This study tested whether the angiotensin-converting enzyme inhibitor
(ACEI) benazepril can improve the insulin resistance and glucose toler
ance in uremia. Fifteen uremic hypertensive patients were treated with
benazepril in a dose of 10-20 mg per day for ten weeks, and ten healt
hy subjects, matched in age, sex ratio and body mass index (BMI), serv
ed as the control group. Before and after the treatment, an oral 75 g
glucose tolerance test (OGTT) and insulin release test (IRT) were perf
ormed in two groups above, and the blood glucose and serum insulin con
centrations at 0, 60, 120 and 180 minutes after glucose load were exam
ined, and the insulin glycoregulatory activity, including insulin sens
itivity index (ISI), glucose uptake rate (M), total areas under the gl
ucose and insulin curves during OGTTs (AUCG AUCINS), was calculated. T
he changes of serum potassium and renal function before and after trea
tment were observed. It showed that (1) benazepril could reduce blood
pressure significantly (SBP decreased from 174.8 +/- 12.0 mmHg to 151.
5 +/- 9.0 mmHg, p < 0.001; DBP decreased from 108.0 +/- 8.2 mmHg to 95
.3 +/- 9.0 mmHg, p <0.001). The total response rate was 86.7%. (2) Aft
er treatment with benazepril for ten weeks, the blood glucose and seru
m insulin concentrations after glucose load and AUCG, AUCINS values in
the uremic patients were significantly lower than before treatment, b
ut were still significantly higher than in the controls. The values of
ISI and M in the uremic patients after treatment were much higher tha
n before treatment, but were still significantly lower than in the con
trol subjects. (3) The differences of serum potassium and creatinine l
evels before and after treatment were not significant. These findings
indicate that benazepril can not only reduce blood pressure effectivel
y and safely, but also partly improve insulin resistance, hyperinsulin
emia and glucose intolerance in uremia.