Growth hormone treatment does not augment the anti-diabetic effects of liraglutide in UCD-T2DM rats.
Endocrinol Diabetes Metab · 2023
Last updated 2026-05-28In a study on rats with obesity and insulin resistance, daily liraglutide treatment (0.2 mg/kg) delayed the onset of type 2 diabetes by over 4 months, reduced body weight, improved blood sugar control, and lowered fat levels in the liver and blood. Adding growth hormone (0.3 mg/kg) did not enhance these benefits, as it did not improve diabetes-related outcomes or blood sugar control beyond what liraglutide alone provided.
AI summary of the abstract below.
| Journal | Endocrinol Diabetes Metab, 2023 |
|---|---|
| Citations | 1 |
| Relative citation ratio | 0.14 |
| NIH percentile | 10 |
| Molecules | liraglutide |
| Conditions studied | Type 2 Diabetes |
Abstract
INTRODUCTION: The incretin hormone glucagon-like peptide-1 (GLP-1) slows gastric emptying, increases satiety and enhances insulin secretion. GLP-1 receptor agonists, such as liraglutide, are used therapeutically in humans to improve glycaemic control and delay the onset of type 2 diabetes mellitus (T2DM). In UCD-T2DM rats, a model of polygenic obesity and insulin resistance, we have previously reported that daily liraglutide administration delayed diabetes onset by >4 months. Growth hormone (GH) may exert anti-diabetic effects, including increasing β-cell mass and insulin secretion, while disrupting GH signalling in mice reduces both the size and number of pancreatic islets. We therefore hypothesized that GH supplementation would augment liraglutide's anti-diabetic effects.
METHODS: Male UCD-T2DM rats were treated daily with GH (0.3 mg/kg) and/or liraglutide (0.2 mg/kg) from 2 months of age. Control (vehicle) and food-restricted (with food intake matched to liraglutide-treated rats) groups were also studied. The effects of treatment on diabetes onset and weight gain were assessed, as well as measures of glucose tolerance, lipids and islet morphology.
RESULTS: Liraglutide treatment significantly reduced food intake and body weight and improved glucose tolerance and insulin sensitivity, relative to controls. After 4.5 months, none of the liraglutide-treated rats had developed T2DM (overall p = .019). Liraglutide-treated rats also displayed lower fasting triglyceride (TG) concentrations and lower hepatic TG content, compared to control rats. Islet morphology was improved in liraglutide-treated rats, with significantly increased pancreatic insulin content (p < .05 vs. controls). Although GH treatment tended to increase body weight (and gastrocnemius muscle weight), there were no obvious effects on diabetes onset or other diabetes-related outcomes.
CONCLUSION: GH supplementation did not augment the anti-diabetic effects of liraglutide.
Verbatim abstract via PubMed 36480511 ↗
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