Effects of prolonged exendin-4 administration on hypothalamic-pituitary-adrenal axis activity and water balance.
Am J Physiol Endocrinol Metab · 2013
Last updated 2026-05-28In a study on rats, daily injections of the GLP-1 drug exendin-4 (5 micrograms per kilogram) for at least 7 days led to increased stress hormone activity, disrupted daily hormone rhythms, and enlarged adrenal glands. The rats also drank and urinated more—three times and one and a half times their normal amounts, respectively—though the increased drinking stopped after removal of the adrenal glands.
AI summary of the abstract below.
| Journal | Am J Physiol Endocrinol Metab, 2013 |
|---|---|
| Citations | 26 |
| Relative citation ratio | 0.90 |
| NIH percentile | 47 |
| Molecules | — |
Abstract
Exendin-4 (Ex-4) is a natural agonist of the glucagon-like peptide-1 (GLP-1) receptor, currently being used as a treatment for type 2 diabetes mellitus due to its insulinotropic properties. Previous studies have revealed that acute administration of both GLP-1 and, in particular, Ex-4 potently stimulates hypothalamic-pituitary-adrenal (HPA) axis activity. In this work, the effects of prolonged Ex-4 exposure on HPA function were explored. To this end, Sprague-Dawley rats were subjected to a daily regimen of two Ex-4 injections (5 μg/kg sc) for a minimum of 7 days. We found that subchronic Ex-4 administration produced a number of effects that resemble chronic stress situations, including hyperactivation of the HPA axis during the trough hours, disruption of glucocorticoid circadian secretion, hypertrophy of the adrenal gland, decreased adrenal gland sensitivity, impaired pituitary-adrenal stress responses, and reductions in both food intake and body weight. In addition, a threefold increase in diuresis was observed followed by a 1.5-fold increase in water intake; these latter effects were abolished by adrenalectomy. Together, these findings indicate that Ex-4 induces a profound dysregulation of HPA axis activity that may also affect renal function.
Verbatim abstract via PubMed 23531615 ↗