Pulmonary perfusion imaging in the rodent lung using dynamic contrast-enhanced MRI

With the development of various models of pulmonary disease, there is tremendous interest in quantitative regional assessment of pulmonary function. While ventilation imaging has been addressed to a certain extent, perfusion imaging for small animals has not kept pace. In humans and large animals pe...

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Bibliographic Details
Published inMagnetic resonance in medicine Vol. 59; no. 2; pp. 289 - 297
Main Authors Mistry, Nilesh N., Pollaro, James, Song, Jiayu, De Lin, Ming, Johnson, G. Allan
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.02.2008
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Summary:With the development of various models of pulmonary disease, there is tremendous interest in quantitative regional assessment of pulmonary function. While ventilation imaging has been addressed to a certain extent, perfusion imaging for small animals has not kept pace. In humans and large animals perfusion can be assessed using dynamic contrast‐enhanced (DCE) MRI with a single bolus injection of a gadolinium (Gd)‐based contrast agent. But the method developed for the clinic cannot be translated directly to image the rodent due to the combined requirements of higher spatial and temporal resolution. This work describes a novel image acquisition technique staggered over multiple, repeatable bolus injections of contrast agent using an automated microinjector, synchronized with image acquisition to achieve dynamic first‐pass contrast enhancement in the rat lung. This allows dynamic first‐pass imaging that can be used to quantify pulmonary perfusion. Further improvements are made in the spatial and temporal resolution by combining the multiple injection acquisition method with Interleaved Radial Imaging and “Sliding window‐keyhole” reconstruction (IRIS). The results demonstrate a simultaneous increase in spatial resolution (<200 μm) and temporal resolution (<200 ms) over previous methods, with a limited loss in signal‐to‐noise‐ratio. Magn Reson Med 59:289–297, 2008. © 2008 Wiley‐Liss, Inc.
Bibliography:NCRR - No. P41-RR005959
ArticleID:MRM21353
istex:F96D1BD18851D5483F2153BBB2C0800E45454138
National Cancer Institute (NCI) - No. U24 CA092656
ark:/67375/WNG-92M8ZM6P-P
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0740-3194
1522-2594
DOI:10.1002/mrm.21353