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Diazoxide-mediated insulin suppression in obese men: a dose-response study
T Schreuder1, M Karreman, A Rennings
1Department of Internal Medicine, Ziekenhuis Rijnstate, Wagnerlaan 55, 6800 TA Arnhem, The Netherlands.
Background:
It has been suggested that diazoxide (DZX)-mediated insulin suppression may be useful to promote weight loss in obese subjects.
Aim:
To assess the DZX-dose range that is safe to use in obese hyperinsulinaemic men.
Methods:
Assessment of DZX efficacy and safety was based on plasma glucose and insulin responses to a standardized 500-kcal breakfast, taken on the sixth day of treatment. Basic information regarding the potential efficacy of DZX treatment was first evaluated in an open-label study in five non-obese men. Subsequently, a double-blind, randomized, placebo-controlled study was performed in 12 obese but otherwise healthy men, comparing placebo treatment with DZX in doses of 50, 75 and 100 mg three times daily for 6 days.
Results:
In non-obese subjects, DZX 50 mg decreased peak insulin levels by +/-28% and raised peak glucose concentration from 7.1 +/- 0.6 to 7.8 +/- 0.6 mmol/l (p < 0.05). DZX 100 mg reduced peak insulin levels by 45% and caused a rise in peak glucose levels from 7.1 +/- 0.6 to 9.0 +/- 0.9 mmol/l (p < 0.05). In obese men, the 50 and 75 mg doses had no significant effects on glucose or insulin levels. DZX 100 mg reduced the peak insulin levels and insulin area under the curve by +/-20% (p < 0.05) but did not affect fasting or postprandial glucose levels. The relatively limited insulin-suppressive effects in obese subjects were attributed to the low plasma DZX levels that were achieved in this group. For comparable doses, plasma DZX levels were about 30% lower in obese than in non-obese men. Plasma DZX levels were highly dependent on dose (p < 0.001) and body weight (p < 0.001). Ninety-two percent of the total variability in DZX levels was explained by these two parameters.
Conclusion:
DZX-mediated insulin suppression is dose dependent in normal and in obese men. However, the efficacy of DZX is much less in obese than in non-obese subjects. This is attributed to weight-dependent differences in distribution volume that lead to markedly lower plasma DZX levels in obese subjects. Weight-adjusted doses will be needed to achieve biologically effective plasma DZX levels. Extrapolation of the data suggests that effective insulin suppression in obese men will at least require a daily dose of 3.2-4.2 mg/kg.
Insights
Diazoxide (DZX) shows dose-dependent insulin suppression, but its efficacy is reduced in obese individuals due to lower plasma DZX levels. Weight-adjusted dosing is crucial for effective insulin suppression in obese men.
Area of Science:
- Pharmacology
- Endocrinology
- Metabolic Disorders
Background:
- Diazoxide (DZX) is investigated for its potential to suppress insulin and promote weight loss in obese individuals.
- Hyperinsulinemia in obese subjects necessitates exploring effective insulin-suppressing agents.
Purpose of the Study:
- To determine a safe and effective dose range of diazoxide (DZX) for obese, hyperinsulinemic men.
- To compare the efficacy and safety of DZX in obese versus non-obese individuals.
Main Methods:
- Open-label study in non-obese men to assess DZX efficacy.
- Double-blind, placebo-controlled trial in obese men using DZX doses of 50, 75, and 100 mg thrice daily for 6 days.
- Evaluation of plasma glucose and insulin responses to a standardized breakfast on day 6 of treatment.
Main Results:
- In non-obese men, DZX (50-100 mg) dose-dependently reduced peak insulin levels and increased peak glucose levels.
- In obese men, DZX doses of 50 and 75 mg showed no significant effects on glucose or insulin.
- DZX 100 mg reduced peak insulin by ~20% in obese men, but fasting/postprandial glucose remained unaffected. Obese subjects exhibited ~30% lower plasma DZX levels than non-obese subjects at comparable doses, attributed to weight-dependent distribution.
- Plasma DZX levels were significantly correlated with dose (p < 0.001) and body weight (p < 0.001).
Conclusions:
- Diazoxide-mediated insulin suppression is dose-dependent but significantly less effective in obese individuals compared to non-obese individuals.
- Lower plasma DZX levels in obese subjects, due to increased distribution volume, limit its efficacy.
- Weight-adjusted DZX doses, estimated at 3.2-4.2 mg/kg daily, are required to achieve effective insulin suppression in obese men.
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