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Three-dimensional Confocal Analysis of Microglia/macrophage Markers of Polarization in Experimental Brain Injury
Published on: September 4, 2013
In vivo MRI analysis of an inflammatory injury in the developing brain
G A Lodygensky1, T West, M Stump
1Department of the Child and Adolescent, Pediatric and Neonatal ICU, University of Geneva, Geneva, Switzerland. gregory.lodygensky@unige.ch
Insights
Inflammation in preterm infant brains causes injury. This study used MR imaging in rat pups to show how inflammation affects brain development and imaging characteristics, revealing early changes in white matter.
Area of Science:
- Neuroscience
- Developmental Biology
- Medical Imaging
Background:
- Cerebral periventricular white matter injury is a major cause of long-term impairment in preterm infants.
- Prenatal and neonatal inflammation are implicated in brain injury in premature infants.
- Understanding the impact of inflammation on developing brain MR imaging is crucial.
Purpose of the Study:
- To investigate the effects of an inflammatory insult on magnetic resonance (MR) imaging characteristics of the developing brain.
- To correlate MR imaging findings with histological changes following inflammation in a rat pup model.
Main Methods:
- Rat pups were induced with lipopolysaccharide (LPS) on postnatal day 5 (P5) to simulate inflammation.
- High-resolution conventional and diffusion MR imaging (including Diffusion Tensor Imaging - DTI) were performed at 11.7 T on days 0, 2, and 4 post-injury.
- Brains were subsequently analyzed using immunohistochemistry and histology.
Main Results:
- Diffusion Tensor Imaging (DTI) revealed an initial decrease in apparent diffusion coefficient (ADC) in white matter, followed by an increase.
- Increased ADC values and T2 relaxation time constants were observed, along with increased radial diffusivity in the corpus callosum.
- Significant ventricular enlargement (10-fold increase) and histological evidence of astrogliosis were noted.
- Increased radial diffusivity occurred despite the absence of myelin, challenging typical interpretations.
Conclusions:
- Inflammatory insults in the developing brain cause significant changes detectable by high-resolution MR imaging.
- MR imaging can reveal early signs of white matter injury and subsequent tissue changes, including astrogliosis.
- The findings highlight the utility of advanced MR techniques in studying inflammatory brain injury in early development, even in the absence of mature myelin.
Abstract:
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.
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