Literature DB >> 28128026

Amide proton transfer-weighted MRI detection of traumatic brain injury in rats.

Hong Zhang1,2, Wenzhu Wang3,4, Shanshan Jiang1, Yi Zhang1, Hye-Young Heo1, Xianlong Wang1, Yun Peng2, Jian Wang3, Jinyuan Zhou1.   

Abstract

The purpose of this study was to explore the capability and uniqueness of amide proton transfer-weighted (APTw) imaging in the detection of primary and secondary injury after controlled cortical impact (CCI)-induced traumatic brain injury (TBI) in rats. Eleven adult rats had craniotomy plus CCI surgery under isoflurane anesthesia. Multi-parameter MRI data were acquired at 4.7 T, at eight time points (1, 6 h, and 1, 2, 3, 7, 14, and 28 days after TBI). At one and six hours post-injury, average APTw signal intensities decreased significantly in the impacted and peri-lesional areas due to tissue acidosis. A slightly high APTw signal was seen in the core lesion area with respect to the peri-lesional area, which was due to hemorrhage, as shown by T2*w. After the initial drop, the APTw signals dramatically increased in some peri-lesional areas at two and three days post-injury, likely due to the secondary inflammatory response. The use of APTw MRI has the potential to introduce a novel molecular neuroimaging approach for the simultaneous detection of ischemia, hemorrhage, and neuroinflammation in TBI.

Entities:  

Keywords:  Amide proton transfer-weighted imaging; hemorrhage; ischemia; neuroinflammation; traumatic brain injury

Mesh:

Substances:

Year:  2017        PMID: 28128026      PMCID: PMC5624391          DOI: 10.1177/0271678X17690165

Source DB:  PubMed          Journal:  J Cereb Blood Flow Metab        ISSN: 0271-678X            Impact factor:   6.200


  54 in total

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5.  Improving Amide Proton Transfer-Weighted MRI Reconstruction Using T2-Weighted Images.

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9.  Amide Proton Transfer-Weighted (APTw) Imaging of Intracranial Infection in Children: Initial Experience and Comparison with Gadolinium-Enhanced T1-Weighted Imaging.

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Review 10.  Current understanding of neuroinflammation after traumatic brain injury and cell-based therapeutic opportunities.

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