Pa. Seeldrayers et al., MAGNETIC-RESONANCE-IMAGING INVESTIGATION OF BLOOD-BRAIN-BARRIER DAMAGE IN ADOPTIVE TRANSFER EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS, Journal of neuroimmunology, 46(1-2), 1993, pp. 199-206
Recent advances in fast magnetic resonance imaging (MRI) techniques ha
ve allowed quantification of parameters such as Tl relaxation time, wh
ich can be modified by changes in the water content of a tissue. We ha
ve used this new method to study the evolution of blood-brain barrier
(BBB) changes after adoptive transfer of MBP-specific (AT-EAE) and ova
lbumin-specific T cell lines in Lewis rats. Measurable changes in Tl r
elaxation time suggesting widespread increase in BBB permeability were
found, starting on day 3 post inoculation (p.i.), in the midbrain and
brainstem of AT-EAE rats. In addition, we noted a significant decreas
e in Tl relaxation time before injection of a paramagnetic agent, in t
he cisternal cerebrospinal fluid (CSF) of diseased animals, starting o
n day 5 p.i. In vitro measurement of Tl in CSF containing various conc
entrations of albumin, IgM and glucose showed that, at physiological c
oncentrations, a Tl decrease is mainly associated with an increase in
albumin concentration. A moderate increase in BBB and blood-CSF barrie
r permeability was found as early as 4-8 h p.i., in rats injected with
MBP-specific as in animals injected with ovalbumin-specific T cell li
nes, suggesting a non-specific mechanism. Experimental MRI may become
a powerful tool to sequentially analyse changes in barrier dynamics, f
or example following pharmacological intervention.