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Cardiovascular Effects of Chronic GIPR and GLP-1R Agonism in Lean and Diet-Induced Obese Mice : Sex Differences and Dose-Dependent Remodeling

Göktaş, Sevilay ŞahoŞlu ; Francisco, Annelise LU orcid ; Duarte, João M N LU orcid ; Meissner, Anja LU orcid and Magnusson, Martin LU orcid (2026) In American Journal of Physiology - Heart and Circulatory Physiology
Abstract

Glucose‑dependent insulinotropic polypeptide (GIP) and glucagon‑like peptide‑1 (GLP‑1) regulate metabolism and are increasingly targeted in therapies for type 2 diabetes and obesity. Although GLP‑1 receptor agonists confer cardiovascular benefits, the cardiovascular effects of GIP receptor (GIPR) stimulation remain controversial. This study aimed at defining the short-term cardiovascular consequences GIPR and GLP‑1 receptor (GLP‑1R) agonism in lean and diet‑induced obese mice, with emphasis on sex‑specific cardiac remodeling patterns. Male and female mice received continuous infusion of a GIPR or GLP‑1R agonist for one month at 0.1, 0.4, 0.8 and 1.0 mg/kg/day under chow feeding, or an effective dose of 0.8 mg/kg/day after 2 months of... (More)

Glucose‑dependent insulinotropic polypeptide (GIP) and glucagon‑like peptide‑1 (GLP‑1) regulate metabolism and are increasingly targeted in therapies for type 2 diabetes and obesity. Although GLP‑1 receptor agonists confer cardiovascular benefits, the cardiovascular effects of GIP receptor (GIPR) stimulation remain controversial. This study aimed at defining the short-term cardiovascular consequences GIPR and GLP‑1 receptor (GLP‑1R) agonism in lean and diet‑induced obese mice, with emphasis on sex‑specific cardiac remodeling patterns. Male and female mice received continuous infusion of a GIPR or GLP‑1R agonist for one month at 0.1, 0.4, 0.8 and 1.0 mg/kg/day under chow feeding, or an effective dose of 0.8 mg/kg/day after 2 months of high‑fat diet (HFD)-induced obesity. Cardiovascular phenotyping included tail‑cuff blood pressure, cardiac magnetic resonance imaging, metabolic testing, and assessment of plasma biomarkers of cardiac stress (ST2 or NT‑proBNP). In lean mice, GIPR agonism dose-dependently increased end‑diastolic volume (EDV), while GLP‑1R agonism increased end‑diastolic left‑ventricular (LV) mass in male mice, resulting in divergent remodeling patterns without affecting systolic function. These structural changes occurred without alterations in ST2 or NT‑proBNP, suggesting remodeling in the absence of overt myocardial stress. In obese mice, both agonists lowered mean arterial pressure and improved systolic function. GIPR agonism primarily increased LV volume in males, whereas GLP‑1R agonism increased LV mass in females. While ST2 levels were largely driven by HFD, NT‑proBNP was reduced by both treatments, consistent with improved cardiac loading conditions. In conclusion, short-term incretin receptor agonism induces distinct, context-dependent cardiovascular remodeling patterns that depended on receptor specificity, metabolic state, and sex. While both GIPR and GLP‑1R agonists exerted beneficial hemodynamic and functional effects in obesity, GIPR stimulation in lean mice increased ventricular volume and GLP‑1R stimulation increases mass without overt functional deterioration. These findings demonstrate distinct cardiac actions of incretin pathways and highlight the importance of metabolic context in their therapeutic effects.

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Contribution to journal
publication status
epub
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in
American Journal of Physiology - Heart and Circulatory Physiology
publisher
American Physiological Society
external identifiers
  • pmid:42734425
ISSN
1522-1539
DOI
10.1152/ajpheart.00204.2026
language
English
LU publication?
yes
id
6f4e6f2f-996a-47f6-9b78-98a9c0c60847
date added to LUP
2026-09-15 14:39:51
date last changed
2026-09-15 16:11:33
@article{6f4e6f2f-996a-47f6-9b78-98a9c0c60847,
  abstract     = {{<p>Glucose‑dependent insulinotropic polypeptide (GIP) and glucagon‑like peptide‑1 (GLP‑1) regulate metabolism and are increasingly targeted in therapies for type 2 diabetes and obesity. Although GLP‑1 receptor agonists confer cardiovascular benefits, the cardiovascular effects of GIP receptor (GIPR) stimulation remain controversial. This study aimed at defining the short-term cardiovascular consequences GIPR and GLP‑1 receptor (GLP‑1R) agonism in lean and diet‑induced obese mice, with emphasis on sex‑specific cardiac remodeling patterns. Male and female mice received continuous infusion of a GIPR or GLP‑1R agonist for one month at 0.1, 0.4, 0.8 and 1.0 mg/kg/day under chow feeding, or an effective dose of 0.8 mg/kg/day after 2 months of high‑fat diet (HFD)-induced obesity. Cardiovascular phenotyping included tail‑cuff blood pressure, cardiac magnetic resonance imaging, metabolic testing, and assessment of plasma biomarkers of cardiac stress (ST2 or NT‑proBNP). In lean mice, GIPR agonism dose-dependently increased end‑diastolic volume (EDV), while GLP‑1R agonism increased end‑diastolic left‑ventricular (LV) mass in male mice, resulting in divergent remodeling patterns without affecting systolic function. These structural changes occurred without alterations in ST2 or NT‑proBNP, suggesting remodeling in the absence of overt myocardial stress. In obese mice, both agonists lowered mean arterial pressure and improved systolic function. GIPR agonism primarily increased LV volume in males, whereas GLP‑1R agonism increased LV mass in females. While ST2 levels were largely driven by HFD, NT‑proBNP was reduced by both treatments, consistent with improved cardiac loading conditions. In conclusion, short-term incretin receptor agonism induces distinct, context-dependent cardiovascular remodeling patterns that depended on receptor specificity, metabolic state, and sex. While both GIPR and GLP‑1R agonists exerted beneficial hemodynamic and functional effects in obesity, GIPR stimulation in lean mice increased ventricular volume and GLP‑1R stimulation increases mass without overt functional deterioration. These findings demonstrate distinct cardiac actions of incretin pathways and highlight the importance of metabolic context in their therapeutic effects.</p>}},
  author       = {{Göktaş, Sevilay ŞahoŞlu and Francisco, Annelise and Duarte, João M N and Meissner, Anja and Magnusson, Martin}},
  issn         = {{1522-1539}},
  language     = {{eng}},
  month        = {{09}},
  publisher    = {{American Physiological Society}},
  series       = {{American Journal of Physiology - Heart and Circulatory Physiology}},
  title        = {{Cardiovascular Effects of Chronic GIPR and GLP-1R Agonism in Lean and Diet-Induced Obese Mice : Sex Differences and Dose-Dependent Remodeling}},
  url          = {{http://dx.doi.org/10.1152/ajpheart.00204.2026}},
  doi          = {{10.1152/ajpheart.00204.2026}},
  year         = {{2026}},
}