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Beneficial Effect of Diazoxide in Obese Hyperinsulinemic Adults1
Hyperinsulinemia, insulin resistance, and increased adipose tissue are hallmarks of the obesity state in both humans and experimental animals. The role of hyperinsulinemia as a possible preceding event in the development of obesity has been proposed. We previously demonstrated that administration of...
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Published in: | The journal of clinical endocrinology and metabolism 1998-06, Vol.83 (6), p.1911-1915 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Hyperinsulinemia, insulin resistance, and increased adipose tissue are
hallmarks of the obesity state in both humans and experimental animals.
The role of hyperinsulinemia as a possible preceding event in the
development of obesity has been proposed. We previously demonstrated
that administration of diazoxide (DZ), an inhibitor of insulin
secretion, to obese hyperinsulinemic Zucker rats resulted in less
weight gain, enhanced insulin sensitivity, and improved glucose
tolerance. Assuming that hyperinsulinemia plays a major role in the
development of human obesity, then its reversal should have therapeutic
potential. To test this hypothesis, we conducted a randomized
placebo-controlled trial in 24 hyperinsulinemic adults [body mass
index (BMI) > 30 kg/m2]. All subjects were placed on a
low-calorie (1260 for females and 1570 for males) Optifast (Sandoz,
Minneapolis, MN) diet. After an initial 1-week lead-in period, 12
subjects (mean ± se for age and BMI, 31 ± 1 and
40 ± 2, respectively) received DZ (2 mg/kg BW·day; maximum, 200
mg/day, divided into 3 doses) for 8 weeks; and 12 subjects (mean±
se for age and BMI, 28 ± 1 and 43 ± 1,
respectively) received placebo. Compared with the placebo group, DZ
subjects had greater weight loss (9.5 ± 0.69% vs.
4.6 ± 0.61%, P < 0.001), greater decrease
in body fat (P < 0.01), greater increase in
fat-free mass to body fat ratio (P < 0.01), and
greater attenuation of acute insulin response to glucose
(P < 0.01). However, there was no significant
difference in insulin sensitivity and glucose effectiveness, as
determined by the insulin-modified iv glucose tolerance test
(Bergman’s minimal model) and no significant difference in
glycohemoglobin values. Conclusion: 8 weeks treatment with DZ had a
significant antiobesity effect in hyperinsulinemic obese adults without
inducing hyperglycemia. |
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ISSN: | 0021-972X 1945-7197 |
DOI: | 10.1210/jcem.83.6.4852 |