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Published on: August 14, 2019
Characterization of Ionic and Lipid Gradients within Corpus Callosum White Matter after Diffuse Traumatic Brain
David Hartnell1,2, Kate Gillespie-Jones3, Cristina Ciornei3
1Curtin Institute for Functional Molecules and Interfaces, School of Molecular and Life Sciences , Curtin University , Perth , Western Australia , Australia 6845.
Abstract:
There is increased recognition of the effects of diffuse traumatic brain injury (dTBI), which can initiate yet unknown biochemical cascades, resulting in delayed secondary brain degeneration and long-term neurological sequela. There is limited availability of therapies that minimize the effect of secondary brain damage on the quality of life of people who have suffered TBI, many of which were otherwise healthy adults. Understanding the cascade of biochemical events initiated in specific brain regions in the acute phase of dTBI and how this spreads into adjacent brain structures may provide the necessary insight into drive development of improved therapies. In this study, we have used direct biochemical imaging techniques (Fourier transform infrared spectroscopic imaging) and elemental mapping (X-ray fluorescence microscopy) to characterize biochemical and elemental alterations that occur in corpus callosum white matter in the acute phase of dTBI. The results provide direct visualization of differential biochemical and ionic changes that occur in the highly vulnerable medial corpus callosum white matter relative to the less vulnerable lateral regions of the corpus callosum. Specifically, the results suggest that altered ionic gradients manifest within mechanically damaged medial corpus callosum, potentially spreading to and inducing lipid alterations to white matter structures in lateral brain regions.
Insights
Diffuse traumatic brain injury (dTBI) triggers biochemical changes in the brain. This study visualizes early ionic and lipid alterations in the corpus callosum following dTBI, offering insights for new therapies.
Area of Science:
- Neuroscience
- Biochemistry
- Medical Imaging
Background:
- Diffuse traumatic brain injury (dTBI) can cause delayed secondary brain degeneration and long-term neurological issues.
- Limited therapies exist to mitigate the impact of secondary brain damage after TBI.
- Understanding acute biochemical cascades in dTBI is crucial for developing effective treatments.
Purpose of the Study:
- To characterize biochemical and elemental alterations in the corpus callosum during the acute phase of dTBI.
- To visualize the spatial spread of these changes within the white matter.
Main Methods:
- Fourier transform infrared spectroscopic imaging (FTIR) for biochemical analysis.
- X-ray fluorescence microscopy (XRF) for elemental mapping.
- Direct biochemical imaging of corpus callosum white matter.
Main Results:
- Differential biochemical and ionic changes were observed in the medial versus lateral corpus callosum.
- Altered ionic gradients were identified in mechanically damaged medial regions.
- These ionic changes may spread and induce lipid alterations in lateral white matter.
Conclusions:
- The study provides direct visualization of acute dTBI-induced biochemical and ionic changes in the corpus callosum.
- Findings highlight the vulnerability of medial white matter and potential spread of damage.
- This research may inform the development of targeted therapies for TBI.
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