Troglitazone Amplifies Counterregulatory Responses to Hypoglycemia in Nondiabetic Subjects1
Abstract
As insulin sensitizers, thiazolidinediones could affect the hormonal counterregulatory response to hypoglycemia via the modulatory effect of insulin on counterregulation. In addition, recent studies suggest that thiazolidinediones may influence key steps in glucose sensing and glucoregulatory hormone secretion. We therefore evaluated the effects of a short course of troglitazone on counterregulatory hormones in response to mild hypoglycemia in eight lean nondiabetic subjects. Subjects received either troglitazone (400 mg/day) or placebo for 7 days before stepped hypoglycemia clamp studies (5.0, 4.4, 3.9, and 3.3 mmol/L target plasma glucose steps, 50 min each). The glycemic thresholds for secretion of epinephrine (3.77 +/- 0.05 mmol/L) and glucagon (3.83 +/- 0.11 mmol/L) were reset to a higher plasma glucose concentration after troglitazone [4.05 +/- 0.05 mmol/L (P = 0.003) and 4.10 +/- 0.05 mmol/L (P = 0.03), respectively]. In addition, the magnitude of the rise in epinephrine and glucagon concentrations was higher with troglitazone (28% and 11%, respectively; P < 0.05 for both), whereas plasma norepinephrine, GH, and cortisol were comparable in both sets of studies. Endogenous glucose production, measured with [3-(3)H]glucose, rose by 33% (P < 0.05) in the troglitazone studies compared with 17% (P = NS) after placebo. We conclude that thiazolidinediones may induce an amplification of the counterregulatory response to hypoglycemia characterized by a shift in the glycemic threshold for and an increase in the magnitude of glucagon and epinephrine secretion, and subsequent activation of glucose production.
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The large variability in glycaemic thresholds in type 1 diabetes can probably be explained by different prior hypoglycaemia exposure rates between individuals, the loss of glucagon secretion within years after diagnosis, blunted catecholamine responses and impaired hypoglycaemic awareness.
“This large variability in glycaemic thresholds in type 1 diabetes can probably be explained by different prior hypoglycaemia exposure rates between individuals [7], the loss of glucagon secretion within years after diagnosis [9, 10], blunted catecholamine responses and impaired hypoglycaemic awareness [11, 12].”
From Glycaemic thresholds for counterregulatory hormone and symptom responses to hypoglycaemia in people with and without type 1 diabetes: a systematic review (2022) · cites this paper as [12]
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References 51 · Cited by 11
- Authors
- Gabriely, I., Wozniak, R., Hawkins, M., & Shamoon, H.
- Affiliations
- Albert Einstein College of Medicine (US)
- Venue
- The Journal of Clinical Endocrinology & Metabolism
- Publisher
- The Endocrine Society
- Published
- 2001-02
- Volume
- 86
- Issue
- 2
- Pages
- 521-528
- ISSN
- 0021-972X (ISSN-L)
- 1945-7197
- OpenAlex
- W2072457904
- Cited by
- 11
- References
- 51
- Citations by year
- 2025: 1 · 2022: 1 · 2017: 1 · 2015: 1
- FWCI
- 0.68
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Clinical Endocrinology & Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Center for Research Resources (M01RR012248, RR-12248)
- NIH Clinical Center
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Keywords
- troglitazone, thiazolidinediones, hypoglycemia, counterregulatory response, epinephrine, glucagon, glycemic thresholds, endogenous glucose production, insulin sensitizers, non-diabetic patients, glucose detection
- MeSH terms
- Troglitazone, Insulin Secretion, Adult, Blood Glucose, Chromans, Epinephrine, Female, Glucagon, Homeostasis, Humans, Hydrocortisone, Hypoglycemia, Hypoglycemic Agents, Insulin, Male, Norepinephrine, Reference Values, Thiazoles, Time Factors, Glucose Clamp Technique, Human Growth Hormone, Thiazolidinediones
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