To determine the long-term effects of the angiotensin-converting enzyme inhibitor captopril on insulin sensitivity in subjects with type II diabetes and arterial hypertension. The chronic effects of angiotensin-converting enzyme inhibition on insulin-sensitive individuals are presently controversial.
Sixteen subjects, with type II diabetes (on diet and/or diet plus oral hypoglycemic agents) and arterial hypertension, were studied. During a 1-mo run-in period no antihypertensive drugs were administered, but oral hypoglycemic agents were continued in subjects already in therapy. The subjects were then randomly assigned to two 3-mo treatment periods, with either captopril or placebo (single blind, cross-over design). At the end of each treatment period, insulin sensitivity was assessed by means of a euglycemic-hyperinsulinemic clamp (2 sequential steps, 2-h each, insulin infusion 0.25 and 1 mU ·kg−1 ·min−1, steps 1 and 2, respectively), combined with infusion of [3-3H]glucose (for calculation of hepatic glucose output and peripheral glucose utilization, rates of glucose disappearance), and indirect calorimetry (for calculation of glucose oxidation, nonoxidative glucose metabolism, and lipid oxidation). The percentage of HbAlc was measured to assess long-term glycemic control.
Comparing data at the end of placebo and captopril treatment, captopril resulted in: lower blood pressure (systolic 154 ± 2 vs. 163 ± 3 mmHg and diastolic 93 ± 2 vs. 101 ± 2 mmHg); greater insulin sensitivity in hyperglycemic conditions (total amount of insulin infused and time of insulin infusion required to reach euglycemia, 1.73 ± 0.54 vs. 2.08 ± 0.60 U and 58 ± 8 vs. 70 ± 11 min, captopril and placebo, respectively, P < 0.05); greater insulin sensitivity in euglycemic conditions at liver level (hepatic glucose output 4.11 ± 0.55 vs. 5.2 ± 0.4 μmol · kg−1 · min−1, step 1 of the clamp), muscle level (rates of glucose disappearance 26.1 ± 2.3 vs. 23.8 ± 2.1 μmol · kg−1 · min−1, step 2 of the clamp), primarily attributable to ∼29% increase in nonoxidative glucose metabolism, and adipose tissue level (plasma free fatty acid 0.185 ± 0.03 vs. 0.24 ± 0.02 mM and lipid oxidation 1.9 ± 0.3 vs. 2.21 ± 0.04 μmol · kg−1 · min−1 in step 1); and lower HbA1c (6.7 ± 0.2 vs. 7.3 ± 0.2%, P < 0.05).
Long-term captopril administration in type II diabetic subjects improves insulin sensitivity in the postprandial state, not in the fasting state, and improves glycemic control.