Ex Vivo MRI Analytical Methods and Brain Pathology in Preterm Lambs Treated with Postnatal Dexamethasone

• Published in: Brain sciences Vol. 10; no. 4; p. 211
• Main Authors: Yates, Nathanael J, Feindel, Kirk W, Mehnert, Andrew, Beare, Richard, Quick, Sophia, Blache, Dominique, Pillow, J Jane, Hunt, Rod W
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 03.04.2020; MDPI
• Subjects: Age; Animal models; Brain; Cerebral hemispheres; Cortex (frontal); Cortex (parietal); Dexamethasone; Fetuses; Gestation; Glucocorticoids; Hippocampus; Histology; Infants; Lung diseases; Magnetic resonance imaging; Neurodevelopment; Neuroimaging; Neuropathology; Newborn babies; Occipital lobe; Parahippocampal gyrus; Software; Substantia alba; Substantia grisea; Ventilators; Sydney New South Wales Australia; Australia; United States > US; dexamethasone; magnetic resonance imaging; premature; neonatal; animals; glucocorticoids; infant; neurodevelopmental disorders; neurology; neuropathology
• ISSN: 2076-3425; 2076-3425
• DOI: 10.3390/brainsci10040211

Postnatal glucocorticoids such as dexamethasone are effective in promoting lung development in preterm infants, but are prescribed cautiously due to concerns of neurological harm. We developed an analysis pipeline for post-mortem magnetic resonance imaging (MRI) to assess brain development and hence the neurological safety profile of postnatal dexamethasone in preterm lambs. Lambs were delivered via caesarean section at 129 days' (d) gestation (full term ≈ 150 d) with saline-vehicle control (Saline, = 9), low-dose tapered dexamethasone (cumulative dose = 0.75 mg/kg, = 8), or high-dose tapered dexamethasone (cumulative dose = 2.67 mg/kg, = 8), for seven days. Naïve fetal lambs (136 d gestation) were used as end-point maturation controls. The left-brain hemispheres were immersion-fixed in 10 % formalin (24 h), followed by paraformaldehyde (>6 months). Image sequences were empirically optimized for T1- and T2-weighted MRI and analysed using accessible methods. Spontaneous lesions detected in the white matter of the frontal cortex, temporo-parietal cortex, occipital lobe, and deep to the parahippocampal gyrus were confirmed with histology. Neither postnatal dexamethasone treatment nor gestation showed any associations with lesion incidence, frontal cortex (total, white, or grey matter) or hippocampal volume (all > 0.05). Postnatal dexamethasone did not appear to adversely affect neurodevelopment. Our post-mortem MRI analysis pipeline is suitable for other animal models of brain development.