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Dissecting abdominal aortic aneurysm in angiotensin II-infused mice: the importance of imaging

(2015) CURRENT PHARMACEUTICAL DESIGN. 21(28). p.4049-4060
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Abstract
Introduction. Since the initial publication in 2000, Angiotensin II-infused mice have become one of the most popular models to study abdominal aortic aneurysm in a pre-clinical setting. We recently used phase contrast X-ray based computed tomography to demonstrate that these animals develop an apparent luminal dilatation and an intramural hematoma, both related to mural ruptures in the tunica media in the vicinity of suprarenal side branches. Aims. The aim of this narrative review was to provide an extensive overview of small animal applicable techniques that have provided relevant insight into the pathogenesis and morphology of dissecting AAA in mice, and to relate findings from these techniques to each other and to our recent PCXTM-based results. Combining insights from recent and consolidated publications we aimed to enhance our understanding of dissecting AAA morphology and anatomy. Results and conclusion. We analyzed in vivo and ex vivo images of aortas obtained from macroscopic anatomy, histology, high-frequency ultrasound, contrast-enhanced micro-CT, micro-MRI and PCXTM. We demonstrate how in almost all publications the aorta has been subdivided into a part in which an intact lumen lies adjacent to a remodeled wall/hematoma, and a part in which elastic lamellae are ruptured and the lumen appears to be dilated. We show how the novel paradigm fits within the existing one, and how 3D images can explain and connect previously published 2D structures. We conclude that PCXTM-based findings are in line with previous results, and all evidence points towards the fact that dissecting AAAs in Angiotensin II-infused mice are actually caused by ruptures of the tunica media in the immediate vicinity of small side branches.
Keywords
DENSITY-LIPOPROTEIN, MURINE MODEL, REDUCES ATHEROSCLEROSIS, MOUSE MODEL, E-DEFICIENT MICE, mouse model, angiotensin II, MRI, micro-CT, PCXTM, high-frequency ultrasound, dissecting aneurysm, small animal imaging, Abdominal aortic aneurysms, PROGRESSION, RUPTURE, INHIBITOR, INFLAMMATION, DILATATION

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Citation

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Chicago
Trachet, Bram, Rodrigo Fraga-Silva, Alessandra Piersigilli, Patrick Segers, and Nikolaos Stergiopulos. 2015. “Dissecting Abdominal Aortic Aneurysm in Angiotensin II-infused Mice: The Importance of Imaging.” Current Pharmaceutical Design 21 (28): 4049–4060.
APA
Trachet, B., Fraga-Silva, R., Piersigilli, A., Segers, P., & Stergiopulos, N. (2015). Dissecting abdominal aortic aneurysm in angiotensin II-infused mice: the importance of imaging. CURRENT PHARMACEUTICAL DESIGN, 21(28), 4049–4060.
Vancouver
1.
Trachet B, Fraga-Silva R, Piersigilli A, Segers P, Stergiopulos N. Dissecting abdominal aortic aneurysm in angiotensin II-infused mice: the importance of imaging. CURRENT PHARMACEUTICAL DESIGN. Bentham; 2015;21(28):4049–60.
MLA
Trachet, Bram, Rodrigo Fraga-Silva, Alessandra Piersigilli, et al. “Dissecting Abdominal Aortic Aneurysm in Angiotensin II-infused Mice: The Importance of Imaging.” CURRENT PHARMACEUTICAL DESIGN 21.28 (2015): 4049–4060. Print.
@article{6922232,
  abstract     = {Introduction. Since the initial publication in 2000, Angiotensin II-infused mice have become one of the most popular models to study abdominal aortic aneurysm in a pre-clinical setting. We recently used phase contrast X-ray based computed tomography to demonstrate that these animals develop an apparent luminal dilatation and an intramural hematoma, both related to mural ruptures in the tunica media in the vicinity of suprarenal side branches. 

Aims. The aim of this narrative review was to provide an extensive overview of small animal applicable techniques that have provided relevant insight into the pathogenesis and morphology of dissecting AAA in mice, and to relate findings from these techniques to each other and to our recent PCXTM-based results. Combining insights from recent and consolidated publications we aimed to enhance our understanding of dissecting AAA morphology and anatomy. 

Results and conclusion. We analyzed in vivo and ex vivo images of aortas obtained from macroscopic anatomy, histology, high-frequency ultrasound, contrast-enhanced micro-CT, micro-MRI and PCXTM. We demonstrate how in almost all publications the aorta has been subdivided into a part in which an intact lumen lies adjacent to a remodeled wall/hematoma, and a part in which elastic lamellae are ruptured and the lumen appears to be dilated. We show how the novel paradigm fits within the existing one, and how 3D images can explain and connect previously published 2D structures. We conclude that PCXTM-based findings are in line with previous results, and all evidence points towards the fact that dissecting AAAs in Angiotensin II-infused mice are actually caused by ruptures of the tunica media in the immediate vicinity of small side branches.},
  author       = {Trachet, Bram and Fraga-Silva, Rodrigo and Piersigilli, Alessandra and Segers, Patrick and Stergiopulos, Nikolaos},
  issn         = {1381-6128},
  journal      = {CURRENT PHARMACEUTICAL DESIGN},
  keyword      = {DENSITY-LIPOPROTEIN,MURINE MODEL,REDUCES ATHEROSCLEROSIS,MOUSE MODEL,E-DEFICIENT MICE,mouse model,angiotensin II,MRI,micro-CT,PCXTM,high-frequency ultrasound,dissecting aneurysm,small animal imaging,Abdominal aortic aneurysms,PROGRESSION,RUPTURE,INHIBITOR,INFLAMMATION,DILATATION},
  language     = {eng},
  number       = {28},
  pages        = {4049--4060},
  publisher    = {Bentham},
  title        = {Dissecting abdominal aortic aneurysm in angiotensin II-infused mice: the importance of imaging},
  url          = {http://dx.doi.org/10.2174/1381612821666150826094746},
  volume       = {21},
  year         = {2015},
}

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