Early life outcomes of prenatal exposure to alcohol and synthetic cannabinoids in mice

Siara K. Rouzer, McKay Domen, Aisley George, Abigail Bowring, Rajesh C. Miranda
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Abstract

Purpose

This study investigated the effects of prenatal co-exposure to alcohol and synthetic cannabinoids on offspring viability, physical development, and neurobehavioral outcomes in young adulthood. The goal of this investigation was to determine whether prenatal co-exposure produced distinct outcomes from single-drug exposures, including sex-specific vulnerabilities in motor coordination and exploratory behaviors.

Methods

Pregnant C57Bl/6 J mice were randomly assigned to one of four treatment groups: drug-free controls, alcohol (ALC)-exposed, cannabinoid (CP-55,940, CB)-exposed or ALC+CB-exposed, with drug exposure occurring between Gestational Days 12–15. Offspring viability, physical malformations, and developmental delays were first assessed at birth. Then, behavioral evaluations, including rotarod and open field tests, were conducted on young adult offspring (Postnatal Days 100–120).

Results

ALC+CB exposure significantly decreased litter survival (p = 0.006) and offspring viability compared to controls. Non-viable offspring exhibited craniofacial abnormalities, limb malformations, and developmental delays. Assessments of rotarod performance revealed that all exposures reduced motor coordination in males compared to controls (p < 0.05), while ALC and CB exposures alone produced this outcome in females. Open field tests indicated that ALC+CB exposure reduced time in the center of the arena in male offspring exclusively, while this same exposure increased hyperactivity compared to single-drug and control groups, independent of sex (p < 0.05).

Conclusions

Prenatal co-exposure to alcohol and synthetic cannabinoids exacerbated offspring mortality and induced sex-specific deficits in neurobehavioral motor outcomes. These findings highlight the distinct risks of polysubstance exposure during pregnancy and underscore the need for targeted interventions to mitigate the effects of prenatal polysubstance exposure on offspring health outcomes.
小鼠产前暴露于酒精和合成大麻素的早期生活结果
目的本研究探讨了产前酒精和合成大麻素共同暴露对后代生存能力、身体发育和成年后神经行为结果的影响。本研究的目的是确定产前共同暴露是否会产生与单一药物暴露不同的结果,包括运动协调和探索性行为的性别特异性脆弱性。方法将妊娠C57Bl/6 J小鼠随机分为4组:无药物对照组、酒精(ALC)暴露组、大麻素(CP-55,940, CB)暴露组和ALC+CB暴露组,暴露时间为妊娠12 ~ 15天。在出生时首先评估后代的生存能力、身体畸形和发育迟缓。然后,对成年幼崽(出生后100-120天)进行行为学评价,包括轮轮试验和野外试验。结果与对照组相比,salc +CB暴露显著降低产仔存活率(p = 0.006)和子代存活率。不能存活的后代表现为颅面异常、肢体畸形和发育迟缓。对旋转棒性能的评估显示,与对照组相比,所有暴露都降低了男性的运动协调能力(p < 0.05),而单独暴露于ALC和CB会在女性中产生这种结果。野外试验表明,与单药组和对照组相比,ALC+CB暴露只减少了雄性后代在竞技场中心的时间,而同样的暴露增加了多动症,与性别无关(p < 0.05)。结论:产前同时暴露于酒精和合成大麻素会增加后代的死亡率,并导致神经行为运动结果的性别特异性缺陷。这些发现强调了怀孕期间多物质暴露的明显风险,并强调需要采取有针对性的干预措施,以减轻产前多物质暴露对后代健康结果的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug and alcohol dependence reports
Drug and alcohol dependence reports Psychiatry and Mental Health
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