 observations, In T-1095-treated beta-cells, the time lag to peak [Ca2+]i levels in the 16.7 mM glucose stimulation was significantly reduced (259.1 +/- 15.3 sec, p < 0.01) compared to untreated GK rats (524.7 +/- 52.9 sec). Thus, improvement of hyperglycemia by T-1095 ameliorates beta-cell function by relieving [Ca2+]i response.
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