Neonatal Faculty Member Directory

Professor of Pediatrics and Associate Division Head for Scholarship and Research
Fellowship Training Program Director
Fellowship Training Program Director
Email: sjuul@u.washington.edu
Dr. Juul's research interests are focused in two primary areas:
- Factors which impact normal neurodevelopment:
In collaboration with Dr. Chris Gleason, Dr. Juul is investigating the acute and long-term effects of neonatal stress and its treatment with sedative and analgesic agents such as morphine and Ativan. These drugs are used commonly in the management of non-surgical ELBW babies, yet little is known about their effects on the developing brain. To study the potential effects of each factor separately as well as potential interaction effects of morphine, Ativan and stress, they have developed mouse and rat models of neonatal stress which mimic the multiple stressors experienced by preterm infants in the NICU. In projects funded by the NIH (NINDS) these models are used to study the cerebrovascular, neuropathologic, and behavioral effects of neonatal stress and neurotropic drug use. - Possible neuroprotective therapies for brain injury:
In research funded by the NIH (Institute of Child Health and Development, and NINDS), and private foundations, the neuroprotective effects of erythropoietin (Epo) is studied in neonatal models of brain injury. Dr. Juul has identified Epo and its receptor in the developing human and rodent brain, studied the penetration of Epo across the blood brain barrier, and examined the safety and neuroprotective effects of high dose Epo in a variety of brain injury models. Her research shows that Epo protects the neonatal brain from injury due to hypoxia and oxidative injury. Dr. Juul will now be moving this research from the bench to the bedside, with phase I/II studies of both preterm and term neonates. She is also in the planning phase of a multicenter randomized clinical trial to test the efficacy of Epo in preterm infants.
- Juul SE, Zerzan JC, Strandjord TP, Woodrum DE. Zinc Protoporphyrin/Heme as an Indicator of Iron Status in NICU Patients. J Pediatr 142:273-8, 2003
- Kellert B, McPherson RJ, and Juul SE. A Comparison of High Dose Erythropoietin Treatment Regimens in Brain Injured Neonatal Rats. Pediatric Res. 61(4): 451-455, 2007
- Statler PA, McPherson RJ, Bauer LA, Juul SE. Pharmacokinetics of High Dose Erythropoietin in Plasma and Brain of Neonatal Rats. Pediatric Res. 61 (6): 671-675, 2007
- Juul SE, Aylward E, Richards T, McPherson RJ, Kuratani J, Burbacher T. Prenatal Cord Clamping in Newborn Macaca nemestrina: a model of perinatal asphyxia. Developmental Neuroscience 29;311–320, 2007
- Juul SE, McPherson RJ, Bauer LA, Ledbetter KJ, Gleason CA, Mayock DE. A Phase I/II Trial of High Dose Erythropoietin in Extremely Low Birth Weight Infants: Pharmacokinetics and Safety. Pediatrics 2008; 122: 383-391. DOI: 10.1542/peds.2007-2711
Teaching, Research and Clinical Activities
Dr. Juul's research interests are focused in two primary areas:
- Factors which impact normal neurodevelopment:
In collaboration with Dr. Chris Gleason, Dr. Juul is investigating the acute and long-term effects of neonatal stress and its treatment with sedative and analgesic agents such as morphine and Ativan. These drugs are used commonly in the management of non-surgical ELBW babies, yet little is known about their effects on the developing brain. To study the potential effects of each factor separately as well as potential interaction effects of morphine, Ativan and stress, they have developed mouse and rat models of neonatal stress which mimic the multiple stressors experienced by preterm infants in the NICU. In projects funded by the NIH (NINDS) these models are used to study the cerebrovascular, neuropathologic, and behavioral effects of neonatal stress and neurotropic drug use. - Possible neuroprotective therapies for brain injury:
In research funded by the NIH (Institute of Child Health and Development, and NINDS), and private foundations, the neuroprotective effects of erythropoietin (Epo) is studied in neonatal models of brain injury. Dr. Juul has identified Epo and its receptor in the developing human and rodent brain, studied the penetration of Epo across the blood brain barrier, and examined the safety and neuroprotective effects of high dose Epo in a variety of brain injury models. Her research shows that Epo protects the neonatal brain from injury due to hypoxia and oxidative injury. Dr. Juul will now be moving this research from the bench to the bedside, with phase I/II studies of both preterm and term neonates. She is also in the planning phase of a multicenter randomized clinical trial to test the efficacy of Epo in preterm infants.
Recent Publications
- Juul SE, Zerzan JC, Strandjord TP, Woodrum DE. Zinc Protoporphyrin/Heme as an Indicator of Iron Status in NICU Patients. J Pediatr 142:273-8, 2003
- Kellert B, McPherson RJ, and Juul SE. A Comparison of High Dose Erythropoietin Treatment Regimens in Brain Injured Neonatal Rats. Pediatric Res. 61(4): 451-455, 2007
- Statler PA, McPherson RJ, Bauer LA, Juul SE. Pharmacokinetics of High Dose Erythropoietin in Plasma and Brain of Neonatal Rats. Pediatric Res. 61 (6): 671-675, 2007
- Juul SE, Aylward E, Richards T, McPherson RJ, Kuratani J, Burbacher T. Prenatal Cord Clamping in Newborn Macaca nemestrina: a model of perinatal asphyxia. Developmental Neuroscience 29;311–320, 2007
- Juul SE, McPherson RJ, Bauer LA, Ledbetter KJ, Gleason CA, Mayock DE. A Phase I/II Trial of High Dose Erythropoietin in Extremely Low Birth Weight Infants: Pharmacokinetics and Safety. Pediatrics 2008; 122: 383-391. DOI: 10.1542/peds.2007-2711
