The Conflicting Role of Caffeine Supplementation on Hyperoxia-Induced Injury on the Cerebellar Granular Cell Neurogenesis of Newborn Rats.
Vivien GiszasEvelyn StraußChristoph BührerStefanie EndesfelderPublished in: Oxidative medicine and cellular longevity (2022)
Preterm birth disrupts cerebellar development, which may be mediated by systemic oxidative stress that damages neuronal developmental stages. Impaired cerebellar neurogenesis affects several downstream targets important for cognition, emotion, and speech. In this study, we demonstrate that oxidative stress induced with high oxygen (80%) for three or five postnatal days (P3/P5) could significantly damage neurogenesis and proliferative capacity of granular cell precursor and Purkinje cells in rat pups. Reversal of cellular neuronal damage after recovery to room air (P15) was augmented by treatment with caffeine. However, downstream transcripts important for migration and differentiation of postmitotic granular cells were irreversibly reduced by hyperoxia, without rescue by caffeine. Protective effects of caffeine in the cerebellum were limited to neuronal survival but failed to restore important transcript signatures.
Keyphrases
- oxidative stress
- induced apoptosis
- cerebral ischemia
- preterm birth
- diabetic rats
- cell cycle arrest
- single cell
- cell therapy
- dna damage
- endoplasmic reticulum stress
- low birth weight
- neural stem cells
- signaling pathway
- stem cells
- rna seq
- ischemia reperfusion injury
- subarachnoid hemorrhage
- brain injury
- gestational age
- blood brain barrier
- depressive symptoms
- cell death
- high glucose
- gene expression
- drug induced
- bone marrow
- dna methylation
- replacement therapy
- hearing loss
- free survival