Focus: defining the mechanisms which determine lean body mass in premature infants Rationale: growth failure is common in premature infants in the neonatal ICU Major findings: the etiology of decreased lean body mass among premature infants is multi-factorial
Focus: Defining treatment strategies to improve the care of infants with neonatal abstinence syndrome (NAS) Rationale: there are currently no scientifically-proven effective therapies to treat infants with NAS
Past
Focus: understanding how hyperoxia modulates protein synthesis in the lung Rationale: lung injury and abnormal lung growth and development are common findings among premature infants in the neonatal intensive care unit where infants are commonly exposed to high inspired concentrations of oxygen Major Findings: modulation of global protein synthesis during hyperoxia is part of complex adaptive signal transduction program known as the integrated stress response which slows translation to conserve energy and induces the expression of transcription factors that enhance the synthesis of chaperones, immune-modulators, and factors integral to redox balance
Focus: delineating the capacity for hyperoxia to enhance the translation of mRNA via non-classical (cap-independent) processes Rationale: in the presence of global repression of mRNA translation, the expression of select proteins is commonly enhanced Major findings: the translational efficiencies of some transcripts containing internal ribosome entry sites (IRES) are enhanced in O2-induced lung injury and O2-induced retinopathy
Jeffrey Scott Shenberger
Associate Professor
: (413) 794-0093
DEPARTMENTDepartment of Pediatrics
Newborn Medicine
Bay state Children’s Hospital