An Animal Model of Neonatal Intensive Care Unit Exposure to Light and Sound
Project Number1R21HD114995-01
Contact PI/Project LeaderMOWERY, TODD M.
Awardee OrganizationRUTGERS BIOMEDICAL AND HEALTH SCIENCES
Description
Abstract Text
SUMMARY:
According to the World Health Organization, approximately 15 million children are born prematurely each year.
Many of these infants end up spending days to weeks in a neonatal intensive care unit (NICU). Infants who are
born prematurely are often exposed to noise and light levels that affect auditory and visual development.
Subsequently, these children can have long-term impairments in cognition, visuospatial processing, hearing, and
language. We have developed a rodent model of NICU exposure to light and sound using the Mongolian gerbil
(Meriones unguiculatus), which has a low frequency human-like audiogram and is altricial. To simulate preterm
infancy the eyes and ears will be opened prematurely, followed by exposure to the NICU-like sensory
environment throughout the gerbil’s cortical critical period of auditory development. Here, natural eye-opening
closes the critical period ~ P18, and early eye opening simulates the effect of preterm birth, by closing the critical
period precociously (Mowery et al., 2016). This motivated the core hypothesis that early eye opening induces
precocious closure of auditory development through feed forward peripheral visual excitatory input onto cross
modal synapses located in auditory cortex. Recent research has provided preliminary validation for the effect of
early light and noise exposure on long-term brain development (Gay et al., 2023). We will test this hypothesis
with three aims. The first aim will track electrophysiological development of inhibition within the auditory cortex
after NICU (early eye/ear opening) or noise only (early ear opening) exposed neonates, juveniles, and adults.
The second aim will track the development of physiological peripheral measures for auditory (auditory brainstem
response) and visual (visual evoked potentials) function in NICU (early eye/ear opening) or noise only (early ear
opening) exposed neonates as they develop into juveniles and then adults. Histological measurements of the
white and grey matter along the visual and auditory neuraxes will be generated and correlated with any
impairments to peripheral physiology thresholds of each animal in AIM 2. The third aim will behaviorally test
measures of auditory and visual based decision-making impairments in NICU (early eye/ear opening) or noise
only (early ear opening) exposed animals after they have become adults. Together, the findings from this project
will introduce a new animal model of the NICU preterm infant, with which mitigative and treatment-based
approaches to early light and sound exposure can be ethically carried out by the research community. We hope
to establish this animal model to create a bridge between clinical pediatric physician researchers and the animal
research community to advance clinical treatments and care for the NICU-exposed preterm infant.
Public Health Relevance Statement
Premature infants can spend weeks in the neonatal intensive care unit (NICU), where they are exposed to
damaging levels of noise and light. The proposed project will establish an animal model of NICU exposure that
will allow researchers to investigate the impact of the NICU on sensory system development and learning.
Eunice Kennedy Shriver National Institute of Child Health and Human Development
CFDA Code
865
DUNS Number
090299830
UEI
YVVTQD8CJC79
Project Start Date
10-September-2024
Project End Date
31-August-2026
Budget Start Date
10-September-2024
Budget End Date
31-August-2025
Project Funding Information for 2024
Total Funding
$235,500
Direct Costs
$150,000
Indirect Costs
$85,500
Year
Funding IC
FY Total Cost by IC
2024
Eunice Kennedy Shriver National Institute of Child Health and Human Development
$235,500
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 1R21HD114995-01
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The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
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Clinical Studies
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