Cheng Yu-Yen, Lin Chen-Cheng, Tung Che-Se, Liu Cheng-Che, Liu Yia-Ping
Graduate Institute of Life Sciences, National Defense Medical Center, Taipei 11490, Taiwan; Laboratory of Cognitive Neuroscience, Department of Physiology, National Defense Medical Center, Taipei 11490, Taiwan.
Laboratory of Cognitive Neuroscience, Department of Physiology, National Defense Medical Center, Taipei 11490, Taiwan; Department of Physiology, National Defense Medical Center, Taipei 11490, Taiwan.
Brain Res Bull. 2025 Sep;229:111472. doi: 10.1016/j.brainresbull.2025.111472. Epub 2025 Jul 18.
Increasing evidence suggests that alterations in the gut microbiota play a crucial role in the pathophysiology of psychiatric disorders, including post-traumatic stress disorder (PTSD). This implies that restoring gut microbiota might serve as a therapeutic strategy, with autologous fecal microbiota transplantation (FMT) being the most promising treatment due to its effectiveness and fewer pharmacological side effects. However, the hypothesis that adjusting gut microbiota may help to restore the impairment of fear memory is still less examined. To evaluate this hypothesis, we employed single prolonged stress (SPS) rat model to examine the impact of autologous FMT on PTSD-related fear memory extinction retention deficits and increased anxiety, and to investigate changes in the levels of gut microbiota, central monoamines, and plasma corticosterone. The correlations between gut microbiota and central serotonin (5-HT) with fear extinction retention deficits and anxiety were analyzed. Note that littermates were used in the gut microbiota analysis to minimize individual differences. Our results demonstrated that autologous FMT significantly ameliorated SPS-induced deficits in fear extinction retention and conditioned anxiety but did not mitigate unconditioned anxiety. These improvements were significantly correlated with the restoration of 5-HT levels in the medial prefrontal cortex (mPFC), dorsal hippocampus (dHPC), and hypothalamus (HT). Autologous FMT also reversed SPS-induced reductions in plasma corticosterone level. Additionally, fecal microbiota analysis revealed significant changes at the genus level, with the relative abundance of the Prevotellaceae Ga6A1 group reduced after SPS, and Intestinimonas increased by FMT, as well as some taxa significantly correlated with fear extinction retention deficits. This study suggests that autologous FMT offers potential as a novel therapeutic strategy for PTSD.
越来越多的证据表明,肠道微生物群的改变在包括创伤后应激障碍(PTSD)在内的精神疾病病理生理学中起关键作用。这意味着恢复肠道微生物群可能是一种治疗策略,自体粪便微生物群移植(FMT)因其有效性和较少的药物副作用而成为最有前景的治疗方法。然而,调节肠道微生物群可能有助于恢复恐惧记忆损伤这一假设仍较少被研究。为了评估这一假设,我们采用单次长时间应激(SPS)大鼠模型来研究自体FMT对PTSD相关恐惧记忆消退保持缺陷和焦虑增加的影响,并调查肠道微生物群、中枢单胺和血浆皮质酮水平的变化。分析了肠道微生物群与中枢5-羟色胺(5-HT)与恐惧消退保持缺陷和焦虑之间的相关性。请注意,在肠道微生物群分析中使用了同窝仔以尽量减少个体差异。我们的结果表明,自体FMT显著改善了SPS诱导的恐惧消退保持缺陷和条件性焦虑,但并未减轻非条件性焦虑。这些改善与内侧前额叶皮质(mPFC)、背侧海马体(dHPC)和下丘脑(HT)中5-HT水平的恢复显著相关。自体FMT还逆转了SPS诱导的血浆皮质酮水平降低。此外,粪便微生物群分析显示在属水平上有显著变化,SPS后普雷沃氏菌科Ga6A1组的相对丰度降低,FMT使肠单胞菌增加,以及一些分类群与恐惧消退保持缺陷显著相关。这项研究表明,自体FMT作为一种治疗PTSD的新型治疗策略具有潜力。