scholarly journals In vivo USPIO Magnetic Resonance Imaging Shows That Minocycline Mitigates Macrophage Recruitment to a Peripheral Nerve Injury

2012 ◽  
Vol 8 ◽  
pp. 1744-8069-8-49 ◽  
Author(s):  
Pejman Ghanouni ◽  
Deepak Behera ◽  
Jin Xie ◽  
Xiaoyuan Chen ◽  
Michael Moseley ◽  
...  
Neurosurgery ◽  
1994 ◽  
Vol 35 (6) ◽  
pp. 1077???1086 ◽  
Author(s):  
G. Alexander West ◽  
David R. Haynor ◽  
Robert Goodkin ◽  
Jay S. Tsuruda ◽  
Andrew D. Bronstein ◽  
...  

Neurosurgery ◽  
1994 ◽  
Vol 35 (6) ◽  
pp. 1077-1086 ◽  
Author(s):  
G. Alexander West ◽  
David R. Haynor ◽  
Robert Goodkin ◽  
Jay S. Tsuruda ◽  
Andrew D. Bronstein ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Elisa Giorgetti ◽  
Michael Obrecht ◽  
Marie Ronco ◽  
Moh Panesar ◽  
Christian Lambert ◽  
...  

Abstract Assessment of myelin integrity in peripheral nerve injuries and pathologies has largely been limited to post-mortem analysis owing to the difficulty in obtaining biopsies without affecting nerve function. This is further encumbered  by the small size of the tissue and its location. Therefore, the development of robust, non-invasive methods is highly attractive. In this study, we used magnetic resonance imaging (MRI) techniques, including magnetization transfer ratio (MTR), to longitudinally and non-invasively characterize both the sciatic nerve crush and lysolecithin (LCP) demyelination models of peripheral nerve injury in rodents. Electrophysiological, gene expression and histological assessments complemented the extensive MRI analyses in young and aged animals. In the nerve crush model, MTR analysis indicated a slower recovery in regions distal to the site of injury in aged animals, as well as incomplete recovery at six weeks post-crush when analyzing across the entire nerve surface. Similar regional impairments were also found in the LCP demyelination model. This research underlines the power of MTR for the study of peripheral nerve injury in small tissues such as the sciatic nerve of rodents and contributes new knowledge to the effect of aging on recovery after injury. A particular advantage of the approach is the translational potential to human neuropathies.


NeuroImage ◽  
2007 ◽  
Vol 38 (4) ◽  
pp. 669-676 ◽  
Author(s):  
Katarzyna Majcher ◽  
Boguslaw Tomanek ◽  
Ursula I. Tuor ◽  
Andrzej Jasinski ◽  
Tadeusz Foniok ◽  
...  

2020 ◽  
Vol 145 (4) ◽  
pp. 949-956
Author(s):  
Angel F. Farinas ◽  
Isaac V. Manzanera Esteve ◽  
Alonda C. Pollins ◽  
Nancy L. Cardwell ◽  
Christodoulos Kaoutzanis ◽  
...  

F1000Research ◽  
2019 ◽  
Vol 8 ◽  
pp. 1803 ◽  
Author(s):  
Yongsheng Chen ◽  
E. Mark Haacke ◽  
Jun Li

Magnetic resonance imaging (MRI) has been used extensively in revealing pathological changes in the central nervous system. However, to date, MRI is very much underutilized in evaluating the peripheral nervous system (PNS). This underutilization is generally due to two perceived weaknesses in MRI: first, the need for very high resolution to image the small structures within the peripheral nerves to visualize morphological changes; second, the lack of normative data in MRI of the PNS and this makes reliable interpretation of the data difficult. This article reviews current state-of-the-art capabilities in in vivo MRI of human peripheral nerves. It aims to identify areas where progress has been made and those that still require further improvement. In particular, with many new therapies on the horizon, this review addresses how MRI can be used to provide non-invasive and objective biomarkers in the evaluation of peripheral neuropathies. Although a number of techniques are available in diagnosing and tracking pathologies in the PNS, those techniques typically target the distal peripheral nerves, and distal nerves may be completely degenerated during the patient’s first clinic visit. These techniques may also not be able to access the proximal nerves deeply embedded in the tissue. Peripheral nerve MRI would be an alternative to circumvent these problems. In order to address the pressing clinical needs, this review closes with a clinical protocol at 3T that will allow high-resolution, high-contrast, quantitative MRI of the proximal peripheral nerves.


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