Susceptibility-weighted imaging in the experimental autoimmune encephalomyelitis model of multiple sclerosis indicates elevated deoxyhemoglobin, iron deposition and demyelination

Mult Scler. 2013 May;19(6):721-31. doi: 10.1177/1352458512460602. Epub 2012 Oct 1.

Abstract

Background: Susceptibility-weighted imaging (SWI) is an iron-sensitive magnetic resonance imaging (MRI) method that has shown iron-related lesions in multiple sclerosis (MS) patients. The contribution of deoxyhemoglobin to the signals seen in SWI has not been well characterized in MS.

Objectives: To determine if SWI lesions (seen as focal hypointensities) exist in the experimental autoimmune encephalomyelitis (EAE) animal model of MS, and to determine whether the lesions relate to iron deposits, inflammation, demyelination, and/or deoxyhemoglobin in the vasculature.

Methods: We performed SWI on the lumbar spinal cord and cerebellum of EAE and control mice (both complete Freund's adjuvant/pertussis toxin (CFA/PTX)-immunized and naive). We also performed SWI on mice before and after perfusion (to remove blood from vessels). SWI lesions were counted and their locations were compared to histology for iron, myelin and inflammation.

Results: SWI lesions were found to exist in the EAE model. Many lesions seen by SWI were not present after perfusion, especially at the grey/white matter boundary of the lumbar spinal cord and in the cerebellum, indicating that these lesion signals were associated with deoxyhemoglobin present in the lumen of vessels. We also observed SWI lesions in the white matter of the lumbar spinal cord that corresponded to iron deposition, inflammation and demyelination. In the cerebellum, SWI lesions were present in white matter tracts, where we found histological evidence of inflammatory perivascular cuffs.

Conclusions: SWI lesions exist in EAE mice. Many lesions seen in SWI were a result of deoxyhemoglobin in the blood, and so may indicate areas of hypoxia. A smaller number of SWI lesions coincided with parenchymal iron, demyelination, and/or inflammation.

Keywords: Cerebellum; demyelination; deoxyhemoglobin; experimental autoimmune encephalomyelitis; hypoxia; iron deposits; magnetic resonance imaging; multiple sclerosis; spinal cord; susceptibility-weighted imaging.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal
  • Biomarkers / metabolism
  • Cerebellum / metabolism*
  • Cerebellum / pathology*
  • Encephalomyelitis, Autoimmune, Experimental / diagnosis*
  • Encephalomyelitis, Autoimmune, Experimental / metabolism
  • Encephalomyelitis, Autoimmune, Experimental / pathology
  • Encephalomyelitis, Autoimmune, Experimental / psychology
  • Female
  • Freund's Adjuvant
  • Hemoglobins / metabolism*
  • Iron / metabolism*
  • Magnetic Resonance Imaging / methods*
  • Mice, Inbred C57BL
  • Myelin Sheath / metabolism*
  • Pertussis Toxin
  • Predictive Value of Tests
  • Spinal Cord / metabolism*
  • Spinal Cord / pathology*
  • White Matter / metabolism
  • White Matter / pathology

Substances

  • Biomarkers
  • Hemoglobins
  • Freund's Adjuvant
  • deoxyhemoglobin
  • Iron
  • Pertussis Toxin