Prenatal Opioid and Alcohol Exposures: Association with Altered Placental Serotonin Transporter Structure and/or Expression

Fetal exposures to many drugs of abuse, e.g., opioids and alcohol (EtOH), are associated with adverse neurodevelopmental problems in early childhood, including abnormalities in activity of the serotonin (5HT) transporter (SERT), which transports 5HT across the placenta. Little is known about the effects of these drugs on SERT expression. Pregnant women who used EtOH or opioids were compared to gestational age-matched controls using a structured questionnaire to determine prenatal substance exposure. Following elective pregnancy termination, placental membranous vesicles and exosomes were prepared from first and second trimester human placentas. Changes in EtOH- or opioid-exposed placental SERT expression and modifications were assessed by quantitative western blot. Novel SERT isoforms were sequenced and analyzed. Opioid-exposed but not EtOH-exposed maternal placentas showed SERT cleavage and formation of new SERT fragments (isoforms). Alcohol-exposed cases showed reduced SERT levels. Antibodies to the N-terminal SERT region did not recognize either of the two cleavage products, while antibodies to the central and C-terminal regions recognized both bands. The secondary band seen in the opioid group may represent a hypophosphorylated SERT fragment. These changes in SERT modifications and expression may result in altered fetal brain serotonergic neurotransmission, which could have neurodevelopmental implications.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2024-10-28
DOI
https://doi.org/10.3390/ijms252111570
Citations
2
Primary Topic
Prenatal Substance Exposure Effects
Type
article
Field-Weighted Citation Impact
2.22

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article

Prenatal Opioid and Alcohol Exposures: Association with Altered Placental Serotonin Transporter Structure and/or Expression

Mary F. Morrison, Michael E. Selzer, Armine Darbinyan, Gabriel Tatevosian et al.
2 citations
International Journal of Molecular Sciences
Prenatal Substance Exposure Effects
2.22
article

Prenatal Opioid and Alcohol Exposures: Association with Altered Placental Serotonin Transporter Structure and/or Expression

Mary F. Morrison, Michael E. Selzer, Armine Darbinyan, Gabriel Tatevosian, Nana Merabova, Sandra Adele, Laura Goetzl, C. Lindsay DeVane, Sammanda Ramamoorthy, Nune Darbinian
article en
2 citations

Abstract

Fetal exposures to many drugs of abuse, e.g., opioids and alcohol (EtOH), are associated with adverse neurodevelopmental problems in early childhood, including abnormalities in activity of the serotonin (5HT) transporter (SERT), which transports 5HT across the placenta. Little is known about the effects of these drugs on SERT expression. Pregnant women who used EtOH or opioids were compared to gestational age-matched controls using a structured questionnaire to determine prenatal substance exposure. Following elective pregnancy termination, placental membranous vesicles and exosomes were prepared from first and second trimester human placentas. Changes in EtOH- or opioid-exposed placental SERT expression and modifications were assessed by quantitative western blot. Novel SERT isoforms were sequenced and analyzed. Opioid-exposed but not EtOH-exposed maternal placentas showed SERT cleavage and formation of new SERT fragments (isoforms). Alcohol-exposed cases showed reduced SERT levels. Antibodies to the N-terminal SERT region did not recognize either of the two cleavage products, while antibodies to the central and C-terminal regions recognized both bands. The secondary band seen in the opioid group may represent a hypophosphorylated SERT fragment. These changes in SERT modifications and expression may result in altered fetal brain serotonergic neurotransmission, which could have neurodevelopmental implications.

International Journal of Molecular SciencesVol. 25(21)
Medical University of South Carolina (US), Virginia Commonwealth University (US), Medical College of Wisconsin (US), Yale University (US), University of Oxford (GB), Medawar Building for Pathogen Research (GB), Prevea Health (US), Temple University Hospital (US), Temple University (US), The University of Texas Health Science Center at Houston (US)
Bill and Melinda Gates Foundation, National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism, National Institute of Neurological Disorders and Stroke
Good health and well-being
Openalex Percentile: Top 11%
Prenatal Substance Exposure Effects
2.22
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