Tanelian Arax, Nankova Bistra, Cheriyan Anish, Arens Christopher, Hu Furong, Sabban Esther L
Department of Biochemistry and Molecular Biology, New York Medical College, Valhalla, NY, USA.
Division of Newborn Medicine, Departments of Pediatrics, Biochemistry and Molecular Biology, New York Medical College, Valhalla, NY, USA.
Neurobiol Stress. 2023 Mar 9;24:100533. doi: 10.1016/j.ynstr.2023.100533. eCollection 2023 May.
Exposure to traumatic stress is a major risk factor for the development of neuropsychiatric disorders in a subpopulation of individuals, whereas others remain resilient. The determinants of resilience and susceptibility remain unclear. Here, we aimed to characterize the microbial, immunological, and molecular differences between stress-susceptible and stress-resilient female rats before and after exposure to a traumatic experience. Animals were randomly divided into unstressed controls (n = 10) and experimental groups (n = 16) exposed to Single Prolonged Stress (SPS), an animal model of PTSD. Fourteen days later, all rats underwent a battery of behavioral tests and were sacrificed the following day to collect different organs. Stool samples were collected before and after SPS. Behavioral analyses revealed divergent responses to SPS. The SPS treated animals were further subdivided into SPS-resilient (SPS-R) and SPS-susceptible (SPS-S) subgroups. Comparative analysis of fecal 16S sequencing before and after SPS exposure indicated significant differences in the gut microbial composition, functionality, and metabolites of the SPS-R and SPS-S subgroups. In line with the observed distinct behavioral phenotypes, the SPS-S subgroup displayed higher blood-brain barrier permeability and neuroinflammation relative to the SPS-R and/or controls. These results indicate, for the first time, pre-existing and trauma-induced differences in the gut microbial composition and functionality of female rats that relate to their ability to cope with traumatic stress. Further characterization of these factors will be crucial for understanding susceptibility and fostering resilience, especially in females, who are more likely than males to develop mood disorders.
对于一部分个体而言,遭受创伤性应激是发生神经精神障碍的主要风险因素,而其他个体则保持 resilient(此处 resilient 可理解为“有恢复力的”“适应力强的”)。恢复力和易感性的决定因素仍不清楚。在此,我们旨在描述应激易感性和应激恢复力的雌性大鼠在经历创伤性事件之前和之后在微生物、免疫和分子方面的差异。动物被随机分为未受应激的对照组(n = 10)和暴露于单次长时间应激(SPS,创伤后应激障碍的动物模型)的实验组(n = 16)。十四天后,所有大鼠接受一系列行为测试,并在第二天处死以收集不同器官。在 SPS 前后收集粪便样本。行为分析揭示了对 SPS 的不同反应。接受 SPS 处理的动物进一步细分为 SPS 恢复力强(SPS - R)和 SPS 易感性(SPS - S)亚组。对 SPS 暴露前后粪便 16S 测序的比较分析表明,SPS - R 和 SPS - S 亚组在肠道微生物组成、功能和代谢物方面存在显著差异。与观察到的不同行为表型一致,SPS - S 亚组相对于 SPS - R 和/或对照组表现出更高的血脑屏障通透性和神经炎症。这些结果首次表明,雌性大鼠在肠道微生物组成和功能方面存在预先存在的以及创伤诱导的差异,这些差异与它们应对创伤性应激的能力有关。进一步表征这些因素对于理解易感性和培养恢复力至关重要,尤其是对于女性,她们比男性更易患情绪障碍。