In rabbits, lixisenatide increased fibrotic plaque components versus saline: 66.30 ± 2.06% versus 75.14 ± 2.62% in the reported pair (p < 0.01).
In plain wordsIn rabbits, lixisenatide increased fibrotic plaque components compared with saline.
- Peptide
- Lixisenatide
- Outcome
- IncreaseIVUS fibrotic plaque area
- Study
Rabbitn = 10
Watanabe heritable hyperlipidemic rabbits- Comparator
- Normal saline
- Outcome group
- Atherosclerotic plaque composition · Cardiovascular
- Studied dose
- 30 nmoL/kg/day · osmotic pump · 12 weeksAs given in this study (Rabbit).
Source sentences
iMAP-IVUS analysis revealed larger fibrotic plaque components and smaller necrotic and calcified plaque components in the GLP-1 group than in the control group; %fibrotic area: 66.30 ± 2.06% vs. 75.14 ± 2.62%, p < 0.01,
2 context sentences(design, population, supporting numbers)
After confirmation of atherosclerotic plaques in brachiocephalic arteries by iMap intravascular ultrasound (iMAP-IVUS), GLP-1 receptor agonist lixisenatide was administered to WHHL rabbits at 30 nmoL/kg/day for 12 weeks by osmotic pump.
An equal volume of normal saline was administered in a control group.