Maternal ingestion of cannabidiol (CBD) in mice leads to sex-dependent changes in memory, anxiety, and metabolism in the adult offspring, and causes a decrease in survival to weaning age.

IF 3.3 3区 心理学 Q1 BEHAVIORAL SCIENCES
Martina Krakora Compagno, Claudia Rose Silver, Alexis Cox-Holmes, Kari B Basso, Caroline Bishop, Amber Michal Bernstein, Aidan Carley, Joshua Cazorla, Jenna Claydon, Ashleigh Crane, Chloe Crespi, Emma Curley, Tyla Dolezel, Ezabelle Franck, Katie Heiden, Carley Marie Huffstetler, Ashley M Loeven, Camilla Ann May, Nicholas Maykut, Alejandro Narvarez, Franklin A Pacheco, Olivia Turner, Debra Ann Fadool
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引用次数: 0

Abstract

Rationale: The consequences of perinatal cannabidiol (CBD) exposure are severely understudied, but are important, given its widespread use and believed safety as a natural supplement.

Objective: The objective of this study was to test the health, metabolic, and behavioral consequences of perinatal CBD exposure on dams and their offspring raised to adult.

Methods: Primiparous female C57BL/6J mice were orally administered 100 mg/kg CBD in strawberry jam to expose offspring during gestation, lactation, or both using a cross-fostering design. Adult offspring were metabolically profiled using indirect calorimetry and intraperitoneal glucose tolerance testing. Adults were behaviorally phenotyped, video recorded, and mouse position tracked using DeepLabCut.

Results: CBD was detected in maternal plasma using LC-MS 10-min post consumption (34.2 ± 1.7 ng/μl) and peaked within 30 min (371.0 ± 34.0 ng/μl). Fetal exposure to CBD significantly decreased survival of the pups, and decreased male postnatal development, but did not alter litter size, maternal body weight or pup birth weight. We observed many sex-dependent effects of perinatal CBD exposure. Exposure to CBD during gestation and lactation increased meal size, caloric intake, and respiratory exchange ratio for adult male offspring, while exposure during lactation decreased fasting glucose, but had no effect on clearance. Adult female offspring exposed to CBD during lactation showed increased drink size. Perinatal CBD exposure increased obsessive compulsive- and decreased anxiety-like behaviors (marble burying, light-dark box, elevated-plus maze) in female mice, decreased long-term object memory in male mice, and had no effect on attention tasks for either sex.

Conclusions: We conclude that orally-administered CBD during pregnancy affects behavior and metabolism in a sex-dependent manner, and mice are differentially sensitive to exposure during gestation vs. lactation, or both. Because long-term changes are observed following perinatal exposure to the drug, and exposure significantly decreases survival to weaning, more research during development is warranted.

母鼠摄入大麻二酚(CBD)会导致成年后代的记忆、焦虑和新陈代谢发生性别依赖性变化,并导致断奶后存活率下降。
理由:对围产期接触大麻二酚(CBD)的后果的研究严重不足,但鉴于大麻二酚作为一种天然补充剂被广泛使用并被认为是安全的,因此这种研究非常重要:本研究的目的是测试围产期接触大麻二酚对母鼠及其养育至成年的后代的健康、代谢和行为的影响:初产雌性 C57BL/6 J 小鼠口服 100 毫克/千克含 CBD 的草莓酱,在妊娠期、哺乳期或两者同时暴露于 CBD。成年后代采用间接量热法和腹腔葡萄糖耐量试验进行代谢分析。使用 DeepLabCut 对成年后代进行行为表型、视频记录和小鼠位置跟踪:使用 LC-MS 检测母体血浆中的 CBD 含量(34.2 ± 1.7 ng/ul),CBD 含量在服用后 10 分钟内达到峰值(371.0 ± 34.0 ng/ul)。胎儿暴露于 CBD 会明显降低幼崽的存活率,并降低雄性的产后发育,但不会改变产仔数、母体体重或幼崽出生体重。我们观察到围产期暴露于CBD会产生许多性别依赖性影响。妊娠期和哺乳期接触CBD会增加成年雄性后代的进食量、热量摄入和呼吸交换比,而哺乳期接触CBD会降低空腹血糖,但对清除率没有影响。在哺乳期暴露于 CBD 的成年雌性后代的饮水量增加。围产期暴露于CBD会增加雌性小鼠的强迫症行为,减少焦虑样行为(埋大理石、光暗箱、高架加迷宫),减少雄性小鼠的长期物体记忆,但对雌雄小鼠的注意力任务均无影响:我们得出结论:妊娠期口服 CBD 会以性别依赖的方式影响小鼠的行为和新陈代谢,而且小鼠对妊娠期与哺乳期或两者的暴露敏感度不同。由于围产期暴露于该药物后会观察到长期变化,而且暴露会显著降低小鼠断奶前的存活率,因此有必要在发育期开展更多研究。
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
CiteScore
6.40
自引率
2.80%
发文量
122
审稿时长
38 days
期刊介绍: Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.
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