Université de Bordeaux, INRAE, Bordeaux INP, NutriNeuro, UMR 1286, Bordeaux, France.
Worcester Biomedical Research Group, School of Science and the Environment, University of Worcester, Henwick Grove, Worcester, WR2 6AJ, UK.
Sci Rep. 2024 Nov 30;14(1):29807. doi: 10.1038/s41598-024-80770-y.
Elective and emergency Caesarean section (C-section) procedures are on the rise, exceeding the recommended guidelines by the World Health Organization. Higher morbidities and long-term health conditions are correlated to C-section deliveries, including neurodevelopmental disorders. During C-section delivery, newborns are not exposed to the vaginal commensal flora, which impedes the early establishment of the gut microbiota. The latter is essential for adequate neuro-immune processes to take place during infancy. In this study, we used a validated model of mice born by C-section (CSD), which mimics clinical observations of dysregulated gut microbiota. Animals were either born naturally or by CSD, before being adopted by dams who underwent delivery within the 12 preceding hours. Behavioural analyses were conducted at post-natal day (PND) 21 and 55. Our results indicate that animals born by C-section present significantly higher body weight in late (PND40-P53) but not early adolescence (PND21-P27), compared to animals born by vaginal delivery (VD). Male animals delivered by C-section presented significantly lower exploration time of the novel arm in the Y Maze test at PND55. However, at PND21, abnormal social interaction was witnessed in male and female animals born by CSD, with significantly decreased time spent interacting during the social interaction test. At both PND21 and PND55, animals from both sexes born by C-section presented significantly decreased time spent in the open arm of the Elevated Plus Maze test, compared to control animals. We then measured the expression of genes associated to neuroimmune interactions (microglia phenotype), inflammatory mediators and lipids in several brain structures of VD and CSD mice at PND21 and PND55. At weaning, animals born by CSD presented altered microglia, inflammatory and lipid metabolism signatures, with increased expression of Cd36, Csf1r and Tnfα in different brain regions of males, but not in females. At PND64, Csf1r, Tmem119 as well as C3ar1 were significantly increased in males born by C-section, but not in females. In males born by vaginal delivery, the expression of Cd36 at PND64 was correlated to anxiety at PND55, whilst a correlation between the expression of Clec7a and the number of head dippings in the elevated plus maze was also noted in males born by CSD. Altogether, our study shows altered emotional behaviour in animals delivered by CSD, which is likely explained by underlying neuro-inflammatory processes in different brain regions. Our work further supports the long-term consequences of CSD on brain health.
择期和紧急剖宫产(CSD)手术的数量不断增加,超过了世界卫生组织的建议标准。CSD 分娩与更高的发病率和长期健康状况相关,包括神经发育障碍。在 CSD 分娩过程中,新生儿不会接触到阴道共生菌群,这阻碍了肠道微生物群的早期建立。后者对于婴儿期适当的神经免疫过程至关重要。在这项研究中,我们使用了一种经过验证的 CSD 出生小鼠模型,该模型模拟了肠道微生物群失调的临床观察。动物要么自然分娩,要么通过 CSD 分娩,然后被在 12 小时前分娩的母鼠收养。在产后第 21 天(PND21)和第 55 天(PND55)进行行为分析。我们的结果表明,与阴道分娩(VD)出生的动物相比,CSD 出生的动物在晚期(PND40-P53)但不在早期青春期(PND21-P27)体重显著增加。CSD 出生的雄性动物在 PND55 的 Y 迷宫测试中,新臂的探索时间显著减少。然而,在 PND21 时,CSD 出生的雄性和雌性动物的社会互动异常,在社会互动测试中,互动时间明显减少。在 PND21 和 PND55 时,与对照组相比,CSD 出生的雄性和雌性动物在高架十字迷宫测试中开放臂的时间明显减少。然后,我们在 PND21 和 PND55 时测量了与神经免疫相互作用(小胶质细胞表型)、炎症介质和脂质相关的基因在 VD 和 CSD 小鼠的几个大脑结构中的表达。在断奶时,CSD 出生的动物表现出小胶质细胞、炎症和脂质代谢特征的改变,雄性动物不同脑区的 Cd36、Csf1r 和 Tnfα 表达增加,但雌性动物没有。在 PND64 时,CSD 出生的雄性动物的 Csf1r、Tmem119 和 C3ar1 显著增加,但雌性动物没有。在阴道分娩出生的雄性动物中,PND64 时 Cd36 的表达与 PND55 时的焦虑相关,而 CSD 出生的雄性动物中 Clec7a 的表达与高架十字迷宫中的头部浸入次数之间也存在相关性。总的来说,我们的研究表明,CSD 分娩的动物表现出情绪行为改变,这可能是由于不同脑区潜在的神经炎症过程所致。我们的工作进一步支持了 CSD 对大脑健康的长期影响。