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Published on: June 11, 2020
Mild Neonatal Brain Hypoxia-Ischemia in Very Immature Rats Causes Long-Term Behavioral and Cerebellar Abnormalities
Eduardo Farias Sanches1, Yohan van de Looij1,2, Audrey Toulotte1
1Division of Child Development and Growth, Department of Pediatrics, School of Medicine, University of Geneva, Geneva, Switzerland.
Insights
Neonatal hypoxia-ischemia (HI) in young rats causes hyperactivity and metabolic brain changes into adulthood. This study reveals long-term cerebellar alterations and reduced neuronal markers following early-life HI.
Area of Science:
- Neuroscience
- Developmental Biology
- Biochemistry
Background:
- Systemic hypoxia-ischemia (HI) is a common complication during preterm birth.
- HI can cause brain injuries, particularly in forebrain structures.
- These injuries may lead to long-term functional disturbances in distant brain regions like the cerebellum.
Purpose of the Study:
- To investigate long-term behavioral, metabolic, and molecular changes in the cerebellum following early postnatal HI.
- To evaluate the impact of mild neonatal HI on cerebellar function and structure in adult rats.
Main Methods:
- Mild HI was induced in the right forebrain of PND3 rats.
- Behavioral assessments were performed from PND45 onwards.
- In vivo 1H magnetic resonance spectroscopy (1H MRS) was used to analyze cerebellar metabolism.
- Protein expression of GFAP, NeuN, and MBP was determined in the left cerebellum.
Main Results:
- HI rats showed increased locomotion but no motor coordination deficits.
- 1H MRS revealed significant global glutamine increase and altered glutamate, glycine, and total choline levels in the left cerebellum of HI rats.
- Decreased expression of myelin basic protein (MBP) and NeuN (neuronal marker) was observed in the left cerebellum, without reactive astrogliosis.
Conclusions:
- Neonatal HI induces hyperactivity and long-term metabolic alterations in the cerebellum.
- The findings suggest a potential disruption of the glutamate-glutamine cycle in the cerebellum post-HI.
- HI can cause cell death and myelin deficits in the cerebellum, a region distant from the primary injury site.
Abstract:
Systemic hypoxia-ischemia (HI) often occurs during preterm birth in human. HI induces injuries to hinder brain cells mainly in the ipsilateral forebrain structures. Such HI injuries may cause lifelong disturbances in the distant regions, such as the contralateral side of the cerebellum. We aimed to evaluate behavior associated with the cerebellum, to acquire cerebellar abundant metabolic alterations using in vivo 1H magnetic resonance spectroscopy (1H MRS), and to determine GFAP, NeuN, and MBP protein expression in the left cerebellum, in adult rats after mild early postnatal HI on the right forebrain at day 3 (PND3). From PND45, HI animals exhibited increased locomotion in the open field while there is neither asymmetrical forelimb use nor coordination deficits in the motor tasks. Despite the fact that metabolic differences between two cerebellar hemispheres were noticeable, a global increase in glutamine of HI rats was observed and became significant in the left cerebellum compared to the sham-operated group. Furthermore, increases in glutamate, glycine, the sum of glutamate and glutamine and total choline, only occurred in the left cerebellum of HI rats. Remarkably, there were decreased expression of MBP and NeuN but no detectable reactive astrogliosis in the contralateral side of the cerebellum of HI rats. Taken together, the detected alterations observed in the left cerebellum of HI rats may reflect disequilibrium in the glutamate-glutamine cycle and a delay in the return of glutamine from astrocytes to neurons from hypoxic-ischemic origin. Our data provides in vivo evidence of long-term changes in the corresponding cerebellum following mild neonatal HI in very immature rats, supporting the notion that systemic HI could cause cell death in the cerebellum, a distant region from the expected injury site.
Highlights:
-Neonatal hypoxia-ischemia (HI) in very immature rats induces hyperactivity toward adulthood.-1H magnetic resonance spectroscopy detects long-term cerebellar metabolic changes in adult rats after neonatal HI at postnatal day 3.-Substantial decreases of expression of neuronal and myelin markers in adult rats cerebellum after neonatal cortical mild HI.
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