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实验性腹主动脉瘤的分子成像

Molecular imaging of experimental abdominal aortic aneurysms.

作者信息

Ramaswamy Aneesh K, Hamilton Mark, Joshi Rucha V, Kline Benjamin P, Li Rui, Wang Pu, Goergen Craig J

机构信息

Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN 47907, USA.

出版信息

ScientificWorldJournal. 2013 Apr 23;2013:973150. doi: 10.1155/2013/973150. Print 2013.

Abstract

Current laboratory research in the field of abdominal aortic aneurysm (AAA) disease often utilizes small animal experimental models induced by genetic manipulation or chemical application. This has led to the use and development of multiple high-resolution molecular imaging modalities capable of tracking disease progression, quantifying the role of inflammation, and evaluating the effects of potential therapeutics. In vivo imaging reduces the number of research animals used, provides molecular and cellular information, and allows for longitudinal studies, a necessity when tracking vessel expansion in a single animal. This review outlines developments of both established and emerging molecular imaging techniques used to study AAA disease. Beyond the typical modalities used for anatomical imaging, which include ultrasound (US) and computed tomography (CT), previous molecular imaging efforts have used magnetic resonance (MR), near-infrared fluorescence (NIRF), bioluminescence, single-photon emission computed tomography (SPECT), and positron emission tomography (PET). Mouse and rat AAA models will hopefully provide insight into potential disease mechanisms, and the development of advanced molecular imaging techniques, if clinically useful, may have translational potential. These efforts could help improve the management of aneurysms and better evaluate the therapeutic potential of new treatments for human AAA disease.

摘要

目前腹主动脉瘤(AAA)疾病领域的实验室研究通常利用通过基因操作或化学方法诱导的小动物实验模型。这促使了多种高分辨率分子成像方式的使用和发展,这些成像方式能够追踪疾病进展、量化炎症作用并评估潜在治疗方法的效果。体内成像减少了所用实验动物的数量,提供分子和细胞信息,并允许进行纵向研究,这在追踪单个动物血管扩张时是必要的。本综述概述了用于研究AAA疾病的既定和新兴分子成像技术的发展情况。除了用于解剖成像的典型方式,包括超声(US)和计算机断层扫描(CT)外,以往的分子成像研究还使用了磁共振(MR)、近红外荧光(NIRF)、生物发光、单光子发射计算机断层扫描(SPECT)和正电子发射断层扫描(PET)。小鼠和大鼠AAA模型有望为潜在疾病机制提供见解,而先进分子成像技术的发展,如果具有临床实用性,可能具有转化潜力。这些努力有助于改善动脉瘤的管理,并更好地评估针对人类AAA疾病的新治疗方法的治疗潜力。

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