Abstract 4369369: Sex Differences in GLP-1 Receptor Mediated Effects on Exercising Blood Pressure Responses in Peripheral Artery Diseas

Background: Glucagon-like peptide-1 receptor agonists (GLP-1RA) are currently prescribed for diabetes and obesity and may also have beneficial effects for atherosclerotic conditions such as peripheral artery disease (PAD). We recently reported that the GLP-1RA liraglutide (lira) attenuated the exaggerated BP response to exercise in both male and female normoglycemic, non-obese rats with chronically ligated femoral arteries (PAD model). Whether the effect of lira was mediated entirely through GLP-1R stimulation or also involved a non-receptor dependent mechanism is unknown. Purpose: We investigated whether the attenuating effect of lira on the blood pressure response to treadmill exercise we previously reported in “ligated” rats was produced via a GLP-1 receptor dependent mechanism. Methods: Male (n=4) and female (n=4) rats had both femoral arteries ligated ~72 hrs prior to experiments. On experiment day, a carotid artery and jugular vein were cannulated for BP measurement and drug administration, respectively. Treadmill exercise was performed (4 min; 15 m/min, 1° incline) while BP was measured continuously. The GLP-1R antagonist exendin-3 (Ex-3, 400mg/kg) was infused followed 10 min later by lira (20mg /kg). 20 min after lira infusion, a second treadmill exercise bout was performed. The BP response to exercise before (control) and after (Ex-3+lira) drug infusions was compared between conditions and across sexes. Data are mean±SEM. Results: The mean arterial pressure (MAP) response to exercise was significantly reduced following Ex-3+lira compared to control in female rats (Peak ΔMAP control: 22±3; Ex-3+Lira: 17±2mmHg; P=0.013*). However, this effect of lira was significantly reduced when compared to our previous experiments in which lira was infused alone. There was no effect of Ex-3+lira on the MAP response to exercise in male rats ( n =4, Peak ΔMAP control: 24±2; Ex-3+Lira: 25±1mmHg; P=0.499). Conclusions: The attenuating effect of lira on the BP response to exercise was abolished by prior GLP-1 receptor blockade in ligated male rats but not female rats. Thus, the attenuating effect of lira on the BP response to exercise in male rats is entirely GLP-1 receptor dependent whereas in female rats the effect is mediated by both GLP-1R dependent and independent mechanisms.

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Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4369369
Primary Topic
Peripheral Artery Disease Management
Type
article
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article

Abstract 4369369: Sex Differences in GLP-1 Receptor Mediated Effects on Exercising Blood Pressure Responses in Peripheral Artery Diseas

Steven W. Copp, Cherise A. Rowan, Britton Scheuermann, Carl J. Ade et al.
Circulation
Peripheral Artery Disease Management
article

Abstract 4369369: Sex Differences in GLP-1 Receptor Mediated Effects on Exercising Blood Pressure Responses in Peripheral Artery Diseas

Steven W. Copp, Cherise A. Rowan, Britton Scheuermann, Carl J. Ade, Ashley Baranczuk, Raimi Carroll
article en

Abstract

Background: Glucagon-like peptide-1 receptor agonists (GLP-1RA) are currently prescribed for diabetes and obesity and may also have beneficial effects for atherosclerotic conditions such as peripheral artery disease (PAD). We recently reported that the GLP-1RA liraglutide (lira) attenuated the exaggerated BP response to exercise in both male and female normoglycemic, non-obese rats with chronically ligated femoral arteries (PAD model). Whether the effect of lira was mediated entirely through GLP-1R stimulation or also involved a non-receptor dependent mechanism is unknown. Purpose: We investigated whether the attenuating effect of lira on the blood pressure response to treadmill exercise we previously reported in “ligated” rats was produced via a GLP-1 receptor dependent mechanism. Methods: Male (n=4) and female (n=4) rats had both femoral arteries ligated ~72 hrs prior to experiments. On experiment day, a carotid artery and jugular vein were cannulated for BP measurement and drug administration, respectively. Treadmill exercise was performed (4 min; 15 m/min, 1° incline) while BP was measured continuously. The GLP-1R antagonist exendin-3 (Ex-3, 400mg/kg) was infused followed 10 min later by lira (20mg /kg). 20 min after lira infusion, a second treadmill exercise bout was performed. The BP response to exercise before (control) and after (Ex-3+lira) drug infusions was compared between conditions and across sexes. Data are mean±SEM. Results: The mean arterial pressure (MAP) response to exercise was significantly reduced following Ex-3+lira compared to control in female rats (Peak ΔMAP control: 22±3; Ex-3+Lira: 17±2mmHg; P=0.013*). However, this effect of lira was significantly reduced when compared to our previous experiments in which lira was infused alone. There was no effect of Ex-3+lira on the MAP response to exercise in male rats ( n =4, Peak ΔMAP control: 24±2; Ex-3+Lira: 25±1mmHg; P=0.499). Conclusions: The attenuating effect of lira on the BP response to exercise was abolished by prior GLP-1 receptor blockade in ligated male rats but not female rats. Thus, the attenuating effect of lira on the BP response to exercise in male rats is entirely GLP-1 receptor dependent whereas in female rats the effect is mediated by both GLP-1R dependent and independent mechanisms.

CirculationVol. 152(Suppl_3)
Kansas State University (US)
Openalex Percentile: Top 50%
Peripheral Artery Disease Management
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