Effects of maternal edible THC consumption on offspring lung growth and function in a rhesus macaque model.

IF 3.6 2区 医学 Q1 PHYSIOLOGY
Lyndsey E Shorey-Kendrick, B Adam Crosland, Matthias C Schabel, Ilhem Messaoudi, Minzhe Guo, Matthew G Drake, Zhenying Nie, R Clayton Edenfield, Issac Cinco, Michael H Davies, Jason A Graham, Olivia L Hagen, Owen J T McCarty, Cindy T McEvoy, Eliot R Spindel, Jamie O Lo
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引用次数: 0

Abstract

Prenatal cannabis use is rising, in part due to legalization and perceptions of safety. The impact of prenatal cannabis exposure on offspring development, especially respiratory health, remains largely unknown. The objective of this study was to determine whether in utero exposure to delta-9-tetrahydrocannabinol (THC), the main psychoactive component of cannabis, is deleterious to offspring lung development and function using a rhesus macaque model. Female rhesus macaques received a daily edible containing either THC (2.5 mg/7 kg/day, equivalent to a heavy medical cannabis dose) or placebo during gestation and postnatally. Serial in utero magnetic resonance imaging (MRI) was performed during pregnancy at approximately gestational days (G)110 and G150. At 6 mo of age, infants underwent pulmonary function testing, followed by tissue collection for molecular analysis (bulk RNAseq, whole genome bisulfite sequencing, and spatial RNAseq). THC-exposed infants displayed significantly reduced forced residual capacity, which correlated with nonsignificant decreases in total lung capacity, lung diffusion capacity and lower fetal lung perfusion, oxygen availability, and lung volume measured by MRI. Consistent with these decreases in volume indices, levels of pulmonary growth factors were decreased in bronchial alveolar lavage at 6 mo. Molecular analysis of infant lungs revealed altered epigenetic regulation of gene expression, including at genes involved in extracellular matrix organization and lung development, and activation of immune signaling. Our study suggests that exposure to prenatal edible THC alters epigenetic regulation of lung gene expression and may negatively affect offspring lung development and function. Data from this study will help guide healthcare provider counseling on cannabis use in pregnancy.NEW & NOTEWORTHY In a translational rhesus macaque model, chronic prenatal delta-9-tetrahydrocannabinol exposure resulted in decreased lung volumes in offspring measured at 6 mo of age. These decreases correlated with altered DNA methylation in the lung, including at genes involved in extracellular matrix organization, lung development, and activation of immune signaling, and changes in lung cell composition as measured by spatial transcriptomics. These findings add to the growing evidence that prenatal cannabis exposure may adversely affect offspring development.

产前使用大麻的人数正在上升,部分原因是大麻合法化和人们对大麻安全的认识。产前接触大麻对后代发育(尤其是呼吸系统健康)的影响在很大程度上仍是未知数。本研究的目的是利用猕猴模型确定子宫内接触大麻的主要精神活性成分δ-9-四氢大麻酚(THC)是否会对后代的肺部发育和功能造成损害。雌性猕猴在妊娠期和产后每天服用含有四氢大麻酚(2.5 毫克/7 千克/天,相当于医用大麻的大剂量)或安慰剂的食品。在怀孕期间,大约在 G110 和 G150 时进行了连续的子宫内磁共振成像(MRI)检查。婴儿在 6 个月大时接受肺功能测试,然后采集组织进行分子分析(大量核糖核酸序列分析、全基因组亚硫酸氢盐测序和空间核糖核酸序列分析)。暴露于四氢大麻酚的婴儿显示出明显的强迫残余肺活量(FRC)下降,这与总肺活量(TLC)、肺弥散能力(DLCO)的非显著下降以及核磁共振成像测量的胎儿肺灌注量、氧供应量和肺容积的降低有关。与肺活量指数的下降相一致,6 个月时支气管肺泡灌洗液中的肺生长因子水平也有所下降。对婴儿肺部的分子分析表明,基因表达的表观遗传调控发生了改变,包括参与细胞外基质组织和肺发育的基因,以及免疫信号的激活。我们的研究表明,暴露于可食用的产前四氢大麻酚会改变肺部基因表达的表观遗传调控,并可能对后代的肺部发育和功能产生负面影响。这项研究的数据将有助于指导医疗保健提供者就孕期使用大麻问题提供咨询。
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
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.
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