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Published on: July 29, 2019
Long-Term Effects of Developmental Exposure to Oxycodone on Gut Microbiota and Relationship to Adult Behaviors and
Zhen Lyu1, Robert R Schmidt2,3, Rachel E Martin2,3
1Department of Electrical Engineering and Computer Science, University of Missourigrid.134936.a, Columbia, Missouri, USA.
Insights
Developmental exposure to oxycodone (OXY) in mice causes lasting changes in gut bacteria, impacting adult metabolism. These findings in rodents raise concerns for children exposed to opioids in utero.
Area of Science:
- Microbiology
- Neuroscience
- Toxicology
Background:
- Opioid analgesics are frequently prescribed to pregnant women, potentially exposing the developing fetus.
- Prenatal opioid exposure may disrupt the maternal and infant gut microbiome, but long-term effects remain unclear.
Purpose of the Study:
- To investigate the enduring effects of developmental oxycodone (OXY) exposure on gut microbiota composition.
- To determine if these microbiota alterations correlate with neurobehavioral and metabolic changes in adult offspring.
Main Methods:
- Female mice received daily oxycodone (OXY) or saline (control) before and during gestation.
- Offspring were assessed for gut microbiota, neurobehavioral, and metabolic profiles in adulthood.
Main Results:
- OXY exposure led to sex-specific alterations in adult gut bacterial abundance, including changes in Bacteroidetes and Clostridia.
- Gut microbiota shifts were associated with altered predictive metabolic pathways and correlated with metabolic, but not behavioral, changes in offspring.
Conclusions:
- Developmental exposure to oxycodone induces persistent changes in the gut microbiome that are linked to host metabolic alterations.
- These findings highlight potential risks for children exposed to opioids during development, warranting further investigation into host-microbiome interactions.
Abstract:
Opioid drugs are commonly prescribed analgesic to pregnant women. Direct exposure to such drugs may slow gut motility, alter gut permeability, and affect the gut microbiome. While such drugs affect gut microbiome in infants, no study to date has determined whether developmental exposure to such drugs results in longstanding effects on gut microbiota and correspondingly on host responses. We hypothesized developmental exposure to oxycodone (OXY) leads to enduring effects on gut microbiota and such changes are associated with adult neurobehavioral and metabolic changes. Female mice were treated daily with 5 mg OXY/kg or saline solution (control [CTL]) for 2 weeks prior to breeding and then throughout gestation. Male and female offspring pups were weaned, tested with a battery of behavioral and metabolic tests, and fecal boli were collected adulthood (120 days of age). In females, relative abundance of Butyricimonas spp., Bacteroidetes, Anaeroplasma spp., TM7, Enterococcus spp., and Clostridia were greater in OXY versus CTL individuals. In males, relative abundance of Coriobacteriaceae, Roseburia spp., Sutterella spp., and Clostridia were elevated in OXY exposed individuals. Bacterial changes were also associated with predictive metabolite pathway alterations that also varied according to sex. In males and females, affected gut microbiota correlated with metabolic but not behavioral alterations. The findings suggest that developmental exposure to OXY leads to lasting effects on adult gut microbiota that might affect host metabolism, possibly through specific bacterial metabolites or other bacterial-derived products. Further work is needed to characterize how developmental exposure to OXY affects host responses through the gut microbiome. IMPORTANCE This is the first work to show in a rodent model that in utero exposure to an opioid drug can lead to longstanding effects on the gut microbiota when examined at adulthood. Further, such bacterial changes are associated with metabolic host responses. Given the similarities between rodent and human microbiomes, it raises cause for concern that similar effects may become evident in children born to mothers taking oxycodone and other opioid drugs.
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