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Updated: Oct 13, 2026

Homogeneous Time-resolved Förster Resonance Energy Transfer-based Assay for Detection of Insulin Secretion
Published on: May 10, 2018
[Effect of arotinolol on insulin secretion and insulin clearance rate in patients with Graves' disease]
Abstract:
Glucose-induced insulin secretion, 24-h urinary C-peptide (CPR) and euglycemic clamp were examined in five patients with hyperthyroid Graves' disease before and 2 weeks after treatment with arotinolol (20 mg/day, p.o.). Plasma glucose and insulin responses to oral administration of 75 g glucose were not changed by arotinolol treatment. 24-h urinary CPR and basal posthepatic insulin delivery rate (BPIDR) as an indicator of insulin secretion were significantly suppressed by arotinolol. Glucose infusion rate (GIR) as an indicator of insulin sensitivity and glucose clearance rate (GCR) were not influenced by arotinolol therapy. Insulin clearance rate (ICR) was significantly suppressed by arotinolol. These findings suggest that arotinolol inhibits insulin secretion by decreasing ICR but does not attenuate insulin release induced by glucose in hyperthyroid patients, and that insulin sensitivity and GCR are not affected by arotinolol.
Insights
Arotinolol treatment in hyperthyroid patients suppressed insulin secretion by reducing insulin clearance rate (ICR). However, it did not affect glucose-induced insulin release or insulin sensitivity.
Area of Science:
- Endocrinology
- Metabolic Research
Background:
- Hyperthyroidism can alter glucose metabolism and insulin dynamics.
- Understanding the effects of medications on these processes is crucial for patient management.
Purpose of the Study:
- To investigate the impact of arotinolol on glucose-induced insulin secretion and insulin sensitivity in hyperthyroid Graves' disease patients.
Main Methods:
- Evaluated five hyperthyroid Graves' disease patients before and after arotinolol treatment.
- Assessed glucose-induced insulin secretion, 24-h urinary C-peptide (CPR), basal posthepatic insulin delivery rate (BPIDR), glucose infusion rate (GIR), glucose clearance rate (GCR), and insulin clearance rate (ICR) using euglycemic clamp techniques.
Main Results:
- Arotinolol did not alter plasma glucose or insulin responses to oral glucose.
- 24-h urinary CPR and BPIDR were significantly suppressed by arotinolol.
- Insulin clearance rate (ICR) was significantly suppressed.
- Insulin sensitivity (GIR) and glucose clearance rate (GCR) remained unaffected.
Conclusions:
- Arotinolol inhibits insulin secretion in hyperthyroid patients primarily by decreasing insulin clearance rate (ICR).
- Arotinolol does not impair glucose-induced insulin release or affect insulin sensitivity in this patient group.
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