G. Bonner et al., EFFECT OF BUNAZOSIN AND ATENOLOL ON GLUCOSE-METABOLISM IN OBESE, NONDIABETIC - PATIENTS WITH PRIMARY HYPERTENSION, Cardiovascular drugs and therapy, 11(1), 1997, pp. 21-26
Citations number
22
Categorie Soggetti
Pharmacology & Pharmacy","Cardiac & Cardiovascular System
Antihypertensive drugs, recommended by the World Health Organization f
or use in monotherapy, exert different effects on glucose and lipid me
tabolism. In our study we compared the effects of the beta-blocker ate
nolol (AT) and the alpha(1)-blocker bunazosin (BU) on glucose metaboli
sm. The doses administered were chosen to produce similar antihyperten
sive effects with both drugs. The study was conducted as a bicenter, p
arallel, controlled, and double-blind study. All patients suffered fro
m mild to moderate primary hypertension, were obese (body mass index >
26 kg/m(2)), but were nondiabetic. After a drug-free period of 4 weeks
, patients were treated either with 6 and 12 mg of bunazosin (n = 15)
or with 50 and 100 mg of atenolol (n = 17) once daily for 12 weeks. Gl
ucose metabolism was measured by the iv glucose tolerance test (GTT) a
nd the euglycemic hyperinsulinemic clamp test. The results show a simi
lar blood pressure reduction with both drugs. However, their effects o
n glucose metabolism were significantly (p < 0.05) different: The area
under the curve (AUC) of glucose in the iv GTT increased 26.8% during
atenolol treatment but decreased 30% during bunazosin treatment. The
same influence on the AUC of insulin was observed [AT +-478.5 +/- 441.
8 (+22%) vs. BU, -588.5 +/- 411.1 (-22%)]. Similar changes were found
in the glucose clamp test. The metabolic clearance rate increased 11.4
% during bunazosin use and decreased 8.4% during atenolol nse to the s
ame degree that the insulin sensitivity index changed (BU +13.2% vs. A
T -21.9%). The differences between the two treatment regimes were stat
istically significant (p < 0.05). These results in obese hypertensives
confirm the well-known negative effects of beta-blockers on glucose m
etabolism. Additionally, they demonstrate that an alpha(1)-blocker suc
h as bunazosin develops the same blood pressure-lowering effect as bet
ablockers, but with a significantly better profile with regard to gluc
ose metabolism. Therefore, the use of alpha(1)-blockers can be recomme
nded for obese hypertensives without any special care for glucose meta
bolism.