TY - JOUR
T1 - In vivo MRI analysis of an inflammatory injury in the developing brain
AU - Lodygensky, G. A.
AU - West, T.
AU - Stump, M.
AU - Holtzman, D. M.
AU - Inder, T. E.
AU - Neil, J. J.
N1 - Funding Information:
This work was supported by the Green Fund, NIH Grant P50-NS35902 and the Reuter Foundation. The authors are grateful to Professor S.-K. Song for his helpful discussions, Professor Alpay Ozcan and M.D. Budde for their help in advanced computational signal post-processing, C.G. Hamontree for his contribution in building an MRI compatible neonatal rodent head holder and M. Parsadanian for her help and advice regarding histology.
PY - 2010/7
Y1 - 2010/7
N2 - Cerebral periventricular white matter injury stands as a leading cause of cognitive, behavioral and motor impairment in preterm infants. There is epidemiological and histopathological evidence demonstrating the role of prenatal or neonatal inflammation in brain injury in preterm infants. In order to define the effect of an inflammatory insult in the developing brain on magnetic resonance (MR) imaging, we obtained high resolution conventional and diffusion MR images of the brain of rat pups after an inflammatory injury. Rat pups were subjected on postnatal day 5 (P5) to a stereotaxic injection of lipopolysaccharide in the corpus callosum and then imaged at 11.7. T on days 0, 2 and 4 following the injury. They were subsequently sacrificed for immunohistochemistry. Diffusion tensor imaging (DTI) acquired at high spatial resolution showed an initial reduction of the apparent diffusion coefficient (ADC) in the white matter. This was followed by an increase in ADC value and in T2 relaxation time constant in the white matter, with an associated increase of radial diffusivity of the corpus callosum, and a 10-fold increase in ventricular size. On histology, these MR changes corresponded to widespread astrogliosis, and decreased proportion of the section areas containing cresyl violet positive stain. The increase in radial diffusivity, typically attributed to myelin loss, occurred in this case despite the absence of myelin at this developmental stage.
AB - Cerebral periventricular white matter injury stands as a leading cause of cognitive, behavioral and motor impairment in preterm infants. There is epidemiological and histopathological evidence demonstrating the role of prenatal or neonatal inflammation in brain injury in preterm infants. In order to define the effect of an inflammatory insult in the developing brain on magnetic resonance (MR) imaging, we obtained high resolution conventional and diffusion MR images of the brain of rat pups after an inflammatory injury. Rat pups were subjected on postnatal day 5 (P5) to a stereotaxic injection of lipopolysaccharide in the corpus callosum and then imaged at 11.7. T on days 0, 2 and 4 following the injury. They were subsequently sacrificed for immunohistochemistry. Diffusion tensor imaging (DTI) acquired at high spatial resolution showed an initial reduction of the apparent diffusion coefficient (ADC) in the white matter. This was followed by an increase in ADC value and in T2 relaxation time constant in the white matter, with an associated increase of radial diffusivity of the corpus callosum, and a 10-fold increase in ventricular size. On histology, these MR changes corresponded to widespread astrogliosis, and decreased proportion of the section areas containing cresyl violet positive stain. The increase in radial diffusivity, typically attributed to myelin loss, occurred in this case despite the absence of myelin at this developmental stage.
KW - Apparent diffusion coefficient
KW - Diffusion tensor imaging
KW - High field MRI
KW - Inflammation
KW - Lipopolysaccharide
KW - Myelin
KW - Periventricular leukomalacia
KW - Radial diffusivity
KW - White matter injury
UR - http://www.scopus.com/inward/record.url?scp=77953609280&partnerID=8YFLogxK
U2 - 10.1016/j.bbi.2009.11.005
DO - 10.1016/j.bbi.2009.11.005
M3 - Article
C2 - 19945527
AN - SCOPUS:77953609280
SN - 0889-1591
VL - 24
SP - 759
EP - 767
JO - Brain, Behavior, and Immunity
JF - Brain, Behavior, and Immunity
IS - 5
ER -