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孕期慢性不可预知轻度应激诱导的大鼠子代情绪行为损伤中,海马 BDNF/CREB 信号通路和肠道菌群的作用。

Contribution of hippocampal BDNF/CREB signaling pathway and gut microbiota to emotional behavior impairment induced by chronic unpredictable mild stress during pregnancy in rats offspring.

机构信息

Ningxia Key Laboratory of Cerebrocranial Disease, Ningxia Medical University, Yinchuan, Ningxia, China.

Key Laboratory of Environmental Factors and Chronic Disease Control, Ningxia Medical University, Yinchuan, Ningxia, China.

出版信息

PeerJ. 2022 Jun 24;10:e13605. doi: 10.7717/peerj.13605. eCollection 2022.

Abstract

BACKGROUND

Numerous studies have shown that exposure to prenatal maternal stress (PMS) is associated with various psychopathological outcomes of offspring. The accumulating evidence linking bacteria in the gut and neurons in the brain (the microbiota-gut-brain axis) has been aconsensus; however, there is a lack of research on the involvement mechanism of gut microbiota in the regulation of the BDNF/CREB signaling pathway in the hippocampus of prenatally stressed offspring.

METHODS

Pregnant rats were subjected to chronic unpredictable mild stress (CUMS) to establish the prenatal maternal stress model. The body weight was measured and the behavioral changes were recorded. Offspring were tested to determine emotional state using sucrose preference test (SPT), open-field test (OFT) and suspended tail test (STT). Gut microbiota was evaluated by sequencing the microbial 16S rRNA V3-V4 region, and the interactive analysis of bacterial community structure and diversity was carried out. The expression of hippocampal BDNF, TrkB and CREB mRNA and proteins were respectively measured using RT-PCR and Western blotting.

RESULTS

Prenatal maternal stress increased maternal plasma corticosterone levels, slowed maternal weight gain and caused depression-like behaviors (all < 0.05). In offspring, prenatal maternal stress increased plasma corticosterone levels ( < 0.05) and emotional behavior changes (depression-like state) were observed ( < 0.05). The species abundance, diversity and composition of the offspring's gut microbiota changed after the maternal stress during pregnancy ( < 0.05). Compared with the control group's offspring, the species abundance of was dropped, while the abundance of the species abundance was risen. Concurrent, changes in the hippocampal structure of the offspring and decreases in expression of BDNF/CREB signaling were noted ( < 0.05).

CONCLUSIONS

Prenatal maternal stress leads to high corticosterone status and abnormal emotion behavior of offspring, which may be associated with the abnormal BDNF/CREB signaling in hippocampus of offspring caused by the change of gut microbiota composition.

摘要

背景

许多研究表明,产前母体应激(PMS)暴露与后代的各种精神病理学结果有关。肠道细菌和大脑神经元(微生物群-肠-脑轴)之间的联系已经得到共识;然而,关于肠道微生物群在调节产前应激后代海马体中 BDNF/CREB 信号通路中的作用机制的研究还很少。

方法

对怀孕大鼠进行慢性不可预测轻度应激(CUMS),建立产前母体应激模型。测量体重,记录行为变化。通过蔗糖偏好测试(SPT)、旷场测试(OFT)和悬尾测试(STT)测试后代的情绪状态。通过测序微生物 16S rRNA V3-V4 区评估肠道微生物群,进行细菌群落结构和多样性的交互分析。采用 RT-PCR 和 Western blotting 分别测定海马体 BDNF、TrkB 和 CREB mRNA 和蛋白的表达。

结果

产前母体应激增加了母鼠血浆皮质酮水平,减缓了母鼠体重增加,并导致抑郁样行为(均<0.05)。在后代中,产前母体应激增加了血浆皮质酮水平(<0.05)并观察到情绪行为变化(抑郁状态)(<0.05)。母鼠孕期应激后,后代肠道微生物群的物种丰度、多样性和组成发生变化(<0.05)。与对照组后代相比,的物种丰度下降,而的物种丰度上升。同时,观察到后代海马体结构的变化和 BDNF/CREB 信号表达的减少(<0.05)。

结论

产前母体应激导致后代皮质酮水平升高和情绪行为异常,这可能与肠道微生物群组成改变导致后代海马体中 BDNF/CREB 信号异常有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b37f/9235812/f1004ec435af/peerj-10-13605-g001.jpg

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