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A Calcium Phosphate-Induced Mouse Abdominal Aortic Aneurysm Model
Published on: November 18, 2022
Colchicine Does Not Reduce Abdominal Aortic Aneurysm Growth in a Mouse Model
James Phie1, Shivshankar Thanigaimani1, Pacific Huynh1
1The Vascular Biology Unit, Queensland Research Centre for Peripheral Vascular Disease, James Cook University, Townsville, Queensland, Australia.
The nacht domain, leucine-rich repeat, and pyrin domain-containing protein 3 (NLRP3) inflammasome is activated in a mouse model of abdominal aortic aneurysm (AAA). However, colchicine did not limit AAA growth in this study.
Area of Science:
- Cardiovascular Research
- Inflammation Biology
- Atherosclerosis Research
Background:
- The nacht domain, leucine-rich repeat, and pyrin domain-containing protein 3 (NLRP3) inflammasome is implicated in abdominal aortic aneurysm (AAA) pathogenesis.
- Its precise role in AAA development and progression remains to be fully elucidated.
Purpose of the Study:
- To investigate NLRP3 inflammasome activation in a murine model of AAA.
- To evaluate the efficacy of colchicine, an inflammasome inhibitor, in limiting AAA expansion.
Main Methods:
- Abdominal aortic aneurysm (AAA) was induced in C57BL6/J mice using elastase and 3-aminopropionitrile (E-BAPN).
- Inflammasome activation markers (IL-1β, caspase-1) and aortic diameter were assessed.
- Mice received daily oral colchicine or vehicle control for 13 weeks post-AAA induction.
Main Results:
- NLRP3 inflammasome markers (IL-1β and caspase-1) were significantly upregulated in AAA samples compared to controls.
- Aortic diameter significantly increased in mice with induced AAA versus sham controls.
- Colchicine treatment did not significantly reduce the rate of aortic diameter increase.
Conclusions:
- The NLRP3 inflammasome is activated during the development of AAA in this mouse model.
- Daily oral administration of colchicine failed to attenuate AAA growth.
- Further research is needed to explore therapeutic strategies targeting the NLRP3 inflammasome in AAA.
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