Prenatal methadone exposure disrupts behavioral development and alters motor neuron intrinsic properties and local circuitry
Year: 2021
Type: article
Abstract: Despite the rising prevalence of methadone treatment in pregnant women with opioid use disorder, the effects of methadone on neurobehavioral development remain unclear. We developed a translational mouse model of prenatal methadone exposure (PME) that resembles the typical pattern of opioid use by pregnant women who first use oxycodone then switch to methadone maintenance pharmacotherapy, and subsequently become pregnant while maintained on methadone. We investigated the effects of PME on physical development, sensorimotor behavior, and motor neuron properties using a multidisciplinary approach of physical, biochemical, and behavioral assessments along with brain slice electrophysiology and in vivo magnetic resonance imaging. Methadone accumulated in the placenta and fetal brain, but methadone levels in offspring dropped rapidly at birth which was associated with symptoms and behaviors consistent with neonatal opioid withdrawal. PME produced substantial impairments in offspring physical growth, activity in an open field, and sensorimotor milestone acquisition. Furthermore, these behavioral alterations were associated with reduced neuronal density in the motor cortex and a disruption in motor neuron intrinsic properties and local circuit connectivity. The present study adds to the limited body of work examining PME by providing a comprehensive, translationally relevant characterization of how PME disrupts offspring physical and neurobehavioral development.
Source: eLife
DOI: 10.7554/elife.66230
Authors: Gregory G. Grecco, Briana Mork, Jui Yen Huang, Corinne E. Metzger, David L. Haggerty, Kaitlin C. Reeves, Yong Gao, Hunter Hoffman, Simon N. Katner, Andrea R. Masters, Cameron W. Morris, Erin A. Newell, Eric A. Engleman, Anthony J. Baucum, Jieun Kim, Bryan K. Yamamoto, Matthew R. Allen, Yu-Chien Wu, Hui-Chen Lu, Patrick L. Sheets, Brady K. Atwood
Language: English
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,500
Funders: Indiana University, Indiana University Health, National Institutes of Health, School of Medicine, Indiana University, Melvin and Bren Simon Cancer Center, Indiana University, National Institute on Alcohol Abuse and Alcoholism, National Institute on Aging, National Institute on Drug Abuse, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke
Awards: Modeling Axonal Density and Inflammation-Associated Cellularity in Alzheimer’s Disease Using Hybrid Diffusion Imaging, G1628476732, G437567452, G4615147670, G4616508932, Indiana Medical Scientist/Engineer Training Program, G6130783537, G6447529026, G8082619168, G9000025480, G9000127741, G9000212862, G911238075, Synapse-specific interactions between ethanol and opioid receptor-mediated synaptic depression in dorsal striatum
OpenAlex ID: W3136301338
