开发实验模型以研究母体肠道微生物组紊乱对围产期窒息影响的尝试与错误》(The Trials and Errors of Developing an Experimental Model to Study the Impact of Maternal Gut Microbiome Disruption on Perinatal Asphyxia)。

IF 2.8 Q2 REPRODUCTIVE BIOLOGY Reproduction & fertility Pub Date : 2024-11-06 Print Date: 2024-10-01 DOI:10.1530/RAF-24-0050
Mara Ioana Ionescu, Ana Maria Catrina, Ioana Alexandra Dogaru, Didina Catalina Barbalata, Cristian Ciotei, Cerasela Haidoiu, Vladimir Suhaianu, Gratiela Gradisteanu Pircalabioru, Siobhain M O'Mahony, Ana-Maria Zagrean
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引用次数: 0

摘要

母体肠道微生物组的损伤因其在影响后代神经发育结果中的潜在作用而备受关注,尤其是在围产期窒息(PA)等增加大脑脆弱性的情况下。母体微生物组和胎儿大脑之间的相互作用是母体健康和后代神经发育之间的关键环节。本研究旨在建立一个模型,以评估妊娠期服用抗生素和 PA 引起的母体菌群失调对后代神经发育的影响。从妊娠第 11 天开始,Wistar 大鼠在饮用水中添加抗生素,直至出生。出生后第6天,幼鼠接受PA/缺氧治疗,分为四个实验组:对照组-缺氧组、抗生素组-缺氧组、对照组-窒息组和抗生素组-窒息组。早期行为测试在出生后第 7 到 9 天进行。与对照组相比,最初的抗菌鸡尾酒疗法(氨苄西林、万古霉素、新霉素、克林霉素、两性霉素-B)导致流产次数增加、孕期体重增加缓慢、后代体重下降以及母体肠道微生物组发生变化。PA 组和抗生素组的后代神经发育反射均受损,海马神经炎症增加。由于这些不利影响,第二次实验中使用了对妊娠更安全的鸡尾酒抗生素(氨苄西林、万古霉素、新霉素、美罗培南)。结果没有出现流产或孕期体重减轻,但仍与肠道微生物群破坏有关。PA 会损害神经发育反射并增加神经炎症,而服用抗生素会放大这种影响。这些初步发现揭示了母体菌群失调和 PA 对神经发育损害的累积潜力,强调了妊娠期抗菌药物使用的谨慎性。进一步的研究应包括后代的长期跟踪和母体行为,并结合益生菌来抵消抗生素的影响。
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MICROBIOME: The trials and errors of developing an experimental model to study the impact of maternal gut microbiome disruption on perinatal asphyxia.

Abstract: Maternal gut microbiome impairment has garnered attention for its potential role in influencing neurodevelopmental outcomes in offspring, especially in situations that increase brain vulnerability such as perinatal asphyxia (PA). Maternal microbiome and fetal brain interplay emerge as a critical link between maternal health and offspring neurodevelopment. This study aims to generate a model to assess the impact of maternal dysbiosis triggered by gestational antibiotic administration and PA on offspring neurodevelopment. Wistar rats were subjected to antibiotics in drinking water from the 11th gestational day until birth. On the 6th postnatal day, pups were subjected to PA/normoxia, resulting in four experimental groups: control-normoxia, antibiotics-normoxia, control-asphyxia, and antibiotics-asphyxia. Early-life behavioral tests were conducted between postnatal days 7 and 9. The initial antimicrobial cocktail (ampicillin, vancomycin, neomycin, clindamycin, amphotericin-B) led to an increased number of miscarriages, poor weight gain during pregnancy, reduced offspring weight, and changes in the maternal gut microbiome compared to control. Offspring presented impaired neurodevelopmental reflexes in both PA and antibiotic groups and increased hippocampal neuroinflammation. Due to these detrimental effects, a more pregnancy-safe antibiotic cocktail was used for a second experiment (ampicillin, vancomycin, neomycin, meropenem). This resulted in no miscarriages or pregnancy-weight loss but was still linked to gut microbiome disruption. PA impaired neurodevelopmental reflexes and increased neuroinflammation, effects amplified by antibiotic administration. These preliminary findings reveal the cumulative potential of maternal dysbiosis and PA on neurodevelopment impairment, emphasizing caution in gestational antimicrobial use. Further investigations should include offspring long-term follow-up and maternal behavior and integrate probiotics to counteract antibiotic effects.

Graphical abstract:

Lay summary: This study investigates the impact of maternal gut microbiome disruptions caused by gestational antibiotic treatment and low oxygen exposure shortly after birth on the development of the rats' babies. We found that both antibiotic exposure and reduced oxygen levels led to changes in early behavior and increased inflammation of the nervous tissue in the baby rats. Although using a different, potentially safer antibiotic combination reduced pregnancy complications, it still changed the bacteria in the mother's gut and worsened early behavior. These findings show that antibiotics during pregnancy can affect the developing brain of baby rats and careful consideration should be used before prescribing them. Future research will explore longer-term effects and potential medicines.

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