Abstract

Remyelination is a naturally occurring response to demyelination and has a central role in the pathophysiology of multiple sclerosis and traumatic brain injury. Recently we demonstrated that a novel MRI technique entitled Relaxation Along a Fictitious Field (RAFF) in the rotating frame of rank n (RAFFn) achieved exceptional sensitivity in detecting the demyelination processes induced by lysophosphatidylcholine (LPC) in rat brain. In the present work, our aim was to test whether RAFF4, along with magnetization transfer (MT) and diffusion tensor imaging (DTI), would be capable of detecting the changes in the myelin content and microstructure caused by modifications of myelin sheets around axons or by gliosis during the remyelination phase after LPC-induced demyelination in the corpus callosum of rats. We collected MRI data with RAFF4, MT and DTI at 3 days after injection (demyelination stage) and at 38 days after injection (remyelination stage) of LPC (n = 12) or vehicle (n = 9). Cell density and myelin content were assessed by histology. All MRI metrics detected differences between LPC-injected and control groups of animals in the demyelination stage, on day 3. In the remyelination phase (day 38), RAFF4, MT parameters, fractional anisotropy, and axial diffusivity detected signs of a partial recovery consistent with the remyelination evident in histology. Radial diffusivity had undergone a further increase from day 3 to 38 and mean diffusivity revealed a complete recovery correlating with the histological assessment of cell density attributed to gliosis. The combination of RAFF4, MT and DTI has the potential to differentiate between normal, demyelinated and remyelinated axons and gliosis and thus it may be able to provide a more detailed assessment of white matter pathologies in several neurological diseases.

Highlights

  • Myelin is essential for the proper functioning of the central nervous system

  • This is consistent with the demyelination/remyelination process described for the LPC model in white matter (Woodruff and Franklin, 1999)

  • The largest relative differences were detected by RAFF4, fractional anisotropy (FA) and axial diffusivity (AD) (48, –50, –54%, respectively), while magnetization transfer ratio (MTR), T1sat and radial diffusivity (RD) showed more modest (–18, 21, 26%) but still very clear changes between the demyelinated ipsilateral area and a similar area in vehicle treated animals (Table 1)

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Summary

Introduction

Myelin is essential for the proper functioning of the central nervous system. It accelerates the propagation of electrical impulses along myelinated fibers, but it provides protection and nutrients to neurons (Saab and Nave, 2017). Remyelination is a natural regenerative response to demyelination Both acquired and genetic demyelinations are followed by remyelination, and this has been found to play an important role especially in multiple sclerosis (Prineas and Connell, 1979; Hirano, 1989) and traumatic brain injury (Armstrong et al, 2016b). Remyelination is a key step in the patient’s recovery process, as electrical impulses propagate too slowly along demyelinated axons to allow normal brain function. Non-invasive quantitative imaging of changes in myelin content and microstructure can provide critical information about demyelination and remyelination processes and be useful for monitoring the progression of diseases and responses to treatment

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