[HTML][HTML] Rapamycin suppresses experimental aortic aneurysm growth

DM Lawrence, RS Singh, DP Franklin, DJ Carey… - Journal of vascular …, 2004 - Elsevier
DM Lawrence, RS Singh, DP Franklin, DJ Carey, JR Elmore
Journal of vascular surgery, 2004Elsevier
OBJECTIVE: Inflammatory modulators are important in the pathogenesis of aneurysmal
disease. Gene expression profiling of experimental abdominal aortic aneurysm (AAA) tissue
demonstrated upregulation of the FK506BP12 (rapamycin binding protein) gene product.
Rapamycin is a potent immunosuppressor that prevents recurrent stenosis. However, its
effect on aneurysm formation has not been studied. We therefore examined the effect of
rapamycin in an experimental rat AAA model. METHODS: Adult male Wistar rats underwent …
OBJECTIVE
Inflammatory modulators are important in the pathogenesis of aneurysmal disease. Gene expression profiling of experimental abdominal aortic aneurysm (AAA) tissue demonstrated upregulation of the FK506BP12 (rapamycin binding protein) gene product. Rapamycin is a potent immunosuppressor that prevents recurrent stenosis. However, its effect on aneurysm formation has not been studied. We therefore examined the effect of rapamycin in an experimental rat AAA model.
METHODS
Adult male Wistar rats underwent elastase infusion into isolated infrarenal aortas to create experimental aneurysms. Rats were randomized to receive either rapamycin or placebo via gastric lavage daily starting on the day of surgery. On postoperative day 7 the aneurysm was measured, the infrarenal aorta was harvested, and the rats were euthanized. NFκB was measured with Western blotting as a marker of inflammation. Matrix metalloproteinase (MMP)–9 protein levels were measured. Hematoxylin-eosin and elastin staining were used to examine tissue inflammation and elastin preservation.
RESULTS
Aneurysms were significantly smaller in diameter in the rapamycin-treated group (3.3 ± 0.7 mm vs 4.5 ± 0.5 mm; P < .0001). NFκB levels were significantly reduced by 64% ± 14% in rapamycin-treated aortas (P = .023). MMP-9 was reduced in rapamycin-treated aortas by 54% ± 22% (P = .043). Hematoxylin-eosin and elastin staining showed no changes in inflammatory infiltrate or degradation of elastin fibers in elastase-infused aortic segments in rapamycin-treated rats.
CONCLUSION
Rapamycin significantly reduces the rate of aneurysm expansion in the experimental AAA rat model by 40%. Biochemical evidence suggests that this is related to suppression of inflammatory signaling and decreased MMP-9 levels. Rapamycin could provide a new treatment for small aneurysms.
Elsevier